[{"id":"265557","variation":"chr11:110045629:->G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*362_*363insC","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs35355844","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265558","variation":"chr11:110045631:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*360C>T","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs574729414","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":"3","otoscope_aj_an":"400","otoscope_aj_af":"0.0075","otoscope_co_ac":"1","otoscope_co_an":"320","otoscope_co_af":"0.003125","otoscope_us_ac":"0","otoscope_us_an":"320","otoscope_us_af":"0","otoscope_jp_ac":"0","otoscope_jp_an":"400","otoscope_jp_af":"0","otoscope_es_ac":"0","otoscope_es_an":"360","otoscope_es_af":"0","otoscope_tr_ac":"0","otoscope_tr_an":"200","otoscope_tr_af":"0","otoscope_all_ac":"4","otoscope_all_an":"2000","otoscope_all_af":"0.002","tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265559","variation":"chr11:110045677:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*314G>A","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs543700466","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265560","variation":"chr11:110045691:C>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*300delG","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs141414335","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"32","tg_afr_an":"1322","tg_afr_af":"0.0242","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"34","tg_all_an":"5008","tg_all_af":"0.00678914","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265561","variation":"chr11:110045716:A>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*275T>G","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs749021295","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265562","variation":"chr11:110045725:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*266G>A","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs564392751","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265563","variation":"chr11:110045726:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*265C>T","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs563666683","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":"0","otoscope_aj_an":"400","otoscope_aj_af":"0","otoscope_co_ac":"1","otoscope_co_an":"320","otoscope_co_af":"0.003125","otoscope_us_ac":"0","otoscope_us_an":"320","otoscope_us_af":"0","otoscope_jp_ac":"0","otoscope_jp_an":"400","otoscope_jp_af":"0","otoscope_es_ac":"1","otoscope_es_an":"360","otoscope_es_af":"0.00277778","otoscope_tr_ac":"0","otoscope_tr_an":"200","otoscope_tr_af":"0","otoscope_all_ac":"2","otoscope_all_an":"2000","otoscope_all_af":"0.001","tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265564","variation":"chr11:110045731:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*260A>G","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs7941903","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"877","tg_afr_an":"1322","tg_afr_af":"0.6634","tg_eur_ac":"514","tg_eur_an":"1006","tg_eur_af":"0.5109","tg_amr_ac":"445","tg_amr_an":"694","tg_amr_af":"0.6412","tg_eas_ac":"825","tg_eas_an":"1008","tg_eas_af":"0.8185","tg_sas_ac":"506","tg_sas_an":"978","tg_sas_af":"0.5174","tg_all_ac":"3167","tg_all_an":"5008","tg_all_af":"0.632388","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265565","variation":"chr11:110045787:GTG>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*204_*208delCAC","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs113179222","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"192","tg_afr_an":"1322","tg_afr_af":"0.1452","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"7","tg_amr_an":"694","tg_amr_af":"0.0101","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"199","tg_all_an":"5008","tg_all_af":"0.0397364","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265566","variation":"chr11:110045791:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*200A>C","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":null,"summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":"0","otoscope_aj_an":"400","otoscope_aj_af":"0","otoscope_co_ac":"0","otoscope_co_an":"320","otoscope_co_af":"0","otoscope_us_ac":"0","otoscope_us_an":"320","otoscope_us_af":"0","otoscope_jp_ac":"0","otoscope_jp_an":"400","otoscope_jp_af":"0","otoscope_es_ac":"0","otoscope_es_an":"360","otoscope_es_af":"0","otoscope_tr_ac":"0","otoscope_tr_an":"200","otoscope_tr_af":"0","otoscope_all_ac":"0","otoscope_all_an":"2000","otoscope_all_af":"0","tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265567","variation":"chr11:110045804:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*187A>C","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":null,"summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":"0","otoscope_aj_an":"400","otoscope_aj_af":"0","otoscope_co_ac":"0","otoscope_co_an":"320","otoscope_co_af":"0","otoscope_us_ac":"0","otoscope_us_an":"320","otoscope_us_af":"0","otoscope_jp_ac":"0","otoscope_jp_an":"400","otoscope_jp_af":"0","otoscope_es_ac":"0","otoscope_es_an":"360","otoscope_es_af":"0","otoscope_tr_ac":"0","otoscope_tr_an":"200","otoscope_tr_af":"0","otoscope_all_ac":"0","otoscope_all_an":"2000","otoscope_all_af":"0","tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265568","variation":"chr11:110045805:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*186A>C","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs546509729","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265569","variation":"chr11:110045830:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*161A>C","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":null,"summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":"0","otoscope_aj_an":"400","otoscope_aj_af":"0","otoscope_co_ac":"0","otoscope_co_an":"320","otoscope_co_af":"0","otoscope_us_ac":"0","otoscope_us_an":"320","otoscope_us_af":"0","otoscope_jp_ac":"0","otoscope_jp_an":"400","otoscope_jp_af":"0","otoscope_es_ac":"0","otoscope_es_an":"360","otoscope_es_af":"0","otoscope_tr_ac":"0","otoscope_tr_an":"200","otoscope_tr_af":"0","otoscope_all_ac":"0","otoscope_all_an":"2000","otoscope_all_af":"0","tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265570","variation":"chr11:110045862:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*129G>A","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs766454192","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265571","variation":"chr11:110045865:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*126C>T","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs568233897","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265572","variation":"chr11:110045883:C>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*108delG","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs147377597","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"27","tg_afr_an":"1322","tg_afr_af":"0.0204","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"28","tg_all_an":"5008","tg_all_af":"0.00559105","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265573","variation":"chr11:110045940:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*51G>A","variantlocale":"THREE_PRIME_EXON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":null,"summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":"0","otoscope_aj_an":"400","otoscope_aj_af":"0","otoscope_co_ac":"0","otoscope_co_an":"320","otoscope_co_af":"0","otoscope_us_ac":"0","otoscope_us_an":"320","otoscope_us_af":"0","otoscope_jp_ac":"0","otoscope_jp_an":"400","otoscope_jp_af":"0","otoscope_es_ac":"1","otoscope_es_an":"360","otoscope_es_af":"0.00277778","otoscope_tr_ac":"0","otoscope_tr_an":"200","otoscope_tr_af":"0","otoscope_all_ac":"1","otoscope_all_an":"2000","otoscope_all_af":"0.0005","tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265574","variation":"chr11:110046025:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-66A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs184503043","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"5","tg_eas_an":"1008","tg_eas_af":"0.005","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"11","tg_all_an":"5008","tg_all_af":"0.00219649","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265575","variation":"chr11:110046039:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-80C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs753981820","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265576","variation":"chr11:110046059:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-100G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs771726371","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265577","variation":"chr11:110046096:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-137G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs548674145","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265578","variation":"chr11:110046139:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-180G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs569783151","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"9","tg_afr_an":"1322","tg_afr_af":"0.0068","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265579","variation":"chr11:110046153:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-194C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs189437915","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265580","variation":"chr11:110046204:A>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-245T>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs558507831","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265581","variation":"chr11:110046207:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-248A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs570844394","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265582","variation":"chr11:110046219:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-260G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs113993941","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"56","tg_afr_an":"1322","tg_afr_af":"0.0424","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"58","tg_all_an":"5008","tg_all_af":"0.0115815","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265583","variation":"chr11:110046231:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-272C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs10749956","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"807","tg_afr_an":"1322","tg_afr_af":"0.6104","tg_eur_ac":"509","tg_eur_an":"1006","tg_eur_af":"0.506","tg_amr_ac":"444","tg_amr_an":"694","tg_amr_af":"0.6398","tg_eas_ac":"814","tg_eas_an":"1008","tg_eas_af":"0.8075","tg_sas_ac":"493","tg_sas_an":"978","tg_sas_af":"0.5041","tg_all_ac":"3067","tg_all_an":"5008","tg_all_af":"0.61242","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265584","variation":"chr11:110046343:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-384A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs574980485","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"5","tg_afr_an":"1322","tg_afr_af":"0.0038","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"10","tg_all_an":"5008","tg_all_af":"0.00199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265585","variation":"chr11:110046367:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-408C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs542016269","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265586","variation":"chr11:110046379:->C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-420_*32-419insG","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs35469828","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265587","variation":"chr11:110046392:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-433C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs760440320","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265588","variation":"chr11:110046401:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-442G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs557034697","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265589","variation":"chr11:110046442:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-483A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs192706080","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265590","variation":"chr11:110046451:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-492G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs377756826","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265591","variation":"chr11:110046459:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-500A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs564053902","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265592","variation":"chr11:110046509:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-550T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs765922342","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265593","variation":"chr11:110046529:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-570G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs528434578","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265594","variation":"chr11:110046540:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-581T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs150072925","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"10","tg_afr_an":"1322","tg_afr_af":"0.0076","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"19","tg_all_an":"5008","tg_all_af":"0.00379393","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265595","variation":"chr11:110046640:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-681C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs561797280","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265596","variation":"chr11:110046695:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-736A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs529103777","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265597","variation":"chr11:110046699:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-740C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs765384494","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265598","variation":"chr11:110046722:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-763C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs753312169","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265599","variation":"chr11:110046725:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-766C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs145405905","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"4","tg_eur_an":"1006","tg_eur_af":"0.004","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"4","tg_sas_an":"978","tg_sas_af":"0.0041","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265600","variation":"chr11:110046761:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-802C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs569844296","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265601","variation":"chr11:110046763:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-804C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs149139315","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"19","tg_afr_an":"1322","tg_afr_af":"0.0144","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"19","tg_all_an":"5008","tg_all_af":"0.00379393","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265602","variation":"chr11:110046776:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-817G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs552194338","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265603","variation":"chr11:110046778:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-819G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs368530119","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265604","variation":"chr11:110046799:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-840G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs184709828","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265605","variation":"chr11:110046800:TTTTTCTT>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-841_*32-832delAAGAAAAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs112239146","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265606","variation":"chr11:110046806:TT>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-847_*32-844delAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs367710666","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265607","variation":"chr11:110046811:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-852A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs12420617","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"301","tg_afr_an":"1322","tg_afr_af":"0.2277","tg_eur_ac":"230","tg_eur_an":"1006","tg_eur_af":"0.2286","tg_amr_ac":"223","tg_amr_an":"694","tg_amr_af":"0.3213","tg_eas_ac":"498","tg_eas_an":"1008","tg_eas_af":"0.494","tg_sas_ac":"315","tg_sas_an":"978","tg_sas_af":"0.3221","tg_all_ac":"1567","tg_all_an":"5008","tg_all_af":"0.312899","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265608","variation":"chr11:110046814:->T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-855_*32-854insA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs778430261","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265609","variation":"chr11:110046814:->TT","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-855_*32-854insAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs778430261","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265610","variation":"chr11:110046814:T>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-855delA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs796290070","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265611","variation":"chr11:110046823:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-864A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11213289","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"154","tg_afr_an":"1322","tg_afr_af":"0.1165","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"7","tg_amr_an":"694","tg_amr_af":"0.0101","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"161","tg_all_an":"5008","tg_all_af":"0.0321486","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265612","variation":"chr11:110046841:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-882G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs188996659","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"3","tg_afr_an":"1322","tg_afr_af":"0.0023","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265613","variation":"chr11:110046842:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-883C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs568625263","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265614","variation":"chr11:110046884:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-925G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs745985752","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265615","variation":"chr11:110046906:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-947C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs113599141","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"59","tg_afr_an":"1322","tg_afr_af":"0.0446","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"61","tg_all_an":"5008","tg_all_af":"0.0121805","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265616","variation":"chr11:110046921:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-962A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs557565002","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265617","variation":"chr11:110046935:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-976G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs34603046","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"3","tg_afr_an":"1322","tg_afr_af":"0.0023","tg_eur_ac":"26","tg_eur_an":"1006","tg_eur_af":"0.0258","tg_amr_ac":"16","tg_amr_an":"694","tg_amr_af":"0.0231","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"9","tg_sas_an":"978","tg_sas_af":"0.0092","tg_all_ac":"57","tg_all_an":"5008","tg_all_af":"0.0113818","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265618","variation":"chr11:110046936:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-977C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs539528942","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265619","variation":"chr11:110046977:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1018G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs140584921","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"59","tg_afr_an":"1322","tg_afr_af":"0.0446","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"61","tg_all_an":"5008","tg_all_af":"0.0121805","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265620","variation":"chr11:110046978:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1019C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs181440439","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265621","variation":"chr11:110046988:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1029G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs539815721","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265622","variation":"chr11:110047010:A>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1051T>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs562039959","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265623","variation":"chr11:110047048:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1089A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs10891072","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1030","tg_afr_an":"1322","tg_afr_af":"0.7791","tg_eur_ac":"510","tg_eur_an":"1006","tg_eur_af":"0.507","tg_amr_ac":"454","tg_amr_an":"694","tg_amr_af":"0.6542","tg_eas_ac":"816","tg_eas_an":"1008","tg_eas_af":"0.8095","tg_sas_ac":"489","tg_sas_an":"978","tg_sas_af":"0.5","tg_all_ac":"3299","tg_all_an":"5008","tg_all_af":"0.658746","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265624","variation":"chr11:110047084:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1125G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs544431436","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265625","variation":"chr11:110047105:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1146T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs562334992","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265626","variation":"chr11:110047204:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1245T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs145679071","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265627","variation":"chr11:110047231:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1272C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs79082554","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"8","tg_eur_an":"1006","tg_eur_af":"0.008","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265628","variation":"chr11:110047234:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1275C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs138706981","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"6","tg_afr_an":"1322","tg_afr_af":"0.0045","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"6","tg_all_an":"5008","tg_all_af":"0.00119808","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265629","variation":"chr11:110047272:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1313A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs780672128","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265630","variation":"chr11:110047305:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1346A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs141735208","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265631","variation":"chr11:110047349:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1390G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs150809887","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"3","tg_eur_an":"1006","tg_eur_af":"0.003","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"4","tg_eas_an":"1008","tg_eas_af":"0.004","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"7","tg_all_an":"5008","tg_all_af":"0.00139776","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265632","variation":"chr11:110047363:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1404G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs185775636","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"3","tg_afr_an":"1322","tg_afr_af":"0.0023","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265633","variation":"chr11:110047388:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1429A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs189455727","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265634","variation":"chr11:110047477:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1518T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs550874420","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265635","variation":"chr11:110047478:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1519C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs181849649","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"10","tg_afr_an":"1322","tg_afr_af":"0.0076","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"10","tg_all_an":"5008","tg_all_af":"0.00199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265636","variation":"chr11:110047482:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1523C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs186145996","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265637","variation":"chr11:110047531:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1572G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs565718756","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"3","tg_sas_an":"978","tg_sas_af":"0.0031","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265638","variation":"chr11:110047532:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1573C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs190848779","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265639","variation":"chr11:110047535:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1576C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs572825525","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265640","variation":"chr11:110047536:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1577C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs533813715","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265641","variation":"chr11:110047540:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1581A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs181313336","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265642","variation":"chr11:110047547:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1588C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs186378156","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265643","variation":"chr11:110047561:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1602C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11604195","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"4","tg_afr_an":"1322","tg_afr_af":"0.003","tg_eur_ac":"50","tg_eur_an":"1006","tg_eur_af":"0.0497","tg_amr_ac":"23","tg_amr_an":"694","tg_amr_af":"0.0331","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"37","tg_sas_an":"978","tg_sas_af":"0.0378","tg_all_ac":"116","tg_all_an":"5008","tg_all_af":"0.0231629","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265644","variation":"chr11:110047576:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1617G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs768348797","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265645","variation":"chr11:110047618:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1659G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs778801511","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265646","variation":"chr11:110047619:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1660C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs138060899","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"11","tg_afr_an":"1322","tg_afr_af":"0.0083","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"11","tg_all_an":"5008","tg_all_af":"0.00219649","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265647","variation":"chr11:110047623:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1664A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs149459653","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265648","variation":"chr11:110047667:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1708C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs143852991","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"10","tg_eas_an":"1008","tg_eas_af":"0.0099","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"10","tg_all_an":"5008","tg_all_af":"0.00199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265649","variation":"chr11:110047667:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1708C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs143852991","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265650","variation":"chr11:110047686:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1727T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs6589117","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1026","tg_afr_an":"1322","tg_afr_af":"0.7761","tg_eur_ac":"509","tg_eur_an":"1006","tg_eur_af":"0.506","tg_amr_ac":"454","tg_amr_an":"694","tg_amr_af":"0.6542","tg_eas_ac":"826","tg_eas_an":"1008","tg_eas_af":"0.8194","tg_sas_ac":"489","tg_sas_an":"978","tg_sas_af":"0.5","tg_all_ac":"3304","tg_all_an":"5008","tg_all_af":"0.659744","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265651","variation":"chr11:110047697:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1738C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs770687446","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265652","variation":"chr11:110047715:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1756G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs776155514","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265653","variation":"chr11:110047721:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1762C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs759174364","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265654","variation":"chr11:110047780:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1821A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs564262424","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265655","variation":"chr11:110047782:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1823A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs528556180","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265656","variation":"chr11:110047806:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1847G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs540654439","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265657","variation":"chr11:110047816:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1857C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs114412816","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"22","tg_afr_an":"1322","tg_afr_af":"0.0166","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"22","tg_all_an":"5008","tg_all_af":"0.00439297","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265658","variation":"chr11:110047825:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1866T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs548951819","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265659","variation":"chr11:110047848:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1889C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs983624","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265660","variation":"chr11:110047884:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1925A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs190733088","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"3","tg_eur_an":"1006","tg_eur_af":"0.003","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265661","variation":"chr11:110047905:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1946G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs534340807","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"32","tg_sas_an":"978","tg_sas_af":"0.0327","tg_all_ac":"32","tg_all_an":"5008","tg_all_af":"0.00638978","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265662","variation":"chr11:110047925:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1966C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs533591705","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265663","variation":"chr11:110047926:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1967C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs765542110","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265664","variation":"chr11:110047953:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-1994C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs983623","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265665","variation":"chr11:110047963:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2004G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs551984595","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265666","variation":"chr11:110047964:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2005C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs566598654","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265667","variation":"chr11:110047989:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2030C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs140276758","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265668","variation":"chr11:110048030:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2071C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs555389550","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"4","tg_sas_an":"978","tg_sas_af":"0.0041","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265669","variation":"chr11:110048057:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2098C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11824716","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"27","tg_afr_an":"1322","tg_afr_af":"0.0204","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"28","tg_all_an":"5008","tg_all_af":"0.00559105","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265670","variation":"chr11:110048062:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2103C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs537408171","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265671","variation":"chr11:110048067:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2108A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs556054266","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265672","variation":"chr11:110048071:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2112A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs577487982","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265673","variation":"chr11:110048148:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2189G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs147376800","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"2","tg_eur_an":"1006","tg_eur_af":"0.002","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265674","variation":"chr11:110048243:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2284C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs553668940","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265675","variation":"chr11:110048356:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2397C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs573325918","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265676","variation":"chr11:110048379:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2420A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs540366504","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265677","variation":"chr11:110048399:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2440C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs562161943","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265678","variation":"chr11:110048415:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2456C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs773923050","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265679","variation":"chr11:110048428:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2469G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs529312508","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"7","tg_sas_an":"978","tg_sas_af":"0.0072","tg_all_ac":"7","tg_all_an":"5008","tg_all_af":"0.00139776","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265680","variation":"chr11:110048443:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2484T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs183139407","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"10","tg_eur_an":"1006","tg_eur_af":"0.0099","tg_amr_ac":"4","tg_amr_an":"694","tg_amr_af":"0.0058","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"15","tg_all_an":"5008","tg_all_af":"0.00299521","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265681","variation":"chr11:110048453:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2494G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs563205445","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265682","variation":"chr11:110048457:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2498G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs533653918","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265683","variation":"chr11:110048461:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2502C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs140134598","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"16","tg_eur_an":"1006","tg_eur_af":"0.0159","tg_amr_ac":"7","tg_amr_an":"694","tg_amr_af":"0.0101","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"5","tg_sas_an":"978","tg_sas_af":"0.0051","tg_all_ac":"29","tg_all_an":"5008","tg_all_af":"0.00579073","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265684","variation":"chr11:110048478:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2519C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs566949511","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265685","variation":"chr11:110048498:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2539G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs535188738","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265686","variation":"chr11:110048500:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2541G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs12363857","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"153","tg_afr_an":"1322","tg_afr_af":"0.1157","tg_eur_ac":"256","tg_eur_an":"1006","tg_eur_af":"0.2545","tg_amr_ac":"119","tg_amr_an":"694","tg_amr_af":"0.1715","tg_eas_ac":"87","tg_eas_an":"1008","tg_eas_af":"0.0863","tg_sas_ac":"151","tg_sas_an":"978","tg_sas_af":"0.1544","tg_all_ac":"766","tg_all_an":"5008","tg_all_af":"0.152955","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265687","variation":"chr11:110048500:CA>TG","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":null,"variantlocale":null,"pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs386757403","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265688","variation":"chr11:110048501:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2542T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs7945686","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1024","tg_afr_an":"1322","tg_afr_af":"0.7746","tg_eur_ac":"501","tg_eur_an":"1006","tg_eur_af":"0.498","tg_amr_ac":"406","tg_amr_an":"694","tg_amr_af":"0.585","tg_eas_ac":"724","tg_eas_an":"1008","tg_eas_af":"0.7183","tg_sas_ac":"474","tg_sas_an":"978","tg_sas_af":"0.4847","tg_all_ac":"3129","tg_all_an":"5008","tg_all_af":"0.6248","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265689","variation":"chr11:110048505:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2546C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs567321628","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265690","variation":"chr11:110048537:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2578G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs776765529","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265691","variation":"chr11:110048549:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2590G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs537468935","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"3","tg_sas_an":"978","tg_sas_af":"0.0031","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265692","variation":"chr11:110048560:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2601G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs142899160","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"23","tg_eas_an":"1008","tg_eas_af":"0.0228","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"23","tg_all_an":"5008","tg_all_af":"0.00459265","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265693","variation":"chr11:110048574:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2615A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs756320207","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265694","variation":"chr11:110048601:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2642G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs151119367","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"11","tg_afr_an":"1322","tg_afr_af":"0.0083","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"12","tg_all_an":"5008","tg_all_af":"0.00239617","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265695","variation":"chr11:110048602:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2643C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs113992515","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265696","variation":"chr11:110048623:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2664G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs796957781","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265697","variation":"chr11:110048643:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2684G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11213290","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"309","tg_afr_an":"1322","tg_afr_af":"0.2337","tg_eur_ac":"245","tg_eur_an":"1006","tg_eur_af":"0.2435","tg_amr_ac":"229","tg_amr_an":"694","tg_amr_af":"0.33","tg_eas_ac":"543","tg_eas_an":"1008","tg_eas_af":"0.5387","tg_sas_ac":"323","tg_sas_an":"978","tg_sas_af":"0.3303","tg_all_ac":"1649","tg_all_an":"5008","tg_all_af":"0.329273","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265698","variation":"chr11:110048653:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2694G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs572148056","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265699","variation":"chr11:110048654:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2695A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs77392428","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"162","tg_afr_an":"1322","tg_afr_af":"0.1225","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"7","tg_amr_an":"694","tg_amr_af":"0.0101","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"169","tg_all_an":"5008","tg_all_af":"0.033746","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265700","variation":"chr11:110048655:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2696G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs191209661","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265701","variation":"chr11:110048667:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2708G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs758466099","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265702","variation":"chr11:110048676:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2717G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs752754683","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265703","variation":"chr11:110048680:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2721G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs74924161","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"16","tg_eur_an":"1006","tg_eur_af":"0.0159","tg_amr_ac":"9","tg_amr_an":"694","tg_amr_af":"0.013","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"5","tg_sas_an":"978","tg_sas_af":"0.0051","tg_all_ac":"30","tg_all_an":"5008","tg_all_af":"0.00599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265704","variation":"chr11:110048681:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2722G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs764455558","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265705","variation":"chr11:110048692:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2733C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs544653060","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265706","variation":"chr11:110048720:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2761A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs111982770","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265707","variation":"chr11:110048722:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2763G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs141079792","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"10","tg_eas_an":"1008","tg_eas_af":"0.0099","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"10","tg_all_an":"5008","tg_all_af":"0.00199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265708","variation":"chr11:110048729:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2770G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs578261891","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265709","variation":"chr11:110048741:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2782T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs746898732","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265710","variation":"chr11:110048771:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2812G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11825268","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"84","tg_afr_an":"1322","tg_afr_af":"0.0635","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"4","tg_amr_an":"694","tg_amr_af":"0.0058","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"89","tg_all_an":"5008","tg_all_af":"0.0177716","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265711","variation":"chr11:110048799:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2840C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs149777457","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265712","variation":"chr11:110048834:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2875G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs527895364","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265713","variation":"chr11:110048839:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2880G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs549525884","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265714","variation":"chr11:110048857:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2898A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs776158818","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265715","variation":"chr11:110048863:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2904T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs560677444","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"4","tg_eas_an":"1008","tg_eas_af":"0.004","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265716","variation":"chr11:110048890:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2931T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs199819025","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265717","variation":"chr11:110048915:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2956G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs146795038","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265718","variation":"chr11:110048916:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2957C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs549405666","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265719","variation":"chr11:110048942:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-2983G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs745542747","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265720","variation":"chr11:110048982:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3023A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs751989777","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265721","variation":"chr11:110048999:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3040C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs775884640","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265722","variation":"chr11:110049026:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3067A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs558776592","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265723","variation":"chr11:110049066:G>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3107delC","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs34198814","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"927","tg_afr_an":"1322","tg_afr_af":"0.7012","tg_eur_ac":"507","tg_eur_an":"1006","tg_eur_af":"0.504","tg_amr_ac":"402","tg_amr_an":"694","tg_amr_af":"0.5793","tg_eas_ac":"730","tg_eas_an":"1008","tg_eas_af":"0.7242","tg_sas_ac":"474","tg_sas_an":"978","tg_sas_af":"0.4847","tg_all_ac":"3040","tg_all_an":"5008","tg_all_af":"0.607029","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265724","variation":"chr11:110049071:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3112A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs140558675","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265725","variation":"chr11:110049090:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3131A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs763293814","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265726","variation":"chr11:110049098:A>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3139T>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs140494371","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"6","tg_afr_an":"1322","tg_afr_af":"0.0045","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"6","tg_all_an":"5008","tg_all_af":"0.00119808","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265727","variation":"chr11:110049105:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3146G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs764374054","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265728","variation":"chr11:110049121:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3162A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs547381958","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"3","tg_eur_an":"1006","tg_eur_af":"0.003","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265729","variation":"chr11:110049142:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3183C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs565930157","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265730","variation":"chr11:110049166:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3207T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs183859614","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265731","variation":"chr11:110049190:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3231C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs762329571","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265732","variation":"chr11:110049199:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3240T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs12272356","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"3","tg_afr_an":"1322","tg_afr_af":"0.0023","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265733","variation":"chr11:110049202:A>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3243T>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs574227976","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265734","variation":"chr11:110049213:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3254C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs538342317","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265735","variation":"chr11:110049292:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3333G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs145733872","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"6","tg_all_an":"5008","tg_all_af":"0.00119808","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265736","variation":"chr11:110049327:A>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3368T>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs577310576","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"6","tg_all_an":"5008","tg_all_af":"0.00119808","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265737","variation":"chr11:110049337:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3378C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs146575288","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265738","variation":"chr11:110049424:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3465C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs140341216","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265739","variation":"chr11:110049457:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3498G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs572676773","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"4","tg_eas_an":"1008","tg_eas_af":"0.004","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265740","variation":"chr11:110049458:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3499C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs542886083","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265741","variation":"chr11:110049461:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3502C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs561135275","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265742","variation":"chr11:110049475:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3516C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs750484844","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265743","variation":"chr11:110049508:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3549C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs117970929","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265744","variation":"chr11:110049534:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3575T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs372865372","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265745","variation":"chr11:110049553:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3594G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs80080100","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"3","tg_afr_an":"1322","tg_afr_af":"0.0023","tg_eur_ac":"19","tg_eur_an":"1006","tg_eur_af":"0.0189","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"95","tg_eas_an":"1008","tg_eas_af":"0.0942","tg_sas_ac":"5","tg_sas_an":"978","tg_sas_af":"0.0051","tg_all_ac":"123","tg_all_an":"5008","tg_all_af":"0.0245607","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265746","variation":"chr11:110049594:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3635G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs766694563","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265747","variation":"chr11:110049629:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3670G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs755760980","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265748","variation":"chr11:110049632:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3673A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11828352","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"38","tg_afr_an":"1322","tg_afr_af":"0.0287","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"39","tg_all_an":"5008","tg_all_af":"0.00778754","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265749","variation":"chr11:110049658:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3699G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs779545861","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265750","variation":"chr11:110049676:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3717G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs372961319","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265751","variation":"chr11:110049702:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3743G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs546481593","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265752","variation":"chr11:110049703:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3744C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs559447990","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265753","variation":"chr11:110049839:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3880C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs192586032","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265754","variation":"chr11:110049861:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3902A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs541954855","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265755","variation":"chr11:110049862:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3903G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs536540532","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265756","variation":"chr11:110049936:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3977C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs757178503","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265757","variation":"chr11:110049945:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-3986A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs548133019","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265758","variation":"chr11:110049991:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4032G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs780610867","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265759","variation":"chr11:110049992:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4033C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs61209308","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"94","tg_afr_an":"1322","tg_afr_af":"0.0711","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"35","tg_amr_an":"694","tg_amr_af":"0.0504","tg_eas_ac":"108","tg_eas_an":"1008","tg_eas_af":"0.1071","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"237","tg_all_an":"5008","tg_all_af":"0.0473243","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265760","variation":"chr11:110049994:->G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4035_*32-4034insC","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs34210361","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265761","variation":"chr11:110050042:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4083G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs778755519","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265762","variation":"chr11:110050063:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4104C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs769496609","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265763","variation":"chr11:110050184:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4225G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs538199617","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265764","variation":"chr11:110050229:->G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4270_*32-4269insC","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs71476069","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265765","variation":"chr11:110050256:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4297C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs148063975","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"6","tg_afr_an":"1322","tg_afr_af":"0.0045","tg_eur_ac":"2","tg_eur_an":"1006","tg_eur_af":"0.002","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"12","tg_all_an":"5008","tg_all_af":"0.00239617","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265766","variation":"chr11:110050262:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4303G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs748879564","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265767","variation":"chr11:110050263:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4304G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs184863753","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265768","variation":"chr11:110050315:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4356A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs769028234","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265769","variation":"chr11:110050319:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4360T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs578124617","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265770","variation":"chr11:110050324:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4365G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs550762568","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265771","variation":"chr11:110050359:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4400C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs187106445","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"3","tg_eur_an":"1006","tg_eur_af":"0.003","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265772","variation":"chr11:110050390:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4431G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs141803396","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265773","variation":"chr11:110050409:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4450T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs543301968","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265774","variation":"chr11:110050481:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4522T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs78105833","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265775","variation":"chr11:110050482:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4523C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs74525053","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265777","variation":"chr11:110050502:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4543G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs11213291","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265776","variation":"chr11:110050502:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4543G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11213291","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1037","tg_afr_an":"1322","tg_afr_af":"0.7844","tg_eur_ac":"503","tg_eur_an":"1006","tg_eur_af":"0.5","tg_amr_ac":"451","tg_amr_an":"694","tg_amr_af":"0.6499","tg_eas_ac":"843","tg_eas_an":"1008","tg_eas_af":"0.8363","tg_sas_ac":"488","tg_sas_an":"978","tg_sas_af":"0.499","tg_all_ac":"3322","tg_all_an":"5008","tg_all_af":"0.663339","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265778","variation":"chr11:110050530:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4571A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs576235755","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"4","tg_afr_an":"1322","tg_afr_af":"0.003","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265779","variation":"chr11:110050547:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4588A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs543573287","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265780","variation":"chr11:110050571:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4612G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs12288953","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265781","variation":"chr11:110050575:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4616C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs564658115","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265782","variation":"chr11:110050601:->TTCTTT","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4642_*32-4641insAAAGAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs776601251","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265783","variation":"chr11:110050601:TTCTTT>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4642_*32-4635delAAAGAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs201577302","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265784","variation":"chr11:110050616:->T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4657_*32-4656insA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs199908880","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265785","variation":"chr11:110050622:->T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4663_*32-4662insA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs748106952","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265786","variation":"chr11:110050622:TTTTTT>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4663_*32-4656delAAAAAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs769880153","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265787","variation":"chr11:110050629:->T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4670_*32-4669insA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs528601645","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"718","tg_afr_an":"1322","tg_afr_af":"0.5431","tg_eur_ac":"427","tg_eur_an":"1006","tg_eur_af":"0.4245","tg_amr_ac":"373","tg_amr_an":"694","tg_amr_af":"0.5375","tg_eas_ac":"518","tg_eas_an":"1008","tg_eas_af":"0.5139","tg_sas_ac":"392","tg_sas_an":"978","tg_sas_af":"0.4008","tg_all_ac":"2428","tg_all_an":"5008","tg_all_af":"0.484824","exac_afr_ac":"13","exac_afr_an":"60","exac_afr_af":"0.216667","exac_amr_ac":"8","exac_amr_an":"44","exac_amr_af":"0.181818","exac_eas_ac":"28","exac_eas_an":"86","exac_eas_af":"0.325581","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"172","exac_nfe_an":"898","exac_nfe_af":"0.191537","exac_oth_ac":"7","exac_oth_an":"40","exac_oth_af":"0.175","exac_sas_ac":"387","exac_sas_an":"2366","exac_sas_af":"0.163567","exac_all_ac":"615","exac_all_an":"3494","exac_all_af":"0.176016"},{"id":"265788","variation":"chr11:110050629:->TT","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4670_*32-4669insAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs528601645","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":"12","exac_afr_an":"60","exac_afr_af":"0.2","exac_amr_ac":"2","exac_amr_an":"44","exac_amr_af":"0.0454545","exac_eas_ac":"23","exac_eas_an":"86","exac_eas_af":"0.267442","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"79","exac_nfe_an":"898","exac_nfe_af":"0.0879733","exac_oth_ac":"3","exac_oth_an":"40","exac_oth_af":"0.075","exac_sas_ac":"239","exac_sas_an":"2366","exac_sas_af":"0.101014","exac_all_ac":"358","exac_all_an":"3494","exac_all_af":"0.102461"},{"id":"265789","variation":"chr11:110050629:->TTT","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4670_*32-4669insAAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs528601645","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":"0","exac_afr_an":"60","exac_afr_af":"0","exac_amr_ac":"2","exac_amr_an":"44","exac_amr_af":"0.0454545","exac_eas_ac":"2","exac_eas_an":"86","exac_eas_af":"0.0232558","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"13","exac_nfe_an":"898","exac_nfe_af":"0.0144766","exac_oth_ac":"1","exac_oth_an":"40","exac_oth_af":"0.025","exac_sas_ac":"51","exac_sas_an":"2366","exac_sas_af":"0.0215554","exac_all_ac":"69","exac_all_an":"3494","exac_all_af":"0.0197481"},{"id":"265790","variation":"chr11:110050629:T>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4670delA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs763180188","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":"6","exac_afr_an":"60","exac_afr_af":"0.1","exac_amr_ac":"6","exac_amr_an":"44","exac_amr_af":"0.136364","exac_eas_ac":"4","exac_eas_an":"86","exac_eas_af":"0.0465116","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"127","exac_nfe_an":"898","exac_nfe_af":"0.141425","exac_oth_ac":"7","exac_oth_an":"40","exac_oth_af":"0.175","exac_sas_ac":"367","exac_sas_an":"2366","exac_sas_af":"0.155114","exac_all_ac":"517","exac_all_an":"3494","exac_all_af":"0.147968"},{"id":"265791","variation":"chr11:110050629:TT>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4670_*32-4667delAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs773171221","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":"3","exac_afr_an":"60","exac_afr_af":"0.05","exac_amr_ac":"1","exac_amr_an":"44","exac_amr_af":"0.0227273","exac_eas_ac":"0","exac_eas_an":"86","exac_eas_af":"0","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"32","exac_nfe_an":"898","exac_nfe_af":"0.0356347","exac_oth_ac":"2","exac_oth_an":"40","exac_oth_af":"0.05","exac_sas_ac":"89","exac_sas_an":"2366","exac_sas_af":"0.0376162","exac_all_ac":"127","exac_all_an":"3494","exac_all_af":"0.036348"},{"id":"265792","variation":"chr11:110050629:TTT>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4670_*32-4666delAAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs768012559","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":"0","exac_afr_an":"60","exac_afr_af":"0","exac_amr_ac":"1","exac_amr_an":"44","exac_amr_af":"0.0227273","exac_eas_ac":"0","exac_eas_an":"86","exac_eas_af":"0","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"14","exac_nfe_an":"898","exac_nfe_af":"0.0155902","exac_oth_ac":"0","exac_oth_an":"40","exac_oth_af":"0","exac_sas_ac":"28","exac_sas_an":"2366","exac_sas_af":"0.0118343","exac_all_ac":"43","exac_all_an":"3494","exac_all_af":"0.0123068"},{"id":"265793","variation":"chr11:110050632:->C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4673_*32-4672insG","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs753210614","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265794","variation":"chr11:110050632:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4673A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs191613836","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"8","tg_eur_an":"1006","tg_eur_af":"0.008","tg_amr_ac":"8","tg_amr_an":"694","tg_amr_af":"0.0115","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"10","tg_sas_an":"978","tg_sas_af":"0.0102","tg_all_ac":"26","tg_all_an":"5008","tg_all_af":"0.00519169","exac_afr_ac":"1","exac_afr_an":"146","exac_afr_af":"0.00684932","exac_amr_ac":"1","exac_amr_an":"80","exac_amr_af":"0.0125","exac_eas_ac":"0","exac_eas_an":"132","exac_eas_af":"0","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"116","exac_nfe_an":"2310","exac_nfe_af":"0.0502165","exac_oth_ac":"3","exac_oth_an":"100","exac_oth_af":"0.03","exac_sas_ac":"159","exac_sas_an":"6462","exac_sas_af":"0.0246054","exac_all_ac":"280","exac_all_an":"9230","exac_all_af":"0.0303359"},{"id":"265795","variation":"chr11:110050633:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4674A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs774264169","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":"0","exac_afr_an":"162","exac_afr_af":"0","exac_amr_ac":"0","exac_amr_an":"86","exac_amr_af":"0","exac_eas_ac":"0","exac_eas_an":"132","exac_eas_af":"0","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"11","exac_nfe_an":"2378","exac_nfe_af":"0.00462574","exac_oth_ac":"1","exac_oth_an":"102","exac_oth_af":"0.00980392","exac_sas_ac":"13","exac_sas_an":"6630","exac_sas_af":"0.00196078","exac_all_ac":"25","exac_all_an":"9490","exac_all_af":"0.00263435"},{"id":"265796","variation":"chr11:110050634:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4675A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs746077888","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":"0","exac_afr_an":"162","exac_afr_af":"0","exac_amr_ac":"0","exac_amr_an":"88","exac_amr_af":"0","exac_eas_ac":"1","exac_eas_an":"128","exac_eas_af":"0.0078125","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"4","exac_nfe_an":"2386","exac_nfe_af":"0.00167645","exac_oth_ac":"0","exac_oth_an":"100","exac_oth_af":"0","exac_sas_ac":"2","exac_sas_an":"6644","exac_sas_af":"0.000301023","exac_all_ac":"7","exac_all_an":"9508","exac_all_af":"0.000736222"},{"id":"265797","variation":"chr11:110050635:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4676A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs540712226","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":"0","exac_afr_an":"162","exac_afr_af":"0","exac_amr_ac":"0","exac_amr_an":"88","exac_amr_af":"0","exac_eas_ac":"1","exac_eas_an":"126","exac_eas_af":"0.00793651","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"3","exac_nfe_an":"2390","exac_nfe_af":"0.00125523","exac_oth_ac":"0","exac_oth_an":"104","exac_oth_af":"0","exac_sas_ac":"2","exac_sas_an":"6654","exac_sas_af":"0.000300571","exac_all_ac":"6","exac_all_an":"9524","exac_all_af":"0.000629987"},{"id":"265798","variation":"chr11:110050645:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4686C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs74482276","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265799","variation":"chr11:110050653:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4694C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs775528881","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":"0","exac_afr_an":"134","exac_afr_af":"0","exac_amr_ac":"0","exac_amr_an":"74","exac_amr_af":"0","exac_eas_ac":"0","exac_eas_an":"126","exac_eas_af":"0","exac_fin_ac":"0","exac_fin_an":"0","exac_fin_af":"0","exac_nfe_ac":"0","exac_nfe_an":"1898","exac_nfe_af":"0","exac_oth_ac":"0","exac_oth_an":"80","exac_oth_af":"0","exac_sas_ac":"1","exac_sas_an":"5344","exac_sas_af":"0.000187126","exac_all_ac":"1","exac_all_an":"7656","exac_all_af":"0.000130617"},{"id":"265800","variation":"chr11:110050656:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4697A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs1784668","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265801","variation":"chr11:110050683:G>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4724delC","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs756580652","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265802","variation":"chr11:110050690:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4731T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs546912000","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265803","variation":"chr11:110050735:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4776A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs759840972","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265804","variation":"chr11:110050745:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4786C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs559301116","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265805","variation":"chr11:110050775:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4816G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs529614211","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265806","variation":"chr11:110050786:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4827G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs377523357","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"5","tg_afr_an":"1322","tg_afr_af":"0.0038","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265807","variation":"chr11:110050828:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4869A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs569931570","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265808","variation":"chr11:110050846:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4887G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs530749059","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"9","tg_afr_an":"1322","tg_afr_af":"0.0068","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265809","variation":"chr11:110050847:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4888C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs371016750","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265810","variation":"chr11:110050884:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4925G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11826652","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"53","tg_afr_an":"1322","tg_afr_af":"0.0401","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"55","tg_all_an":"5008","tg_all_af":"0.0109824","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265811","variation":"chr11:110050887:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4928T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11821931","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"55","tg_afr_an":"1322","tg_afr_af":"0.0416","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"57","tg_all_an":"5008","tg_all_af":"0.0113818","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265812","variation":"chr11:110050896:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4937T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11821933","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"53","tg_afr_an":"1322","tg_afr_af":"0.0401","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"55","tg_all_an":"5008","tg_all_af":"0.0109824","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265813","variation":"chr11:110050900:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4941A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs139517540","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"55","tg_afr_an":"1322","tg_afr_af":"0.0416","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"56","tg_all_an":"5008","tg_all_af":"0.0111821","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265814","variation":"chr11:110050917:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4958C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs566068219","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265815","variation":"chr11:110050919:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4960C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs113933301","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265816","variation":"chr11:110050925:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-4966G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs760802525","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265817","variation":"chr11:110050963:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5004T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11821948","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"31","tg_afr_an":"1322","tg_afr_af":"0.0234","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"33","tg_all_an":"5008","tg_all_af":"0.00658946","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265818","variation":"chr11:110050975:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5016T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs114468260","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"55","tg_afr_an":"1322","tg_afr_af":"0.0416","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"56","tg_all_an":"5008","tg_all_af":"0.0111821","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265819","variation":"chr11:110050977:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5018A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs144323624","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"7","tg_eur_an":"1006","tg_eur_af":"0.007","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"11","tg_all_an":"5008","tg_all_af":"0.00219649","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265820","variation":"chr11:110051005:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5046A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs759784463","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265821","variation":"chr11:110051018:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5059A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs764012905","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265822","variation":"chr11:110051075:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5116G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs549113490","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265823","variation":"chr11:110051096:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5137G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs751341412","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265824","variation":"chr11:110051099:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5140C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs543646102","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265825","variation":"chr11:110051116:A>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5157T>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs118189409","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"14","tg_eur_an":"1006","tg_eur_af":"0.0139","tg_amr_ac":"8","tg_amr_an":"694","tg_amr_af":"0.0115","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"4","tg_sas_an":"978","tg_sas_af":"0.0041","tg_all_ac":"28","tg_all_an":"5008","tg_all_af":"0.00559105","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265826","variation":"chr11:110051123:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5164G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs548652895","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265827","variation":"chr11:110051155:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5196C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs115377543","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"55","tg_afr_an":"1322","tg_afr_af":"0.0416","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"56","tg_all_an":"5008","tg_all_af":"0.0111821","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265828","variation":"chr11:110051162:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5203C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs541127321","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265829","variation":"chr11:110051164:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5205C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs148764372","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"18","tg_afr_an":"1322","tg_afr_af":"0.0136","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"18","tg_all_an":"5008","tg_all_af":"0.00359425","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265830","variation":"chr11:110051183:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5224A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs749971525","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265831","variation":"chr11:110051233:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5274G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs529708686","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265832","variation":"chr11:110051234:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5275G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs541819499","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"4","tg_afr_an":"1322","tg_afr_af":"0.003","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265833","variation":"chr11:110051234:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5275G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs541819499","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265834","variation":"chr11:110051240:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5281T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs60529536","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"8","tg_afr_an":"1322","tg_afr_af":"0.0061","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"8","tg_all_an":"5008","tg_all_af":"0.00159744","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265835","variation":"chr11:110051258:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5299G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs11213292","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265836","variation":"chr11:110051281:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5322C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs188929784","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"4","tg_afr_an":"1322","tg_afr_af":"0.003","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265837","variation":"chr11:110051290:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5331A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs377432700","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265838","variation":"chr11:110051304:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5345G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs114584215","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"55","tg_afr_an":"1322","tg_afr_af":"0.0416","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"56","tg_all_an":"5008","tg_all_af":"0.0111821","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265839","variation":"chr11:110051316:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5357G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs537569081","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265840","variation":"chr11:110051343:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5384C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs570622443","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265841","variation":"chr11:110051362:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5403T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs371836358","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265842","variation":"chr11:110051376:G>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5417delC","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11295042","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"24","tg_afr_an":"1322","tg_afr_af":"0.0182","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"3","tg_amr_an":"694","tg_amr_af":"0.0043","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"28","tg_all_an":"5008","tg_all_af":"0.00559105","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265843","variation":"chr11:110051380:T>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5421delA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11295043","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"953","tg_afr_an":"1322","tg_afr_af":"0.7209","tg_eur_ac":"500","tg_eur_an":"1006","tg_eur_af":"0.497","tg_amr_ac":"405","tg_amr_an":"694","tg_amr_af":"0.5836","tg_eas_ac":"718","tg_eas_an":"1008","tg_eas_af":"0.7123","tg_sas_ac":"482","tg_sas_an":"978","tg_sas_af":"0.4928","tg_all_ac":"3058","tg_all_an":"5008","tg_all_af":"0.610623","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265844","variation":"chr11:110051404:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5445G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs528226381","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265845","variation":"chr11:110051439:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5480C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs142475062","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"13","tg_afr_an":"1322","tg_afr_af":"0.0098","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"13","tg_all_an":"5008","tg_all_af":"0.00259585","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265846","variation":"chr11:110051443:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5484A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs557084941","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265847","variation":"chr11:110051471:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5512A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs748967537","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265848","variation":"chr11:110051487:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5528C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs768261718","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265849","variation":"chr11:110051508:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5549G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs577379037","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265850","variation":"chr11:110051509:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5550C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs536266876","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265851","variation":"chr11:110051527:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5568A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs554519236","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265852","variation":"chr11:110051584:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5625G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs539735613","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265853","variation":"chr11:110051594:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5635C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs11213293","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265854","variation":"chr11:110051599:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5640G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs371124169","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265855","variation":"chr11:110051599:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5640G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs371124169","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265856","variation":"chr11:110051601:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5642A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs570057083","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265857","variation":"chr11:110051608:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5649A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs146875154","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265858","variation":"chr11:110051612:CC>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5653_*32-5650delGG","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs781484523","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265859","variation":"chr11:110051625:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5666A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs560852448","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265860","variation":"chr11:110051638:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5679C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs558781244","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265861","variation":"chr11:110051672:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5713C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs373951874","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265862","variation":"chr11:110051680:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5721G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs60138353","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"26","tg_afr_an":"1322","tg_afr_af":"0.0197","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"4","tg_eas_an":"1008","tg_eas_af":"0.004","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"31","tg_all_an":"5008","tg_all_af":"0.0061901","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265863","variation":"chr11:110051735:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5776C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs534872707","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265864","variation":"chr11:110051766:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5807C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs376726592","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265865","variation":"chr11:110051807:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5848C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs4754426","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"971","tg_afr_an":"1322","tg_afr_af":"0.7345","tg_eur_ac":"500","tg_eur_an":"1006","tg_eur_af":"0.497","tg_amr_ac":"404","tg_amr_an":"694","tg_amr_af":"0.5821","tg_eas_ac":"732","tg_eas_an":"1008","tg_eas_af":"0.7262","tg_sas_ac":"456","tg_sas_an":"978","tg_sas_af":"0.4663","tg_all_ac":"3063","tg_all_an":"5008","tg_all_af":"0.611621","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265866","variation":"chr11:110051826:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5867G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs761208928","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265867","variation":"chr11:110051834:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5875C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs144175851","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265868","variation":"chr11:110051838:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5879A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs367625800","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265869","variation":"chr11:110051867:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5908C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs28668919","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"12","tg_afr_an":"1322","tg_afr_af":"0.0091","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"12","tg_all_an":"5008","tg_all_af":"0.00239617","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265871","variation":"chr11:110051890:T>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5931delA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs34297768","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265870","variation":"chr11:110051890:TT>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5931_*32-5928delAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs60581788","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1051","tg_afr_an":"1322","tg_afr_af":"0.795","tg_eur_ac":"567","tg_eur_an":"1006","tg_eur_af":"0.5636","tg_amr_ac":"434","tg_amr_an":"694","tg_amr_af":"0.6254","tg_eas_ac":"773","tg_eas_an":"1008","tg_eas_af":"0.7669","tg_sas_ac":"495","tg_sas_an":"978","tg_sas_af":"0.5061","tg_all_ac":"3320","tg_all_an":"5008","tg_all_af":"0.662939","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265872","variation":"chr11:110051890:TTT>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5931_*32-5927delAAA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs769712541","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265873","variation":"chr11:110051909:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5950G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs575655343","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265874","variation":"chr11:110051910:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5951C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs182138682","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265875","variation":"chr11:110051934:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5975A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs564184030","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265876","variation":"chr11:110051943:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5984T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs140970468","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"6","tg_sas_an":"978","tg_sas_af":"0.0061","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265877","variation":"chr11:110051953:A>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5994T>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs4754427","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1029","tg_afr_an":"1322","tg_afr_af":"0.7784","tg_eur_ac":"500","tg_eur_an":"1006","tg_eur_af":"0.497","tg_amr_ac":"406","tg_amr_an":"694","tg_amr_af":"0.585","tg_eas_ac":"735","tg_eas_an":"1008","tg_eas_af":"0.7292","tg_sas_ac":"462","tg_sas_an":"978","tg_sas_af":"0.4724","tg_all_ac":"3132","tg_all_an":"5008","tg_all_af":"0.625399","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265878","variation":"chr11:110051957:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-5998C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs559823858","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"6","tg_afr_an":"1322","tg_afr_af":"0.0045","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"6","tg_all_an":"5008","tg_all_af":"0.00119808","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265879","variation":"chr11:110051973:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6014G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs185529210","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"4","tg_eas_an":"1008","tg_eas_af":"0.004","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265880","variation":"chr11:110051980:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6021G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs150355207","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"42","tg_afr_an":"1322","tg_afr_af":"0.0318","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"43","tg_all_an":"5008","tg_all_af":"0.00858626","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265881","variation":"chr11:110052031:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6072C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs569720241","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265882","variation":"chr11:110052056:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6097A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs113305504","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"8","tg_afr_an":"1322","tg_afr_af":"0.0061","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"8","tg_all_an":"5008","tg_all_af":"0.00159744","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265883","variation":"chr11:110052091:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6132C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs552851214","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265884","variation":"chr11:110052094:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6135C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs571029593","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265885","variation":"chr11:110052139:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6180C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs535250533","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265886","variation":"chr11:110052150:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6191C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs189244035","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265887","variation":"chr11:110052159:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6200A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs145024472","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"42","tg_afr_an":"1322","tg_afr_af":"0.0318","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"43","tg_all_an":"5008","tg_all_af":"0.00858626","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265888","variation":"chr11:110052171:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6212C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs556910227","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265889","variation":"chr11:110052180:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6221G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs180790845","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265890","variation":"chr11:110052183:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6224C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs149084029","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265891","variation":"chr11:110052189:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6230C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs535539741","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265892","variation":"chr11:110052209:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6250G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs767837949","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265893","variation":"chr11:110052235:->GCCCCTTCCCAGTATCTTCCACT","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6276_*32-6275insAGTGGAAGATACTGGGAAGGGGC","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs558148374","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"4","tg_afr_an":"1322","tg_afr_af":"0.003","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265894","variation":"chr11:110052306:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6347G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs751792688","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265895","variation":"chr11:110052328:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6369G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs557048654","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265896","variation":"chr11:110052335:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6376C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs750721126","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265897","variation":"chr11:110052358:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6399T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs12279365","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265898","variation":"chr11:110052411:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6452C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs542280735","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265899","variation":"chr11:110052430:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6471C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs146268454","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"10","tg_eur_an":"1006","tg_eur_af":"0.0099","tg_amr_ac":"4","tg_amr_an":"694","tg_amr_af":"0.0058","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"4","tg_sas_an":"978","tg_sas_af":"0.0041","tg_all_ac":"18","tg_all_an":"5008","tg_all_af":"0.00359425","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265900","variation":"chr11:110052474:GG>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6515_*32-6512delCC","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs777860562","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265901","variation":"chr11:110052476:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6517G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs765479980","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265902","variation":"chr11:110052477:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6518C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs138881106","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265903","variation":"chr11:110052483:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6524C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs573030693","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265904","variation":"chr11:110052548:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6589C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs117058925","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":"0","otoscope_aj_an":"400","otoscope_aj_af":"0","otoscope_co_ac":"0","otoscope_co_an":"320","otoscope_co_af":"0","otoscope_us_ac":"0","otoscope_us_an":"320","otoscope_us_af":"0","otoscope_jp_ac":"21","otoscope_jp_an":"400","otoscope_jp_af":"0.0525","otoscope_es_ac":"0","otoscope_es_an":"360","otoscope_es_af":"0","otoscope_tr_ac":"0","otoscope_tr_an":"200","otoscope_tr_af":"0","otoscope_all_ac":"21","otoscope_all_an":"2000","otoscope_all_af":"0.0105","tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"4","tg_eur_an":"1006","tg_eur_af":"0.004","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"87","tg_eas_an":"1008","tg_eas_af":"0.0863","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"93","tg_all_an":"5008","tg_all_af":"0.0185703","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265905","variation":"chr11:110052567:A>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6608delT","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs34758357","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265906","variation":"chr11:110052571:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6612T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs142703254","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265907","variation":"chr11:110052590:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6631A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs529010430","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265908","variation":"chr11:110052593:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6634C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs761666099","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265909","variation":"chr11:110052595:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6636C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs76516736","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265910","variation":"chr11:110052634:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6675A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs146922256","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"5","tg_afr_an":"1322","tg_afr_af":"0.0038","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265911","variation":"chr11:110052640:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6681G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs575782842","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265912","variation":"chr11:110052673:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6714C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs563410144","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265913","variation":"chr11:110052681:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6722G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs750393806","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265914","variation":"chr11:110052692:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6733C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs796656527","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265915","variation":"chr11:110052705:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6746G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs530835161","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265916","variation":"chr11:110052713:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6754G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs756002414","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265917","variation":"chr11:110052714:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6755G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs552267282","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265918","variation":"chr11:110052721:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6762C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs544726300","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265919","variation":"chr11:110052728:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6769G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs372099112","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265920","variation":"chr11:110052730:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6771A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs12273407","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"179","tg_afr_an":"1322","tg_afr_af":"0.1354","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"9","tg_amr_an":"694","tg_amr_af":"0.013","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"188","tg_all_an":"5008","tg_all_af":"0.0375399","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265921","variation":"chr11:110052732:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6773C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs185874439","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"4","tg_afr_an":"1322","tg_afr_af":"0.003","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265922","variation":"chr11:110052733:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6774C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs753457607","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265923","variation":"chr11:110052783:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6824C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs565555871","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265924","variation":"chr11:110052821:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6862C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs564114485","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265925","variation":"chr11:110052868:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6909G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs61900201","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265926","variation":"chr11:110052872:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6913C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs547217321","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265927","variation":"chr11:110052877:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6918A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs754682921","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265928","variation":"chr11:110052887:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6928A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs138036974","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265929","variation":"chr11:110052890:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6931C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs898845","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"968","tg_afr_an":"1322","tg_afr_af":"0.7322","tg_eur_ac":"512","tg_eur_an":"1006","tg_eur_af":"0.5089","tg_amr_ac":"405","tg_amr_an":"694","tg_amr_af":"0.5836","tg_eas_ac":"733","tg_eas_an":"1008","tg_eas_af":"0.7272","tg_sas_ac":"456","tg_sas_an":"978","tg_sas_af":"0.4663","tg_all_ac":"3074","tg_all_an":"5008","tg_all_af":"0.613818","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265930","variation":"chr11:110052897:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6938T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs141696729","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"12","tg_afr_an":"1322","tg_afr_af":"0.0091","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"12","tg_all_an":"5008","tg_all_af":"0.00239617","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265931","variation":"chr11:110052909:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6950C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs747686298","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265932","variation":"chr11:110052934:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-6975G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs190390257","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"15","tg_eas_an":"1008","tg_eas_af":"0.0149","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"15","tg_all_an":"5008","tg_all_af":"0.00299521","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265933","variation":"chr11:110052979:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7020A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs181261921","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"4","tg_eas_an":"1008","tg_eas_af":"0.004","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265934","variation":"chr11:110052994:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7035A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs73553533","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"118","tg_afr_an":"1322","tg_afr_af":"0.0893","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"3","tg_amr_an":"694","tg_amr_af":"0.0043","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"121","tg_all_an":"5008","tg_all_af":"0.0241613","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265935","variation":"chr11:110053028:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7069T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs114525685","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"110","tg_afr_an":"1322","tg_afr_af":"0.0832","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"6","tg_amr_an":"694","tg_amr_af":"0.0086","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"116","tg_all_an":"5008","tg_all_af":"0.0231629","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265936","variation":"chr11:110053041:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7082T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs540161542","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265937","variation":"chr11:110053043:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7084C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs555204554","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"5","tg_sas_an":"978","tg_sas_af":"0.0051","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265938","variation":"chr11:110053063:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7104T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs573518682","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265939","variation":"chr11:110053136:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7177C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs543974936","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265940","variation":"chr11:110053149:A>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7190T>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs563471255","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265941","variation":"chr11:110053154:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7195G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs540131167","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265942","variation":"chr11:110053155:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7196C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs530897415","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"4","tg_eas_an":"1008","tg_eas_af":"0.004","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265943","variation":"chr11:110053178:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7219G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs898846","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1025","tg_afr_an":"1322","tg_afr_af":"0.7753","tg_eur_ac":"529","tg_eur_an":"1006","tg_eur_af":"0.5258","tg_amr_ac":"412","tg_amr_an":"694","tg_amr_af":"0.5937","tg_eas_ac":"733","tg_eas_an":"1008","tg_eas_af":"0.7272","tg_sas_ac":"460","tg_sas_an":"978","tg_sas_af":"0.4703","tg_all_ac":"3159","tg_all_an":"5008","tg_all_af":"0.630791","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265944","variation":"chr11:110053186:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7227A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs186097876","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265945","variation":"chr11:110053195:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7236T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs528438397","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"6","tg_afr_an":"1322","tg_afr_af":"0.0045","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"6","tg_all_an":"5008","tg_all_af":"0.00119808","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265946","variation":"chr11:110053198:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7239G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs546986268","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265947","variation":"chr11:110053208:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7249G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs568736285","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265948","variation":"chr11:110053219:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7260C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs529531159","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265949","variation":"chr11:110053231:TGGGAGGATGGTTTAAGCCTGAGAGA>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7272_*32-7245delTCTCTCAGGCTTAAACCATCCTCCCA","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs559818681","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"230","tg_afr_an":"1322","tg_afr_af":"0.174","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"13","tg_amr_an":"694","tg_amr_af":"0.0187","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"243","tg_all_an":"5008","tg_all_af":"0.0485224","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265950","variation":"chr11:110053237:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7278C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs190466333","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"22","tg_eas_an":"1008","tg_eas_af":"0.0218","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"22","tg_all_an":"5008","tg_all_af":"0.00439297","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265951","variation":"chr11:110053256:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7297T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs625747","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1322","tg_afr_an":"1322","tg_afr_af":"1","tg_eur_ac":"1006","tg_eur_an":"1006","tg_eur_af":"1","tg_amr_ac":"694","tg_amr_an":"694","tg_amr_af":"1","tg_eas_ac":"1008","tg_eas_an":"1008","tg_eas_af":"1","tg_sas_ac":"978","tg_sas_an":"978","tg_sas_af":"1","tg_all_ac":"5008","tg_all_an":"5008","tg_all_af":"1","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265952","variation":"chr11:110053284:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7325G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs539148897","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265953","variation":"chr11:110053288:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7329C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs575156185","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"3","tg_sas_an":"978","tg_sas_af":"0.0031","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265954","variation":"chr11:110053288:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7329C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs575156185","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265955","variation":"chr11:110053327:->AAC","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7368_*32-7367insGTT","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs140588360","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"13","tg_eas_an":"1008","tg_eas_af":"0.0129","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"13","tg_all_an":"5008","tg_all_af":"0.00259585","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265956","variation":"chr11:110053327:->AACAACAACAAC","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7368_*32-7367insGTTGTTGTTGTT","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs140588360","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"186","tg_afr_an":"1322","tg_afr_af":"0.1407","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"7","tg_amr_an":"694","tg_amr_af":"0.0101","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"193","tg_all_an":"5008","tg_all_af":"0.0385383","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265957","variation":"chr11:110053341:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7382G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs188940057","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265958","variation":"chr11:110053349:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7390A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs150531810","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"6","tg_eur_an":"1006","tg_eur_af":"0.006","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"6","tg_all_an":"5008","tg_all_af":"0.00119808","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265959","variation":"chr11:110053408:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7449C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs4754428","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"93","tg_afr_an":"1322","tg_afr_af":"0.0703","tg_eur_ac":"201","tg_eur_an":"1006","tg_eur_af":"0.1998","tg_amr_ac":"72","tg_amr_an":"694","tg_amr_af":"0.1037","tg_eas_ac":"110","tg_eas_an":"1008","tg_eas_af":"0.1091","tg_sas_ac":"82","tg_sas_an":"978","tg_sas_af":"0.0838","tg_all_ac":"558","tg_all_an":"5008","tg_all_af":"0.111422","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265960","variation":"chr11:110053409:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7450C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs573577530","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265961","variation":"chr11:110053457:G>-","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7498delC","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs35093720","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265962","variation":"chr11:110053497:G>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7538C>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs139924113","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265963","variation":"chr11:110053500:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7541A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11821648","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"45","tg_afr_an":"1322","tg_afr_af":"0.034","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"46","tg_all_an":"5008","tg_all_af":"0.0091853","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265964","variation":"chr11:110053501:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7542C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs772957390","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265965","variation":"chr11:110053504:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7545G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs116375479","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"38","tg_afr_an":"1322","tg_afr_af":"0.0287","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"4","tg_amr_an":"694","tg_amr_af":"0.0058","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"43","tg_all_an":"5008","tg_all_af":"0.00858626","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265966","variation":"chr11:110053505:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7546C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs545982704","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265967","variation":"chr11:110053576:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7617G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs564562560","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265968","variation":"chr11:110053577:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7618C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs149403013","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"24","tg_afr_an":"1322","tg_afr_af":"0.0182","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"8","tg_amr_an":"694","tg_amr_af":"0.0115","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"32","tg_all_an":"5008","tg_all_af":"0.00638978","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265969","variation":"chr11:110053592:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7633C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs746747060","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265970","variation":"chr11:110053603:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7644C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs191891824","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"5","tg_afr_an":"1322","tg_afr_af":"0.0038","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265971","variation":"chr11:110053618:A>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7659T>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs562393575","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265972","variation":"chr11:110053622:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7663T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs146393833","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"31","tg_afr_an":"1322","tg_afr_af":"0.0234","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"32","tg_all_an":"5008","tg_all_af":"0.00638978","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265973","variation":"chr11:110053623:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7664A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs551234565","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265974","variation":"chr11:110053635:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7676G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs754519383","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265975","variation":"chr11:110053642:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7683A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs764592434","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265976","variation":"chr11:110053654:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7695G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs4754429","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"113","tg_afr_an":"1322","tg_afr_af":"0.0855","tg_eur_ac":"200","tg_eur_an":"1006","tg_eur_af":"0.1988","tg_amr_ac":"79","tg_amr_an":"694","tg_amr_af":"0.1138","tg_eas_ac":"98","tg_eas_an":"1008","tg_eas_af":"0.0972","tg_sas_ac":"76","tg_sas_an":"978","tg_sas_af":"0.0777","tg_all_ac":"566","tg_all_an":"5008","tg_all_af":"0.113019","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265977","variation":"chr11:110053664:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7705C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs139735729","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265978","variation":"chr11:110053706:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7747T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs551206377","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"3","tg_afr_an":"1322","tg_afr_af":"0.0023","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265979","variation":"chr11:110053735:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7776C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs566537380","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265980","variation":"chr11:110053738:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7779A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs551102726","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265981","variation":"chr11:110053795:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7836G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs775898378","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265982","variation":"chr11:110053811:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7852G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs182982560","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"2","tg_eas_an":"1008","tg_eas_af":"0.002","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265983","variation":"chr11:110053830:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7871C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs116159351","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"31","tg_afr_an":"1322","tg_afr_af":"0.0234","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"32","tg_all_an":"5008","tg_all_af":"0.00638978","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265984","variation":"chr11:110053836:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7877G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs12294712","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"225","tg_afr_an":"1322","tg_afr_af":"0.1702","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"20","tg_amr_an":"694","tg_amr_af":"0.0288","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"245","tg_all_an":"5008","tg_all_af":"0.0489217","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265985","variation":"chr11:110053837:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7878C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs186620031","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265986","variation":"chr11:110053866:->AAAAAAAC","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7907_*32-7906insGTTTTTTT","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs148648049","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265987","variation":"chr11:110053866:->AAAAAAC","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7907_*32-7906insGTTTTTT","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs148648049","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265988","variation":"chr11:110053877:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7918C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs555991588","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265989","variation":"chr11:110053897:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7938C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs191871701","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"6","tg_afr_an":"1322","tg_afr_af":"0.0045","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"6","tg_all_an":"5008","tg_all_af":"0.00119808","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265990","variation":"chr11:110053934:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7975G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs183816074","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"23","tg_afr_an":"1322","tg_afr_af":"0.0174","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"8","tg_amr_an":"694","tg_amr_af":"0.0115","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"31","tg_all_an":"5008","tg_all_af":"0.0061901","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265991","variation":"chr11:110053942:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7983A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs557992458","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"4","tg_afr_an":"1322","tg_afr_af":"0.003","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"4","tg_all_an":"5008","tg_all_af":"0.000798722","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265992","variation":"chr11:110053954:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7995G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs542135414","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265993","variation":"chr11:110053955:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-7996C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs187404399","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"6","tg_eas_an":"1008","tg_eas_af":"0.006","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"6","tg_all_an":"5008","tg_all_af":"0.00119808","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265994","variation":"chr11:110053994:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8035G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs763249591","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265995","variation":"chr11:110054036:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8077A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs540663323","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265996","variation":"chr11:110054053:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8094G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs562052819","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265997","variation":"chr11:110054070:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8111C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs757901202","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265998","variation":"chr11:110054073:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8114G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs60617819","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"227","tg_afr_an":"1322","tg_afr_af":"0.1717","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"13","tg_amr_an":"694","tg_amr_af":"0.0187","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"240","tg_all_an":"5008","tg_all_af":"0.0479233","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"265999","variation":"chr11:110054077:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8118G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs544933247","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"3","tg_afr_an":"1322","tg_afr_af":"0.0023","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266000","variation":"chr11:110054078:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8119C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs372067937","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266001","variation":"chr11:110054111:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8152C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs533386279","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266002","variation":"chr11:110054139:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8180T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs769937349","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266003","variation":"chr11:110054147:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8188C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs140730001","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266004","variation":"chr11:110054158:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8199A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs193043193","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"7","tg_eur_an":"1006","tg_eur_af":"0.007","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266005","variation":"chr11:110054191:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8232A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs560024782","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266006","variation":"chr11:110054193:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8234G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs144209585","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"23","tg_afr_an":"1322","tg_afr_af":"0.0174","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"8","tg_amr_an":"694","tg_amr_af":"0.0115","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"31","tg_all_an":"5008","tg_all_af":"0.0061901","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266007","variation":"chr11:110054201:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8242G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs548616209","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266008","variation":"chr11:110054202:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8243C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs566927538","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"3","tg_afr_an":"1322","tg_afr_af":"0.0023","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266009","variation":"chr11:110054211:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8252G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs146538449","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266010","variation":"chr11:110054219:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8260A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs549679506","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266011","variation":"chr11:110054223:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8264A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs73553537","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266012","variation":"chr11:110054260:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8301T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs538484655","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266013","variation":"chr11:110054287:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8328C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs115151525","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"43","tg_afr_an":"1322","tg_afr_af":"0.0325","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"8","tg_amr_an":"694","tg_amr_af":"0.0115","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"52","tg_all_an":"5008","tg_all_af":"0.0103834","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266014","variation":"chr11:110054301:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8342A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11213294","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"443","tg_afr_an":"1322","tg_afr_af":"0.3351","tg_eur_ac":"201","tg_eur_an":"1006","tg_eur_af":"0.1998","tg_amr_ac":"95","tg_amr_an":"694","tg_amr_af":"0.1369","tg_eas_ac":"109","tg_eas_an":"1008","tg_eas_af":"0.1081","tg_sas_ac":"81","tg_sas_an":"978","tg_sas_af":"0.0828","tg_all_ac":"929","tg_all_an":"5008","tg_all_af":"0.185503","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266015","variation":"chr11:110054303:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8344G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs148713627","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"8","tg_afr_an":"1322","tg_afr_af":"0.0061","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"8","tg_all_an":"5008","tg_all_af":"0.00159744","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266016","variation":"chr11:110054399:T>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8440A>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs555848951","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266017","variation":"chr11:110054406:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8447A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs574100023","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266018","variation":"chr11:110054409:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8450A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs553377774","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266019","variation":"chr11:110054414:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8455C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs142373722","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"17","tg_afr_an":"1322","tg_afr_af":"0.0129","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"2","tg_amr_an":"694","tg_amr_af":"0.0029","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"19","tg_all_an":"5008","tg_all_af":"0.00379393","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266020","variation":"chr11:110054433:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8474A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs11213295","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"251","tg_afr_an":"1322","tg_afr_af":"0.1899","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"21","tg_amr_an":"694","tg_amr_af":"0.0303","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"272","tg_all_an":"5008","tg_all_af":"0.0543131","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266021","variation":"chr11:110054457:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8498A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs764835890","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266022","variation":"chr11:110054477:A>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8518T>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs578184700","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266023","variation":"chr11:110054489:C>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8530G>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs560771418","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266024","variation":"chr11:110054531:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8572T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs185651402","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"5","tg_eur_an":"1006","tg_eur_af":"0.005","tg_amr_ac":"3","tg_amr_an":"694","tg_amr_af":"0.0043","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"17","tg_sas_an":"978","tg_sas_af":"0.0174","tg_all_ac":"25","tg_all_an":"5008","tg_all_af":"0.00499201","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266025","variation":"chr11:110054545:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8586G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs190759605","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"23","tg_afr_an":"1322","tg_afr_af":"0.0174","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"8","tg_amr_an":"694","tg_amr_af":"0.0115","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"31","tg_all_an":"5008","tg_all_af":"0.0061901","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266026","variation":"chr11:110054564:G>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8605C>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs763829069","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266027","variation":"chr11:110054580:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8621G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs536180359","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266028","variation":"chr11:110054581:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8622C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs548677272","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266029","variation":"chr11:110054589:A>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8630T>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs61900202","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"48","tg_eur_an":"1006","tg_eur_af":"0.0477","tg_amr_ac":"18","tg_amr_an":"694","tg_amr_af":"0.0259","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"68","tg_all_an":"5008","tg_all_af":"0.0135783","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266030","variation":"chr11:110054622:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8663C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs151274100","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"6","tg_afr_an":"1322","tg_afr_af":"0.0045","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"3","tg_eas_an":"1008","tg_eas_af":"0.003","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"9","tg_all_an":"5008","tg_all_af":"0.00179712","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266031","variation":"chr11:110054631:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8672C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs549344678","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"2","tg_afr_an":"1322","tg_afr_af":"0.0015","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266032","variation":"chr11:110054641:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8682T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs757703216","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266033","variation":"chr11:110054682:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8723C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs571482835","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266034","variation":"chr11:110054683:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8724A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs532425526","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266035","variation":"chr11:110054685:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8726C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs768012930","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266036","variation":"chr11:110054722:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8763A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs182041850","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266037","variation":"chr11:110054734:A>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8775T>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs565869381","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266038","variation":"chr11:110054773:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8814A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs536418774","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"2","tg_sas_an":"978","tg_sas_af":"0.002","tg_all_ac":"2","tg_all_an":"5008","tg_all_af":"0.000399361","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266039","variation":"chr11:110054775:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8816A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs746405452","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266040","variation":"chr11:110054792:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8833T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs17110940","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"251","tg_afr_an":"1322","tg_afr_af":"0.1899","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"21","tg_amr_an":"694","tg_amr_af":"0.0303","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"272","tg_all_an":"5008","tg_all_af":"0.0543131","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266041","variation":"chr11:110054882:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8923C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs780227175","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266042","variation":"chr11:110054888:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8929C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs567744212","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266043","variation":"chr11:110054891:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8932C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs144367762","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"1","tg_eur_an":"1006","tg_eur_af":"0.001","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"3","tg_all_an":"5008","tg_all_af":"0.000599042","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266044","variation":"chr11:110054896:T>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8937A>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs371971124","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266045","variation":"chr11:110054906:A>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-8947T>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs796901014","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266046","variation":"chr11:110054972:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9013C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs147854560","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"5","tg_afr_an":"1322","tg_afr_af":"0.0038","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"5","tg_all_an":"5008","tg_all_af":"0.000998403","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266047","variation":"chr11:110054987:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9028G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs578221737","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266048","variation":"chr11:110054988:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9029C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs141409818","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"11","tg_afr_an":"1322","tg_afr_af":"0.0083","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"12","tg_all_an":"5008","tg_all_af":"0.00239617","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266049","variation":"chr11:110055043:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9084G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs7120342","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"38","tg_afr_an":"1322","tg_afr_af":"0.0287","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"3","tg_amr_an":"694","tg_amr_af":"0.0043","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"41","tg_all_an":"5008","tg_all_af":"0.0081869","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266050","variation":"chr11:110055075:C>G","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9116G>C","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs572319607","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"1","tg_afr_an":"1322","tg_afr_af":"0.0008","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266051","variation":"chr11:110055078:C>T","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9119G>A","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs542782875","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"1","tg_eas_an":"1008","tg_eas_af":"0.001","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266052","variation":"chr11:110055115:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9156A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Benign","disease":null,"pubmed_id":null,"dbsnp":"rs17110941","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"250","tg_afr_an":"1322","tg_afr_af":"0.1891","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"21","tg_amr_an":"694","tg_amr_af":"0.0303","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"271","tg_all_an":"5008","tg_all_af":"0.0541134","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266053","variation":"chr11:110055118:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9159C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs768988227","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":null,"tg_afr_an":null,"tg_afr_af":null,"tg_eur_ac":null,"tg_eur_an":null,"tg_eur_af":null,"tg_amr_ac":null,"tg_amr_an":null,"tg_amr_af":null,"tg_eas_ac":null,"tg_eas_an":null,"tg_eas_af":null,"tg_sas_ac":null,"tg_sas_an":null,"tg_sas_af":null,"tg_all_ac":null,"tg_all_an":null,"tg_all_af":null,"exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266054","variation":"chr11:110055144:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9185C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs183949890","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"1","tg_amr_an":"694","tg_amr_af":"0.0014","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"0","tg_sas_an":"978","tg_sas_af":"0","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266055","variation":"chr11:110055145:T>C","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9186A>G","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs543088310","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":null,"mutationtaster_score":null,"mutationtaster_pred":null,"gerp_nr":null,"gerp_rs":null,"gerp_pred":null,"evs_ea_ac":null,"evs_ea_an":null,"evs_ea_af":null,"evs_aa_ac":null,"evs_aa_an":null,"evs_aa_af":null,"evs_all_ac":null,"evs_all_an":null,"evs_all_af":null,"otoscope_aj_ac":null,"otoscope_aj_an":null,"otoscope_aj_af":null,"otoscope_co_ac":null,"otoscope_co_an":null,"otoscope_co_af":null,"otoscope_us_ac":null,"otoscope_us_an":null,"otoscope_us_af":null,"otoscope_jp_ac":null,"otoscope_jp_an":null,"otoscope_jp_af":null,"otoscope_es_ac":null,"otoscope_es_an":null,"otoscope_es_af":null,"otoscope_tr_ac":null,"otoscope_tr_an":null,"otoscope_tr_af":null,"otoscope_all_ac":null,"otoscope_all_an":null,"otoscope_all_af":null,"tg_afr_ac":"0","tg_afr_an":"1322","tg_afr_af":"0","tg_eur_ac":"0","tg_eur_an":"1006","tg_eur_af":"0","tg_amr_ac":"0","tg_amr_an":"694","tg_amr_af":"0","tg_eas_ac":"0","tg_eas_an":"1008","tg_eas_af":"0","tg_sas_ac":"1","tg_sas_an":"978","tg_sas_af":"0.001","tg_all_ac":"1","tg_all_an":"5008","tg_all_af":"0.000199681","exac_afr_ac":null,"exac_afr_an":null,"exac_afr_af":null,"exac_amr_ac":null,"exac_amr_an":null,"exac_amr_af":null,"exac_eas_ac":null,"exac_eas_an":null,"exac_eas_af":null,"exac_fin_ac":null,"exac_fin_an":null,"exac_fin_af":null,"exac_nfe_ac":null,"exac_nfe_an":null,"exac_nfe_af":null,"exac_oth_ac":null,"exac_oth_an":null,"exac_oth_af":null,"exac_sas_ac":null,"exac_sas_an":null,"exac_sas_af":null,"exac_all_ac":null,"exac_all_an":null,"exac_all_af":null},{"id":"266056","variation":"chr11:110055150:G>A","gene":"RDX","hgvs_protein_change":null,"hgvs_nucleotide_change":"NM_001260493:c.*32-9191C>T","variantlocale":"THREE_PRIME_INTRON","pathogenicity":"Unknown significance","disease":null,"pubmed_id":null,"dbsnp":"rs564891244","summary_insilico":null,"summary_frequency":null,"summary_published":null,"comments":"This variant is a VUS because it does not have enough information.","lrt_omega":null,"phylop_score":null,"phylop_pred":null,"sift_score":null,"sift_pred":null,"polyphen2_score":null,"polyphen2_pred":null,"lrt_score":null,"lrt_pred":nu