id variation gene hgvs_protein_change hgvs_nucleotide_change variantlocale pathogenicity disease pubmed_id dbsnp summary_insilico summary_frequency summary_published comments lrt_omega phylop_score phylop_pred sift_score sift_pred polyphen2_score polyphen2_pred lrt_score lrt_pred mutationtaster_score mutationtaster_pred gerp_nr gerp_rs gerp_pred evs_ea_ac evs_ea_an evs_ea_af evs_aa_ac evs_aa_an evs_aa_af evs_all_ac evs_all_an evs_all_af otoscope_aj_ac otoscope_aj_an otoscope_aj_af otoscope_co_ac otoscope_co_an otoscope_co_af otoscope_us_ac otoscope_us_an otoscope_us_af otoscope_jp_ac otoscope_jp_an otoscope_jp_af otoscope_es_ac otoscope_es_an otoscope_es_af otoscope_tr_ac otoscope_tr_an otoscope_tr_af otoscope_all_ac otoscope_all_an otoscope_all_af tg_afr_ac tg_afr_an tg_afr_af tg_eur_ac tg_eur_an tg_eur_af tg_amr_ac tg_amr_an tg_amr_af tg_eas_ac tg_eas_an tg_eas_af tg_sas_ac tg_sas_an tg_sas_af tg_all_ac tg_all_an tg_all_af exac_afr_ac exac_afr_an exac_afr_af exac_amr_ac exac_amr_an exac_amr_af exac_eas_ac exac_eas_an exac_eas_af exac_fin_ac exac_fin_an exac_fin_af exac_nfe_ac exac_nfe_an exac_nfe_af exac_oth_ac exac_oth_ant exac_oth_af exac_sas_ac exac_sas_an exac_sas_af exac_all_ac exac_all_an exac_all_af
307450 "chr12:80838125:G>A" "PTPRQ" "NM_001145026:c.0G>A" "FIVE_PRIME_FLANK" "Unknown significance" "rs538419954" "This variant is a VUS because it does not have enough information." 1 2122 0.000471254 0 406 0 0 614 0 0 34 0 5 8404 0.000594955 0 190 0 1 7898 0.000126614 7 19668 0.000355908
307451 "chr12:80838153:C>T" "PTPRQ" "NM_001145026:p.Leu10Phe" "NM_001145026:c.28C>T" "EXON1" "Unknown significance" "rs553967336" "This variant is a VUS because it does not have enough information." 0.062 "N" 0.999904 "N" "1.87" "C" 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307452 "chr12:80838154:T>C" "PTPRQ" "NM_001145026:p.Leu10Pro" "NM_001145026:c.29T>C" "EXON1" "Unknown significance" "rs762742378" "This variant is a VUS because it does not have enough information." 0.125 "N" 0.997629 "D" "4.66" "C"
307453 "chr12:80838164:G>C" "PTPRQ" "NM_001145026:p.Gly13Gly" "NM_001145026:c.39G>C" "EXON1" "Unknown significance" "rs571284105" "This variant is a VUS because it does not have enough information." 0 2112 0 0 402 0 0 614 0 0 32 0 1 8386 0.000119246 0 190 0 0 7900 0 1 19636 0.0000509269
307454 "chr12:80838175:C>T" "PTPRQ" "NM_001145026:p.Thr17Ile" "NM_001145026:c.50C>T" "EXON1" "Benign" "rs60216135" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.045 "N" 0.999986 "P" "3.9" "C" 16 400 0.04 34 320 0.10625 9 320 0.028125 31 400 0.0775 8 360 0.0222222 3 200 0.015 101 2000 0.0505 387 1322 0.2927 21 1006 0.0209 62 694 0.0893 37 1008 0.0367 101 978 0.1033 608 5008 0.121406 525 2102 0.249762 31 400 0.0775 24 614 0.0390879 2 32 0.0625 168 8380 0.0200477 13 190 0.0684211 704 7900 0.0891139 1467 19618 0.0747783
307455 "chr12:80838182:A>G" "PTPRQ" "NM_001145026:c.54+3A>G" "INTRON1" "Pathogenic" "Non-syndromic deafness, autosomal recessive, DFNB84A" "26969326" "rs778471583" 0 2094 0 0 398 0 0 612 0 0 32 0 1 8376 0.000119389 0 190 0 0 7896 0 1 19598 0.0000510256
307456 "chr12:80838186:C>T" "PTPRQ" "NM_001145026:c.54+7C>T" "INTRON1" "Unknown significance" "rs750110116" "This variant is a VUS because it does not have enough information." 1 400 0.0025 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 1 2000 0.0005 3 2094 0.00143266 0 398 0 0 612 0 0 32 0 2 8374 0.000238834 0 188 0 1 7898 0.000126614 6 19596 0.000306185
307457 "chr12:80838187:G>A" "PTPRQ" "NM_001145026:c.54+8G>A" "INTRON1" "Unknown significance" "rs372908419" "This variant is a VUS because it does not have enough information." 0 3180 0 2 1384 0.00144509 2 4564 0.000438212 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042 3 2092 0.00143403 0 398 0 0 612 0 0 32 0 1 8368 0.000119503 0 188 0 1 7892 0.000126711 5 19582 0.000255337
307458 "chr12:80838213:A>G" "PTPRQ" "NM_001145026:c.54+34A>G" "INTRON1" "Unknown significance" "rs554531597" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 2090 0.000478469 0 398 0 0 612 0 0 32 0 0 8354 0 0 188 0 0 7890 0 1 19564 0.0000511143
307459 "chr12:80838251:G>T" "PTPRQ" "NM_001145026:c.54+72G>T" "INTRON1" "Unknown significance" "rs373778372" "This variant is a VUS because it does not have enough information."
307460 "chr12:80838257:T>C" "PTPRQ" "NM_001145026:c.54+78T>C" "INTRON1" "Unknown significance" "rs575986955" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307461 "chr12:80838258:G>A" "PTPRQ" "NM_001145026:c.54+79G>A" "INTRON1" "Unknown significance" "rs553661471" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307462 "chr12:80838306:C>T" "PTPRQ" "NM_001145026:c.54+127C>T" "INTRON1" "Unknown significance" "rs559382274" "This variant is a VUS because it does not have enough information."
307463 "chr12:80838307:G>A" "PTPRQ" "NM_001145026:c.54+128G>A" "INTRON1" "Unknown significance" "rs756143041" "This variant is a VUS because it does not have enough information."
307464 "chr12:80838308:C>T" "PTPRQ" "NM_001145026:c.54+129C>T" "INTRON1" "Unknown significance" "rs565204614" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307465 "chr12:80838313:C>T" "PTPRQ" "NM_001145026:c.54+134C>T" "INTRON1" "Unknown significance" "rs577286716" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
307466 "chr12:80838355:->ATATG" "PTPRQ" "NM_001145026:c.55-166_55-165insATATG" "INTRON1" "Benign" "rs112125750" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 577 1322 0.4365 71 1006 0.0706 61 694 0.0879 0 1008 0 49 978 0.0501 758 5008 0.151358
307467 "chr12:80838359:A>G" "PTPRQ" "NM_001145026:c.55-162A>G" "INTRON1" "Unknown significance" "rs201307498" "This variant is a VUS because it does not have enough information."
307468 "chr12:80838380:A>G" "PTPRQ" "NM_001145026:c.55-141A>G" "INTRON1" "Unknown significance" "rs754373298" "This variant is a VUS because it does not have enough information."
307469 "chr12:80838391:T>A" "PTPRQ" "NM_001145026:c.55-130T>A" "INTRON1" "Unknown significance" "rs184246077" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307470 "chr12:80838440:T>G" "PTPRQ" "NM_001145026:c.55-81T>G" "INTRON1" "Unknown significance" "rs73143190" "This variant is a VUS because it does not have enough information."
307471 "chr12:80838497:A>G" "PTPRQ" "NM_001145026:c.55-24A>G" "INTRON1" "Unknown significance" "rs374547044" "This variant is a VUS because it does not have enough information."
307472 "chr12:80838499:C>A" "PTPRQ" "NM_001145026:c.55-22C>A" "INTRON1" "Unknown significance" "rs747325115" "This variant is a VUS because it does not have enough information." 0 2146 0 0 410 0 0 622 0 0 34 0 1 8474 0.000118008 0 190 0 0 7910 0 1 19786 0.0000505408
307473 "chr12:80838501:A>G" "PTPRQ" "NM_001145026:c.55-20A>G" "INTRON1" "Unknown significance" "rs559926582" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042 0 2146 0 0 410 0 0 622 0 0 34 0 0 8474 0 0 190 0 14 7912 0.00176946 14 19788 0.000707499
307474 "chr12:80838531:C>T" "PTPRQ" "NM_001145026:p.Ser22Phe" "NM_001145026:c.65C>T" "EXON2" "Likely benign" "rs781735530" "Pathogenicity is based on prediction data only. 1 out of 5 predictions were pathogenic." -0.347 "N" "0.993;0.088;0.806;.;." "T;T;T;.;." "0.003" "B" 0.999938 "N" "1.99" "C"
307475 "chr12:80838538:C>T" "PTPRQ" "NM_001145026:p.Val24Val" "NM_001145026:c.72C>T" "EXON2" "Unknown significance" "rs542507106" "This variant is a VUS because it does not have enough information."
307476 "chr12:80838557:G>A" "PTPRQ" "NM_001145026:p.Asp31Asn" "NM_001145026:c.91G>A" "EXON2" "Likely benign" "rs530416889" "Pathogenicity is based on prediction data only. 2 out of 5 predictions were pathogenic." 1.036 "C" "0.432;0.488;0.558;.;." "T;T;T;.;." "0.002" "B" 1 "N" "1.33" "C" 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307477 "chr12:80838558:A>T" "PTPRQ" "NM_001145026:p.Asp31Val" "NM_001145026:c.92A>T" "EXON2" "Likely benign" "rs368090643" "Pathogenicity is based on prediction data only. 1 out of 5 predictions were pathogenic." -0.138 "N" "0.218;0.283;0.299;.;." "T;T;T;.;." "0.081" "B" 1 "N" "4.67" "C"
307478 "chr12:80838564:C>T" "PTPRQ" "NM_001145026:p.Thr33Ile" "NM_001145026:c.98C>T" "EXON2" "Benign" "rs78857302" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.925 "N" "0.014;0.54;0.029;.;." "D;T;D;.;." "1.0" "D" 0.961681 "D" "4.94" "C" 61 3182 0.0191703 43 1384 0.0310694 104 4566 0.022777 10 400 0.025 27 320 0.084375 9 320 0.028125 35 400 0.0875 7 360 0.0194444 2 200 0.01 90 2000 0.045 47 1322 0.0356 21 1006 0.0209 45 694 0.0648 37 1008 0.0367 101 978 0.1033 251 5008 0.0501198 87 2146 0.0405405 26 410 0.0634146 24 622 0.0385852 2 34 0.0588235 137 8478 0.0161595 9 190 0.0473684 702 7912 0.088726 987 19792 0.0498686
307479 "chr12:80838564:C>A" "PTPRQ" "NM_001145026:p.Thr33Asn" "NM_001145026:c.98C>A" "EXON2" "Unknown significance" "rs78857302" "This variant is a VUS because it does not have enough information." 0.925 "N" "0.005;0.136;0.251;.;." "D;T;T;.;." "1.0" "D" 0.955524 "D" "4.94" "C" 0 2146 0 0 410 0 0 622 0 0 34 0 1 8478 0.000117952 0 190 0 0 7912 0 1 19792 0.0000505255
307480 "chr12:80838587:T>C" "PTPRQ" "NM_001145026:p.Tyr41His" "NM_001145026:c.121T>C" "EXON2" "Unknown significance" "rs369812501" "This variant is a VUS because it does not have enough information." 1.049 "C" "0.3;0.006;0.54;.;." "T;D;T;.;." "0.975" "D" 1 "N" "3.41" "C" 1 3182 0.000314268 0 1384 0 1 4566 0.00021901 0 2146 0 0 410 0 0 622 0 0 34 0 1 8474 0.000118008 0 190 0 0 7910 0 1 19786 0.0000505408
307481 "chr12:80838608:A>C" "PTPRQ" "NM_001145026:p.Ile48Leu" "NM_001145026:c.142A>C" "EXON2" "Likely benign" "rs771093567" "Pathogenicity is based on prediction data only. 2 out of 5 predictions were pathogenic." 1.184 "C" "0.12;0.142;0.227;.;." "T;T;T;.;." "0.0" "B" 0.999723 "N" "4.67" "C" 0 2146 0 0 410 0 0 622 0 0 34 0 0 8470 0 0 190 0 1 7910 0.000126422 1 19782 0.000050551
307482 "chr12:80838609:T>C" "PTPRQ" "NM_001145026:p.Ile48Thr" "NM_001145026:c.143T>C" "EXON2" "Likely benign" "rs779591577" "Pathogenicity is based on prediction data only. 1 out of 5 predictions were pathogenic." 0.055 "N" "1.0;1.0;0.461;.;." "T;T;T;.;." "0.0" "B" 0.998924 "N" "2.61" "C"
307483 "chr12:80838611:GTGACAACAAAT>-" "PTPRQ" "NM_001145026:c.145_156delGTGACAACAAAT" "EXON2" "Unknown significance" "rs368946018" "This variant is a VUS because it does not have enough information."
307484 "chr12:80838615:C>T" "PTPRQ" "NM_001145026:p.Thr50Ile" "NM_001145026:c.149C>T" "EXON2" "Likely benign" "rs775295841" "Pathogenicity is based on prediction data only. 1 out of 5 predictions were pathogenic." 0.925 "N" "0.064;0.307;0.513;.;." "T;T;T;.;." "0.017" "B" 0.999337 "N" "4.94" "C" 0 2146 0 0 410 0 1 622 0.00160772 0 34 0 0 8460 0 0 190 0 0 7910 0 1 19772 0.0000505766
307485 "chr12:80838648:T>C" "PTPRQ" "NM_001145026:c.163+19T>C" "INTRON2" "Unknown significance" "rs760396351" "This variant is a VUS because it does not have enough information." 0 2146 0 0 410 0 0 622 0 0 34 0 0 8448 0 0 190 0 1 7908 0.000126454 1 19758 0.0000506124
307486 "chr12:80838649:T>G" "PTPRQ" "NM_001145026:c.163+20T>G" "INTRON2" "Unknown significance" "rs764030443" "This variant is a VUS because it does not have enough information." 0 2146 0 0 410 0 0 622 0 0 34 0 1 8444 0.000118427 0 190 0 0 7906 0 1 19752 0.0000506278
307487 "chr12:80838654:T>C" "PTPRQ" "NM_001145026:c.163+25T>C" "INTRON2" "Unknown significance" "rs551750005" "This variant is a VUS because it does not have enough information."
307488 "chr12:80838675:C>T" "PTPRQ" "NM_001145026:c.163+46C>T" "INTRON2" "Unknown significance" "rs371767925" "This variant is a VUS because it does not have enough information."
307489 "chr12:80838716:T>C" "PTPRQ" "NM_001145026:c.163+87T>C" "INTRON2" "Benign" "rs74625318" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 1 978 0.001 41 5008 0.0081869
307490 "chr12:80838746:A>G" "PTPRQ" "NM_001145026:c.163+117A>G" "INTRON2" "Unknown significance" "rs531285757" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307491 "chr12:80838786:C>T" "PTPRQ" "NM_001145026:c.163+157C>T" "INTRON2" "Unknown significance" "rs549770980" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307492 "chr12:80838790:A>G" "PTPRQ" "NM_001145026:c.163+161A>G" "INTRON2" "Benign" "rs56711652" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 540 1322 0.4085 71 1006 0.0706 58 694 0.0836 0 1008 0 49 978 0.0501 718 5008 0.143371
307493 "chr12:80838822:A>G" "PTPRQ" "NM_001145026:c.163+193A>G" "INTRON2" "Unknown significance" "rs772496024" "This variant is a VUS because it does not have enough information."
307494 "chr12:80838837:->T" "PTPRQ" "NM_001145026:c.163+208_163+209insT" "INTRON2" "Unknown significance" "rs528260554" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
307495 "chr12:80838885:A>G" "PTPRQ" "NM_001145026:c.163+256A>G" "INTRON2" "Benign" "rs60520650" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 539 1322 0.4077 71 1006 0.0706 58 694 0.0836 0 1008 0 49 978 0.0501 717 5008 0.143171
307496 "chr12:80838886:C>T" "PTPRQ" "NM_001145026:c.163+257C>T" "INTRON2" "Benign" "rs78776778" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 32 1322 0.0242 0 1006 0 0 694 0 0 1008 0 0 978 0 32 5008 0.00638978
307497 "chr12:80838991:C>T" "PTPRQ" "NM_001145026:c.164-280C>T" "INTRON2" "Unknown significance" "rs371759807" "This variant is a VUS because it does not have enough information."
307498 "chr12:80838995:G>A" "PTPRQ" "NM_001145026:c.164-276G>A" "INTRON2" "Unknown significance" "rs373818915" "This variant is a VUS because it does not have enough information."
307499 "chr12:80838997:G>A" "PTPRQ" "NM_001145026:c.164-274G>A" "INTRON2" "Unknown significance" "rs565578338" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307500 "chr12:80839021:A>G" "PTPRQ" "NM_001145026:c.164-250A>G" "INTRON2" "Unknown significance" "rs567882044" "This variant is a VUS because it does not have enough information."
307501 "chr12:80839024:T>C" "PTPRQ" "NM_001145026:c.164-247T>C" "INTRON2" "Unknown significance" "rs746718919" "This variant is a VUS because it does not have enough information."
307502 "chr12:80839030:C>T" "PTPRQ" "NM_001145026:c.164-241C>T" "INTRON2" "Unknown significance" "rs536044803" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307503 "chr12:80839064:A>G" "PTPRQ" "NM_001145026:c.164-207A>G" "INTRON2" "Unknown significance" "rs551601043" "This variant is a VUS because it does not have enough information."
307504 "chr12:80839114:T>C" "PTPRQ" "NM_001145026:c.164-157T>C" "INTRON2" "Unknown significance" "rs527297905" "This variant is a VUS because it does not have enough information."
307505 "chr12:80839131:T>C" "PTPRQ" "NM_001145026:c.164-140T>C" "INTRON2" "Benign" "rs142077279" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 36 5008 0.0071885
307506 "chr12:80839139:C>A" "PTPRQ" "NM_001145026:c.164-132C>A" "INTRON2" "Unknown significance" "rs575949786" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307507 "chr12:80839151:T>C" "PTPRQ" "NM_001145026:c.164-120T>C" "INTRON2" "Unknown significance" "rs540986020" "This variant is a VUS because it does not have enough information."
307508 "chr12:80839220:A>T" "PTPRQ" "NM_001145026:c.164-51A>T" "INTRON2" "Benign" "rs60509052" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 245 1322 0.1853 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 263 5008 0.052516
307509 "chr12:80839290:C>T" "PTPRQ" "NM_001145026:p.Phe61Phe" "NM_001145026:c.183C>T" "EXON3" "Unknown significance" "rs768055115" "This variant is a VUS because it does not have enough information."
307510 "chr12:80839295:C>-" "PTPRQ" "NM_001145026:c.188delC" "EXON3" "Unknown significance" "rs773511370" "This variant is a VUS because it does not have enough information." 0 1792 0 0 268 0 0 400 0 0 6 0 0 7420 0 0 180 0 1 7752 0.000128999 1 17818 0.000056123
307511 "chr12:80839296:C>T" "PTPRQ" "NM_001145026:p.Ala63Ala" "NM_001145026:c.189C>T" "EXON3" "Unknown significance" "rs558947480" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 1810 0 0 268 0 0 406 0 0 6 0 1 7480 0.00013369 0 182 0 0 7762 0 1 17914 0.0000558223
307512 "chr12:80839302:A>G" "PTPRQ" "NM_001145026:p.Glu65Glu" "NM_001145026:c.195A>G" "EXON3" "Unknown significance" "rs577247628" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307513 "chr12:80839303:A>G" "PTPRQ" "NM_001145026:p.Arg66Gly" "NM_001145026:c.196A>G" "EXON3" "Unknown significance" "rs761805006" "This variant is a VUS because it does not have enough information." 1.126 "C" "0.03;.;." "D;.;." "0.98" "D" 0.96505 "D" "4.65" "C" 0 1846 0 0 284 0 0 432 0 0 8 0 0 7620 0 0 184 0 1 7804 0.000128139 1 18178 0.0000550116
307514 "chr12:80839308:C>T" "PTPRQ" "NM_001145026:p.Val67Val" "NM_001145026:c.201C>T" "EXON3" "Benign" "rs187435968" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 3180 0 10 1384 0.00722543 10 4564 0.00219106 13 1322 0.0098 1 1006 0.001 0 694 0 0 1008 0 0 978 0 14 5008 0.00279553 17 1880 0.00904255 0 290 0 0 456 0 0 10 0 0 7730 0 0 188 0 0 7810 0 17 18364 0.000925724
307515 "chr12:80839309:G>A" "PTPRQ" "NM_001145026:p.Gly68Arg" "NM_001145026:c.202G>A" "EXON3" "Benign" "rs61729303" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.985 "C" "0.0;.;." "D;.;." "1.0" "D" 0.999987 "D" "5.83" "C" 0 3180 0 4 1384 0.00289017 4 4564 0.000876424 0 400 0 6 320 0.01875 0 320 0 0 400 0 0 360 0 0 200 0 6 2000 0.003 0 1322 0 0 1006 0 17 694 0.0245 0 1008 0 0 978 0 17 5008 0.00339457 6 1884 0.00318471 12 302 0.0397351 0 460 0 0 10 0 1 7752 0.000128999 0 188 0 0 7816 0 19 18412 0.00103194
307516 "chr12:80839313:C>G" "PTPRQ" "NM_001145026:p.Ser69Cys" "NM_001145026:c.206C>G" "EXON3" "Benign" "rs61729302" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.881 "N" "0.0;.;." "D;.;." "1.0" "D" 0.9999 "D" "5.83" "C" 0 3180 0 21 1384 0.0151734 21 4564 0.00460123 30 1322 0.0227 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 33 5008 0.00658946 29 1910 0.0151832 0 310 0 0 486 0 0 12 0 0 7814 0 0 188 0 0 7832 0 29 18552 0.00156317
307517 "chr12:80839313:C>A" "PTPRQ" "NM_001145026:p.Ser69Tyr" "NM_001145026:c.206C>A" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 0.881 "N" "0.0;.;." "D;.;." "1.0" "D" 0.999943 "D" "5.83" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
307518 "chr12:80839318:G>A" "PTPRQ" "NM_001145026:p.Gly71Arg" "NM_001145026:c.211G>A" "EXON3" "Unknown significance" "rs766087465" "This variant is a VUS because it does not have enough information." 0.985 "C" "0.0;.;." "D;.;." "1.0" "D" 0.999985 "D" "5.83" "C" 0 1916 0 0 320 0 0 508 0 0 12 0 1 7902 0.00012655 0 188 0 0 7842 0 1 18688 0.0000535103
307519 "chr12:80839332:T>C" "PTPRQ" "NM_001145026:p.Ser75Ser" "NM_001145026:c.225T>C" "EXON3" "Unknown significance" "rs767425598" "This variant is a VUS because it does not have enough information."
307520 "chr12:80839350:T>C" "PTPRQ" "NM_001145026:p.Asn81Asn" "NM_001145026:c.243T>C" "EXON3" "Unknown significance" "rs769654922" "This variant is a VUS because it does not have enough information."
307521 "chr12:80839362:G>A" "PTPRQ" "NM_001145026:p.Arg85Arg" "NM_001145026:c.255G>A" "EXON3" "Benign" "rs184871373" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 400 0 0 320 0 0 320 0 0 400 0 1 360 0.00277778 0 200 0 1 2000 0.0005 0 1322 0 3 1006 0.003 1 694 0.0014 0 1008 0 0 978 0 4 5008 0.000798722 0 2016 0 0 362 0 0 590 0 1 34 0.0294118 5 8098 0.000617436 0 190 0 1 7872 0.000127033 7 19162 0.000365306
307522 "chr12:80839363:A>T" "PTPRQ" "NM_001145026:p.Ile86Phe" "NM_001145026:c.256A>T" "EXON3" "Unknown significance" "rs763472295" "This variant is a VUS because it does not have enough information." 1.126 "C" "0.0;.;." "D;.;." "0.999" "D" 0.999441 "D" "5.72" "C"
307523 "chr12:80839372:T>G" "PTPRQ" "NM_001145026:p.Tyr89Asp" "NM_001145026:c.265T>G" "EXON3" "Unknown significance" "rs755453927" "This variant is a VUS because it does not have enough information." 0.998 "C" "0.0;.;." "D;.;." "1.0" "D" 0.998541 "D" "5.72" "C" 0 2012 0 0 364 0 0 590 0 0 32 0 0 8100 0 0 190 0 1 7874 0.000127 1 19162 0.0000521866
307524 "chr12:80839393:G>A" "PTPRQ" "NM_001145026:p.Val96Ile" "NM_001145026:c.286G>A" "EXON3" "Benign" "rs148527546" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.985 "C" "0.032;.;." "D;.;." "0.992" "D" 0.744938 "D" "4.83" "C" 0 3180 0 23 1384 0.0166185 23 4564 0.00503944 20 1322 0.0151 0 1006 0 0 694 0 0 1008 0 0 978 0 20 5008 0.00399361 32 2016 0.015873 0 366 0 0 594 0 0 32 0 0 8084 0 0 190 0 0 7874 0 32 19156 0.00167049
307525 "chr12:80839401:G>A" "PTPRQ" "NM_001145026:p.Pro98Pro" "NM_001145026:c.294G>A" "EXON3" "Unknown significance" "rs748647118" "This variant is a VUS because it does not have enough information." 0 2010 0 0 366 0 0 594 0 0 32 0 0 8088 0 0 190 0 2 7874 0.000254001 2 19154 0.000104417
307526 "chr12:80839427:T>A" "PTPRQ" "NM_001145026:p.Val107Asp" "NM_001145026:c.320T>A" "EXON3" "Benign" "rs531266049" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.998 "C" "0.002;.;." "D;.;." "0.879" "P" 0.999997 "D" "3.29" "C" 0 400 0 0 320 0 0 320 0 2 400 0.005 0 360 0 0 200 0 2 2000 0.001 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307527 "chr12:80839436:A>G" "PTPRQ" "NM_001145026:p.Lys110Arg" "NM_001145026:c.329A>G" "EXON3" "Unknown significance" "rs756626854" "This variant is a VUS because it does not have enough information." 1.126 "C" "0.286;.;." "T;.;." "0.979" "D" 0.759142 "D" "5.82" "C" 0 1988 0 0 362 0 1 590 0.00169492 0 32 0 0 8052 0 0 182 0 0 7872 0 1 19078 0.0000524164
307528 "chr12:80839459:C>T" "PTPRQ" "NM_001145026:p.Leu118Phe" "NM_001145026:c.352C>T" "EXON3" "Unknown significance" "rs777738298" "This variant is a VUS because it does not have enough information." 0.881 "N" "0.0;.;." "D;.;." "1.0" "D" 0.999592 "D" "5.82" "C" 0 1948 0 0 346 0 1 580 0.00172414 0 32 0 1 7910 0.000126422 0 178 0 0 7836 0 2 18830 0.000106213
307529 "chr12:80839492:A>T" "PTPRQ" "NM_001145026:p.Ile129Phe" "NM_001145026:c.385A>T" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 1.126 "C" "0.0;.;." "D;.;." "1.0" "D" 0.999993 "D" "5.82" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
307530 "chr12:80839494:T>C" "PTPRQ" "NM_001145026:p.Ile129Ile" "NM_001145026:c.387T>C" "EXON3" "Unknown significance" "rs749326611" "This variant is a VUS because it does not have enough information." 0 1852 0 0 334 0 0 564 0 0 32 0 0 7704 0 0 176 0 1 7802 0.000128172 1 18464 0.0000541594
307531 "chr12:80839499:T>A" "PTPRQ" "NM_001145026:p.Val131Glu" "NM_001145026:c.392T>A" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 0.998 "C" 0.999991 "D" "5.82" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
307532 "chr12:80839515:G>T" "PTPRQ" "NM_001145026:c.392+16G>T" "INTRON3" "Benign" "rs190463905" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 4 1006 0.004 2 694 0.0029 0 1008 0 1 978 0.001 7 5008 0.00139776 2 1790 0.00111732 1 322 0.00310559 0 552 0 0 30 0 77 7500 0.0102667 1 176 0.00568182 22 7746 0.00284018 103 18116 0.00568558
307533 "chr12:80839528:T>C" "PTPRQ" "NM_001145026:c.392+29T>C" "INTRON3" "Unknown significance" "rs564939738" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307534 "chr12:80839533:C>T" "PTPRQ" "NM_001145026:c.392+34C>T" "INTRON3" "Unknown significance" "rs764016474" "This variant is a VUS because it does not have enough information." 0 1670 0 0 294 0 0 530 0 0 30 0 1 7208 0.000138735 0 174 0 0 7688 0 1 17594 0.0000568376
307535 "chr12:80839535:T>G" "PTPRQ" "NM_001145026:c.392+36T>G" "INTRON3" "Unknown significance" "rs151025918" "This variant is a VUS because it does not have enough information." 0 1658 0 0 288 0 0 526 0 0 30 0 3 7186 0.000417478 0 176 0 1 7686 0.000130107 4 17550 0.00022792
307536 "chr12:80839549:A>G" "PTPRQ" "NM_001145026:c.392+50A>G" "INTRON3" "Unknown significance" "rs532097338" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 0 1584 0 0 280 0 0 512 0 0 28 0 1 7022 0.00014241 0 172 0 0 7604 0 1 17202 0.0000581328
307537 "chr12:80839583:T>C" "PTPRQ" "NM_001145026:c.392+84T>C" "INTRON3" "Unknown significance" "rs761005570" "This variant is a VUS because it does not have enough information."
307538 "chr12:80839669:A>T" "PTPRQ" "NM_001145026:c.392+170A>T" "INTRON3" "Unknown significance" "rs139658553" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307539 "chr12:80839676:C>T" "PTPRQ" "NM_001145026:c.392+177C>T" "INTRON3" "Unknown significance" "rs13378038" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 1 1008 0.001 0 978 0 2 5008 0.000399361
307540 "chr12:80839779:C>T" "PTPRQ" "NM_001145026:c.392+280C>T" "INTRON3" "Unknown significance" "rs549349553" "This variant is a VUS because it does not have enough information."
307541 "chr12:80839800:A>C" "PTPRQ" "NM_001145026:c.392+301A>C" "INTRON3" "Unknown significance" "rs182134475" "This variant is a VUS because it does not have enough information."
307542 "chr12:80839825:C>G" "PTPRQ" "NM_001145026:c.392+326C>G" "INTRON3" "Benign" "rs7311006" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 563 1322 0.4259 252 1006 0.2505 167 694 0.2406 40 1008 0.0397 203 978 0.2076 1225 5008 0.244609
307543 "chr12:80839856:G>A" "PTPRQ" "NM_001145026:c.392+357G>A" "INTRON3" "Unknown significance" "rs547995201" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307544 "chr12:80839885:A>G" "PTPRQ" "NM_001145026:c.392+386A>G" "INTRON3" "Unknown significance" "rs569602716" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307545 "chr12:80839900:G>T" "PTPRQ" "NM_001145026:c.392+401G>T" "INTRON3" "Unknown significance" "rs531718311" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 4 1006 0.004 0 694 0 0 1008 0 2 978 0.002 7 5008 0.00139776
307546 "chr12:80839901:C>G" "PTPRQ" "NM_001145026:c.392+402C>G" "INTRON3" "Unknown significance" "rs558678923" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307547 "chr12:80839927:A>G" "PTPRQ" "NM_001145026:c.392+428A>G" "INTRON3" "Benign" "rs7296335" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 563 1322 0.4259 249 1006 0.2475 165 694 0.2378 41 1008 0.0407 204 978 0.2086 1222 5008 0.24401
307548 "chr12:80839958:T>C" "PTPRQ" "NM_001145026:c.392+459T>C" "INTRON3" "Benign" "rs144515164" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 27 1322 0.0204 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 28 5008 0.00559105
307549 "chr12:80839967:C>T" "PTPRQ" "NM_001145026:c.392+468C>T" "INTRON3" "Benign" "rs7311157" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1135 1322 0.8585 323 1006 0.3211 227 694 0.3271 40 1008 0.0397 251 978 0.2566 1976 5008 0.394569
307550 "chr12:80839968:G>C" "PTPRQ" "NM_001145026:c.392+469G>C" "INTRON3" "Unknown significance" "rs184334488" "This variant is a VUS because it does not have enough information."
307551 "chr12:80840007:->TT" "PTPRQ" "NM_001145026:c.392+508_392+509insTT" "INTRON3" "Benign" "rs530783702" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 174 1322 0.1316 230 1006 0.2286 109 694 0.1571 4 1008 0.004 103 978 0.1053 620 5008 0.123802
307552 "chr12:80840049:G>A" "PTPRQ" "NM_001145026:c.392+550G>A" "INTRON3" "Benign" "rs73143194" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 102 978 0.1043 616 5008 0.123003
307553 "chr12:80840066:T>C" "PTPRQ" "NM_001145026:c.392+567T>C" "INTRON3" "Unknown significance" "rs542407761" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307554 "chr12:80840186:T>C" "PTPRQ" "NM_001145026:c.392+687T>C" "INTRON3" "Benign" "rs59243263" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 236 5008 0.0471246
307555 "chr12:80840221:T>A" "PTPRQ" "NM_001145026:c.392+722T>A" "INTRON3" "Benign" "rs78809205" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 71 1006 0.0706 32 694 0.0461 0 1008 0 48 978 0.0491 158 5008 0.0315495
307556 "chr12:80840269:T>C" "PTPRQ" "NM_001145026:c.392+770T>C" "INTRON3" "Unknown significance" "rs571506177" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
307557 "chr12:80840284:T>C" "PTPRQ" "NM_001145026:c.392+785T>C" "INTRON3" "Unknown significance" "rs189234115" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
307558 "chr12:80840292:G>A" "PTPRQ" "NM_001145026:c.392+793G>A" "INTRON3" "Unknown significance" "rs532082693" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307559 "chr12:80840297:T>C" "PTPRQ" "NM_001145026:c.392+798T>C" "INTRON3" "Unknown significance" "rs540691420" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307560 "chr12:80840321:G>C" "PTPRQ" "NM_001145026:c.392+822G>C" "INTRON3" "Unknown significance" "rs558986144" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307561 "chr12:80840338:T>C" "PTPRQ" "NM_001145026:c.392+839T>C" "INTRON3" "Unknown significance" "rs756897595" "This variant is a VUS because it does not have enough information."
307562 "chr12:80840390:C>T" "PTPRQ" "NM_001145026:c.392+891C>T" "INTRON3" "Benign" "rs74701794" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 53 1322 0.0401 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 59 5008 0.0117812
307563 "chr12:80840447:G>A" "PTPRQ" "NM_001145026:c.392+948G>A" "INTRON3" "Unknown significance" "rs370004538" "This variant is a VUS because it does not have enough information."
307564 "chr12:80840453:G>A" "PTPRQ" "NM_001145026:c.392+954G>A" "INTRON3" "Unknown significance" "rs547963398" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
307565 "chr12:80840507:G>A" "PTPRQ" "NM_001145026:c.392+1008G>A" "INTRON3" "Unknown significance" "rs11114443" "This variant is a VUS because it does not have enough information."
307566 "chr12:80840510:C>-" "PTPRQ" "NM_001145026:c.392+1011delC" "INTRON3" "Benign" "rs112211776" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 71 1006 0.0706 34 694 0.049 0 1008 0 48 978 0.0491 187 5008 0.0373403
307567 "chr12:80840549:T>C" "PTPRQ" "NM_001145026:c.392+1050T>C" "INTRON3" "Unknown significance" "rs181139033" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307568 "chr12:80840550:G>A" "PTPRQ" "NM_001145026:c.392+1051G>A" "INTRON3" "Unknown significance" "rs745326256" "This variant is a VUS because it does not have enough information."
307569 "chr12:80840568:G>T" "PTPRQ" "NM_001145026:c.392+1069G>T" "INTRON3" "Unknown significance" "rs530708666" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307570 "chr12:80840571:G>A" "PTPRQ" "NM_001145026:c.392+1072G>A" "INTRON3" "Unknown significance" "rs552409884" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307571 "chr12:80840601:G>A" "PTPRQ" "NM_001145026:c.392+1102G>A" "INTRON3" "Unknown significance" "rs570658785" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307572 "chr12:80840637:G>T" "PTPRQ" "NM_001145026:c.392+1138G>T" "INTRON3" "Unknown significance" "rs373016028" "This variant is a VUS because it does not have enough information."
307573 "chr12:80840660:G>A" "PTPRQ" "NM_001145026:c.392+1161G>A" "INTRON3" "Unknown significance" "rs534990822" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 2 5008 0.000399361
307574 "chr12:80840662:G>T" "PTPRQ" "NM_001145026:c.392+1163G>T" "INTRON3" "Unknown significance" "rs553420128" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307575 "chr12:80840667:G>A" "PTPRQ" "NM_001145026:c.392+1168G>A" "INTRON3" "Unknown significance" "rs185586190" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307576 "chr12:80840668:G>T" "PTPRQ" "NM_001145026:c.392+1169G>T" "INTRON3" "Unknown significance" "rs535999219" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
307577 "chr12:80840668:G>C" "PTPRQ" "NM_001145026:c.392+1169G>C" "INTRON3" "Unknown significance" "rs535999219" "This variant is a VUS because it does not have enough information."
307578 "chr12:80840691:C>A" "PTPRQ" "NM_001145026:c.392+1192C>A" "INTRON3" "Unknown significance" "rs113769020" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307579 "chr12:80840753:G>C" "PTPRQ" "NM_001145026:c.392+1254G>C" "INTRON3" "Unknown significance" "rs575752932" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307580 "chr12:80840767:C>T" "PTPRQ" "NM_001145026:c.392+1268C>T" "INTRON3" "Unknown significance" "rs376290915" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
307581 "chr12:80840770:C>T" "PTPRQ" "NM_001145026:c.392+1271C>T" "INTRON3" "Unknown significance" "rs201730046" "This variant is a VUS because it does not have enough information."
307582 "chr12:80840771:G>A" "PTPRQ" "NM_001145026:c.392+1272G>A" "INTRON3" "Benign" "rs7311270" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 904 1322 0.6838 323 1006 0.3211 220 694 0.317 40 1008 0.0397 251 978 0.2566 1738 5008 0.347045
307583 "chr12:80840814:A>C" "PTPRQ" "NM_001145026:c.392+1315A>C" "INTRON3" "Unknown significance" "rs761543655" "This variant is a VUS because it does not have enough information."
307584 "chr12:80840816:T>C" "PTPRQ" "NM_001145026:c.392+1317T>C" "INTRON3" "Unknown significance" "rs556113318" "This variant is a VUS because it does not have enough information."
307585 "chr12:80840876:T>C" "PTPRQ" "NM_001145026:c.392+1377T>C" "INTRON3" "Unknown significance" "rs573471905" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307586 "chr12:80840923:T>G" "PTPRQ" "NM_001145026:c.392+1424T>G" "INTRON3" "Unknown significance" "rs540606006" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307587 "chr12:80840949:T>-" "PTPRQ" "NM_001145026:c.392+1450delT" "INTRON3" "Unknown significance" "rs556117137" "This variant is a VUS because it does not have enough information."
307588 "chr12:80840978:G>A" "PTPRQ" "NM_001145026:c.392+1479G>A" "INTRON3" "Unknown significance" "rs558954568" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307589 "chr12:80841116:C>T" "PTPRQ" "NM_001145026:c.392+1617C>T" "INTRON3" "Benign" "rs7979989" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1216 1322 0.9198 887 1006 0.8817 590 694 0.8501 572 1008 0.5675 878 978 0.8978 4143 5008 0.827276
307590 "chr12:80841143:A>T" "PTPRQ" "NM_001145026:c.392+1644A>T" "INTRON3" "Unknown significance" "rs541568480" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307591 "chr12:80841152:C>T" "PTPRQ" "NM_001145026:c.392+1653C>T" "INTRON3" "Unknown significance" "rs759671189" "This variant is a VUS because it does not have enough information."
307592 "chr12:80841153:T>C" "PTPRQ" "NM_001145026:c.392+1654T>C" "INTRON3" "Unknown significance" "rs181681408" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 2 978 0.002 3 5008 0.000599042
307593 "chr12:80841155:T>C" "PTPRQ" "NM_001145026:c.392+1656T>C" "INTRON3" "Unknown significance" "rs765451508" "This variant is a VUS because it does not have enough information."
307594 "chr12:80841183:A>G" "PTPRQ" "NM_001145026:c.392+1684A>G" "INTRON3" "Unknown significance" "rs530684238" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307595 "chr12:80841208:T>G" "PTPRQ" "NM_001145026:c.392+1709T>G" "INTRON3" "Unknown significance" "rs538801525" "This variant is a VUS because it does not have enough information."
307596 "chr12:80841232:C>T" "PTPRQ" "NM_001145026:c.392+1733C>T" "INTRON3" "Unknown significance" "rs79002148" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307597 "chr12:80841232:C>G" "PTPRQ" "NM_001145026:c.392+1733C>G" "INTRON3" "Unknown significance" "rs79002148" "This variant is a VUS because it does not have enough information."
307598 "chr12:80841265:C>T" "PTPRQ" "NM_001145026:c.392+1766C>T" "INTRON3" "Unknown significance" "rs186797741" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307599 "chr12:80841309:T>C" "PTPRQ" "NM_001145026:c.392+1810T>C" "INTRON3" "Benign" "rs147831714" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521
307600 "chr12:80841313:G>A" "PTPRQ" "NM_001145026:c.392+1814G>A" "INTRON3" "Benign" "rs114976260" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 35 1322 0.0265 0 1006 0 0 694 0 0 1008 0 0 978 0 35 5008 0.00698882
307601 "chr12:80841337:A>C" "PTPRQ" "NM_001145026:c.392+1838A>C" "INTRON3" "Unknown significance" "rs568505543" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307602 "chr12:80841346:TAA>-" "PTPRQ" "NM_001145026:c.392+1847_392+1849delTAA" "INTRON3" "Unknown significance" "rs767643209" "This variant is a VUS because it does not have enough information."
307603 "chr12:80841354:G>A" "PTPRQ" "NM_001145026:c.392+1855G>A" "INTRON3" "Unknown significance" "rs539992558" "This variant is a VUS because it does not have enough information."
307604 "chr12:80841380:TT>-" "PTPRQ" "NM_001145026:c.392+1881_392+1882delTT" "INTRON3" "Benign" "rs576261250" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 3 1006 0.003 0 694 0 0 1008 0 12 978 0.0123 15 5008 0.00299521
307605 "chr12:80841403:G>A" "PTPRQ" "NM_001145026:c.392+1904G>A" "INTRON3" "Unknown significance" "rs535859152" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307606 "chr12:80841439:C>-" "PTPRQ" "NM_001145026:c.392+1940delC" "INTRON3" "Benign" "rs201357354" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 21 1006 0.0209 13 694 0.0187 0 1008 0 6 978 0.0061 41 5008 0.0081869
307607 "chr12:80841444:C>A" "PTPRQ" "NM_001145026:c.392+1945C>A" "INTRON3" "Unknown significance" "rs559467757" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307608 "chr12:80841445:C>A" "PTPRQ" "NM_001145026:c.392+1946C>A" "INTRON3" "Unknown significance" "rs528579535" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307609 "chr12:80841457:T>G" "PTPRQ" "NM_001145026:c.392+1958T>G" "INTRON3" "Unknown significance" "rs758891451" "This variant is a VUS because it does not have enough information."
307610 "chr12:80841465:A>G" "PTPRQ" "NM_001145026:c.392+1966A>G" "INTRON3" "Benign" "rs192107274" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 8 5008 0.00159744
307611 "chr12:80841471:T>C" "PTPRQ" "NM_001145026:c.392+1972T>C" "INTRON3" "Unknown significance" "rs572124546" "This variant is a VUS because it does not have enough information."
307612 "chr12:80841481:GTTG>-" "PTPRQ" "NM_001145026:c.392+1982_392+1985delGTTG" "INTRON3" "Unknown significance" "rs773933632" "This variant is a VUS because it does not have enough information."
307613 "chr12:80841487:->AAATAAAGGACCTCTTCAAGGAGAACTACAAACCACTGCTCAA" "PTPRQ" "NM_001145026:c.392+1988_392+1989insAAATAAAGGACCTCTTCAAGGAGAACTACAAACCACTGCTCAA" "INTRON3" "Benign" "rs576743382" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
307614 "chr12:80841492:G>T" "PTPRQ" "NM_001145026:c.392+1993G>T" "INTRON3" "Unknown significance" "rs558101713" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307615 "chr12:80841495:TGTGAC>-" "PTPRQ" "NM_001145026:c.392+1996_392+2001delTGTGAC" "INTRON3" "Benign" "rs536602983" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
307616 "chr12:80841588:T>C" "PTPRQ" "NM_001145026:c.392+2089T>C" "INTRON3" "Unknown significance" "rs573459016" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307617 "chr12:80841591:T>C" "PTPRQ" "NM_001145026:c.392+2092T>C" "INTRON3" "Unknown significance" "rs141348025" "This variant is a VUS because it does not have enough information."
307618 "chr12:80841599:G>A" "PTPRQ" "NM_001145026:c.392+2100G>A" "INTRON3" "Benign" "rs11833433" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 248 1322 0.1876 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 266 5008 0.053115
307619 "chr12:80841603:T>C" "PTPRQ" "NM_001145026:c.392+2104T>C" "INTRON3" "Unknown significance" "rs4284459" "This variant is a VUS because it does not have enough information."
307620 "chr12:80841642:A>G" "PTPRQ" "NM_001145026:c.392+2143A>G" "INTRON3" "Unknown significance" "rs552542125" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307621 "chr12:80841643:G>A" "PTPRQ" "NM_001145026:c.392+2144G>A" "INTRON3" "Unknown significance" "rs183978561" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307622 "chr12:80841698:T>A" "PTPRQ" "NM_001145026:c.392+2199T>A" "INTRON3" "Unknown significance" "rs146975849" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307623 "chr12:80841749:A>-" "PTPRQ" "NM_001145026:c.392+2250delA" "INTRON3" "Benign" "rs58028512" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 21 1006 0.0209 63 694 0.0908 37 1008 0.0367 101 978 0.1033 647 5008 0.129193
307624 "chr12:80841805:G>C" "PTPRQ" "NM_001145026:c.392+2306G>C" "INTRON3" "Unknown significance" "rs563369598" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307625 "chr12:80841864:C>T" "PTPRQ" "NM_001145026:c.392+2365C>T" "INTRON3" "Unknown significance" "rs575261102" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307626 "chr12:80841916:->T" "PTPRQ" "NM_001145026:c.392+2417_392+2418insT" "INTRON3" "Unknown significance" "rs201054857" "This variant is a VUS because it does not have enough information."
307627 "chr12:80841922:T>G" "PTPRQ" "NM_001145026:c.392+2423T>G" "INTRON3" "Benign" "rs10047561" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 272 1322 0.2057 0 1006 0 12 694 0.0173 0 1008 0 0 978 0 284 5008 0.0567093
307628 "chr12:80841924:G>-" "PTPRQ" "NM_001145026:c.392+2425delG" "INTRON3" "Unknown significance" "rs77146600" "This variant is a VUS because it does not have enough information."
307629 "chr12:80841924:G>T" "PTPRQ" "NM_001145026:c.392+2425G>T" "INTRON3" "Benign" "rs12811965" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 104 1322 0.0787 86 1006 0.0855 43 694 0.062 206 1008 0.2044 57 978 0.0583 496 5008 0.0990415
307630 "chr12:80841933:G>A" "PTPRQ" "NM_001145026:c.392+2434G>A" "INTRON3" "Benign" "rs144948588" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 8 5008 0.00159744
307631 "chr12:80841978:T>C" "PTPRQ" "NM_001145026:c.392+2479T>C" "INTRON3" "Unknown significance" "rs182663004" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307632 "chr12:80842026:A>C" "PTPRQ" "NM_001145026:c.392+2527A>C" "INTRON3" "Benign" "rs10047551" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 649 5008 0.129593
307633 "chr12:80842026:A>G" "PTPRQ" "NM_001145026:c.392+2527A>G" "INTRON3" "Benign" "rs10047551" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 305 1322 0.2307 71 1006 0.0706 51 694 0.0735 0 1008 0 49 978 0.0501 476 5008 0.0950479
307634 "chr12:80842035:T>C" "PTPRQ" "NM_001145026:c.392+2536T>C" "INTRON3" "Unknown significance" "rs551007287" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307635 "chr12:80842062:A>T" "PTPRQ" "NM_001145026:c.392+2563A>T" "INTRON3" "Unknown significance" "rs377579377" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
307636 "chr12:80842081:T>A" "PTPRQ" "NM_001145026:c.392+2582T>A" "INTRON3" "Unknown significance" "rs539575163" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307637 "chr12:80842109:A>T" "PTPRQ" "NM_001145026:c.392+2610A>T" "INTRON3" "Benign" "rs80208221" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
307638 "chr12:80842161:->A" "PTPRQ" "NM_001145026:c.392+2662_392+2663insA" "INTRON3" "Benign" "rs553187460" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 5 978 0.0051 5 5008 0.000998403
307639 "chr12:80842161:A>T" "PTPRQ" "NM_001145026:c.392+2662A>T" "INTRON3" "Benign" "rs10047552" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 21 1006 0.0209 64 694 0.0922 37 1008 0.0367 101 978 0.1033 648 5008 0.129393
307640 "chr12:80842177:A>G" "PTPRQ" "NM_001145026:c.392+2678A>G" "INTRON3" "Benign" "rs149048383" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 64 1008 0.0635 3 978 0.0031 67 5008 0.0133786
307641 "chr12:80842195:G>T" "PTPRQ" "NM_001145026:c.392+2696G>T" "INTRON3" "Unknown significance" "rs574283342" "This variant is a VUS because it does not have enough information."
307642 "chr12:80842199:A>C" "PTPRQ" "NM_001145026:c.392+2700A>C" "INTRON3" "Benign" "rs11513908" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 176 1322 0.1331 231 1006 0.2296 105 694 0.1513 3 1008 0.003 102 978 0.1043 617 5008 0.123203
307643 "chr12:80842205:C>A" "PTPRQ" "NM_001145026:c.392+2706C>A" "INTRON3" "Benign" "rs187311410" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
307644 "chr12:80842207:G>T" "PTPRQ" "NM_001145026:c.392+2708G>T" "INTRON3" "Unknown significance" "rs547209903" "This variant is a VUS because it does not have enough information."
307645 "chr12:80842213:T>A" "PTPRQ" "NM_001145026:c.392+2714T>A" "INTRON3" "Unknown significance" "rs535049499" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307646 "chr12:80842221:G>A" "PTPRQ" "NM_001145026:c.392+2722G>A" "INTRON3" "Unknown significance" "rs556718475" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307647 "chr12:80842243:T>C" "PTPRQ" "NM_001145026:c.392+2744T>C" "INTRON3" "Benign" "rs10047565" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 220 694 0.317 40 1008 0.0397 252 978 0.2577 1740 5008 0.347444
307648 "chr12:80842270:A>C" "PTPRQ" "NM_001145026:c.392+2771A>C" "INTRON3" "Unknown significance" "rs61950889" "This variant is a VUS because it does not have enough information."
307649 "chr12:80842300:C>T" "PTPRQ" "NM_001145026:c.392+2801C>T" "INTRON3" "Benign" "rs545620526" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 49 1322 0.0371 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 53 5008 0.0105831
307650 "chr12:80842302:C>A" "PTPRQ" "NM_001145026:c.392+2803C>A" "INTRON3" "Unknown significance" "rs531799989" "This variant is a VUS because it does not have enough information."
307651 "chr12:80842303:A>C" "PTPRQ" "NM_001145026:c.392+2804A>C" "INTRON3" "Unknown significance" "rs61950900" "This variant is a VUS because it does not have enough information."
307652 "chr12:80842362:T>A" "PTPRQ" "NM_001145026:c.392+2863T>A" "INTRON3" "Unknown significance" "rs564217360" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
307653 "chr12:80842392:A>G" "PTPRQ" "NM_001145026:c.392+2893A>G" "INTRON3" "Unknown significance" "rs573027303" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
307654 "chr12:80842399:G>A" "PTPRQ" "NM_001145026:c.392+2900G>A" "INTRON3" "Benign" "rs10047591" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 319 1322 0.2413 21 1006 0.0209 57 694 0.0821 37 1008 0.0367 101 978 0.1033 535 5008 0.106829
307655 "chr12:80842400:C>T" "PTPRQ" "NM_001145026:c.392+2901C>T" "INTRON3" "Benign" "rs561926941" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 0 1006 0 0 694 0 0 1008 0 0 978 0 20 5008 0.00399361
307656 "chr12:80842415:C>-" "PTPRQ" "NM_001145026:c.392+2916delC" "INTRON3" "Unknown significance" "rs201757879" "This variant is a VUS because it does not have enough information."
307657 "chr12:80842415:C>T" "PTPRQ" "NM_001145026:c.392+2916C>T" "INTRON3" "Benign" "rs10047520" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1320 1322 0.9985 973 1006 0.9672 633 694 0.9121 785 1008 0.7788 938 978 0.9591 4649 5008 0.928315
307658 "chr12:80842422:->G" "PTPRQ" "NM_001145026:c.392+2923_392+2924insG" "INTRON3" "Benign" "rs542100785" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 67 1322 0.0507 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 70 5008 0.0139776
307659 "chr12:80842423:C>T" "PTPRQ" "NM_001145026:c.392+2924C>T" "INTRON3" "Benign" "rs61950901" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
307660 "chr12:80842460:T>C" "PTPRQ" "NM_001145026:c.392+2961T>C" "INTRON3" "Benign" "rs10047566" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1212 1322 0.9168 887 1006 0.8817 590 694 0.8501 579 1008 0.5744 880 978 0.8998 4148 5008 0.828275
307661 "chr12:80842465:C>A" "PTPRQ" "NM_001145026:c.392+2966C>A" "INTRON3" "Unknown significance" "rs533459794" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307662 "chr12:80842476:G>A" "PTPRQ" "NM_001145026:c.392+2977G>A" "INTRON3" "Benign" "rs370203843" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 0 1006 0 0 694 0 127 1008 0.126 4 978 0.0041 133 5008 0.0265575
307663 "chr12:80842483:C>G" "PTPRQ" "NM_001145026:c.392+2984C>G" "INTRON3" "Unknown significance" "rs566962962" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307664 "chr12:80842492:T>C" "PTPRQ" "NM_001145026:c.392+2993T>C" "INTRON3" "Unknown significance" "rs527853843" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307665 "chr12:80842509:A>G" "PTPRQ" "NM_001145026:c.392+3010A>G" "INTRON3" "Unknown significance" "rs538205009" "This variant is a VUS because it does not have enough information."
307666 "chr12:80842516:G>C" "PTPRQ" "NM_001145026:c.392+3017G>C" "INTRON3" "Unknown significance" "rs549181527" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
307667 "chr12:80842525:G>A" "PTPRQ" "NM_001145026:c.392+3026G>A" "INTRON3" "Benign" "rs567604733" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
307668 "chr12:80842532:T>A" "PTPRQ" "NM_001145026:c.392+3033T>A" "INTRON3" "Benign" "rs12305917" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 32 1006 0.0318 79 694 0.1138 35 1008 0.0347 109 978 0.1115 680 5008 0.135783
307669 "chr12:80842604:G>A" "PTPRQ" "NM_001145026:c.392+3105G>A" "INTRON3" "Unknown significance" "rs567630463" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 1 1008 0.001 1 978 0.001 4 5008 0.000798722
307670 "chr12:80842644:A>T" "PTPRQ" "NM_001145026:c.392+3145A>T" "INTRON3" "Unknown significance" "rs568717518" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 1 978 0.001 3 5008 0.000599042
307671 "chr12:80842667:C>T" "PTPRQ" "NM_001145026:c.392+3168C>T" "INTRON3" "Benign" "rs539422133" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
307672 "chr12:80842731:C>A" "PTPRQ" "NM_001145026:c.392+3232C>A" "INTRON3" "Unknown significance" "rs557539767" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307673 "chr12:80842776:G>A" "PTPRQ" "NM_001145026:c.392+3277G>A" "INTRON3" "Benign" "rs191807606" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
307674 "chr12:80842777:T>G" "PTPRQ" "NM_001145026:c.392+3278T>G" "INTRON3" "Unknown significance" "rs536225497" "This variant is a VUS because it does not have enough information."
307675 "chr12:80842819:C>G" "PTPRQ" "NM_001145026:c.392+3320C>G" "INTRON3" "Unknown significance" "rs150866250" "This variant is a VUS because it does not have enough information."
307676 "chr12:80842874:G>A" "PTPRQ" "NM_001145026:c.392+3375G>A" "INTRON3" "Benign" "rs184349169" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 8 5008 0.00159744
307677 "chr12:80842889:A>T" "PTPRQ" "NM_001145026:c.392+3390A>T" "INTRON3" "Unknown significance" "rs201459994" "This variant is a VUS because it does not have enough information."
307678 "chr12:80842931:T>C" "PTPRQ" "NM_001145026:c.392+3432T>C" "INTRON3" "Unknown significance" "rs555626640" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361
307679 "chr12:80842941:C>A" "PTPRQ" "NM_001145026:c.392+3442C>A" "INTRON3" "Unknown significance" "rs573977356" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307680 "chr12:80842958:G>C" "PTPRQ" "NM_001145026:c.392+3459G>C" "INTRON3" "Benign" "rs544223455" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 16 5008 0.00319489
307681 "chr12:80842977:C>T" "PTPRQ" "NM_001145026:c.392+3478C>T" "INTRON3" "Unknown significance" "rs796821908" "This variant is a VUS because it does not have enough information."
307682 "chr12:80843042:G>A" "PTPRQ" "NM_001145026:c.392+3543G>A" "INTRON3" "Unknown significance" "rs7958737" "This variant is a VUS because it does not have enough information."
307683 "chr12:80843078:G>A" "PTPRQ" "NM_001145026:c.392+3579G>A" "INTRON3" "Unknown significance" "rs562811993" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307684 "chr12:80843111:T>C" "PTPRQ" "NM_001145026:c.392+3612T>C" "INTRON3" "Benign" "rs138226131" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 85 1006 0.0845 33 694 0.0476 195 1008 0.1935 38 978 0.0389 351 5008 0.0700879
307685 "chr12:80843115:C>T" "PTPRQ" "NM_001145026:c.392+3616C>T" "INTRON3" "Unknown significance" "rs545409294" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307686 "chr12:80843125:A>G" "PTPRQ" "NM_001145026:c.392+3626A>G" "INTRON3" "Unknown significance" "rs558781617" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307687 "chr12:80843140:G>A" "PTPRQ" "NM_001145026:c.392+3641G>A" "INTRON3" "Benign" "rs527815714" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 6 978 0.0061 6 5008 0.00119808
307688 "chr12:80843141:C>A" "PTPRQ" "NM_001145026:c.392+3642C>A" "INTRON3" "Unknown significance" "rs549144825" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
307689 "chr12:80843144:A>G" "PTPRQ" "NM_001145026:c.392+3645A>G" "INTRON3" "Benign" "rs567568656" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 0 1006 0 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744
307690 "chr12:80843185:T>C" "PTPRQ" "NM_001145026:c.392+3686T>C" "INTRON3" "Benign" "rs375679677" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 15 1008 0.0149 33 978 0.0337 48 5008 0.00958466
307691 "chr12:80843223:C>A" "PTPRQ" "NM_001145026:c.392+3724C>A" "INTRON3" "Benign" "rs11503514" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 405 1322 0.3064 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 629 5008 0.125599
307692 "chr12:80843231:A>G" "PTPRQ" "NM_001145026:c.392+3732A>G" "INTRON3" "Unknown significance" "rs571929741" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307693 "chr12:80843249:G>T" "PTPRQ" "NM_001145026:c.392+3750G>T" "INTRON3" "Unknown significance" "rs539028841" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307694 "chr12:80843260:G>T" "PTPRQ" "NM_001145026:c.392+3761G>T" "INTRON3" "Unknown significance" "rs193218066" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307695 "chr12:80843260:G>C" "PTPRQ" "NM_001145026:c.392+3761G>C" "INTRON3" "Unknown significance" "rs193218066" "This variant is a VUS because it does not have enough information."
307696 "chr12:80843265:C>T" "PTPRQ" "NM_001145026:c.392+3766C>T" "INTRON3" "Unknown significance" "rs566548640" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307697 "chr12:80843357:T>C" "PTPRQ" "NM_001145026:c.392+3858T>C" "INTRON3" "Unknown significance" "rs112955268" "This variant is a VUS because it does not have enough information."
307698 "chr12:80843395:C>T" "PTPRQ" "NM_001145026:c.392+3896C>T" "INTRON3" "Unknown significance" "rs11513910" "This variant is a VUS because it does not have enough information."
307699 "chr12:80843415:C>-" "PTPRQ" "NM_001145026:c.392+3916delC" "INTRON3" "Unknown significance" "rs574782010" "This variant is a VUS because it does not have enough information." 0 1322 0 4 1006 0.004 2 694 0.0029 0 1008 0 2 978 0.002 8 5008 0.00159744
307700 "chr12:80843417:C>T" "PTPRQ" "NM_001145026:c.392+3918C>T" "INTRON3" "Benign" "rs11513911" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 480 1322 0.3631 316 1006 0.3141 162 694 0.2334 3 1008 0.003 156 978 0.1595 1117 5008 0.223043
307701 "chr12:80843463:T>G" "PTPRQ" "NM_001145026:c.392+3964T>G" "INTRON3" "Unknown significance" "rs555589848" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307702 "chr12:80843470:A>G" "PTPRQ" "NM_001145026:c.392+3971A>G" "INTRON3" "Unknown significance" "rs573841329" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307703 "chr12:80843473:C>T" "PTPRQ" "NM_001145026:c.392+3974C>T" "INTRON3" "Unknown significance" "rs544401337" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
307704 "chr12:80843485:G>T" "PTPRQ" "NM_001145026:c.392+3986G>T" "INTRON3" "Benign" "rs140691461" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 305 1322 0.2307 71 1006 0.0706 51 694 0.0735 0 1008 0 48 978 0.0491 475 5008 0.0948482
307705 "chr12:80843504:C>T" "PTPRQ" "NM_001145026:c.392+4005C>T" "INTRON3" "Benign" "rs11513912" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 102 978 0.1043 616 5008 0.123003
307706 "chr12:80843517:C>T" "PTPRQ" "NM_001145026:c.392+4018C>T" "INTRON3" "Unknown significance" "rs545059399" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
307707 "chr12:80843541:C>T" "PTPRQ" "NM_001145026:c.392+4042C>T" "INTRON3" "Unknown significance" "rs560142046" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307708 "chr12:80843575:A>C" "PTPRQ" "NM_001145026:c.392+4076A>C" "INTRON3" "Unknown significance" "rs527777273" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307709 "chr12:80843592:T>C" "PTPRQ" "NM_001145026:c.392+4093T>C" "INTRON3" "Unknown significance" "rs542670227" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307710 "chr12:80843631:C>T" "PTPRQ" "NM_001145026:c.392+4132C>T" "INTRON3" "Benign" "rs11114447" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 82 1322 0.062 564 1006 0.5606 363 694 0.5231 537 1008 0.5327 626 978 0.6401 2172 5008 0.433706
307711 "chr12:80843632:G>A" "PTPRQ" "NM_001145026:c.392+4133G>A" "INTRON3" "Benign" "rs531783411" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 0 1006 0 0 694 0 0 1008 0 0 978 0 36 5008 0.0071885
307712 "chr12:80843640:C>T" "PTPRQ" "NM_001145026:c.392+4141C>T" "INTRON3" "Benign" "rs76686191" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 564 1006 0.5606 363 694 0.5231 532 1008 0.5278 627 978 0.6411 2167 5008 0.432708
307713 "chr12:80843644:T>G" "PTPRQ" "NM_001145026:c.392+4145T>G" "INTRON3" "Unknown significance" "rs565421022" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307714 "chr12:80843655:A>T" "PTPRQ" "NM_001145026:c.392+4156A>T" "INTRON3" "Benign" "rs532865758" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 71 1006 0.0706 33 694 0.0476 0 1008 0 48 978 0.0491 186 5008 0.0371406
307715 "chr12:80843703:G>C" "PTPRQ" "NM_001145026:c.392+4204G>C" "INTRON3" "Benign" "rs551391794" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
307716 "chr12:80843713:G>A" "PTPRQ" "NM_001145026:c.392+4214G>A" "INTRON3" "Benign" "rs566512553" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 12 1322 0.0091 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 14 5008 0.00279553
307717 "chr12:80843718:T>C" "PTPRQ" "NM_001145026:c.392+4219T>C" "INTRON3" "Benign" "rs189366868" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 1322 0.0068 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 11 5008 0.00219649
307718 "chr12:80843748:G>A" "PTPRQ" "NM_001145026:c.392+4249G>A" "INTRON3" "Unknown significance" "rs549054278" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307719 "chr12:80843763:C>T" "PTPRQ" "NM_001145026:c.392+4264C>T" "INTRON3" "Unknown significance" "rs567379156" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307720 "chr12:80843764:G>A" "PTPRQ" "NM_001145026:c.392+4265G>A" "INTRON3" "Benign" "rs181019295" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 5 1006 0.005 9 694 0.013 0 1008 0 2 978 0.002 17 5008 0.00339457
307721 "chr12:80843832:T>A" "PTPRQ" "NM_001145026:c.392+4333T>A" "INTRON3" "Unknown significance" "rs556357858" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307722 "chr12:80843873:G>A" "PTPRQ" "NM_001145026:c.392+4374G>A" "INTRON3" "Benign" "rs11519621" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 482 1322 0.3646 326 1006 0.3241 174 694 0.2507 4 1008 0.004 178 978 0.182 1164 5008 0.232428
307723 "chr12:80843897:G>C" "PTPRQ" "NM_001145026:c.392+4398G>C" "INTRON3" "Unknown significance" "rs538971242" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307724 "chr12:80843916:T>G" "PTPRQ" "NM_001145026:c.392+4417T>G" "INTRON3" "Benign" "rs7316849" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1319 1322 0.9977 972 1006 0.9662 632 694 0.9107 783 1008 0.7768 938 978 0.9591 4644 5008 0.927316
307725 "chr12:80843919:A>G" "PTPRQ" "NM_001145026:c.392+4420A>G" "INTRON3" "Benign" "rs572059973" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
307726 "chr12:80843920:T>C" "PTPRQ" "NM_001145026:c.392+4421T>C" "INTRON3" "Unknown significance" "rs11534867" "This variant is a VUS because it does not have enough information."
307727 "chr12:80843924:G>C" "PTPRQ" "NM_001145026:c.392+4425G>C" "INTRON3" "Unknown significance" "rs542633303" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307728 "chr12:80843986:G>A" "PTPRQ" "NM_001145026:c.392+4487G>A" "INTRON3" "Unknown significance" "rs199513857" "This variant is a VUS because it does not have enough information."
307729 "chr12:80844065:G>A" "PTPRQ" "NM_001145026:c.392+4566G>A" "INTRON3" "Unknown significance" "rs369383297" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307730 "chr12:80844096:T>C" "PTPRQ" "NM_001145026:c.392+4597T>C" "INTRON3" "Unknown significance" "rs576515580" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307731 "chr12:80844099:T>G" "PTPRQ" "NM_001145026:c.392+4600T>G" "INTRON3" "Unknown significance" "rs7131785" "This variant is a VUS because it does not have enough information."
307732 "chr12:80844103:A>G" "PTPRQ" "NM_001145026:c.392+4604A>G" "INTRON3" "Unknown significance" "rs561192077" "This variant is a VUS because it does not have enough information."
307733 "chr12:80844140:A>G" "PTPRQ" "NM_001145026:c.392+4641A>G" "INTRON3" "Unknown significance" "rs530114120" "This variant is a VUS because it does not have enough information."
307734 "chr12:80844171:C>A" "PTPRQ" "NM_001145026:c.392+4672C>A" "INTRON3" "Unknown significance" "rs543628968" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307735 "chr12:80844184:C>T" "PTPRQ" "NM_001145026:c.392+4685C>T" "INTRON3" "Benign" "rs150980677" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 2 1006 0.002 0 694 0 18 1008 0.0179 0 978 0 20 5008 0.00399361
307736 "chr12:80844192:A>G" "PTPRQ" "NM_001145026:c.392+4693A>G" "INTRON3" "Unknown significance" "rs532683240" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307737 "chr12:80844215:A>G" "PTPRQ" "NM_001145026:c.392+4716A>G" "INTRON3" "Unknown significance" "rs548067082" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307738 "chr12:80844240:T>G" "PTPRQ" "NM_001145026:c.392+4741T>G" "INTRON3" "Unknown significance" "rs186863426" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307739 "chr12:80844241:T>G" "PTPRQ" "NM_001145026:c.392+4742T>G" "INTRON3" "Benign" "rs190057898" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
307740 "chr12:80844267:C>G" "PTPRQ" "NM_001145026:c.392+4768C>G" "INTRON3" "Benign" "rs182332429" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 9 1008 0.0089 0 978 0 9 5008 0.00179712
307741 "chr12:80844272:C>T" "PTPRQ" "NM_001145026:c.392+4773C>T" "INTRON3" "Benign" "rs7963809" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 264 1322 0.1997 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 282 5008 0.0563099
307742 "chr12:80844274:G>T" "PTPRQ" "NM_001145026:c.392+4775G>T" "INTRON3" "Unknown significance" "rs537974477" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307743 "chr12:80844292:G>A" "PTPRQ" "NM_001145026:c.392+4793G>A" "INTRON3" "Unknown significance" "rs549706893" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
307744 "chr12:80844301:A>G" "PTPRQ" "NM_001145026:c.392+4802A>G" "INTRON3" "Benign" "rs571461802" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 13 1322 0.0098 0 1006 0 0 694 0 0 1008 0 0 978 0 13 5008 0.00259585
307745 "chr12:80844321:A>G" "PTPRQ" "NM_001145026:c.392+4822A>G" "INTRON3" "Benign" "rs538457472" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 36 5008 0.0071885
307746 "chr12:80844353:A>G" "PTPRQ" "NM_001145026:c.392+4854A>G" "INTRON3" "Unknown significance" "rs553621754" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307747 "chr12:80844359:T>C" "PTPRQ" "NM_001145026:c.392+4860T>C" "INTRON3" "Benign" "rs7953180" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1273 1322 0.9629 967 1006 0.9612 616 694 0.8876 783 1008 0.7768 918 978 0.9387 4557 5008 0.909944
307748 "chr12:80844369:C>A" "PTPRQ" "NM_001145026:c.392+4870C>A" "INTRON3" "Benign" "rs7963938" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1273 1322 0.9629 967 1006 0.9612 616 694 0.8876 784 1008 0.7778 918 978 0.9387 4558 5008 0.910144
307749 "chr12:80844370:A>G" "PTPRQ" "NM_001145026:c.392+4871A>G" "INTRON3" "Benign" "rs7978521" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 861 1322 0.6513 316 1006 0.3141 201 694 0.2896 37 1008 0.0367 217 978 0.2219 1632 5008 0.325879
307750 "chr12:80844373:G>A" "PTPRQ" "NM_001145026:c.392+4874G>A" "INTRON3" "Benign" "rs149686375" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 19 1322 0.0144 68 1006 0.0676 30 694 0.0432 0 1008 0 48 978 0.0491 165 5008 0.0329473
307751 "chr12:80844383:G>T" "PTPRQ" "NM_001145026:c.392+4884G>T" "INTRON3" "Unknown significance" "rs182116878" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 2 5008 0.000399361
307752 "chr12:80844406:T>C" "PTPRQ" "NM_001145026:c.392+4907T>C" "INTRON3" "Benign" "rs145477460" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 14 1006 0.0139 0 694 0 0 1008 0 0 978 0 14 5008 0.00279553
307753 "chr12:80844420:C>T" "PTPRQ" "NM_001145026:c.392+4921C>T" "INTRON3" "Benign" "rs7964038" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 448 1322 0.3389 21 1006 0.0209 64 694 0.0922 36 1008 0.0357 98 978 0.1002 667 5008 0.133187
307754 "chr12:80844421:G>A" "PTPRQ" "NM_001145026:c.392+4922G>A" "INTRON3" "Unknown significance" "rs541670003" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 0 978 0 0 5008 0
307755 "chr12:80844438:T>C" "PTPRQ" "NM_001145026:c.392+4939T>C" "INTRON3" "Benign" "rs7953299" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 412 1322 0.3116 21 1006 0.0209 64 694 0.0922 36 1008 0.0357 97 978 0.0992 630 5008 0.125799
307756 "chr12:80844465:G>C" "PTPRQ" "NM_001145026:c.392+4966G>C" "INTRON3" "Benign" "rs185317188" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 14 1008 0.0139 0 978 0 14 5008 0.00279553
307757 "chr12:80844506:G>T" "PTPRQ" "NM_001145026:c.392+5007G>T" "INTRON3" "Unknown significance" "rs542622813" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307758 "chr12:80844520:T>G" "PTPRQ" "NM_001145026:c.392+5021T>G" "INTRON3" "Benign" "rs560985989" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 1 1006 0.001 4 694 0.0058 0 1008 0 1 978 0.001 9 5008 0.00179712
307759 "chr12:80844530:C>A" "PTPRQ" "NM_001145026:c.392+5031C>A" "INTRON3" "Unknown significance" "rs531297622" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307760 "chr12:80844577:T>G" "PTPRQ" "NM_001145026:c.392+5078T>G" "INTRON3" "Unknown significance" "rs766631927" "This variant is a VUS because it does not have enough information."
307761 "chr12:80844586:C>T" "PTPRQ" "NM_001145026:c.392+5087C>T" "INTRON3" "Benign" "rs190130286" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521
307762 "chr12:80844597:A>G" "PTPRQ" "NM_001145026:c.392+5098A>G" "INTRON3" "Unknown significance" "rs183061206" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
307763 "chr12:80844619:C>A" "PTPRQ" "NM_001145026:c.392+5120C>A" "INTRON3" "Unknown significance" "rs532140117" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307764 "chr12:80844633:T>A" "PTPRQ" "NM_001145026:c.392+5134T>A" "INTRON3" "Benign" "rs7953545" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 263 1322 0.1989 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 281 5008 0.0561102
307765 "chr12:80844648:G>T" "PTPRQ" "NM_001145026:c.392+5149G>T" "INTRON3" "Unknown significance" "rs565617080" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307766 "chr12:80844656:G>A" "PTPRQ" "NM_001145026:c.392+5157G>A" "INTRON3" "Unknown significance" "rs193025299" "This variant is a VUS because it does not have enough information."
307767 "chr12:80844666:G>A" "PTPRQ" "NM_001145026:c.392+5167G>A" "INTRON3" "Unknown significance" "rs536189830" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307768 "chr12:80844695:C>T" "PTPRQ" "NM_001145026:c.392+5196C>T" "INTRON3" "Unknown significance" "rs554655094" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307769 "chr12:80844740:T>C" "PTPRQ" "NM_001145026:c.392+5241T>C" "INTRON3" "Unknown significance" "rs796506236" "This variant is a VUS because it does not have enough information."
307770 "chr12:80844743:C>A" "PTPRQ" "NM_001145026:c.392+5244C>A" "INTRON3" "Unknown significance" "rs796614577" "This variant is a VUS because it does not have enough information."
307771 "chr12:80844755:C>T" "PTPRQ" "NM_001145026:c.392+5256C>T" "INTRON3" "Unknown significance" "rs796299639" "This variant is a VUS because it does not have enough information."
307772 "chr12:80844767:G>A" "PTPRQ" "NM_001145026:c.392+5268G>A" "INTRON3" "Benign" "rs140697068" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 27 1322 0.0204 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 29 5008 0.00579073
307773 "chr12:80844772:T>C" "PTPRQ" "NM_001145026:c.392+5273T>C" "INTRON3" "Unknown significance" "rs537052231" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307774 "chr12:80844779:G>A" "PTPRQ" "NM_001145026:c.392+5280G>A" "INTRON3" "Benign" "rs12314556" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 12 1322 0.0091 0 1006 0 0 694 0 1 1008 0.001 1 978 0.001 14 5008 0.00279553
307775 "chr12:80844792:C>A" "PTPRQ" "NM_001145026:c.392+5293C>A" "INTRON3" "Unknown significance" "rs577433019" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307776 "chr12:80844800:C>G" "PTPRQ" "NM_001145026:c.392+5301C>G" "INTRON3" "Benign" "rs7964395" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 21 1006 0.0209 64 694 0.0922 37 1008 0.0367 102 978 0.1043 649 5008 0.129593
307777 "chr12:80844814:C>T" "PTPRQ" "NM_001145026:c.392+5315C>T" "INTRON3" "Unknown significance" "rs12302833" "This variant is a VUS because it does not have enough information."
307778 "chr12:80844841:T>C" "PTPRQ" "NM_001145026:c.392+5342T>C" "INTRON3" "Unknown significance" "rs554663061" "This variant is a VUS because it does not have enough information."
307779 "chr12:80844844:G>T" "PTPRQ" "NM_001145026:c.392+5345G>T" "INTRON3" "Unknown significance" "rs553633828" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307780 "chr12:80844891:G>A" "PTPRQ" "NM_001145026:c.392+5392G>A" "INTRON3" "Unknown significance" "rs575206758" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
307781 "chr12:80844902:G>T" "PTPRQ" "NM_001145026:c.392+5403G>T" "INTRON3" "Unknown significance" "rs200122920" "This variant is a VUS because it does not have enough information."
307782 "chr12:80844928:T>A" "PTPRQ" "NM_001145026:c.392+5429T>A" "INTRON3" "Unknown significance" "rs542585960" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307783 "chr12:80844935:T>C" "PTPRQ" "NM_001145026:c.392+5436T>C" "INTRON3" "Unknown significance" "rs563838258" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307784 "chr12:80844952:G>A" "PTPRQ" "NM_001145026:c.392+5453G>A" "INTRON3" "Benign" "rs11525614" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 564 1006 0.5606 362 694 0.5216 532 1008 0.5278 628 978 0.6421 2167 5008 0.432708
307785 "chr12:80844992:A>G" "PTPRQ" "NM_001145026:c.392+5493A>G" "INTRON3" "Unknown significance" "rs559348140" "This variant is a VUS because it does not have enough information."
307786 "chr12:80845001:A>G" "PTPRQ" "NM_001145026:c.392+5502A>G" "INTRON3" "Unknown significance" "rs796513676" "This variant is a VUS because it does not have enough information."
307787 "chr12:80845002:A>T" "PTPRQ" "NM_001145026:c.392+5503A>T" "INTRON3" "Unknown significance" "rs796557903" "This variant is a VUS because it does not have enough information."
307788 "chr12:80845126:T>C" "PTPRQ" "NM_001145026:c.392+5627T>C" "INTRON3" "Benign" "rs543065630" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 229 1322 0.1732 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 236 5008 0.0471246
307789 "chr12:80845144:G>C" "PTPRQ" "NM_001145026:c.392+5645G>C" "INTRON3" "Unknown significance" "rs564977218" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307790 "chr12:80845153:T>A" "PTPRQ" "NM_001145026:c.392+5654T>A" "INTRON3" "Unknown significance" "rs532103791" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307791 "chr12:80845310:C>T" "PTPRQ" "NM_001145026:c.392+5811C>T" "INTRON3" "Unknown significance" "rs10862117" "This variant is a VUS because it does not have enough information."
307792 "chr12:80845341:T>A" "PTPRQ" "NM_001145026:c.392+5842T>A" "INTRON3" "Unknown significance" "rs11114448" "This variant is a VUS because it does not have enough information."
307793 "chr12:80845350:T>C" "PTPRQ" "NM_001145026:c.392+5851T>C" "INTRON3" "Unknown significance" "rs11114449" "This variant is a VUS because it does not have enough information."
307794 "chr12:80845352:T>C" "PTPRQ" "NM_001145026:c.392+5853T>C" "INTRON3" "Unknown significance" "rs11503517" "This variant is a VUS because it does not have enough information."
307795 "chr12:80845408:T>C" "PTPRQ" "NM_001145026:c.392+5909T>C" "INTRON3" "Unknown significance" "rs4356728" "This variant is a VUS because it does not have enough information."
307796 "chr12:80845408:T>G" "PTPRQ" "NM_001145026:c.392+5909T>G" "INTRON3" "Unknown significance" "rs4356728" "This variant is a VUS because it does not have enough information."
307797 "chr12:80845416:A>T" "PTPRQ" "NM_001145026:c.392+5917A>T" "INTRON3" "Unknown significance" "rs10862119" "This variant is a VUS because it does not have enough information."
307798 "chr12:80845431:G>A" "PTPRQ" "NM_001145026:c.392+5932G>A" "INTRON3" "Unknown significance" "rs11503520" "This variant is a VUS because it does not have enough information."
307799 "chr12:80845479:T>A" "PTPRQ" "NM_001145026:c.392+5980T>A" "INTRON3" "Unknown significance" "rs35060516" "This variant is a VUS because it does not have enough information."
307800 "chr12:80845523:C>T" "PTPRQ" "NM_001145026:c.392+6024C>T" "INTRON3" "Unknown significance" "rs11503521" "This variant is a VUS because it does not have enough information."
307801 "chr12:80845578:C>T" "PTPRQ" "NM_001145026:c.392+6079C>T" "INTRON3" "Unknown significance" "rs11503522" "This variant is a VUS because it does not have enough information."
307802 "chr12:80845646:G>-" "PTPRQ" "NM_001145026:c.392+6147delG" "INTRON3" "Unknown significance" "rs769821023" "This variant is a VUS because it does not have enough information."
307803 "chr12:80845651:A>G" "PTPRQ" "NM_001145026:c.392+6152A>G" "INTRON3" "Unknown significance" "rs202126901" "This variant is a VUS because it does not have enough information."
307804 "chr12:80845655:C>T" "PTPRQ" "NM_001145026:c.392+6156C>T" "INTRON3" "Unknown significance" "rs200463724" "This variant is a VUS because it does not have enough information."
307805 "chr12:80845675:G>A" "PTPRQ" "NM_001145026:c.392+6176G>A" "INTRON3" "Unknown significance" "rs201300978" "This variant is a VUS because it does not have enough information."
307806 "chr12:80845704:G>A" "PTPRQ" "NM_001145026:c.392+6205G>A" "INTRON3" "Unknown significance" "rs757237053" "This variant is a VUS because it does not have enough information."
307807 "chr12:80845769:A>G" "PTPRQ" "NM_001145026:c.392+6270A>G" "INTRON3" "Benign" "rs547183779" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 221 694 0.3184 40 1008 0.0397 250 978 0.2556 1739 5008 0.347244
307808 "chr12:80845843:A>T" "PTPRQ" "NM_001145026:c.392+6344A>T" "INTRON3" "Unknown significance" "rs565576382" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307809 "chr12:80845875:A>G" "PTPRQ" "NM_001145026:c.392+6376A>G" "INTRON3" "Benign" "rs529846556" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
307810 "chr12:80845906:C>G" "PTPRQ" "NM_001145026:c.392+6407C>G" "INTRON3" "Unknown significance" "rs548416370" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307811 "chr12:80845977:G>T" "PTPRQ" "NM_001145026:c.392+6478G>T" "INTRON3" "Benign" "rs569874525" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 231 1322 0.1747 0 1006 0 7 694 0.0101 0 1008 0 1 978 0.001 239 5008 0.0477236
307812 "chr12:80846020:T>G" "PTPRQ" "NM_001145026:c.392+6521T>G" "INTRON3" "Benign" "rs537419829" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 37 5008 0.00738818
307813 "chr12:80846051:A>T" "PTPRQ" "NM_001145026:c.392+6552A>T" "INTRON3" "Benign" "rs60770733" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
307814 "chr12:80846053:G>A" "PTPRQ" "NM_001145026:c.392+6554G>A" "INTRON3" "Unknown significance" "rs570938823" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307815 "chr12:80846069:G>A" "PTPRQ" "NM_001145026:c.392+6570G>A" "INTRON3" "Unknown significance" "rs200380255" "This variant is a VUS because it does not have enough information."
307816 "chr12:80846071:A>G" "PTPRQ" "NM_001145026:c.392+6572A>G" "INTRON3" "Unknown significance" "rs535172637" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
307817 "chr12:80846133:A>C" "PTPRQ" "NM_001145026:c.392+6634A>C" "INTRON3" "Benign" "rs200589835" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 4 694 0.0058 65 1008 0.0645 3 978 0.0031 72 5008 0.014377
307818 "chr12:80846153:C>T" "PTPRQ" "NM_001145026:c.392+6654C>T" "INTRON3" "Unknown significance" "rs61950902" "This variant is a VUS because it does not have enough information."
307819 "chr12:80846176:A>T" "PTPRQ" "NM_001145026:c.392+6677A>T" "INTRON3" "Unknown significance" "rs575046728" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307820 "chr12:80846177:T>A" "PTPRQ" "NM_001145026:c.392+6678T>A" "INTRON3" "Unknown significance" "rs201473214" "This variant is a VUS because it does not have enough information."
307821 "chr12:80846179:C>T" "PTPRQ" "NM_001145026:c.392+6680C>T" "INTRON3" "Unknown significance" "rs188596704" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307822 "chr12:80846185:T>G" "PTPRQ" "NM_001145026:c.392+6686T>G" "INTRON3" "Unknown significance" "rs199797049" "This variant is a VUS because it does not have enough information."
307823 "chr12:80846213:G>A" "PTPRQ" "NM_001145026:c.392+6714G>A" "INTRON3" "Unknown significance" "rs557597011" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307824 "chr12:80846220:G>A" "PTPRQ" "NM_001145026:c.392+6721G>A" "INTRON3" "Unknown significance" "rs575881679" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307825 "chr12:80846222:T>C" "PTPRQ" "NM_001145026:c.392+6723T>C" "INTRON3" "Unknown significance" "rs543383955" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307826 "chr12:80846227:T>C" "PTPRQ" "NM_001145026:c.392+6728T>C" "INTRON3" "Unknown significance" "rs564585313" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307827 "chr12:80846239:C>T" "PTPRQ" "NM_001145026:c.392+6740C>T" "INTRON3" "Unknown significance" "rs576518697" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307828 "chr12:80846249:T>G" "PTPRQ" "NM_001145026:c.392+6750T>G" "INTRON3" "Unknown significance" "rs370644457" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307829 "chr12:80846257:T>G" "PTPRQ" "NM_001145026:c.392+6758T>G" "INTRON3" "Unknown significance" "rs559026071" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307830 "chr12:80846267:T>G" "PTPRQ" "NM_001145026:c.392+6768T>G" "INTRON3" "Unknown significance" "rs529810312" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307831 "chr12:80846283:C>A" "PTPRQ" "NM_001145026:c.392+6784C>A" "INTRON3" "Benign" "rs60874560" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 479 1322 0.3623 302 1006 0.3002 156 694 0.2248 3 1008 0.003 149 978 0.1524 1089 5008 0.217452
307832 "chr12:80846285:G>A" "PTPRQ" "NM_001145026:c.392+6786G>A" "INTRON3" "Unknown significance" "rs192958216" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
307833 "chr12:80846293:T>C" "PTPRQ" "NM_001145026:c.392+6794T>C" "INTRON3" "Unknown significance" "rs753149896" "This variant is a VUS because it does not have enough information."
307834 "chr12:80846305:A>G" "PTPRQ" "NM_001145026:c.392+6806A>G" "INTRON3" "Benign" "rs184037792" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 71 1006 0.0706 33 694 0.0476 1 1008 0.001 48 978 0.0491 187 5008 0.0373403
307835 "chr12:80846327:T>C" "PTPRQ" "NM_001145026:c.392+6828T>C" "INTRON3" "Benign" "rs552539608" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 6 978 0.0061 6 5008 0.00119808
307836 "chr12:80846367:T>C" "PTPRQ" "NM_001145026:c.392+6868T>C" "INTRON3" "Benign" "rs10862120" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 221 694 0.3184 40 1008 0.0397 250 978 0.2556 1739 5008 0.347244
307837 "chr12:80846372:C>T" "PTPRQ" "NM_001145026:c.392+6873C>T" "INTRON3" "Unknown significance" "rs535029041" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
307838 "chr12:80846380:G>T" "PTPRQ" "NM_001145026:c.392+6881G>T" "INTRON3" "Unknown significance" "rs756632838" "This variant is a VUS because it does not have enough information."
307839 "chr12:80846430:T>A" "PTPRQ" "NM_001145026:c.392+6931T>A" "INTRON3" "Unknown significance" "rs547070942" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
307840 "chr12:80846435:G>A" "PTPRQ" "NM_001145026:c.392+6936G>A" "INTRON3" "Unknown significance" "rs568592195" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
307841 "chr12:80846439:C>A" "PTPRQ" "NM_001145026:c.392+6940C>A" "INTRON3" "Benign" "rs10746167" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1322 1322 1 973 1006 0.9672 674 694 0.9712 864 1008 0.8571 942 978 0.9632 4775 5008 0.953474
307842 "chr12:80846471:G>T" "PTPRQ" "NM_001145026:c.392+6972G>T" "INTRON3" "Unknown significance" "rs545275234" "This variant is a VUS because it does not have enough information."
307843 "chr12:80846477:A>G" "PTPRQ" "NM_001145026:c.392+6978A>G" "INTRON3" "Unknown significance" "rs192540234" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307844 "chr12:80846480:C>T" "PTPRQ" "NM_001145026:c.392+6981C>T" "INTRON3" "Unknown significance" "rs575888324" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307845 "chr12:80846497:G>T" "PTPRQ" "NM_001145026:c.392+6998G>T" "INTRON3" "Unknown significance" "rs539785930" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307846 "chr12:80846515:G>C" "PTPRQ" "NM_001145026:c.392+7016G>C" "INTRON3" "Benign" "rs150637357" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 0 1006 0 0 694 0 0 1008 0 0 978 0 20 5008 0.00399361
307847 "chr12:80846528:T>C" "PTPRQ" "NM_001145026:c.392+7029T>C" "INTRON3" "Unknown significance" "rs745331901" "This variant is a VUS because it does not have enough information."
307848 "chr12:80846546:T>C" "PTPRQ" "NM_001145026:c.392+7047T>C" "INTRON3" "Benign" "rs56162313" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 232 1006 0.2306 105 694 0.1513 3 1008 0.003 101 978 0.1033 616 5008 0.123003
307849 "chr12:80846570:C>-" "PTPRQ" "NM_001145026:c.392+7071delC" "INTRON3" "Unknown significance" "rs780774328" "This variant is a VUS because it does not have enough information."
307850 "chr12:80846608:A>C" "PTPRQ" "NM_001145026:c.392+7109A>C" "INTRON3" "Benign" "rs11613004" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 563 1006 0.5596 362 694 0.5216 531 1008 0.5268 628 978 0.6421 2165 5008 0.432308
307851 "chr12:80846626:G>A" "PTPRQ" "NM_001145026:c.392+7127G>A" "INTRON3" "Benign" "rs572321732" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 4 1006 0.004 1 694 0.0014 0 1008 0 5 978 0.0051 10 5008 0.00199681
307852 "chr12:80846627:G>A" "PTPRQ" "NM_001145026:c.392+7128G>A" "INTRON3" "Unknown significance" "rs574483945" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307853 "chr12:80846631:C>T" "PTPRQ" "NM_001145026:c.392+7132C>T" "INTRON3" "Benign" "rs7307497" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1320 1322 0.9985 973 1006 0.9672 633 694 0.9121 786 1008 0.7798 938 978 0.9591 4650 5008 0.928514
307854 "chr12:80846641:G>A" "PTPRQ" "NM_001145026:c.392+7142G>A" "INTRON3" "Benign" "rs561434767" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 4 1006 0.004 1 694 0.0014 0 1008 0 5 978 0.0051 10 5008 0.00199681
307855 "chr12:80846652:T>C" "PTPRQ" "NM_001145026:c.392+7153T>C" "INTRON3" "Unknown significance" "rs183468465" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 3 5008 0.000599042
307856 "chr12:80846658:C>A" "PTPRQ" "NM_001145026:c.392+7159C>A" "INTRON3" "Unknown significance" "rs188248385" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307857 "chr12:80846675:G>A" "PTPRQ" "NM_001145026:c.392+7176G>A" "INTRON3" "Benign" "rs12816407" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 104 1322 0.0787 86 1006 0.0855 43 694 0.062 214 1008 0.2123 60 978 0.0613 507 5008 0.101238
307858 "chr12:80846677:A>C" "PTPRQ" "NM_001145026:c.392+7178A>C" "INTRON3" "Unknown significance" "rs528468918" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307859 "chr12:80846704:T>C" "PTPRQ" "NM_001145026:c.392+7205T>C" "INTRON3" "Unknown significance" "rs547049099" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307860 "chr12:80846719:T>C" "PTPRQ" "NM_001145026:c.392+7220T>C" "INTRON3" "Unknown significance" "rs568542337" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307861 "chr12:80846721:G>C" "PTPRQ" "NM_001145026:c.392+7222G>C" "INTRON3" "Unknown significance" "rs191546813" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307862 "chr12:80846722:A>G" "PTPRQ" "NM_001145026:c.392+7223A>G" "INTRON3" "Benign" "rs11834589" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 263 1322 0.1989 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 281 5008 0.0561102
307863 "chr12:80846735:C>G" "PTPRQ" "NM_001145026:c.392+7236C>G" "INTRON3" "Benign" "rs57814907" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 232 1006 0.2306 105 694 0.1513 3 1008 0.003 101 978 0.1033 616 5008 0.123003
307864 "chr12:80846785:A>G" "PTPRQ" "NM_001145026:c.392+7286A>G" "INTRON3" "Unknown significance" "rs371248065" "This variant is a VUS because it does not have enough information."
307865 "chr12:80846792:G>A" "PTPRQ" "NM_001145026:c.392+7293G>A" "INTRON3" "Unknown significance" "rs540025912" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307866 "chr12:80846819:G>A" "PTPRQ" "NM_001145026:c.392+7320G>A" "INTRON3" "Benign" "rs55773121" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 563 1006 0.5596 362 694 0.5216 532 1008 0.5278 628 978 0.6421 2166 5008 0.432508
307867 "chr12:80846822:T>C" "PTPRQ" "NM_001145026:c.392+7323T>C" "INTRON3" "Unknown significance" "rs573214808" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307868 "chr12:80846833:C>G" "PTPRQ" "NM_001145026:c.392+7334C>G" "INTRON3" "Unknown significance" "rs200790409" "This variant is a VUS because it does not have enough information."
307869 "chr12:80846847:T>G" "PTPRQ" "NM_001145026:c.392+7348T>G" "INTRON3" "Unknown significance" "rs534303822" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307870 "chr12:80846850:T>C" "PTPRQ" "NM_001145026:c.392+7351T>C" "INTRON3" "Unknown significance" "rs552578895" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 6 5008 0.00119808
307871 "chr12:80846885:T>C" "PTPRQ" "NM_001145026:c.392+7386T>C" "INTRON3" "Benign" "rs574473120" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 5 1008 0.005 0 978 0 5 5008 0.000998403
307872 "chr12:80846908:A>G" "PTPRQ" "NM_001145026:c.392+7409A>G" "INTRON3" "Unknown significance" "rs541601569" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307873 "chr12:80846924:C>T" "PTPRQ" "NM_001145026:c.392+7425C>T" "INTRON3" "Unknown significance" "rs557030956" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 2 694 0.0029 0 1008 0 0 978 0 5 5008 0.000998403
307874 "chr12:80846925:C>T" "PTPRQ" "NM_001145026:c.392+7426C>T" "INTRON3" "Benign" "rs56121556" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 563 1006 0.5596 362 694 0.5216 532 1008 0.5278 617 978 0.6309 2155 5008 0.430312
307875 "chr12:80846937:T>C" "PTPRQ" "NM_001145026:c.392+7438T>C" "INTRON3" "Unknown significance" "rs546044393" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307876 "chr12:80846938:C>T" "PTPRQ" "NM_001145026:c.392+7439C>T" "INTRON3" "Unknown significance" "rs373221286" "This variant is a VUS because it does not have enough information."
307877 "chr12:80846952:T>C" "PTPRQ" "NM_001145026:c.392+7453T>C" "INTRON3" "Unknown significance" "rs564339842" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307878 "chr12:80846969:G>A" "PTPRQ" "NM_001145026:c.392+7470G>A" "INTRON3" "Unknown significance" "rs528421945" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 2 694 0.0029 0 1008 0 0 978 0 5 5008 0.000998403
307879 "chr12:80846972:T>C" "PTPRQ" "NM_001145026:c.392+7473T>C" "INTRON3" "Benign" "rs142147100" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 480 1322 0.3631 303 1006 0.3012 155 694 0.2233 3 1008 0.003 148 978 0.1513 1089 5008 0.217452
307880 "chr12:80846975:G>A" "PTPRQ" "NM_001145026:c.392+7476G>A" "INTRON3" "Benign" "rs561978688" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 6 978 0.0061 8 5008 0.00159744
307881 "chr12:80846976:A>T" "PTPRQ" "NM_001145026:c.392+7477A>T" "INTRON3" "Benign" "rs146701991" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 480 1322 0.3631 303 1006 0.3012 155 694 0.2233 3 1008 0.003 148 978 0.1513 1089 5008 0.217452
307882 "chr12:80846980:T>C" "PTPRQ" "NM_001145026:c.392+7481T>C" "INTRON3" "Benign" "rs190165544" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 18 5008 0.00359425
307883 "chr12:80846981:T>C" "PTPRQ" "NM_001145026:c.392+7482T>C" "INTRON3" "Unknown significance" "rs569355041" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307884 "chr12:80847016:T>C" "PTPRQ" "NM_001145026:c.392+7517T>C" "INTRON3" "Benign" "rs7299348" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 304 1322 0.23 71 1006 0.0706 51 694 0.0735 0 1008 0 48 978 0.0491 474 5008 0.0946486
307885 "chr12:80847029:T>C" "PTPRQ" "NM_001145026:c.392+7530T>C" "INTRON3" "Benign" "rs4460866" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 320 1322 0.2421 22 1006 0.0219 58 694 0.0836 37 1008 0.0367 101 978 0.1033 538 5008 0.107428
307886 "chr12:80847045:G>A" "PTPRQ" "NM_001145026:c.392+7546G>A" "INTRON3" "Benign" "rs115790639" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
307887 "chr12:80847051:A>G" "PTPRQ" "NM_001145026:c.392+7552A>G" "INTRON3" "Unknown significance" "rs376860055" "This variant is a VUS because it does not have enough information."
307888 "chr12:80847052:->T" "PTPRQ" "NM_001145026:c.392+7553_392+7554insT" "INTRON3" "Benign" "rs563457385" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 6 1006 0.006 5 694 0.0072 0 1008 0 1 978 0.001 12 5008 0.00239617
307889 "chr12:80847056:T>C" "PTPRQ" "NM_001145026:c.392+7557T>C" "INTRON3" "Unknown significance" "rs534268801" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
307890 "chr12:80847061:T>A" "PTPRQ" "NM_001145026:c.392+7562T>A" "INTRON3" "Unknown significance" "rs552540754" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
307891 "chr12:80847107:C>T" "PTPRQ" "NM_001145026:c.392+7608C>T" "INTRON3" "Unknown significance" "rs200913112" "This variant is a VUS because it does not have enough information."
307892 "chr12:80847108:G>A" "PTPRQ" "NM_001145026:c.392+7609G>A" "INTRON3" "Benign" "rs7310064" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 479 1322 0.3623 305 1006 0.3032 157 694 0.2262 6 1008 0.006 150 978 0.1534 1097 5008 0.21905
307893 "chr12:80847121:C>T" "PTPRQ" "NM_001145026:c.392+7622C>T" "INTRON3" "Unknown significance" "rs535438357" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 2 1006 0.002 3 694 0.0043 0 1008 0 3 978 0.0031 9 5008 0.00179712
307894 "chr12:80847130:C>T" "PTPRQ" "NM_001145026:c.392+7631C>T" "INTRON3" "Unknown significance" "rs556755313" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307895 "chr12:80847132:T>G" "PTPRQ" "NM_001145026:c.392+7633T>G" "INTRON3" "Benign" "rs4460867" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 423 1322 0.32 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 95 978 0.0971 641 5008 0.127995
307896 "chr12:80847133:T>C" "PTPRQ" "NM_001145026:c.392+7634T>C" "INTRON3" "Benign" "rs4400861" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 423 1322 0.32 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 95 978 0.0971 641 5008 0.127995
307897 "chr12:80847164:T>A" "PTPRQ" "NM_001145026:c.392+7665T>A" "INTRON3" "Benign" "rs558029191" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
307898 "chr12:80847184:G>A" "PTPRQ" "NM_001145026:c.392+7685G>A" "INTRON3" "Benign" "rs189276422" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 27 1322 0.0204 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 29 5008 0.00579073
307899 "chr12:80847186:T>G" "PTPRQ" "NM_001145026:c.392+7687T>G" "INTRON3" "Unknown significance" "rs540488894" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307900 "chr12:80847198:T>A" "PTPRQ" "NM_001145026:c.392+7699T>A" "INTRON3" "Unknown significance" "rs562019535" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307901 "chr12:80847206:G>T" "PTPRQ" "NM_001145026:c.392+7707G>T" "INTRON3" "Unknown significance" "rs570137914" "This variant is a VUS because it does not have enough information."
307902 "chr12:80847217:C>G" "PTPRQ" "NM_001145026:c.392+7718C>G" "INTRON3" "Unknown significance" "rs7311203" "This variant is a VUS because it does not have enough information."
307903 "chr12:80847234:G>T" "PTPRQ" "NM_001145026:c.392+7735G>T" "INTRON3" "Benign" "rs529242834" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
307904 "chr12:80847250:C>T" "PTPRQ" "NM_001145026:c.392+7751C>T" "INTRON3" "Benign" "rs544609343" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 13 1322 0.0098 2 1006 0.002 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489
307905 "chr12:80847252:C>G" "PTPRQ" "NM_001145026:c.392+7753C>G" "INTRON3" "Benign" "rs562824601" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 0 1006 0 0 694 0 0 1008 0 0 978 0 20 5008 0.00399361
307906 "chr12:80847279:->A" "PTPRQ" "NM_001145026:c.392+7780_392+7781insA" "INTRON3" "Unknown significance" "rs761620145" "This variant is a VUS because it does not have enough information."
307907 "chr12:80847318:G>A" "PTPRQ" "NM_001145026:c.392+7819G>A" "INTRON3" "Unknown significance" "rs533280487" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
307908 "chr12:80847330:G>C" "PTPRQ" "NM_001145026:c.392+7831G>C" "INTRON3" "Benign" "rs34942782" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 562 1006 0.5586 362 694 0.5216 532 1008 0.5278 628 978 0.6421 2165 5008 0.432308
307909 "chr12:80847377:C>T" "PTPRQ" "NM_001145026:c.392+7878C>T" "INTRON3" "Benign" "rs7488430" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 390 1322 0.295 21 1006 0.0209 62 694 0.0893 37 1008 0.0367 101 978 0.1033 611 5008 0.122005
307910 "chr12:80847461:G>A" "PTPRQ" "NM_001145026:c.392+7962G>A" "INTRON3" "Benign" "rs200238093" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 563 1006 0.5596 362 694 0.5216 531 1008 0.5268 627 978 0.6411 2164 5008 0.432109
307911 "chr12:80847462:A>T" "PTPRQ" "NM_001145026:c.392+7963A>T" "INTRON3" "Unknown significance" "rs113922544" "This variant is a VUS because it does not have enough information."
307912 "chr12:80847487:G>A" "PTPRQ" "NM_001145026:c.392+7988G>A" "INTRON3" "Benign" "rs201186112" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 18 1008 0.0179 0 978 0 18 5008 0.00359425
307913 "chr12:80847557:C>T" "PTPRQ" "NM_001145026:c.392+8058C>T" "INTRON3" "Unknown significance" "rs775912839" "This variant is a VUS because it does not have enough information."
307914 "chr12:80847582:G>C" "PTPRQ" "NM_001145026:c.392+8083G>C" "INTRON3" "Unknown significance" "rs567973101" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307915 "chr12:80847597:G>A" "PTPRQ" "NM_001145026:c.392+8098G>A" "INTRON3" "Unknown significance" "rs772023080" "This variant is a VUS because it does not have enough information."
307916 "chr12:80847625:G>T" "PTPRQ" "NM_001145026:c.392+8126G>T" "INTRON3" "Benign" "rs7975397" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 204 1322 0.1543 6 1006 0.006 27 694 0.0389 15 1008 0.0149 21 978 0.0215 273 5008 0.0545128
307917 "chr12:80847629:G>A" "PTPRQ" "NM_001145026:c.392+8130G>A" "INTRON3" "Benign" "rs7975401" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 49 1322 0.0371 3 1006 0.003 10 694 0.0144 2 1008 0.002 6 978 0.0061 70 5008 0.0139776
307918 "chr12:80847644:G>T" "PTPRQ" "NM_001145026:c.392+8145G>T" "INTRON3" "Unknown significance" "rs7310811" "This variant is a VUS because it does not have enough information."
307919 "chr12:80847703:T>C" "PTPRQ" "NM_001145026:c.392+8204T>C" "INTRON3" "Unknown significance" "rs112620007" "This variant is a VUS because it does not have enough information."
307920 "chr12:80847782:G>T" "PTPRQ" "NM_001145026:c.392+8283G>T" "INTRON3" "Unknown significance" "rs7975548" "This variant is a VUS because it does not have enough information."
307921 "chr12:80847820:T>C" "PTPRQ" "NM_001145026:c.392+8321T>C" "INTRON3" "Unknown significance" "rs7975698" "This variant is a VUS because it does not have enough information."
307922 "chr12:80847854:C>T" "PTPRQ" "NM_001145026:c.392+8355C>T" "INTRON3" "Unknown significance" "rs568855247" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307923 "chr12:80847863:C>T" "PTPRQ" "NM_001145026:c.392+8364C>T" "INTRON3" "Unknown significance" "rs539579881" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307924 "chr12:80847883:C>T" "PTPRQ" "NM_001145026:c.392+8384C>T" "INTRON3" "Unknown significance" "rs36134914" "This variant is a VUS because it does not have enough information."
307925 "chr12:80847930:C>T" "PTPRQ" "NM_001145026:c.392+8431C>T" "INTRON3" "Unknown significance" "rs557893833" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307926 "chr12:80847940:A>G" "PTPRQ" "NM_001145026:c.392+8441A>G" "INTRON3" "Unknown significance" "rs7972803" "This variant is a VUS because it does not have enough information."
307927 "chr12:80847943:C>-" "PTPRQ" "NM_001145026:c.392+8444delC" "INTRON3" "Unknown significance" "rs36129800" "This variant is a VUS because it does not have enough information."
307928 "chr12:80847996:G>A" "PTPRQ" "NM_001145026:c.392+8497G>A" "INTRON3" "Unknown significance" "rs573025094" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 1 1006 0.001 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307929 "chr12:80847999:G>A" "PTPRQ" "NM_001145026:c.392+8500G>A" "INTRON3" "Unknown significance" "rs185172456" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
307930 "chr12:80848059:T>G" "PTPRQ" "NM_001145026:c.392+8560T>G" "INTRON3" "Unknown significance" "rs761749447" "This variant is a VUS because it does not have enough information."
307931 "chr12:80848095:C>T" "PTPRQ" "NM_001145026:c.392+8596C>T" "INTRON3" "Benign" "rs7958430" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 318 1322 0.2405 20 1006 0.0199 54 694 0.0778 36 1008 0.0357 100 978 0.1022 528 5008 0.105431
307932 "chr12:80848096:A>G" "PTPRQ" "NM_001145026:c.392+8597A>G" "INTRON3" "Benign" "rs7972946" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1238 1322 0.9365 407 1006 0.4046 266 694 0.3833 252 1008 0.25 304 978 0.3108 2467 5008 0.492612
307933 "chr12:80848100:C>T" "PTPRQ" "NM_001145026:c.392+8601C>T" "INTRON3" "Unknown significance" "rs544259094" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307934 "chr12:80848102:C>T" "PTPRQ" "NM_001145026:c.392+8603C>T" "INTRON3" "Benign" "rs7958434" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 245 1322 0.1853 0 1006 0 11 694 0.0159 0 1008 0 0 978 0 256 5008 0.0511182
307935 "chr12:80848103:G>A" "PTPRQ" "NM_001145026:c.392+8604G>A" "INTRON3" "Benign" "rs149196119" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 263 1322 0.1989 1 1006 0.001 18 694 0.0259 0 1008 0 1 978 0.001 283 5008 0.0565096
307936 "chr12:80848129:C>T" "PTPRQ" "NM_001145026:c.392+8630C>T" "INTRON3" "Benign" "rs545059225" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 6 1322 0.0045 31 1006 0.0308 14 694 0.0202 0 1008 0 11 978 0.0112 62 5008 0.0123802
307937 "chr12:80848136:C>T" "PTPRQ" "NM_001145026:c.392+8637C>T" "INTRON3" "Unknown significance" "rs560218945" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 1 1006 0.001 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307938 "chr12:80848145:C>T" "PTPRQ" "NM_001145026:c.392+8646C>T" "INTRON3" "Benign" "rs11114451" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 195 1322 0.1475 231 1006 0.2296 105 694 0.1513 4 1008 0.004 101 978 0.1033 636 5008 0.126997
307939 "chr12:80848146:G>A" "PTPRQ" "NM_001145026:c.392+8647G>A" "INTRON3" "Unknown significance" "rs12311761" "This variant is a VUS because it does not have enough information."
307940 "chr12:80848172:G>T" "PTPRQ" "NM_001145026:c.392+8673G>T" "INTRON3" "Benign" "rs7957660" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 408 1322 0.3086 21 1006 0.0209 63 694 0.0908 37 1008 0.0367 101 978 0.1033 630 5008 0.125799
307941 "chr12:80848192:A>G" "PTPRQ" "NM_001145026:c.392+8693A>G" "INTRON3" "Unknown significance" "rs374876850" "This variant is a VUS because it does not have enough information."
307942 "chr12:80848199:C>T" "PTPRQ" "NM_001145026:c.392+8700C>T" "INTRON3" "Unknown significance" "rs561409594" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307943 "chr12:80848200:G>A" "PTPRQ" "NM_001145026:c.392+8701G>A" "INTRON3" "Benign" "rs7957671" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 408 1322 0.3086 21 1006 0.0209 63 694 0.0908 37 1008 0.0367 101 978 0.1033 630 5008 0.125799
307944 "chr12:80848230:C>T" "PTPRQ" "NM_001145026:c.392+8731C>T" "INTRON3" "Benign" "rs11114452" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 101 978 0.1033 615 5008 0.122804
307945 "chr12:80848231:G>A" "PTPRQ" "NM_001145026:c.392+8732G>A" "INTRON3" "Unknown significance" "rs773307185" "This variant is a VUS because it does not have enough information."
307946 "chr12:80848242:C>T" "PTPRQ" "NM_001145026:c.392+8743C>T" "INTRON3" "Unknown significance" "rs568827796" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 3 1008 0.003 0 978 0 4 5008 0.000798722
307947 "chr12:80848247:A>C" "PTPRQ" "NM_001145026:c.392+8748A>C" "INTRON3" "Benign" "rs563743787" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 8 1006 0.008 5 694 0.0072 0 1008 0 3 978 0.0031 16 5008 0.00319489
307948 "chr12:80848266:G>A" "PTPRQ" "NM_001145026:c.392+8767G>A" "INTRON3" "Unknown significance" "rs551473106" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 4 1008 0.004 0 978 0 5 5008 0.000998403
307949 "chr12:80848278:A>G" "PTPRQ" "NM_001145026:c.392+8779A>G" "INTRON3" "Unknown significance" "rs566587141" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 1 1008 0.001 0 978 0 2 5008 0.000399361
307950 "chr12:80848293:C>A" "PTPRQ" "NM_001145026:c.392+8794C>A" "INTRON3" "Unknown significance" "rs367586914" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307951 "chr12:80848301:G>A" "PTPRQ" "NM_001145026:c.392+8802G>A" "INTRON3" "Unknown significance" "rs141804963" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307952 "chr12:80848303:A>G" "PTPRQ" "NM_001145026:c.392+8804A>G" "INTRON3" "Unknown significance" "rs369547383" "This variant is a VUS because it does not have enough information."
307953 "chr12:80848308:T>A" "PTPRQ" "NM_001145026:c.392+8809T>A" "INTRON3" "Unknown significance" "rs573851738" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
307954 "chr12:80848333:A>C" "PTPRQ" "NM_001145026:c.392+8834A>C" "INTRON3" "Unknown significance" "rs373010231" "This variant is a VUS because it does not have enough information."
307955 "chr12:80848352:G>A" "PTPRQ" "NM_001145026:c.392+8853G>A" "INTRON3" "Unknown significance" "rs532565980" "This variant is a VUS because it does not have enough information."
307956 "chr12:80848383:->A" "PTPRQ" "NM_001145026:c.392+8884_392+8885insA" "INTRON3" "Unknown significance" "rs146212962" "This variant is a VUS because it does not have enough information."
307957 "chr12:80848400:A>G" "PTPRQ" "NM_001145026:c.392+8901A>G" "INTRON3" "Unknown significance" "rs56011272" "This variant is a VUS because it does not have enough information."
307958 "chr12:80848413:A>C" "PTPRQ" "NM_001145026:c.392+8914A>C" "INTRON3" "Unknown significance" "rs189980071" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
307959 "chr12:80848434:T>-" "PTPRQ" "NM_001145026:c.392+8935delT" "INTRON3" "Unknown significance" "rs35665506" "This variant is a VUS because it does not have enough information."
307960 "chr12:80848443:->A" "PTPRQ" "NM_001145026:c.392+8944_392+8945insA" "INTRON3" "Benign" "rs150327117" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 103 978 0.1053 617 5008 0.123203
307961 "chr12:80848458:G>A" "PTPRQ" "NM_001145026:c.392+8959G>A" "INTRON3" "Unknown significance" "rs759738546" "This variant is a VUS because it does not have enough information."
307962 "chr12:80848489:C>T" "PTPRQ" "NM_001145026:c.392+8990C>T" "INTRON3" "Unknown significance" "rs559732580" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307963 "chr12:80848528:A>G" "PTPRQ" "NM_001145026:c.392+9029A>G" "INTRON3" "Unknown significance" "rs753057944" "This variant is a VUS because it does not have enough information."
307964 "chr12:80848563:T>C" "PTPRQ" "NM_001145026:c.392+9064T>C" "INTRON3" "Unknown significance" "rs577569084" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307965 "chr12:80848583:A>G" "PTPRQ" "NM_001145026:c.392+9084A>G" "INTRON3" "Unknown significance" "rs545025083" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307966 "chr12:80848586:T>C" "PTPRQ" "NM_001145026:c.392+9087T>C" "INTRON3" "Unknown significance" "rs756720724" "This variant is a VUS because it does not have enough information."
307967 "chr12:80848640:A>G" "PTPRQ" "NM_001145026:c.392+9141A>G" "INTRON3" "Unknown significance" "rs768597489" "This variant is a VUS because it does not have enough information."
307968 "chr12:80848688:A>G" "PTPRQ" "NM_001145026:c.392+9189A>G" "INTRON3" "Unknown significance" "rs560182533" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307969 "chr12:80848702:A>G" "PTPRQ" "NM_001145026:c.392+9203A>G" "INTRON3" "Unknown significance" "rs778716753" "This variant is a VUS because it does not have enough information."
307970 "chr12:80848737:T>A" "PTPRQ" "NM_001145026:c.392+9238T>A" "INTRON3" "Benign" "rs537204411" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 1 1006 0.001 0 694 0 0 1008 0 32 978 0.0327 34 5008 0.00678914
307971 "chr12:80848765:G>A" "PTPRQ" "NM_001145026:c.392+9266G>A" "INTRON3" "Unknown significance" "rs747916178" "This variant is a VUS because it does not have enough information."
307972 "chr12:80848805:A>T" "PTPRQ" "NM_001145026:c.392+9306A>T" "INTRON3" "Unknown significance" "rs778463988" "This variant is a VUS because it does not have enough information."
307973 "chr12:80848806:T>C" "PTPRQ" "NM_001145026:c.392+9307T>C" "INTRON3" "Unknown significance" "rs528366811" "This variant is a VUS because it does not have enough information."
307974 "chr12:80848832:A>G" "PTPRQ" "NM_001145026:c.392+9333A>G" "INTRON3" "Unknown significance" "rs772047230" "This variant is a VUS because it does not have enough information."
307975 "chr12:80848905:G>A" "PTPRQ" "NM_001145026:c.392+9406G>A" "INTRON3" "Benign" "rs542832882" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 0 1006 0 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744
307976 "chr12:80848916:T>C" "PTPRQ" "NM_001145026:c.392+9417T>C" "INTRON3" "Benign" "rs12308829" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
307977 "chr12:80848916:TG>CA" "PTPRQ" "Unknown significance" "rs386764635" "This variant is a VUS because it does not have enough information."
307978 "chr12:80848917:G>A" "PTPRQ" "NM_001145026:c.392+9418G>A" "INTRON3" "Benign" "rs12313529" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
307979 "chr12:80848925:T>G" "PTPRQ" "NM_001145026:c.392+9426T>G" "INTRON3" "Benign" "rs7979859" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 479 1322 0.3623 302 1006 0.3002 156 694 0.2248 3 1008 0.003 150 978 0.1534 1090 5008 0.217652
307980 "chr12:80848952:G>A" "PTPRQ" "NM_001145026:c.392+9453G>A" "INTRON3" "Unknown significance" "rs746643901" "This variant is a VUS because it does not have enough information."
307981 "chr12:80848963:T>C" "PTPRQ" "NM_001145026:c.392+9464T>C" "INTRON3" "Unknown significance" "rs768294988" "This variant is a VUS because it does not have enough information."
307982 "chr12:80848977:C>T" "PTPRQ" "NM_001145026:c.392+9478C>T" "INTRON3" "Unknown significance" "rs796697792" "This variant is a VUS because it does not have enough information."
307983 "chr12:80849017:G>C" "PTPRQ" "NM_001145026:c.392+9518G>C" "INTRON3" "Unknown significance" "rs565597578" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 5 5008 0.000998403
307984 "chr12:80849026:T>A" "PTPRQ" "NM_001145026:c.392+9527T>A" "INTRON3" "Unknown significance" "rs183184343" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 1 694 0.0014 0 1008 0 0 978 0 4 5008 0.000798722
307985 "chr12:80849039:C>T" "PTPRQ" "NM_001145026:c.392+9540C>T" "INTRON3" "Benign" "rs11114453" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
307986 "chr12:80849045:G>C" "PTPRQ" "NM_001145026:c.392+9546G>C" "INTRON3" "Unknown significance" "rs762950070" "This variant is a VUS because it does not have enough information."
307987 "chr12:80849063:T>C" "PTPRQ" "NM_001145026:c.392+9564T>C" "INTRON3" "Benign" "rs7980018" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 324 1006 0.3221 221 694 0.3184 40 1008 0.0397 251 978 0.2566 1741 5008 0.347644
307988 "chr12:80849070:A>G" "PTPRQ" "NM_001145026:c.392+9571A>G" "INTRON3" "Benign" "rs527429143" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 0 1006 0 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744
307989 "chr12:80849086:A>G" "PTPRQ" "NM_001145026:c.392+9587A>G" "INTRON3" "Unknown significance" "rs752066321" "This variant is a VUS because it does not have enough information."
307990 "chr12:80849118:T>C" "PTPRQ" "NM_001145026:c.392+9619T>C" "INTRON3" "Unknown significance" "rs548898060" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307991 "chr12:80849126:C>T" "PTPRQ" "NM_001145026:c.392+9627C>T" "INTRON3" "Unknown significance" "rs550278674" "This variant is a VUS because it does not have enough information."
307992 "chr12:80849168:G>A" "PTPRQ" "NM_001145026:c.392+9669G>A" "INTRON3" "Unknown significance" "rs567413954" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
307993 "chr12:80849175:G>A" "PTPRQ" "NM_001145026:c.392+9676G>A" "INTRON3" "Unknown significance" "rs762233820" "This variant is a VUS because it does not have enough information."
307994 "chr12:80849234:T>G" "PTPRQ" "NM_001145026:c.392+9735T>G" "INTRON3" "Unknown significance" "rs537648514" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
307995 "chr12:80849261:A>C" "PTPRQ" "NM_001145026:c.392+9762A>C" "INTRON3" "Benign" "rs150592597" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
307996 "chr12:80849271:A>G" "PTPRQ" "NM_001145026:c.392+9772A>G" "INTRON3" "Unknown significance" "rs186525522" "This variant is a VUS because it does not have enough information."
307997 "chr12:80849275:C>T" "PTPRQ" "NM_001145026:c.392+9776C>T" "INTRON3" "Unknown significance" "rs767910054" "This variant is a VUS because it does not have enough information."
307998 "chr12:80849279:T>C" "PTPRQ" "NM_001145026:c.392+9780T>C" "INTRON3" "Benign" "rs76775226" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 18 1006 0.0179 4 694 0.0058 0 1008 0 9 978 0.0092 32 5008 0.00638978
307999 "chr12:80849298:G>A" "PTPRQ" "NM_001145026:c.392+9799G>A" "INTRON3" "Unknown significance" "rs191801650" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308000 "chr12:80849299:T>-" "PTPRQ" "NM_001145026:c.392+9800delT" "INTRON3" "Unknown significance" "rs34480167" "This variant is a VUS because it does not have enough information."
308001 "chr12:80849328:G>A" "PTPRQ" "NM_001145026:c.392+9829G>A" "INTRON3" "Benign" "rs4482094" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1216 1322 0.9198 887 1006 0.8817 590 694 0.8501 572 1008 0.5675 878 978 0.8978 4143 5008 0.827276
308002 "chr12:80849329:C>G" "PTPRQ" "NM_001145026:c.392+9830C>G" "INTRON3" "Unknown significance" "rs572195870" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 1 1008 0.001 0 978 0 2 5008 0.000399361
308003 "chr12:80849343:A>G" "PTPRQ" "NM_001145026:c.392+9844A>G" "INTRON3" "Unknown significance" "rs377478735" "This variant is a VUS because it does not have enough information."
308004 "chr12:80849345:A>C" "PTPRQ" "NM_001145026:c.392+9846A>C" "INTRON3" "Unknown significance" "rs543065295" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308005 "chr12:80849348:A>G" "PTPRQ" "NM_001145026:c.392+9849A>G" "INTRON3" "Unknown significance" "rs183258549" "This variant is a VUS because it does not have enough information."
308006 "chr12:80849348:A>T" "PTPRQ" "NM_001145026:c.392+9849A>T" "INTRON3" "Unknown significance" "rs183258549" "This variant is a VUS because it does not have enough information."
308007 "chr12:80849351:T>A" "PTPRQ" "NM_001145026:c.392+9852T>A" "INTRON3" "Unknown significance" "rs554765736" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308008 "chr12:80849388:A>T" "PTPRQ" "NM_001145026:c.392+9889A>T" "INTRON3" "Unknown significance" "rs551266263" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
308009 "chr12:80849389:T>A" "PTPRQ" "NM_001145026:c.392+9890T>A" "INTRON3" "Unknown significance" "rs566401859" "This variant is a VUS because it does not have enough information."
308010 "chr12:80849398:T>C" "PTPRQ" "NM_001145026:c.392+9899T>C" "INTRON3" "Unknown significance" "rs543669790" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308011 "chr12:80849429:C>T" "PTPRQ" "NM_001145026:c.392+9930C>T" "INTRON3" "Unknown significance" "rs534989227" "This variant is a VUS because it does not have enough information."
308012 "chr12:80849430:G>A" "PTPRQ" "NM_001145026:c.392+9931G>A" "INTRON3" "Unknown significance" "rs779710150" "This variant is a VUS because it does not have enough information."
308013 "chr12:80849453:C>T" "PTPRQ" "NM_001145026:c.392+9954C>T" "INTRON3" "Unknown significance" "rs187394184" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 3 5008 0.000599042
308014 "chr12:80849461:G>A" "PTPRQ" "NM_001145026:c.392+9962G>A" "INTRON3" "Unknown significance" "rs573286482" "This variant is a VUS because it does not have enough information."
308015 "chr12:80849462:T>C" "PTPRQ" "NM_001145026:c.392+9963T>C" "INTRON3" "Unknown significance" "rs574955582" "This variant is a VUS because it does not have enough information."
308016 "chr12:80849470:T>C" "PTPRQ" "NM_001145026:c.392+9971T>C" "INTRON3" "Unknown significance" "rs281865414" "This variant is a VUS because it does not have enough information."
308017 "chr12:80849477:G>A" "PTPRQ" "NM_001145026:c.392+9978G>A" "INTRON3" "Unknown significance" "rs762875679" "This variant is a VUS because it does not have enough information."
308018 "chr12:80849500:T>C" "PTPRQ" "NM_001145026:c.392+10001T>C" "INTRON3" "Unknown significance" "rs537607144" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308019 "chr12:80849528:G>T" "PTPRQ" "NM_001145026:c.392+10029G>T" "INTRON3" "Unknown significance" "rs771973896" "This variant is a VUS because it does not have enough information."
308020 "chr12:80849549:G>C" "PTPRQ" "NM_001145026:c.392+10050G>C" "INTRON3" "Unknown significance" "rs777666031" "This variant is a VUS because it does not have enough information."
308021 "chr12:80849559:G>A" "PTPRQ" "NM_001145026:c.392+10060G>A" "INTRON3" "Unknown significance" "rs545018099" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308022 "chr12:80849566:C>G" "PTPRQ" "NM_001145026:c.392+10067C>G" "INTRON3" "Unknown significance" "rs560232222" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308023 "chr12:80849572:G>A" "PTPRQ" "NM_001145026:c.392+10073G>A" "INTRON3" "Unknown significance" "rs746834543" "This variant is a VUS because it does not have enough information."
308024 "chr12:80849580:A>G" "PTPRQ" "NM_001145026:c.392+10081A>G" "INTRON3" "Benign" "rs10862121" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 221 694 0.3184 40 1008 0.0397 251 978 0.2566 1740 5008 0.347444
308025 "chr12:80849585:T>A" "PTPRQ" "NM_001145026:c.392+10086T>A" "INTRON3" "Unknown significance" "rs549016330" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308026 "chr12:80849585:T>C" "PTPRQ" "NM_001145026:c.392+10086T>C" "INTRON3" "Unknown significance" "rs549016330" "This variant is a VUS because it does not have enough information."
308027 "chr12:80849591:C>G" "PTPRQ" "NM_001145026:c.392+10092C>G" "INTRON3" "Unknown significance" "rs567272642" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
308028 "chr12:80849602:T>C" "PTPRQ" "NM_001145026:c.392+10103T>C" "INTRON3" "Unknown significance" "rs531502208" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308029 "chr12:80849603:T>G" "PTPRQ" "NM_001145026:c.392+10104T>G" "INTRON3" "Benign" "rs139609196" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 6 1006 0.006 3 694 0.0043 0 1008 0 0 978 0 9 5008 0.00179712
308030 "chr12:80849606:T>G" "PTPRQ" "NM_001145026:c.392+10107T>G" "INTRON3" "Benign" "rs74108658" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 129 1322 0.0976 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 135 5008 0.0269569
308031 "chr12:80849620:->T" "PTPRQ" "NM_001145026:c.392+10121_392+10122insT" "INTRON3" "Unknown significance" "rs35959993" "This variant is a VUS because it does not have enough information."
308032 "chr12:80849621:A>G" "PTPRQ" "NM_001145026:c.392+10122A>G" "INTRON3" "Unknown significance" "rs567828828" "This variant is a VUS because it does not have enough information."
308033 "chr12:80849632:C>T" "PTPRQ" "NM_001145026:c.392+10133C>T" "INTRON3" "Unknown significance" "rs538597364" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308034 "chr12:80849639:T>C" "PTPRQ" "NM_001145026:c.392+10140T>C" "INTRON3" "Unknown significance" "rs768687946" "This variant is a VUS because it does not have enough information."
308035 "chr12:80849662:C>A" "PTPRQ" "NM_001145026:c.392+10163C>A" "INTRON3" "Unknown significance" "rs546261858" "This variant is a VUS because it does not have enough information."
308036 "chr12:80849682:T>G" "PTPRQ" "NM_001145026:c.392+10183T>G" "INTRON3" "Unknown significance" "rs192388698" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
308037 "chr12:80849682:T>C" "PTPRQ" "NM_001145026:c.392+10183T>C" "INTRON3" "Unknown significance" "rs192388698" "This variant is a VUS because it does not have enough information."
308038 "chr12:80849706:G>A" "PTPRQ" "NM_001145026:c.392+10207G>A" "INTRON3" "Benign" "rs12313966" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
308039 "chr12:80849719:T>C" "PTPRQ" "NM_001145026:c.392+10220T>C" "INTRON3" "Unknown significance" "rs536269790" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308040 "chr12:80849726:T>C" "PTPRQ" "NM_001145026:c.392+10227T>C" "INTRON3" "Unknown significance" "rs183341312" "This variant is a VUS because it does not have enough information."
308041 "chr12:80849742:C>T" "PTPRQ" "NM_001145026:c.392+10243C>T" "INTRON3" "Benign" "rs10862122" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 221 694 0.3184 40 1008 0.0397 250 978 0.2556 1739 5008 0.347244
308042 "chr12:80849794:C>T" "PTPRQ" "NM_001145026:c.392+10295C>T" "INTRON3" "Benign" "rs10862123" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 221 694 0.3184 40 1008 0.0397 250 978 0.2556 1739 5008 0.347244
308043 "chr12:80849800:G>T" "PTPRQ" "NM_001145026:c.392+10301G>T" "INTRON3" "Unknown significance" "rs753488711" "This variant is a VUS because it does not have enough information."
308044 "chr12:80849802:A>T" "PTPRQ" "NM_001145026:c.392+10303A>T" "INTRON3" "Unknown significance" "rs561985088" "This variant is a VUS because it does not have enough information."
308045 "chr12:80849808:A>G" "PTPRQ" "NM_001145026:c.392+10309A>G" "INTRON3" "Unknown significance" "rs543973829" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308046 "chr12:80849890:T>A" "PTPRQ" "NM_001145026:c.392+10391T>A" "INTRON3" "Unknown significance" "rs559241239" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308047 "chr12:80849898:T>G" "PTPRQ" "NM_001145026:c.392+10399T>G" "INTRON3" "Benign" "rs34243691" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 104 1322 0.0787 86 1006 0.0855 43 694 0.062 214 1008 0.2123 60 978 0.0613 507 5008 0.101238
308048 "chr12:80849942:T>A" "PTPRQ" "NM_001145026:c.392+10443T>A" "INTRON3" "Unknown significance" "rs541706863" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308049 "chr12:80849947:C>T" "PTPRQ" "NM_001145026:c.392+10448C>T" "INTRON3" "Unknown significance" "rs560093042" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308050 "chr12:80849960:C>T" "PTPRQ" "NM_001145026:c.392+10461C>T" "INTRON3" "Unknown significance" "rs186611449" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 2 978 0.002 3 5008 0.000599042
308051 "chr12:80849961:G>A" "PTPRQ" "NM_001145026:c.392+10462G>A" "INTRON3" "Benign" "rs78545075" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 22 1322 0.0166 0 1006 0 0 694 0 0 1008 0 0 978 0 22 5008 0.00439297
308052 "chr12:80849979:A>G" "PTPRQ" "NM_001145026:c.392+10480A>G" "INTRON3" "Unknown significance" "rs550315400" "This variant is a VUS because it does not have enough information."
308053 "chr12:80849992:G>T" "PTPRQ" "NM_001145026:c.392+10493G>T" "INTRON3" "Unknown significance" "rs146231883" "This variant is a VUS because it does not have enough information."
308054 "chr12:80850089:G>T" "PTPRQ" "NM_001145026:c.392+10590G>T" "INTRON3" "Unknown significance" "rs367714795" "This variant is a VUS because it does not have enough information."
308055 "chr12:80850095:C>A" "PTPRQ" "NM_001145026:c.392+10596C>A" "INTRON3" "Unknown significance" "rs561024998" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 1 978 0.001 2 5008 0.000399361
308056 "chr12:80850096:A>C" "PTPRQ" "NM_001145026:c.392+10597A>C" "INTRON3" "Unknown significance" "rs758373636" "This variant is a VUS because it does not have enough information."
308057 "chr12:80850127:G>A" "PTPRQ" "NM_001145026:c.392+10628G>A" "INTRON3" "Benign" "rs7300248" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 479 1322 0.3623 302 1006 0.3002 156 694 0.2248 3 1008 0.003 149 978 0.1524 1089 5008 0.217452
308058 "chr12:80850130:G>A" "PTPRQ" "NM_001145026:c.392+10631G>A" "INTRON3" "Unknown significance" "rs191404126" "This variant is a VUS because it does not have enough information."
308059 "chr12:80850168:T>C" "PTPRQ" "NM_001145026:c.392+10669T>C" "INTRON3" "Unknown significance" "rs184841270" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 1 1006 0.001 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308060 "chr12:80850171:T>C" "PTPRQ" "NM_001145026:c.392+10672T>C" "INTRON3" "Unknown significance" "rs535455538" "This variant is a VUS because it does not have enough information."
308061 "chr12:80850187:C>T" "PTPRQ" "NM_001145026:c.392+10688C>T" "INTRON3" "Benign" "rs75757749" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 30 1322 0.0227 0 1006 0 0 694 0 0 1008 0 0 978 0 30 5008 0.00599042
308062 "chr12:80850194:T>A" "PTPRQ" "NM_001145026:c.392+10695T>A" "INTRON3" "Unknown significance" "rs187808104" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308063 "chr12:80850232:T>-" "PTPRQ" "NM_001145026:c.392+10733delT" "INTRON3" "Unknown significance" "rs757770664" "This variant is a VUS because it does not have enough information."
308064 "chr12:80850274:C>T" "PTPRQ" "NM_001145026:c.392+10775C>T" "INTRON3" "Unknown significance" "rs139246959" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 0 694 0 1 1008 0.001 0 978 0 4 5008 0.000798722
308065 "chr12:80850277:C>G" "PTPRQ" "NM_001145026:c.392+10778C>G" "INTRON3" "Unknown significance" "rs765818135" "This variant is a VUS because it does not have enough information."
308066 "chr12:80850320:A>C" "PTPRQ" "NM_001145026:c.392+10821A>C" "INTRON3" "Unknown significance" "rs546220832" "This variant is a VUS because it does not have enough information."
308067 "chr12:80850357:C>T" "PTPRQ" "NM_001145026:c.392+10858C>T" "INTRON3" "Unknown significance" "rs565848689" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308068 "chr12:80850365:C>T" "PTPRQ" "NM_001145026:c.392+10866C>T" "INTRON3" "Unknown significance" "rs751028640" "This variant is a VUS because it does not have enough information."
308069 "chr12:80850408:C>T" "PTPRQ" "NM_001145026:c.392+10909C>T" "INTRON3" "Unknown significance" "rs536633741" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308070 "chr12:80850416:C>T" "PTPRQ" "NM_001145026:c.392+10917C>T" "INTRON3" "Unknown significance" "rs192915183" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
308071 "chr12:80850422:C>T" "PTPRQ" "NM_001145026:c.392+10923C>T" "INTRON3" "Unknown significance" "rs374971747" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 1 978 0.001 2 5008 0.000399361
308072 "chr12:80850440:A>C" "PTPRQ" "NM_001145026:c.392+10941A>C" "INTRON3" "Benign" "rs12809610" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 104 1322 0.0787 86 1006 0.0855 43 694 0.062 214 1008 0.2123 60 978 0.0613 507 5008 0.101238
308073 "chr12:80850443:A>T" "PTPRQ" "NM_001145026:c.392+10944A>T" "INTRON3" "Unknown significance" "rs559103703" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308074 "chr12:80850453:T>C" "PTPRQ" "NM_001145026:c.392+10954T>C" "INTRON3" "Unknown significance" "rs577468717" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308075 "chr12:80850515:A>C" "PTPRQ" "NM_001145026:c.392+11016A>C" "INTRON3" "Unknown significance" "rs371990632" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 1 978 0.001 4 5008 0.000798722
308076 "chr12:80850522:A>T" "PTPRQ" "NM_001145026:c.392+11023A>T" "INTRON3" "Benign" "rs10862124" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 565 1006 0.5616 362 694 0.5216 532 1008 0.5278 625 978 0.6391 2165 5008 0.432308
308077 "chr12:80850532:C>T" "PTPRQ" "NM_001145026:c.392+11033C>T" "INTRON3" "Unknown significance" "rs185051618" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308078 "chr12:80850547:A>G" "PTPRQ" "NM_001145026:c.392+11048A>G" "INTRON3" "Unknown significance" "rs548616669" "This variant is a VUS because it does not have enough information."
308079 "chr12:80850554:C>T" "PTPRQ" "NM_001145026:c.392+11055C>T" "INTRON3" "Unknown significance" "rs542588953" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308080 "chr12:80850555:G>A" "PTPRQ" "NM_001145026:c.392+11056G>A" "INTRON3" "Unknown significance" "rs144040680" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308081 "chr12:80850559:T>C" "PTPRQ" "NM_001145026:c.392+11060T>C" "INTRON3" "Benign" "rs11114454" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 102 978 0.1043 616 5008 0.123003
308082 "chr12:80850560:G>A" "PTPRQ" "NM_001145026:c.392+11061G>A" "INTRON3" "Unknown significance" "rs543064844" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308083 "chr12:80850568:T>C" "PTPRQ" "NM_001145026:c.392+11069T>C" "INTRON3" "Unknown significance" "rs564658260" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308084 "chr12:80850576:T>C" "PTPRQ" "NM_001145026:c.392+11077T>C" "INTRON3" "Benign" "rs11114455" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 324 1322 0.2451 21 1006 0.0209 61 694 0.0879 37 1008 0.0367 101 978 0.1033 544 5008 0.108626
308085 "chr12:80850617:T>C" "PTPRQ" "NM_001145026:c.392+11118T>C" "INTRON3" "Benign" "rs114961525" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 30 1322 0.0227 0 1006 0 0 694 0 0 1008 0 0 978 0 30 5008 0.00599042
308086 "chr12:80850619:T>C" "PTPRQ" "NM_001145026:c.392+11120T>C" "INTRON3" "Unknown significance" "rs761011191" "This variant is a VUS because it does not have enough information."
308087 "chr12:80850629:A>T" "PTPRQ" "NM_001145026:c.392+11130A>T" "INTRON3" "Unknown significance" "rs766716227" "This variant is a VUS because it does not have enough information."
308088 "chr12:80850643:->A" "PTPRQ" "NM_001145026:c.392+11144_392+11145insA" "INTRON3" "Benign" "rs111637311" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 220 694 0.317 40 1008 0.0397 251 978 0.2566 1739 5008 0.347244
308089 "chr12:80850645:A>C" "PTPRQ" "NM_001145026:c.392+11146A>C" "INTRON3" "Benign" "rs189130342" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 1 1006 0.001 0 694 0 6 1008 0.006 0 978 0 7 5008 0.00139776
308090 "chr12:80850648:T>A" "PTPRQ" "NM_001145026:c.392+11149T>A" "INTRON3" "Unknown significance" "rs146431508" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308091 "chr12:80850668:C>T" "PTPRQ" "NM_001145026:c.392+11169C>T" "INTRON3" "Unknown significance" "rs577450221" "This variant is a VUS because it does not have enough information."
308092 "chr12:80850705:G>A" "PTPRQ" "NM_001145026:c.392+11206G>A" "INTRON3" "Unknown significance" "rs548553185" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308093 "chr12:80850736:G>C" "PTPRQ" "NM_001145026:c.392+11237G>C" "INTRON3" "Unknown significance" "rs555042933" "This variant is a VUS because it does not have enough information."
308094 "chr12:80850760:C>A" "PTPRQ" "NM_001145026:c.392+11261C>A" "INTRON3" "Unknown significance" "rs759064616" "This variant is a VUS because it does not have enough information."
308095 "chr12:80850765:T>A" "PTPRQ" "NM_001145026:c.392+11266T>A" "INTRON3" "Unknown significance" "rs181874234" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
308096 "chr12:80850818:C>T" "PTPRQ" "NM_001145026:c.392+11319C>T" "INTRON3" "Unknown significance" "rs148607908" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 1 1006 0.001 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308097 "chr12:80850825:A>G" "PTPRQ" "NM_001145026:c.392+11326A>G" "INTRON3" "Unknown significance" "rs752192510" "This variant is a VUS because it does not have enough information."
308098 "chr12:80850867:C>T" "PTPRQ" "NM_001145026:c.392+11368C>T" "INTRON3" "Unknown significance" "rs552676412" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308099 "chr12:80850877:C>A" "PTPRQ" "NM_001145026:c.392+11378C>A" "INTRON3" "Unknown significance" "rs757999526" "This variant is a VUS because it does not have enough information."
308100 "chr12:80850887:C>T" "PTPRQ" "NM_001145026:c.392+11388C>T" "INTRON3" "Unknown significance" "rs764115113" "This variant is a VUS because it does not have enough information."
308101 "chr12:80850923:A>C" "PTPRQ" "NM_001145026:c.392+11424A>C" "INTRON3" "Benign" "rs142043759" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
308102 "chr12:80850963:A>C" "PTPRQ" "NM_001145026:c.392+11464A>C" "INTRON3" "Unknown significance" "rs751614551" "This variant is a VUS because it does not have enough information."
308103 "chr12:80850968:A>T" "PTPRQ" "NM_001145026:c.392+11469A>T" "INTRON3" "Unknown significance" "rs535217333" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308104 "chr12:80850970:A>C" "PTPRQ" "NM_001145026:c.392+11471A>C" "INTRON3" "Unknown significance" "rs780900830" "This variant is a VUS because it does not have enough information."
308105 "chr12:80850984:A>G" "PTPRQ" "NM_001145026:c.392+11485A>G" "INTRON3" "Unknown significance" "rs151116946" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
308106 "chr12:80851005:A>C" "PTPRQ" "NM_001145026:c.909-11482A>C" "INTRON3" "Unknown significance" "rs745696781" "This variant is a VUS because it does not have enough information."
308107 "chr12:80851009:G>C" "PTPRQ" "NM_001145026:c.909-11478G>C" "INTRON3" "Unknown significance" "rs572204517" "This variant is a VUS because it does not have enough information."
308108 "chr12:80851027:T>C" "PTPRQ" "NM_001145026:c.909-11460T>C" "INTRON3" "Benign" "rs375966906" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 18 978 0.0184 18 5008 0.00359425
308109 "chr12:80851054:A>C" "PTPRQ" "NM_001145026:c.909-11433A>C" "INTRON3" "Unknown significance" "rs535815981" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308110 "chr12:80851071:G>A" "PTPRQ" "NM_001145026:c.909-11416G>A" "INTRON3" "Benign" "rs7969433" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 428 1322 0.3238 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 652 5008 0.130192
308111 "chr12:80851100:G>A" "PTPRQ" "NM_001145026:c.909-11387G>A" "INTRON3" "Unknown significance" "rs141075560" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308112 "chr12:80851104:ATAC>-" "PTPRQ" "NM_001145026:c.909-11383_909-11380delATAC" "INTRON3" "Unknown significance" "rs772021972" "This variant is a VUS because it does not have enough information."
308113 "chr12:80851122:C>T" "PTPRQ" "NM_001145026:c.909-11365C>T" "INTRON3" "Unknown significance" "rs373026335" "This variant is a VUS because it does not have enough information."
308114 "chr12:80851143:A>C" "PTPRQ" "NM_001145026:c.909-11344A>C" "INTRON3" "Benign" "rs11114456" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 479 1322 0.3623 302 1006 0.3002 156 694 0.2248 3 1008 0.003 149 978 0.1524 1089 5008 0.217452
308115 "chr12:80851222:T>C" "PTPRQ" "NM_001145026:c.909-11265T>C" "INTRON3" "Benign" "rs147929319" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521
308116 "chr12:80851266:C>A" "PTPRQ" "NM_001145026:c.909-11221C>A" "INTRON3" "Unknown significance" "rs773700144" "This variant is a VUS because it does not have enough information."
308117 "chr12:80851296:T>C" "PTPRQ" "NM_001145026:c.909-11191T>C" "INTRON3" "Unknown significance" "rs747552990" "This variant is a VUS because it does not have enough information."
308118 "chr12:80851319:A>C" "PTPRQ" "NM_001145026:c.909-11168A>C" "INTRON3" "Unknown significance" "rs185022073" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308119 "chr12:80851337:G>C" "PTPRQ" "NM_001145026:c.909-11150G>C" "INTRON3" "Benign" "rs7969794" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 221 694 0.3184 40 1008 0.0397 250 978 0.2556 1739 5008 0.347244
308120 "chr12:80851390:A>T" "PTPRQ" "NM_001145026:c.909-11097A>T" "INTRON3" "Unknown significance" "rs559325589" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 0 978 0 0 5008 0
308121 "chr12:80851412:A>G" "PTPRQ" "NM_001145026:c.909-11075A>G" "INTRON3" "Unknown significance" "rs373735333" "This variant is a VUS because it does not have enough information."
308122 "chr12:80851430:TAA>-" "PTPRQ" "NM_001145026:c.909-11057_909-11055delTAA" "INTRON3" "Unknown significance" "rs745943547" "This variant is a VUS because it does not have enough information."
308123 "chr12:80851498:A>G" "PTPRQ" "NM_001145026:c.909-10989A>G" "INTRON3" "Unknown significance" "rs55773518" "This variant is a VUS because it does not have enough information."
308124 "chr12:80851508:A>G" "PTPRQ" "NM_001145026:c.909-10979A>G" "INTRON3" "Unknown significance" "rs529908081" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308125 "chr12:80851509:T>A" "PTPRQ" "NM_001145026:c.909-10978T>A" "INTRON3" "Unknown significance" "rs141672025" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308126 "chr12:80851515:T>A" "PTPRQ" "NM_001145026:c.909-10972T>A" "INTRON3" "Unknown significance" "rs563623044" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308127 "chr12:80851518:T>G" "PTPRQ" "NM_001145026:c.909-10969T>G" "INTRON3" "Unknown significance" "rs530894191" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308128 "chr12:80851558:C>A" "PTPRQ" "NM_001145026:c.909-10929C>A" "INTRON3" "Unknown significance" "rs776824586" "This variant is a VUS because it does not have enough information."
308129 "chr12:80851574:C>T" "PTPRQ" "NM_001145026:c.909-10913C>T" "INTRON3" "Benign" "rs147057586" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
308130 "chr12:80851590:C>T" "PTPRQ" "NM_001145026:c.909-10897C>T" "INTRON3" "Benign" "rs2895800" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 80 1322 0.0605 564 1006 0.5606 362 694 0.5216 531 1008 0.5268 628 978 0.6421 2165 5008 0.432308
308131 "chr12:80851619:C>T" "PTPRQ" "NM_001145026:c.909-10868C>T" "INTRON3" "Unknown significance" "rs528646067" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308132 "chr12:80851620:G>A" "PTPRQ" "NM_001145026:c.909-10867G>A" "INTRON3" "Unknown significance" "rs561840390" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 5 5008 0.000998403
308133 "chr12:80851629:->A" "PTPRQ" "NM_001145026:c.909-10858_909-10857insA" "INTRON3" "Benign" "rs138111017" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 422 1322 0.3192 25 1006 0.0249 67 694 0.0965 39 1008 0.0387 105 978 0.1074 658 5008 0.13139
308134 "chr12:80851693:T>G" "PTPRQ" "NM_001145026:c.909-10794T>G" "INTRON3" "Unknown significance" "rs544041148" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308135 "chr12:80851722:A>T" "PTPRQ" "NM_001145026:c.909-10765A>T" "INTRON3" "Unknown significance" "rs762549828" "This variant is a VUS because it does not have enough information."
308136 "chr12:80851741:C>T" "PTPRQ" "NM_001145026:c.909-10746C>T" "INTRON3" "Benign" "rs7971193" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
308137 "chr12:80851742:A>T" "PTPRQ" "NM_001145026:c.909-10745A>T" "INTRON3" "Unknown significance" "rs751522234" "This variant is a VUS because it does not have enough information."
308138 "chr12:80851764:A>G" "PTPRQ" "NM_001145026:c.909-10723A>G" "INTRON3" "Unknown significance" "rs777075153" "This variant is a VUS because it does not have enough information."
308139 "chr12:80851802:G>A" "PTPRQ" "NM_001145026:c.909-10685G>A" "INTRON3" "Unknown significance" "rs757095104" "This variant is a VUS because it does not have enough information."
308140 "chr12:80851812:A>G" "PTPRQ" "NM_001145026:c.909-10675A>G" "INTRON3" "Benign" "rs7294621" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 304 1322 0.23 71 1006 0.0706 51 694 0.0735 0 1008 0 48 978 0.0491 474 5008 0.0946486
308141 "chr12:80851816:C>T" "PTPRQ" "NM_001145026:c.909-10671C>T" "INTRON3" "Unknown significance" "rs569241942" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 2 5008 0.000399361
308142 "chr12:80851879:C>T" "PTPRQ" "NM_001145026:c.909-10608C>T" "INTRON3" "Benign" "rs12306109" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
308143 "chr12:80851924:T>C" "PTPRQ" "NM_001145026:c.909-10563T>C" "INTRON3" "Unknown significance" "rs754578346" "This variant is a VUS because it does not have enough information."
308144 "chr12:80852007:G>T" "PTPRQ" "NM_001145026:c.909-10480G>T" "INTRON3" "Benign" "rs118030698" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 9 1008 0.0089 0 978 0 9 5008 0.00179712
308145 "chr12:80852008:C>T" "PTPRQ" "NM_001145026:c.909-10479C>T" "INTRON3" "Benign" "rs117791757" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 10 1008 0.0099 0 978 0 10 5008 0.00199681
308146 "chr12:80852018:A>T" "PTPRQ" "NM_001145026:c.909-10469A>T" "INTRON3" "Unknown significance" "rs779093940" "This variant is a VUS because it does not have enough information."
308147 "chr12:80852019:A>G" "PTPRQ" "NM_001145026:c.909-10468A>G" "INTRON3" "Benign" "rs138359219" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
308148 "chr12:80852025:G>A" "PTPRQ" "NM_001145026:c.909-10462G>A" "INTRON3" "Unknown significance" "rs553034942" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308149 "chr12:80852076:C>T" "PTPRQ" "NM_001145026:c.909-10411C>T" "INTRON3" "Benign" "rs12306214" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 323 1322 0.2443 21 1006 0.0209 60 694 0.0865 37 1008 0.0367 101 978 0.1033 542 5008 0.108227
308150 "chr12:80852097:A>G" "PTPRQ" "NM_001145026:c.909-10390A>G" "INTRON3" "Unknown significance" "rs758437158" "This variant is a VUS because it does not have enough information."
308151 "chr12:80852130:T>C" "PTPRQ" "NM_001145026:c.909-10357T>C" "INTRON3" "Unknown significance" "rs542025188" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308152 "chr12:80852149:G>A" "PTPRQ" "NM_001145026:c.909-10338G>A" "INTRON3" "Unknown significance" "rs563560663" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308153 "chr12:80852155:A>C" "PTPRQ" "NM_001145026:c.909-10332A>C" "INTRON3" "Unknown significance" "rs149567913" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308154 "chr12:80852208:C>T" "PTPRQ" "NM_001145026:c.909-10279C>T" "INTRON3" "Benign" "rs4545623" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 221 694 0.3184 40 1008 0.0397 250 978 0.2556 1739 5008 0.347244
308155 "chr12:80852216:T>C" "PTPRQ" "NM_001145026:c.909-10271T>C" "INTRON3" "Unknown significance" "rs548916021" "This variant is a VUS because it does not have enough information."
308156 "chr12:80852225:T>C" "PTPRQ" "NM_001145026:c.909-10262T>C" "INTRON3" "Unknown significance" "rs532744414" "This variant is a VUS because it does not have enough information."
308157 "chr12:80852252:A>T" "PTPRQ" "NM_001145026:c.909-10235A>T" "INTRON3" "Unknown significance" "rs370275742" "This variant is a VUS because it does not have enough information."
308158 "chr12:80852254:A>-" "PTPRQ" "NM_001145026:c.909-10233delA" "INTRON3" "Unknown significance" "rs777568362" "This variant is a VUS because it does not have enough information."
308159 "chr12:80852272:A>-" "PTPRQ" "NM_001145026:c.909-10215delA" "INTRON3" "Unknown significance" "rs749045099" "This variant is a VUS because it does not have enough information."
308160 "chr12:80852274:A>C" "PTPRQ" "NM_001145026:c.909-10213A>C" "INTRON3" "Unknown significance" "rs564515588" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308161 "chr12:80852277:T>G" "PTPRQ" "NM_001145026:c.909-10210T>G" "INTRON3" "Unknown significance" "rs143214231" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308162 "chr12:80852391:C>T" "PTPRQ" "NM_001145026:c.909-10096C>T" "INTRON3" "Unknown significance" "rs568701197" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308163 "chr12:80852392:G>A" "PTPRQ" "NM_001145026:c.909-10095G>A" "INTRON3" "Unknown significance" "rs771278018" "This variant is a VUS because it does not have enough information."
308164 "chr12:80852460:A>G" "PTPRQ" "NM_001145026:c.909-10027A>G" "INTRON3" "Unknown significance" "rs534698075" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
308165 "chr12:80852485:G>A" "PTPRQ" "NM_001145026:c.909-10002G>A" "INTRON3" "Benign" "rs373653134" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 15 978 0.0153 15 5008 0.00299521
308166 "chr12:80852493:C>G" "PTPRQ" "NM_001145026:c.909-9994C>G" "INTRON3" "Unknown significance" "rs551181723" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308167 "chr12:80852504:C>T" "PTPRQ" "NM_001145026:c.909-9983C>T" "INTRON3" "Benign" "rs11114457" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 5 1008 0.005 101 978 0.1033 617 5008 0.123203
308168 "chr12:80852521:C>T" "PTPRQ" "NM_001145026:c.909-9966C>T" "INTRON3" "Unknown significance" "rs188271164" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308169 "chr12:80852543:A>T" "PTPRQ" "NM_001145026:c.909-9944A>T" "INTRON3" "Unknown significance" "rs181037660" "This variant is a VUS because it does not have enough information."
308170 "chr12:80852567:A>G" "PTPRQ" "NM_001145026:c.909-9920A>G" "INTRON3" "Benign" "rs79029040" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 0 1006 0 0 694 0 0 1008 0 0 978 0 20 5008 0.00399361
308171 "chr12:80852580:C>T" "PTPRQ" "NM_001145026:c.909-9907C>T" "INTRON3" "Benign" "rs74814860" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 36 5008 0.0071885
308172 "chr12:80852592:T>G" "PTPRQ" "NM_001145026:c.909-9895T>G" "INTRON3" "Unknown significance" "rs534636580" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308173 "chr12:80852658:T>C" "PTPRQ" "NM_001145026:c.909-9829T>C" "INTRON3" "Unknown significance" "rs552759652" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308174 "chr12:80852665:T>C" "PTPRQ" "NM_001145026:c.909-9822T>C" "INTRON3" "Unknown significance" "rs186122794" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308175 "chr12:80852701:G>A" "PTPRQ" "NM_001145026:c.909-9786G>A" "INTRON3" "Unknown significance" "rs541638801" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 1 1008 0.001 0 978 0 3 5008 0.000599042
308176 "chr12:80852704:A>G" "PTPRQ" "NM_001145026:c.909-9783A>G" "INTRON3" "Benign" "rs148275951" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 18 5008 0.00359425
308177 "chr12:80852716:T>C" "PTPRQ" "NM_001145026:c.909-9771T>C" "INTRON3" "Unknown significance" "rs575602265" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308178 "chr12:80852729:G>C" "PTPRQ" "NM_001145026:c.909-9758G>C" "INTRON3" "Unknown significance" "rs770260739" "This variant is a VUS because it does not have enough information."
308179 "chr12:80852738:C>T" "PTPRQ" "NM_001145026:c.909-9749C>T" "INTRON3" "Unknown significance" "rs745779774" "This variant is a VUS because it does not have enough information."
308180 "chr12:80852758:C>T" "PTPRQ" "NM_001145026:c.909-9729C>T" "INTRON3" "Benign" "rs10862125" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 221 694 0.3184 40 1008 0.0397 250 978 0.2556 1739 5008 0.347244
308181 "chr12:80852823:A>T" "PTPRQ" "NM_001145026:c.909-9664A>T" "INTRON3" "Unknown significance" "rs571078665" "This variant is a VUS because it does not have enough information."
308182 "chr12:80852849:A>G" "PTPRQ" "NM_001145026:c.909-9638A>G" "INTRON3" "Unknown significance" "rs540007793" "This variant is a VUS because it does not have enough information."
308183 "chr12:80852902:T>C" "PTPRQ" "NM_001145026:c.909-9585T>C" "INTRON3" "Unknown significance" "rs564377983" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308184 "chr12:80852912:A>G" "PTPRQ" "NM_001145026:c.909-9575A>G" "INTRON3" "Unknown significance" "rs573118531" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308185 "chr12:80852925:A>G" "PTPRQ" "NM_001145026:c.909-9562A>G" "INTRON3" "Benign" "rs59973438" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 306 1322 0.2315 71 1006 0.0706 51 694 0.0735 0 1008 0 48 978 0.0491 476 5008 0.0950479
308186 "chr12:80852930:A>G" "PTPRQ" "NM_001145026:c.909-9557A>G" "INTRON3" "Unknown significance" "rs562018124" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308187 "chr12:80852952:A>G" "PTPRQ" "NM_001145026:c.909-9535A>G" "INTRON3" "Unknown significance" "rs768446168" "This variant is a VUS because it does not have enough information."
308188 "chr12:80852999:A>G" "PTPRQ" "NM_001145026:c.909-9488A>G" "INTRON3" "Unknown significance" "rs141341390" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308189 "chr12:80853044:A>T" "PTPRQ" "NM_001145026:c.909-9443A>T" "INTRON3" "Benign" "rs190999165" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
308190 "chr12:80853054:A>G" "PTPRQ" "NM_001145026:c.909-9433A>G" "INTRON3" "Unknown significance" "rs181482000" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
308191 "chr12:80853055:G>C" "PTPRQ" "NM_001145026:c.909-9432G>C" "INTRON3" "Unknown significance" "rs376587670" "This variant is a VUS because it does not have enough information."
308192 "chr12:80853056:T>C" "PTPRQ" "NM_001145026:c.909-9431T>C" "INTRON3" "Unknown significance" "rs747247371" "This variant is a VUS because it does not have enough information."
308193 "chr12:80853082:G>T" "PTPRQ" "NM_001145026:c.909-9405G>T" "INTRON3" "Unknown significance" "rs533351304" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308194 "chr12:80853085:T>G" "PTPRQ" "NM_001145026:c.909-9402T>G" "INTRON3" "Unknown significance" "rs773957906" "This variant is a VUS because it does not have enough information."
308195 "chr12:80853103:A>-" "PTPRQ" "NM_001145026:c.909-9384delA" "INTRON3" "Benign" "rs550269979" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489
308196 "chr12:80853113:G>T" "PTPRQ" "NM_001145026:c.909-9374G>T" "INTRON3" "Benign" "rs57063468" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 267 5008 0.0533147
308197 "chr12:80853145:A>G" "PTPRQ" "NM_001145026:c.909-9342A>G" "INTRON3" "Unknown significance" "rs566839973" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 0 978 0 0 5008 0
308198 "chr12:80853164:A>G" "PTPRQ" "NM_001145026:c.909-9323A>G" "INTRON3" "Unknown significance" "rs534309179" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308199 "chr12:80853174:A>C" "PTPRQ" "NM_001145026:c.909-9313A>C" "INTRON3" "Unknown significance" "rs185738582" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
308200 "chr12:80853184:T>C" "PTPRQ" "NM_001145026:c.909-9303T>C" "INTRON3" "Unknown significance" "rs568062580" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308201 "chr12:80853213:C>A" "PTPRQ" "NM_001145026:c.909-9274C>A" "INTRON3" "Unknown significance" "rs535579876" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308202 "chr12:80853226:G>A" "PTPRQ" "NM_001145026:c.909-9261G>A" "INTRON3" "Unknown significance" "rs761388194" "This variant is a VUS because it does not have enough information."
308203 "chr12:80853265:T>C" "PTPRQ" "NM_001145026:c.909-9222T>C" "INTRON3" "Benign" "rs4489813" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 388 1322 0.2935 21 1006 0.0209 62 694 0.0893 37 1008 0.0367 101 978 0.1033 609 5008 0.121605
308204 "chr12:80853296:T>C" "PTPRQ" "NM_001145026:c.909-9191T>C" "INTRON3" "Unknown significance" "rs73145112" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 2 694 0.0029 0 1008 0 2 978 0.002 7 5008 0.00139776
308205 "chr12:80853348:T>C" "PTPRQ" "NM_001145026:c.909-9139T>C" "INTRON3" "Unknown significance" "rs558031157" "This variant is a VUS because it does not have enough information."
308206 "chr12:80853359:G>A" "PTPRQ" "NM_001145026:c.909-9128G>A" "INTRON3" "Unknown significance" "rs190640565" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
308207 "chr12:80853363:A>T" "PTPRQ" "NM_001145026:c.909-9124A>T" "INTRON3" "Unknown significance" "rs558066013" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308208 "chr12:80853413:C>T" "PTPRQ" "NM_001145026:c.909-9074C>T" "INTRON3" "Unknown significance" "rs573117699" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308209 "chr12:80853416:C>G" "PTPRQ" "NM_001145026:c.909-9071C>G" "INTRON3" "Unknown significance" "rs760379301" "This variant is a VUS because it does not have enough information."
308210 "chr12:80853424:T>C" "PTPRQ" "NM_001145026:c.909-9063T>C" "INTRON3" "Benign" "rs4439581" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 323 1006 0.3211 221 694 0.3184 40 1008 0.0397 250 978 0.2556 1739 5008 0.347244
308211 "chr12:80853426:A>C" "PTPRQ" "NM_001145026:c.909-9061A>C" "INTRON3" "Unknown significance" "rs562151723" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308212 "chr12:80853518:G>A" "PTPRQ" "NM_001145026:c.909-8969G>A" "INTRON3" "Unknown significance" "rs573958884" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
308213 "chr12:80853559:C>A" "PTPRQ" "NM_001145026:c.909-8928C>A" "INTRON3" "Unknown significance" "rs752891248" "This variant is a VUS because it does not have enough information."
308214 "chr12:80853573:T>A" "PTPRQ" "NM_001145026:c.909-8914T>A" "INTRON3" "Unknown significance" "rs758563786" "This variant is a VUS because it does not have enough information."
308215 "chr12:80853649:G>A" "PTPRQ" "NM_001145026:c.909-8838G>A" "INTRON3" "Benign" "rs11837911" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 480 1322 0.3631 302 1006 0.3002 156 694 0.2248 3 1008 0.003 149 978 0.1524 1090 5008 0.217652
308216 "chr12:80853672:C>-" "PTPRQ" "NM_001145026:c.909-8815delC" "INTRON3" "Benign" "rs539516819" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
308217 "chr12:80853682:A>G" "PTPRQ" "NM_001145026:c.909-8805A>G" "INTRON3" "Unknown significance" "rs751538112" "This variant is a VUS because it does not have enough information."
308218 "chr12:80853695:TTAA>-" "PTPRQ" "NM_001145026:c.909-8792_909-8789delTTAA" "INTRON3" "Unknown significance" "rs369689570" "This variant is a VUS because it does not have enough information."
308219 "chr12:80853723:C>T" "PTPRQ" "NM_001145026:c.909-8764C>T" "INTRON3" "Unknown significance" "rs562664011" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308220 "chr12:80853768:A>G" "PTPRQ" "NM_001145026:c.909-8719A>G" "INTRON3" "Unknown significance" "rs533316636" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308221 "chr12:80853778:T>C" "PTPRQ" "NM_001145026:c.909-8709T>C" "INTRON3" "Unknown significance" "rs757419751" "This variant is a VUS because it does not have enough information."
308222 "chr12:80853797:T>G" "PTPRQ" "NM_001145026:c.909-8690T>G" "INTRON3" "Unknown significance" "rs551593016" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308223 "chr12:80853806:T>A" "PTPRQ" "NM_001145026:c.909-8681T>A" "INTRON3" "Unknown significance" "rs560603151" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308224 "chr12:80853884:T>C" "PTPRQ" "NM_001145026:c.909-8603T>C" "INTRON3" "Benign" "rs139283247" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 11 1322 0.0083 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 12 5008 0.00239617
308225 "chr12:80853998:A>G" "PTPRQ" "NM_001145026:c.909-8489A>G" "INTRON3" "Unknown significance" "rs781550036" "This variant is a VUS because it does not have enough information."
308226 "chr12:80854003:A>G" "PTPRQ" "NM_001145026:c.909-8484A>G" "INTRON3" "Benign" "rs117029569" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 12 1006 0.0119 4 694 0.0058 0 1008 0 10 978 0.0102 26 5008 0.00519169
308227 "chr12:80854040:T>G" "PTPRQ" "NM_001145026:c.909-8447T>G" "INTRON3" "Unknown significance" "rs770032729" "This variant is a VUS because it does not have enough information."
308228 "chr12:80854044:T>C" "PTPRQ" "NM_001145026:c.909-8443T>C" "INTRON3" "Unknown significance" "rs183173124" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308229 "chr12:80854067:A>G" "PTPRQ" "NM_001145026:c.909-8420A>G" "INTRON3" "Unknown significance" "rs535111384" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308230 "chr12:80854071:T>C" "PTPRQ" "NM_001145026:c.909-8416T>C" "INTRON3" "Unknown significance" "rs550670779" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308231 "chr12:80854080:A>G" "PTPRQ" "NM_001145026:c.909-8407A>G" "INTRON3" "Benign" "rs142493840" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
308232 "chr12:80854089:A>G" "PTPRQ" "NM_001145026:c.909-8398A>G" "INTRON3" "Benign" "rs570606375" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 10 978 0.0102 10 5008 0.00199681
308233 "chr12:80854158:A>T" "PTPRQ" "NM_001145026:c.909-8329A>T" "INTRON3" "Benign" "rs11114458" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 91 1006 0.0905 118 694 0.17 9 1008 0.0089 27 978 0.0276 249 5008 0.0497204
308234 "chr12:80854183:C>T" "PTPRQ" "NM_001145026:c.909-8304C>T" "INTRON3" "Unknown significance" "rs767032279" "This variant is a VUS because it does not have enough information."
308235 "chr12:80854203:G>T" "PTPRQ" "NM_001145026:c.909-8284G>T" "INTRON3" "Unknown significance" "rs573043002" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308236 "chr12:80854207:T>C" "PTPRQ" "NM_001145026:c.909-8280T>C" "INTRON3" "Unknown significance" "rs534051679" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308237 "chr12:80854275:->G" "PTPRQ" "NM_001145026:c.909-8212_909-8211insG" "INTRON3" "Unknown significance" "rs142938399" "This variant is a VUS because it does not have enough information."
308238 "chr12:80854279:G>A" "PTPRQ" "NM_001145026:c.909-8208G>A" "INTRON3" "Unknown significance" "rs555376165" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308239 "chr12:80854288:C>T" "PTPRQ" "NM_001145026:c.909-8199C>T" "INTRON3" "Unknown significance" "rs373332655" "This variant is a VUS because it does not have enough information."
308240 "chr12:80854339:T>C" "PTPRQ" "NM_001145026:c.909-8148T>C" "INTRON3" "Unknown significance" "rs199519946" "This variant is a VUS because it does not have enough information."
308241 "chr12:80854342:C>T" "PTPRQ" "NM_001145026:c.909-8145C>T" "INTRON3" "Unknown significance" "rs573950202" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308242 "chr12:80854345:G>T" "PTPRQ" "NM_001145026:c.909-8142G>T" "INTRON3" "Unknown significance" "rs540381555" "This variant is a VUS because it does not have enough information."
308243 "chr12:80854346:G>C" "PTPRQ" "NM_001145026:c.909-8141G>C" "INTRON3" "Unknown significance" "rs544214898" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308244 "chr12:80854373:A>G" "PTPRQ" "NM_001145026:c.909-8114A>G" "INTRON3" "Unknown significance" "rs763778867" "This variant is a VUS because it does not have enough information."
308245 "chr12:80854393:G>A" "PTPRQ" "NM_001145026:c.909-8094G>A" "INTRON3" "Unknown significance" "rs61950906" "This variant is a VUS because it does not have enough information."
308246 "chr12:80854396:->A" "PTPRQ" "NM_001145026:c.909-8091_909-8090insA" "INTRON3" "Benign" "rs113012136" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 868 1322 0.6566 323 1006 0.3211 221 694 0.3184 41 1008 0.0407 252 978 0.2577 1705 5008 0.340455
308247 "chr12:80854405:->T" "PTPRQ" "NM_001145026:c.909-8082_909-8081insT" "INTRON3" "Benign" "rs59826411" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 0 1006 0 0 694 0 0 1008 0 0 978 0 14 5008 0.00279553
308248 "chr12:80854412:C>T" "PTPRQ" "NM_001145026:c.909-8075C>T" "INTRON3" "Unknown significance" "rs556224109" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 1 978 0.001 3 5008 0.000599042
308249 "chr12:80854421:T>C" "PTPRQ" "NM_001145026:c.909-8066T>C" "INTRON3" "Unknown significance" "rs577743249" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308250 "chr12:80854425:C>T" "PTPRQ" "NM_001145026:c.909-8062C>T" "INTRON3" "Benign" "rs61950907" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 97 1322 0.0734 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 98 5008 0.0195687
308251 "chr12:80854426:G>A" "PTPRQ" "NM_001145026:c.909-8061G>A" "INTRON3" "Unknown significance" "rs577912893" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308252 "chr12:80854438:G>A" "PTPRQ" "NM_001145026:c.909-8049G>A" "INTRON3" "Benign" "rs139501633" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 18 1008 0.0179 0 978 0 18 5008 0.00359425
308253 "chr12:80854442:G>A" "PTPRQ" "NM_001145026:c.909-8045G>A" "INTRON3" "Unknown significance" "rs187951915" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308254 "chr12:80854443:C>-" "PTPRQ" "NM_001145026:c.909-8044delC" "INTRON3" "Unknown significance" "rs766241627" "This variant is a VUS because it does not have enough information."
308255 "chr12:80854477:G>A" "PTPRQ" "NM_001145026:c.909-8010G>A" "INTRON3" "Unknown significance" "rs561447865" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308256 "chr12:80854486:G>A" "PTPRQ" "NM_001145026:c.909-8001G>A" "INTRON3" "Unknown significance" "rs528876347" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308257 "chr12:80854500:C>T" "PTPRQ" "NM_001145026:c.909-7987C>T" "INTRON3" "Benign" "rs376520375" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 12 1008 0.0119 0 978 0 12 5008 0.00239617
308258 "chr12:80854501:G>A" "PTPRQ" "NM_001145026:c.909-7986G>A" "INTRON3" "Benign" "rs11608378" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 19 1322 0.0144 71 1006 0.0706 33 694 0.0476 0 1008 0 48 978 0.0491 171 5008 0.0341454
308259 "chr12:80854518:G>A" "PTPRQ" "NM_001145026:c.909-7969G>A" "INTRON3" "Benign" "rs542294434" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 7 1006 0.007 3 694 0.0043 0 1008 0 0 978 0 10 5008 0.00199681
308260 "chr12:80854523:C>T" "PTPRQ" "NM_001145026:c.909-7964C>T" "INTRON3" "Unknown significance" "rs192320550" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308261 "chr12:80854556:G>A" "PTPRQ" "NM_001145026:c.909-7931G>A" "INTRON3" "Unknown significance" "rs566613772" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308262 "chr12:80854562:C>A" "PTPRQ" "NM_001145026:c.909-7925C>A" "INTRON3" "Unknown significance" "rs543208932" "This variant is a VUS because it does not have enough information."
308263 "chr12:80854569:->A" "PTPRQ" "NM_001145026:c.909-7918_909-7917insA" "INTRON3" "Unknown significance" "rs35890290" "This variant is a VUS because it does not have enough information."
308264 "chr12:80854569:A>-" "PTPRQ" "NM_001145026:c.909-7918delA" "INTRON3" "Unknown significance" "rs371429699" "This variant is a VUS because it does not have enough information."
308265 "chr12:80854584:A>G" "PTPRQ" "NM_001145026:c.909-7903A>G" "INTRON3" "Unknown significance" "rs750379333" "This variant is a VUS because it does not have enough information."
308266 "chr12:80854585:C>G" "PTPRQ" "NM_001145026:c.909-7902C>G" "INTRON3" "Unknown significance" "rs562447420" "This variant is a VUS because it does not have enough information."
308267 "chr12:80854598:G>A" "PTPRQ" "NM_001145026:c.909-7889G>A" "INTRON3" "Benign" "rs563614310" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 13 978 0.0133 13 5008 0.00259585
308268 "chr12:80854599:A>C" "PTPRQ" "NM_001145026:c.909-7888A>C" "INTRON3" "Benign" "rs145454931" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 21 1006 0.0209 10 694 0.0144 0 1008 0 6 978 0.0061 39 5008 0.00778754
308269 "chr12:80854603:T>A" "PTPRQ" "NM_001145026:c.909-7884T>A" "INTRON3" "Unknown significance" "rs551312170" "This variant is a VUS because it does not have enough information."
308270 "chr12:80854656:T>C" "PTPRQ" "NM_001145026:c.909-7831T>C" "INTRON3" "Unknown significance" "rs567483371" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308271 "chr12:80854666:G>T" "PTPRQ" "NM_001145026:c.909-7821G>T" "INTRON3" "Unknown significance" "rs537827915" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 0 1008 0 3 978 0.0031 5 5008 0.000998403
308272 "chr12:80854673:C>T" "PTPRQ" "NM_001145026:c.909-7814C>T" "INTRON3" "Unknown significance" "rs556187020" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308273 "chr12:80854674:G>A" "PTPRQ" "NM_001145026:c.909-7813G>A" "INTRON3" "Unknown significance" "rs577708707" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308274 "chr12:80854709:A>G" "PTPRQ" "NM_001145026:c.909-7778A>G" "INTRON3" "Unknown significance" "rs545061144" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308275 "chr12:80854710:A>G" "PTPRQ" "NM_001145026:c.909-7777A>G" "INTRON3" "Benign" "rs7969389" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 267 5008 0.0533147
308276 "chr12:80854720:A>G" "PTPRQ" "NM_001145026:c.909-7767A>G" "INTRON3" "Benign" "rs148809747" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521
308277 "chr12:80854730:C>G" "PTPRQ" "NM_001145026:c.909-7757C>G" "INTRON3" "Benign" "rs144902188" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521
308278 "chr12:80854753:T>C" "PTPRQ" "NM_001145026:c.909-7734T>C" "INTRON3" "Unknown significance" "rs760712015" "This variant is a VUS because it does not have enough information."
308279 "chr12:80854755:G>T" "PTPRQ" "NM_001145026:c.909-7732G>T" "INTRON3" "Unknown significance" "rs78989200" "This variant is a VUS because it does not have enough information."
308280 "chr12:80854776:C>T" "PTPRQ" "NM_001145026:c.909-7711C>T" "INTRON3" "Unknown significance" "rs571120843" "This variant is a VUS because it does not have enough information."
308281 "chr12:80854778:A>G" "PTPRQ" "NM_001145026:c.909-7709A>G" "INTRON3" "Benign" "rs147938575" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 4 1006 0.004 7 694 0.0101 0 1008 0 0 978 0 11 5008 0.00219649
308282 "chr12:80854786:T>C" "PTPRQ" "NM_001145026:c.909-7701T>C" "INTRON3" "Benign" "rs182345722" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 0 1006 0 0 694 0 0 1008 0 0 978 0 20 5008 0.00399361
308283 "chr12:80854787:A>G" "PTPRQ" "NM_001145026:c.909-7700A>G" "INTRON3" "Benign" "rs76856506" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 0 1006 0 0 694 0 0 1008 0 0 978 0 36 5008 0.0071885
308284 "chr12:80854803:T>C" "PTPRQ" "NM_001145026:c.909-7684T>C" "INTRON3" "Unknown significance" "rs759341605" "This variant is a VUS because it does not have enough information."
308285 "chr12:80854827:T>C" "PTPRQ" "NM_001145026:c.909-7660T>C" "INTRON3" "Unknown significance" "rs187947121" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
308286 "chr12:80854834:T>A" "PTPRQ" "NM_001145026:c.909-7653T>A" "INTRON3" "Benign" "rs11114459" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 30 1322 0.0227 0 1006 0 0 694 0 0 1008 0 0 978 0 30 5008 0.00599042
308287 "chr12:80854839:TT>-" "PTPRQ" "NM_001145026:c.909-7648_909-7647delTT" "INTRON3" "Unknown significance" "rs202206927" "This variant is a VUS because it does not have enough information."
308288 "chr12:80854853:A>G" "PTPRQ" "NM_001145026:c.909-7634A>G" "INTRON3" "Unknown significance" "rs112705130" "This variant is a VUS because it does not have enough information."
308289 "chr12:80854857:A>C" "PTPRQ" "NM_001145026:c.909-7630A>C" "INTRON3" "Unknown significance" "rs75843167" "This variant is a VUS because it does not have enough information."
308290 "chr12:80854858:G>C" "PTPRQ" "NM_001145026:c.909-7629G>C" "INTRON3" "Unknown significance" "rs547170514" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308291 "chr12:80854869:A>G" "PTPRQ" "NM_001145026:c.909-7618A>G" "INTRON3" "Unknown significance" "rs566460093" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308292 "chr12:80854884:A>C" "PTPRQ" "NM_001145026:c.909-7603A>C" "INTRON3" "Benign" "rs114172344" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 97 1322 0.0734 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 99 5008 0.0197684
308293 "chr12:80854902:A>C" "PTPRQ" "NM_001145026:c.909-7585A>C" "INTRON3" "Unknown significance" "rs566895097" "This variant is a VUS because it does not have enough information."
308294 "chr12:80854980:TTTG>-" "PTPRQ" "NM_001145026:c.909-7507_909-7504delTTTG" "INTRON3" "Benign" "rs148411196" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 389 1322 0.2943 21 1006 0.0209 62 694 0.0893 38 1008 0.0377 101 978 0.1033 611 5008 0.122005
308295 "chr12:80854988:->TCTGT" "PTPRQ" "NM_001145026:c.909-7499_909-7498insTCTGT" "INTRON3" "Unknown significance" "rs771469404" "This variant is a VUS because it does not have enough information."
308296 "chr12:80855001:G>A" "PTPRQ" "NM_001145026:c.909-7486G>A" "INTRON3" "Unknown significance" "rs548934837" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
308297 "chr12:80855006:G>A" "PTPRQ" "NM_001145026:c.909-7481G>A" "INTRON3" "Unknown significance" "rs767685627" "This variant is a VUS because it does not have enough information."
308298 "chr12:80855007:C>T" "PTPRQ" "NM_001145026:c.909-7480C>T" "INTRON3" "Benign" "rs78400892" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 1 1008 0.001 0 978 0 41 5008 0.0081869
308299 "chr12:80855010:C>T" "PTPRQ" "NM_001145026:c.909-7477C>T" "INTRON3" "Unknown significance" "rs796185835" "This variant is a VUS because it does not have enough information."
308300 "chr12:80855022:G>A" "PTPRQ" "NM_001145026:c.909-7465G>A" "INTRON3" "Unknown significance" "rs537790033" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308301 "chr12:80855029:A>T" "PTPRQ" "NM_001145026:c.909-7458A>T" "INTRON3" "Benign" "rs12582357" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 649 5008 0.129593
308302 "chr12:80855035:G>C" "PTPRQ" "NM_001145026:c.909-7452G>C" "INTRON3" "Benign" "rs571263074" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 7 978 0.0072 7 5008 0.00139776
308303 "chr12:80855043:T>C" "PTPRQ" "NM_001145026:c.909-7444T>C" "INTRON3" "Benign" "rs10862126" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 80 1322 0.0605 564 1006 0.5606 362 694 0.5216 532 1008 0.5278 628 978 0.6421 2166 5008 0.432508
308304 "chr12:80855044:G>A" "PTPRQ" "NM_001145026:c.909-7443G>A" "INTRON3" "Unknown significance" "rs554207216" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308305 "chr12:80855078:C>T" "PTPRQ" "NM_001145026:c.909-7409C>T" "INTRON3" "Benign" "rs192574894" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 7 1006 0.007 2 694 0.0029 0 1008 0 0 978 0 9 5008 0.00179712
308306 "chr12:80855093:C>A" "PTPRQ" "NM_001145026:c.909-7394C>A" "INTRON3" "Unknown significance" "rs536847403" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308307 "chr12:80855102:->C" "PTPRQ" "NM_001145026:c.909-7385_909-7384insC" "INTRON3" "Benign" "rs141012030" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 38 1322 0.0287 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 39 5008 0.00778754
308308 "chr12:80855109:C>A" "PTPRQ" "NM_001145026:c.909-7378C>A" "INTRON3" "Unknown significance" "rs554902680" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308309 "chr12:80855113:G>T" "PTPRQ" "NM_001145026:c.909-7374G>T" "INTRON3" "Unknown significance" "rs576717314" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308310 "chr12:80855118:T>A" "PTPRQ" "NM_001145026:c.909-7369T>A" "INTRON3" "Unknown significance" "rs749605423" "This variant is a VUS because it does not have enough information."
308311 "chr12:80855120:G>A" "PTPRQ" "NM_001145026:c.909-7367G>A" "INTRON3" "Unknown significance" "rs544081232" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308312 "chr12:80855128:G>C" "PTPRQ" "NM_001145026:c.909-7359G>C" "INTRON3" "Unknown significance" "rs565599576" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308313 "chr12:80855134:C>T" "PTPRQ" "NM_001145026:c.909-7353C>T" "INTRON3" "Benign" "rs11114460" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 480 1322 0.3631 302 1006 0.3002 157 694 0.2262 3 1008 0.003 149 978 0.1524 1091 5008 0.217851
308314 "chr12:80855135:G>A" "PTPRQ" "NM_001145026:c.909-7352G>A" "INTRON3" "Unknown significance" "rs577467644" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308315 "chr12:80855137:C>A" "PTPRQ" "NM_001145026:c.909-7350C>A" "INTRON3" "Unknown significance" "rs560171870" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 1 1008 0.001 0 978 0 2 5008 0.000399361
308316 "chr12:80855183:C>T" "PTPRQ" "NM_001145026:c.909-7304C>T" "INTRON3" "Unknown significance" "rs540099981" "This variant is a VUS because it does not have enough information."
308317 "chr12:80855184:G>A" "PTPRQ" "NM_001145026:c.909-7303G>A" "INTRON3" "Unknown significance" "rs527442873" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308318 "chr12:80855188:T>C" "PTPRQ" "NM_001145026:c.909-7299T>C" "INTRON3" "Benign" "rs11837477" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 241 1322 0.1823 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 259 5008 0.0517173
308319 "chr12:80855224:C>T" "PTPRQ" "NM_001145026:c.909-7263C>T" "INTRON3" "Unknown significance" "rs560710133" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308320 "chr12:80855225:G>T" "PTPRQ" "NM_001145026:c.909-7262G>T" "INTRON3" "Unknown significance" "rs531408076" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308321 "chr12:80855227:C>A" "PTPRQ" "NM_001145026:c.909-7260C>A" "INTRON3" "Benign" "rs184292200" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 16 1322 0.0121 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 17 5008 0.00339457
308322 "chr12:80855229:G>A" "PTPRQ" "NM_001145026:c.909-7258G>A" "INTRON3" "Unknown significance" "rs150204307" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308323 "chr12:80855234:G>A" "PTPRQ" "NM_001145026:c.909-7253G>A" "INTRON3" "Unknown significance" "rs369441270" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
308324 "chr12:80855257:C>T" "PTPRQ" "NM_001145026:c.909-7230C>T" "INTRON3" "Unknown significance" "rs547517763" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308325 "chr12:80855280:C>T" "PTPRQ" "NM_001145026:c.909-7207C>T" "INTRON3" "Unknown significance" "rs187442620" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308326 "chr12:80855281:C>T" "PTPRQ" "NM_001145026:c.909-7206C>T" "INTRON3" "Benign" "rs138721507" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 1 1006 0.001 0 694 0 0 1008 0 0 978 0 16 5008 0.00319489
308327 "chr12:80855294:T>G" "PTPRQ" "NM_001145026:c.909-7193T>G" "INTRON3" "Unknown significance" "rs760228730" "This variant is a VUS because it does not have enough information."
308328 "chr12:80855302:G>A" "PTPRQ" "NM_001145026:c.909-7185G>A" "INTRON3" "Unknown significance" "rs772726853" "This variant is a VUS because it does not have enough information."
308329 "chr12:80855307:A>G" "PTPRQ" "NM_001145026:c.909-7180A>G" "INTRON3" "Unknown significance" "rs746529691" "This variant is a VUS because it does not have enough information."
308330 "chr12:80855331:A>G" "PTPRQ" "NM_001145026:c.909-7156A>G" "INTRON3" "Unknown significance" "rs555101933" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308331 "chr12:80855354:T>C" "PTPRQ" "NM_001145026:c.909-7133T>C" "INTRON3" "Unknown significance" "rs56011090" "This variant is a VUS because it does not have enough information."
308332 "chr12:80855356:C>T" "PTPRQ" "NM_001145026:c.909-7131C>T" "INTRON3" "Unknown significance" "rs770799272" "This variant is a VUS because it does not have enough information."
308333 "chr12:80855357:G>A" "PTPRQ" "NM_001145026:c.909-7130G>A" "INTRON3" "Unknown significance" "rs553918672" "This variant is a VUS because it does not have enough information."
308334 "chr12:80855362:T>C" "PTPRQ" "NM_001145026:c.909-7125T>C" "INTRON3" "Unknown significance" "rs370835453" "This variant is a VUS because it does not have enough information."
308335 "chr12:80855363:A>G" "PTPRQ" "NM_001145026:c.909-7124A>G" "INTRON3" "Unknown significance" "rs759325222" "This variant is a VUS because it does not have enough information."
308336 "chr12:80855385:T>C" "PTPRQ" "NM_001145026:c.909-7102T>C" "INTRON3" "Unknown significance" "rs573683526" "This variant is a VUS because it does not have enough information."
308337 "chr12:80855403:C>-" "PTPRQ" "NM_001145026:c.909-7084delC" "INTRON3" "Benign" "rs559380386" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 15 5008 0.00299521
308338 "chr12:80855413:T>A" "PTPRQ" "NM_001145026:c.909-7074T>A" "INTRON3" "Unknown significance" "rs576680460" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308339 "chr12:80855436:C>A" "PTPRQ" "NM_001145026:c.909-7051C>A" "INTRON3" "Unknown significance" "rs763582688" "This variant is a VUS because it does not have enough information."
308340 "chr12:80855454:C>T" "PTPRQ" "NM_001145026:c.909-7033C>T" "INTRON3" "Benign" "rs58822047" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 131 1322 0.0991 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 137 5008 0.0273562
308341 "chr12:80855454:C>A" "PTPRQ" "NM_001145026:c.909-7033C>A" "INTRON3" "Unknown significance" "rs58822047" "This variant is a VUS because it does not have enough information."
308342 "chr12:80855455:G>A" "PTPRQ" "NM_001145026:c.909-7032G>A" "INTRON3" "Unknown significance" "rs373547103" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 1 978 0.001 3 5008 0.000599042
308343 "chr12:80855456:T>C" "PTPRQ" "NM_001145026:c.909-7031T>C" "INTRON3" "Unknown significance" "rs577639945" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308344 "chr12:80855465:A>C" "PTPRQ" "NM_001145026:c.909-7022A>C" "INTRON3" "Unknown significance" "rs753592505" "This variant is a VUS because it does not have enough information."
308345 "chr12:80855466:T>C" "PTPRQ" "NM_001145026:c.909-7021T>C" "INTRON3" "Unknown significance" "rs762046372" "This variant is a VUS because it does not have enough information."
308346 "chr12:80855481:T>G" "PTPRQ" "NM_001145026:c.909-7006T>G" "INTRON3" "Unknown significance" "rs192336485" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
308347 "chr12:80855513:C>T" "PTPRQ" "NM_001145026:c.909-6974C>T" "INTRON3" "Unknown significance" "rs184877337" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308348 "chr12:80855514:C>T" "PTPRQ" "NM_001145026:c.909-6973C>T" "INTRON3" "Unknown significance" "rs761302796" "This variant is a VUS because it does not have enough information."
308349 "chr12:80855559:A>G" "PTPRQ" "NM_001145026:c.909-6928A>G" "INTRON3" "Benign" "rs114312343" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
308350 "chr12:80855584:A>T" "PTPRQ" "NM_001145026:c.909-6903A>T" "INTRON3" "Unknown significance" "rs138082375" "This variant is a VUS because it does not have enough information."
308351 "chr12:80855585:C>T" "PTPRQ" "NM_001145026:c.909-6902C>T" "INTRON3" "Unknown significance" "rs776454475" "This variant is a VUS because it does not have enough information." 0 188 0 0 92 0 0 132 0 0 2 0 0 2668 0 0 116 0 1 7480 0.00013369 1 10678 0.0000936505
308352 "chr12:80855590:T>C" "PTPRQ" "NM_001145026:c.909-6897T>C" "INTRON3" "Unknown significance" "rs531764509" "This variant is a VUS because it does not have enough information."
308353 "chr12:80855597:T>C" "PTPRQ" "NM_001145026:c.909-6890T>C" "INTRON3" "Benign" "rs4499068" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1320 1322 0.9985 973 1006 0.9672 633 694 0.9121 786 1008 0.7798 938 978 0.9591 4650 5008 0.928514 188 188 1 89 92 0.967391 108 132 0.818182 0 0 0 2702 2722 0.992652 114 118 0.966102 7299 7506 0.972422 10500 10758 0.976018
308354 "chr12:80855598:G>A" "PTPRQ" "NM_001145026:c.909-6889G>A" "INTRON3" "Benign" "rs765169241" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 188 0.00531915 0 92 0 0 132 0 0 0 0 0 2712 0 0 118 0 0 7504 0 1 10746 0.0000930579
308355 "chr12:80855635:C>T" "PTPRQ" "NM_001145026:c.909-6852C>T" "INTRON3" "Unknown significance" "rs140434432" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 4 1008 0.004 0 978 0 5 5008 0.000998403
308356 "chr12:80855641:T>C" "PTPRQ" "NM_001145026:c.909-6846T>C" "INTRON3" "Benign" "rs189306719" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361 0 188 0 1 92 0.0108696 0 132 0 0 0 0 10 2722 0.00367377 0 118 0 81 7506 0.0107914 92 10758 0.00855178
308357 "chr12:80855646:T>C" "PTPRQ" "NM_001145026:c.909-6841T>C" "INTRON3" "Unknown significance" "rs573823756" "This variant is a VUS because it does not have enough information." 0 188 0 0 92 0 0 132 0 0 0 0 0 2722 0 0 118 0 8 7506 0.00106581 8 10758 0.000743633
308358 "chr12:80855661:A>G" "PTPRQ" "NM_001145026:c.909-6826A>G" "INTRON3" "Benign" "rs115286176" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722 4 192 0.0208333 0 92 0 0 132 0 0 0 0 0 2726 0 0 118 0 1 7506 0.000133227 5 10766 0.000464425
308359 "chr12:80855663:C>G" "PTPRQ" "NM_001145026:c.909-6824C>G" "INTRON3" "Unknown significance" "rs564831858" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308360 "chr12:80855673:->A" "PTPRQ" "NM_001145026:c.909-6814_909-6813insA" "INTRON3" "Unknown significance" "rs571712629" "This variant is a VUS because it does not have enough information."
308361 "chr12:80855674:C>T" "PTPRQ" "NM_001145026:c.909-6813C>T" "INTRON3" "Unknown significance" "rs751326024" "This variant is a VUS because it does not have enough information." 0 190 0 0 92 0 0 132 0 0 0 0 0 2726 0 0 118 0 4 7506 0.000532907 4 10764 0.000371609
308362 "chr12:80855680:T>G" "PTPRQ" "NM_001145026:c.909-6807T>G" "INTRON3" "Unknown significance" "rs145543871" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
308363 "chr12:80855690:A>C" "PTPRQ" "NM_001145026:c.909-6797A>C" "INTRON3" "Benign" "rs58874695" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 108 1322 0.0817 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 113 5008 0.0225639 11 188 0.0585106 0 92 0 0 132 0 0 0 0 0 2724 0 0 118 0 1 7504 0.000133262 12 10758 0.00111545
308364 "chr12:80855692:C>A" "PTPRQ" "NM_001145026:c.909-6795C>A" "INTRON3" "Unknown significance" "rs182409675" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 4 5008 0.000798722
308365 "chr12:80855698:C>T" "PTPRQ" "NM_001145026:c.909-6789C>T" "INTRON3" "Unknown significance" "rs138095498" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 4 1008 0.004 1 978 0.001 5 5008 0.000998403 0 188 0 0 92 0 0 132 0 0 0 0 0 2724 0 0 118 0 10 7504 0.00133262 10 10758 0.000929541
308366 "chr12:80855698:C>A" "PTPRQ" "NM_001145026:c.909-6789C>A" "INTRON3" "Benign" "rs138095498" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 188 0 0 92 0 0 132 0 0 0 0 0 2724 0 1 118 0.00847458 7 7504 0.000932836 8 10758 0.000743633
308367 "chr12:80855699:G>A" "PTPRQ" "NM_001145026:c.909-6788G>A" "INTRON3" "Unknown significance" "rs142586886" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308368 "chr12:80855703:A>C" "PTPRQ" "NM_001145026:c.909-6784A>C" "INTRON3" "Unknown significance" "rs756611041" "This variant is a VUS because it does not have enough information." 0 188 0 0 92 0 0 132 0 0 0 0 1 2718 0.000367918 0 118 0 0 7502 0 1 10750 0.0000930233
308369 "chr12:80855729:C>A" "PTPRQ" "NM_001145026:c.909-6758C>A" "INTRON3" "Unknown significance" "rs778277428" "This variant is a VUS because it does not have enough information." 0 190 0 0 92 0 0 132 0 0 0 0 0 2700 0 0 118 0 1 7470 0.000133869 1 10702 0.0000934405
308370 "chr12:80855729:C>G" "PTPRQ" "NM_001145026:c.909-6758C>G" "INTRON3" "Unknown significance" "rs778277428" "This variant is a VUS because it does not have enough information." 0 190 0 0 92 0 0 132 0 0 0 0 0 2700 0 0 118 0 1 7470 0.000133869 1 10702 0.0000934405
308371 "chr12:80855730:C>A" "PTPRQ" "NM_001145026:c.909-6757C>A" "INTRON3" "Unknown significance" "rs184204208" "This variant is a VUS because it does not have enough information."
308372 "chr12:80855732:T>C" "PTPRQ" "NM_001145026:c.909-6755T>C" "INTRON3" "Unknown significance" "rs570196806" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308373 "chr12:80855736:C>T" "PTPRQ" "NM_001145026:c.909-6751C>T" "INTRON3" "Benign" "rs145987138" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 12 1006 0.0119 4 694 0.0058 0 1008 0 19 978 0.0194 37 5008 0.00738818 3 190 0.0157895 2 92 0.0217391 0 132 0 0 0 0 34 2692 0.01263 2 118 0.0169492 195 7460 0.0261394 236 10684 0.0220891
308374 "chr12:80855737:G>T" "PTPRQ" "NM_001145026:c.909-6750G>T" "INTRON3" "Benign" "rs559241517" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 7 978 0.0072 7 5008 0.00139776 0 190 0 1 92 0.0108696 0 132 0 0 0 0 0 2698 0 0 118 0 39 7468 0.00522228 40 10698 0.00373902
308375 "chr12:80855737:G>A" "PTPRQ" "NM_001145026:c.909-6750G>A" "INTRON3" "Benign" "rs559241517" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 190 0 0 92 0 0 132 0 0 0 0 0 2698 0 1 118 0.00847458 0 7468 0 1 10698 0.0000934754
308376 "chr12:80855745:A>T" "PTPRQ" "NM_001145026:c.909-6742A>T" "INTRON3" "Benign" "rs55852310" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243 23 190 0.121053 2 92 0.0217391 0 132 0 0 0 0 0 2698 0 0 118 0 2 7462 0.000268025 27 10692 0.00252525
308377 "chr12:80855747:C>G" "PTPRQ" "NM_001145026:c.909-6740C>G" "INTRON3" "Unknown significance" "rs747931060" "This variant is a VUS because it does not have enough information." 0 190 0 0 92 0 0 132 0 0 0 0 0 2694 0 0 118 0 1 7450 0.000134228 1 10676 0.000093668
308378 "chr12:80855748:T>G" "PTPRQ" "NM_001145026:c.909-6739T>G" "INTRON3" "Unknown significance" "rs148230609" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 4 1008 0.004 0 978 0 4 5008 0.000798722
308379 "chr12:80855749:A>G" "PTPRQ" "NM_001145026:c.909-6738A>G" "INTRON3" "Unknown significance" "rs769620650" "This variant is a VUS because it does not have enough information." 0 190 0 0 92 0 0 132 0 0 0 0 0 2698 0 0 118 0 1 7456 0.00013412 1 10686 0.0000935804
308380 "chr12:80855768:C>G" "PTPRQ" "NM_001145026:c.909-6719C>G" "INTRON3" "Unknown significance" "rs553633301" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 0 190 0 0 92 0 0 132 0 0 0 0 0 2696 0 0 118 0 2 7436 0.000268962 2 10664 0.000187547
308381 "chr12:80855771:G>C" "PTPRQ" "NM_001145026:c.909-6716G>C" "INTRON3" "Benign" "rs141202103" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 0 1006 0 0 694 0 0 1008 0 0 978 0 36 5008 0.0071885 2 190 0.0105263 0 92 0 0 132 0 0 2 0 0 2698 0 0 118 0 0 7428 0 2 10660 0.000187617
308382 "chr12:80855774:A>G" "PTPRQ" "NM_001145026:c.909-6713A>G" "INTRON3" "Unknown significance" "rs766030373" "This variant is a VUS because it does not have enough information." 0 190 0 0 92 0 0 132 0 0 2 0 0 2698 0 0 118 0 2 7436 0.000268962 2 10668 0.000187477
308383 "chr12:80855776:T>A" "PTPRQ" "NM_001145026:c.909-6711T>A" "INTRON3" "Unknown significance" "rs773980512" "This variant is a VUS because it does not have enough information." 0 190 0 0 92 0 0 132 0 0 2 0 1 2698 0.000370645 0 118 0 0 7428 0 1 10660 0.0000938086
308384 "chr12:80855788:G>C" "PTPRQ" "NM_001145026:c.909-6699G>C" "INTRON3" "Unknown significance" "rs150726185" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 5 5008 0.000998403
308385 "chr12:80855803:G>A" "PTPRQ" "NM_001145026:c.909-6684G>A" "INTRON3" "Benign" "rs7137294" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 76 1322 0.0575 561 1006 0.5577 361 694 0.5202 519 1008 0.5149 595 978 0.6084 2112 5008 0.421725 44 194 0.226804 53 92 0.576087 67 134 0.5 0 0 0 1600 2712 0.589971 62 118 0.525424 4707 7428 0.633683 6533 10678 0.611819
308386 "chr12:80855809:T>C" "PTPRQ" "NM_001145026:c.909-6678T>C" "INTRON3" "Unknown significance" "rs767158321" "This variant is a VUS because it does not have enough information." 0 192 0 0 92 0 0 132 0 0 0 0 0 2650 0 0 116 0 1 7288 0.000137212 1 10470 0.000095511
308387 "chr12:80855811:C>T" "PTPRQ" "NM_001145026:c.909-6676C>T" "INTRON3" "Unknown significance" "rs753008707" "This variant is a VUS because it does not have enough information."
308388 "chr12:80855815:G>T" "PTPRQ" "NM_001145026:c.909-6672G>T" "INTRON3" "Benign" "rs56760815" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 243 1322 0.1838 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 261 5008 0.0521166 25 196 0.127551 0 92 0 0 132 0 0 0 0 2 2638 0.00075815 0 116 0 2 7226 0.000276778 29 10400 0.00278846
308389 "chr12:80855815:G>A" "PTPRQ" "NM_001145026:c.909-6672G>A" "INTRON3" "Benign" "rs56760815" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 196 0 1 92 0.0108696 0 132 0 0 0 0 0 2638 0 0 116 0 0 7226 0 1 10400 0.0000961538
308390 "chr12:80855816:T>C" "PTPRQ" "NM_001145026:c.909-6671T>C" "INTRON3" "Benign" "rs543201505" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 3 1006 0.003 6 694 0.0086 0 1008 0 0 978 0 9 5008 0.00179712 0 194 0 1 92 0.0108696 0 132 0 0 0 0 3 2634 0.00113895 0 116 0 0 7218 0 4 10386 0.000385134
308391 "chr12:80855818:A>C" "PTPRQ" "NM_001145026:c.909-6669A>C" "INTRON3" "Benign" "rs7976388" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 476 1322 0.3601 302 1006 0.3002 156 694 0.2248 3 1008 0.003 150 978 0.1534 1087 5008 0.217053 69 194 0.35567 20 90 0.222222 0 130 0 0 0 0 760 2622 0.289855 30 116 0.258621 1217 7146 0.170305 2096 10298 0.203535
308392 "chr12:80855818:A>T" "PTPRQ" "NM_001145026:c.909-6669A>T" "INTRON3" "Benign" "rs7976388" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 649 5008 0.129593 40 194 0.206186 7 90 0.0777778 8 130 0.0615385 0 0 0 63 2622 0.0240275 9 116 0.0775862 654 7146 0.0915197 781 10298 0.07584
308393 "chr12:80855825:C>T" "PTPRQ" "NM_001145026:c.909-6662C>T" "INTRON3" "Benign" "rs60342585" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 535 1322 0.4047 71 1006 0.0706 58 694 0.0836 1 1008 0.001 48 978 0.0491 713 5008 0.142372 58 192 0.302083 9 84 0.107143 0 128 0 0 0 0 260 2510 0.103586 9 116 0.0775862 380 6848 0.0554907 716 9878 0.0724843
308394 "chr12:80855826:G>A" "PTPRQ" "NM_001145026:c.909-6661G>A" "INTRON3" "Unknown significance" "rs758576330" "This variant is a VUS because it does not have enough information." 0 188 0 0 80 0 0 128 0 0 0 0 3 2492 0.00120385 0 116 0 0 6788 0 3 9792 0.000306373
308395 "chr12:80855835:C>T" "PTPRQ" "NM_001145026:c.909-6652C>T" "INTRON3" "Benign" "rs11524045" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 232 1006 0.2306 105 694 0.1513 3 1008 0.003 101 978 0.1033 616 5008 0.123003 32 186 0.172043 13 76 0.171053 0 128 0 0 0 0 486 2420 0.200826 21 114 0.184211 820 6558 0.125038 1372 9482 0.144695
308396 "chr12:80855836:G>C" "PTPRQ" "NM_001145026:c.909-6651G>C" "INTRON3" "Unknown significance" "rs530026080" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681 0 182 0 0 74 0 0 128 0 0 0 0 1 2368 0.000422297 0 114 0 0 6424 0 1 9290 0.000107643
308397 "chr12:80855838:G>C" "PTPRQ" "NM_001145026:c.909-6649G>C" "INTRON3" "Unknown significance" "rs769686911" "This variant is a VUS because it does not have enough information."
308398 "chr12:80855844:G>C" "PTPRQ" "NM_001145026:c.909-6643G>C" "INTRON3" "Unknown significance" "rs548630076" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 178 0 0 70 0 0 124 0 0 0 0 0 2260 0 0 112 0 5 6164 0.000811162 5 8908 0.000561293
308399 "chr12:80855851:T>C" "PTPRQ" "NM_001145026:c.909-6636T>C" "INTRON3" "Unknown significance" "rs189523847" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308400 "chr12:80855852:T>C" "PTPRQ" "NM_001145026:c.909-6635T>C" "INTRON3" "Unknown significance" "rs531067139" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 0 178 0 0 68 0 0 124 0 0 0 0 2 2190 0.000913242 0 102 0 17 5890 0.00288625 19 8552 0.0022217
308401 "chr12:80855852:T>G" "PTPRQ" "NM_001145026:c.909-6635T>G" "INTRON3" "Unknown significance" "rs531067139" "This variant is a VUS because it does not have enough information." 0 178 0 0 68 0 0 124 0 0 0 0 0 2190 0 0 102 0 2 5890 0.000339559 2 8552 0.000233863
308402 "chr12:80855853:G>T" "PTPRQ" "NM_001145026:c.909-6634G>T" "INTRON3" "Benign" "rs147541349" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 39 5008 0.00778754 2 176 0.0113636 0 70 0 0 124 0 0 0 0 0 2178 0 0 104 0 1 5820 0.000171821 3 8472 0.000354108
308403 "chr12:80855856:G>A" "PTPRQ" "NM_001145026:c.909-6631G>A" "INTRON3" "Benign" "rs4448754" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 324 1006 0.3221 221 694 0.3184 40 1008 0.0397 251 978 0.2566 1741 5008 0.347644 97 176 0.551136 23 68 0.338235 8 124 0.0645161 0 0 0 712 2160 0.32963 36 110 0.327273 1622 5794 0.279945 2498 8432 0.296252
308404 "chr12:80855875:G>A" "PTPRQ" "NM_001145026:c.909-6612G>A" "INTRON3" "Unknown significance" "rs771637628" "This variant is a VUS because it does not have enough information."
308405 "chr12:80855881:T>A" "PTPRQ" "NM_001145026:c.909-6606T>A" "INTRON3" "Unknown significance" "rs775272032" "This variant is a VUS because it does not have enough information." 0 120 0 0 36 0 0 116 0 0 0 0 1 1244 0.000803859 0 66 0 0 3514 0 1 5096 0.000196232
308406 "chr12:80855883:T>A" "PTPRQ" "NM_001145026:c.909-6604T>A" "INTRON3" "Unknown significance" "rs535244447" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308407 "chr12:80855894:G>C" "PTPRQ" "NM_001145026:c.909-6593G>C" "INTRON3" "Unknown significance" "rs553359096" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308408 "chr12:80855960:A>G" "PTPRQ" "NM_001145026:c.909-6527A>G" "INTRON3" "Benign" "rs4357758" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1322 1322 1 996 1006 0.9901 693 694 0.9986 1006 1008 0.998 964 978 0.9857 4981 5008 0.994609
308409 "chr12:80855960:AG>GA" "PTPRQ" "Unknown significance" "rs386764636" "This variant is a VUS because it does not have enough information."
308410 "chr12:80855961:G>A" "PTPRQ" "NM_001145026:c.909-6526G>A" "INTRON3" "Benign" "rs535827307" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521
308411 "chr12:80855971:AC>-" "PTPRQ" "NM_001145026:c.909-6516_909-6515delAC" "INTRON3" "Unknown significance" "rs777354072" "This variant is a VUS because it does not have enough information."
308412 "chr12:80856000:A>G" "PTPRQ" "NM_001145026:c.909-6487A>G" "INTRON3" "Unknown significance" "rs554194187" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308413 "chr12:80856001:T>G" "PTPRQ" "NM_001145026:c.909-6486T>G" "INTRON3" "Unknown significance" "rs575637952" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
308414 "chr12:80856012:G>T" "PTPRQ" "NM_001145026:c.909-6475G>T" "INTRON3" "Unknown significance" "rs543075084" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308415 "chr12:80856015:C>T" "PTPRQ" "NM_001145026:c.909-6472C>T" "INTRON3" "Benign" "rs61950908" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 7 1006 0.007 13 694 0.0187 8 1008 0.0079 21 978 0.0215 52 5008 0.0103834
308416 "chr12:80856040:G>T" "PTPRQ" "NM_001145026:c.909-6447G>T" "INTRON3" "Unknown significance" "rs181228480" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308417 "chr12:80856072:G>A" "PTPRQ" "NM_001145026:c.909-6415G>A" "INTRON3" "Unknown significance" "rs11114461" "This variant is a VUS because it does not have enough information."
308418 "chr12:80856075:G>A" "PTPRQ" "NM_001145026:c.909-6412G>A" "INTRON3" "Unknown significance" "rs541248819" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308419 "chr12:80856092:G>-" "PTPRQ" "NM_001145026:c.909-6395delG" "INTRON3" "Unknown significance" "rs528687405" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 1 978 0.001 3 5008 0.000599042
308420 "chr12:80856112:G>T" "PTPRQ" "NM_001145026:c.909-6375G>T" "INTRON3" "Unknown significance" "rs75099755" "This variant is a VUS because it does not have enough information."
308421 "chr12:80856123:G>T" "PTPRQ" "NM_001145026:c.909-6364G>T" "INTRON3" "Unknown significance" "rs112074663" "This variant is a VUS because it does not have enough information."
308422 "chr12:80856135:G>A" "PTPRQ" "NM_001145026:c.909-6352G>A" "INTRON3" "Benign" "rs559373546" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 1 1006 0.001 0 694 0 6 1008 0.006 0 978 0 7 5008 0.00139776
308423 "chr12:80856143:G>T" "PTPRQ" "NM_001145026:c.909-6344G>T" "INTRON3" "Unknown significance" "rs530044880" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308424 "chr12:80856173:A>C" "PTPRQ" "NM_001145026:c.909-6314A>C" "INTRON3" "Benign" "rs542241809" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 1 1006 0.001 0 694 0 7 1008 0.0069 0 978 0 8 5008 0.00159744
308425 "chr12:80856200:C>T" "PTPRQ" "NM_001145026:c.909-6287C>T" "INTRON3" "Unknown significance" "rs113845933" "This variant is a VUS because it does not have enough information."
308426 "chr12:80856311:C>A" "PTPRQ" "NM_001145026:c.909-6176C>A" "INTRON3" "Benign" "rs11835227" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 482 1322 0.3646 302 1006 0.3002 156 694 0.2248 3 1008 0.003 149 978 0.1524 1092 5008 0.218051
308427 "chr12:80856326:C>T" "PTPRQ" "NM_001145026:c.909-6161C>T" "INTRON3" "Benign" "rs530936300" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 134 1322 0.1014 10 1006 0.0099 21 694 0.0303 12 1008 0.0119 33 978 0.0337 210 5008 0.0419329
308428 "chr12:80856330:C>A" "PTPRQ" "NM_001145026:c.909-6157C>A" "INTRON3" "Benign" "rs552668335" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 422 1322 0.3192 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 646 5008 0.128994
308429 "chr12:80856494:C>T" "PTPRQ" "NM_001145026:c.909-5993C>T" "INTRON3" "Unknown significance" "rs36148723" "This variant is a VUS because it does not have enough information."
308430 "chr12:80856578:G>A" "PTPRQ" "NM_001145026:c.909-5909G>A" "INTRON3" "Benign" "rs570944396" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 302 1322 0.2284 2 1006 0.002 22 694 0.0317 9 1008 0.0089 21 978 0.0215 356 5008 0.0710863
308431 "chr12:80856613:C>A" "PTPRQ" "NM_001145026:c.909-5874C>A" "INTRON3" "Benign" "rs367870298" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 1 694 0.0014 13 1008 0.0129 4 978 0.0041 18 5008 0.00359425
308432 "chr12:80856622:C>T" "PTPRQ" "NM_001145026:c.909-5865C>T" "INTRON3" "Unknown significance" "rs547202944" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 2 5008 0.000399361
308433 "chr12:80856676:->T" "PTPRQ" "NM_001145026:c.909-5811_909-5810insT" "INTRON3" "Benign" "rs549079014" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 101 978 0.1033 615 5008 0.122804
308434 "chr12:80856695:A>G" "PTPRQ" "NM_001145026:c.909-5792A>G" "INTRON3" "Benign" "rs375222719" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 304 1322 0.23 71 1006 0.0706 51 694 0.0735 0 1008 0 48 978 0.0491 474 5008 0.0946486
308435 "chr12:80856702:AG>-" "PTPRQ" "NM_001145026:c.909-5785_909-5784delAG" "INTRON3" "Benign" "rs550621915" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 101 978 0.1033 615 5008 0.122804
308436 "chr12:80856709:A>-" "PTPRQ" "NM_001145026:c.909-5778delA" "INTRON3" "Benign" "rs200513532" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 78 1322 0.059 563 1006 0.5596 362 694 0.5216 529 1008 0.5248 628 978 0.6421 2160 5008 0.43131
308437 "chr12:80856732:A>C" "PTPRQ" "NM_001145026:c.909-5755A>C" "INTRON3" "Unknown significance" "rs535708092" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308438 "chr12:80856733:G>C" "PTPRQ" "NM_001145026:c.909-5754G>C" "INTRON3" "Unknown significance" "rs550873950" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308439 "chr12:80856748:T>A" "PTPRQ" "NM_001145026:c.909-5739T>A" "INTRON3" "Unknown significance" "rs569278762" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 8 5008 0.00159744
308440 "chr12:80856757:T>A" "PTPRQ" "NM_001145026:c.909-5730T>A" "INTRON3" "Benign" "rs185592160" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 225 1322 0.1702 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 232 5008 0.0463259
308441 "chr12:80856758:G>C" "PTPRQ" "NM_001145026:c.909-5729G>C" "INTRON3" "Benign" "rs4268566" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1322 1322 1 998 1006 0.992 694 694 1 1008 1008 1 964 978 0.9857 4986 5008 0.995607
308442 "chr12:80856762:G>C" "PTPRQ" "NM_001145026:c.909-5725G>C" "INTRON3" "Benign" "rs4512920" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 887 1006 0.8817 583 694 0.8401 572 1008 0.5675 878 978 0.8978 3911 5008 0.78095
308443 "chr12:80856794:G>A" "PTPRQ" "NM_001145026:c.909-5693G>A" "INTRON3" "Unknown significance" "rs534509992" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308444 "chr12:80856796:G>C" "PTPRQ" "NM_001145026:c.909-5691G>C" "INTRON3" "Benign" "rs12300440" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 649 5008 0.129593
308445 "chr12:80856822:A>G" "PTPRQ" "NM_001145026:c.909-5665A>G" "INTRON3" "Benign" "rs574687413" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 1 1006 0.001 0 694 0 0 1008 0 5 978 0.0051 26 5008 0.00519169
308446 "chr12:80856823:A>C" "PTPRQ" "NM_001145026:c.909-5664A>C" "INTRON3" "Benign" "rs542105308" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 1 1006 0.001 0 694 0 0 1008 0 5 978 0.0051 26 5008 0.00519169
308447 "chr12:80856830:G>A" "PTPRQ" "NM_001145026:c.909-5657G>A" "INTRON3" "Unknown significance" "rs563589581" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 6 5008 0.00119808
308448 "chr12:80856833:C>T" "PTPRQ" "NM_001145026:c.909-5654C>T" "INTRON3" "Unknown significance" "rs575679846" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 3 1008 0.003 0 978 0 4 5008 0.000798722
308449 "chr12:80856847:C>T" "PTPRQ" "NM_001145026:c.909-5640C>T" "INTRON3" "Benign" "rs7300448" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 480 1322 0.3631 302 1006 0.3002 156 694 0.2248 3 1008 0.003 149 978 0.1524 1090 5008 0.217652
308450 "chr12:80856895:T>G" "PTPRQ" "NM_001145026:c.909-5592T>G" "INTRON3" "Unknown significance" "rs564406919" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308451 "chr12:80856899:A>G" "PTPRQ" "NM_001145026:c.909-5588A>G" "INTRON3" "Benign" "rs151257824" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
308452 "chr12:80856931:C>G" "PTPRQ" "NM_001145026:c.909-5556C>G" "INTRON3" "Unknown significance" "rs546785557" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308453 "chr12:80856936:C>T" "PTPRQ" "NM_001145026:c.909-5551C>T" "INTRON3" "Unknown significance" "rs562271175" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308454 "chr12:80856944:T>A" "PTPRQ" "NM_001145026:c.909-5543T>A" "INTRON3" "Unknown significance" "rs529463825" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308455 "chr12:80856952:G>A" "PTPRQ" "NM_001145026:c.909-5535G>A" "INTRON3" "Benign" "rs185868922" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 101 978 0.1033 615 5008 0.122804
308456 "chr12:80856980:C>T" "PTPRQ" "NM_001145026:c.909-5507C>T" "INTRON3" "Unknown significance" "rs553756665" "This variant is a VUS because it does not have enough information."
308457 "chr12:80856990:G>A" "PTPRQ" "NM_001145026:c.909-5497G>A" "INTRON3" "Unknown significance" "rs569238691" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308458 "chr12:80857044:C>G" "PTPRQ" "NM_001145026:c.909-5443C>G" "INTRON3" "Unknown significance" "rs191863632" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308459 "chr12:80857095:A>G" "PTPRQ" "NM_001145026:c.909-5392A>G" "INTRON3" "Unknown significance" "rs552190880" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308460 "chr12:80857099:A>G" "PTPRQ" "NM_001145026:c.909-5388A>G" "INTRON3" "Unknown significance" "rs113393215" "This variant is a VUS because it does not have enough information."
308461 "chr12:80857122:C>G" "PTPRQ" "NM_001145026:c.909-5365C>G" "INTRON3" "Benign" "rs570451200" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 19 1322 0.0144 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 20 5008 0.00399361
308462 "chr12:80857136:C>T" "PTPRQ" "NM_001145026:c.909-5351C>T" "INTRON3" "Unknown significance" "rs534666558" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361
308463 "chr12:80857137:G>A" "PTPRQ" "NM_001145026:c.909-5350G>A" "INTRON3" "Benign" "rs140528976" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 70 1006 0.0696 32 694 0.0461 1 1008 0.001 48 978 0.0491 158 5008 0.0315495
308464 "chr12:80857142:T>C" "PTPRQ" "NM_001145026:c.909-5345T>C" "INTRON3" "Unknown significance" "rs574650518" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308465 "chr12:80857143:A>G" "PTPRQ" "NM_001145026:c.909-5344A>G" "INTRON3" "Benign" "rs184104829" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
308466 "chr12:80857144:T>C" "PTPRQ" "NM_001145026:c.909-5343T>C" "INTRON3" "Unknown significance" "rs376706338" "This variant is a VUS because it does not have enough information."
308467 "chr12:80857164:G>A" "PTPRQ" "NM_001145026:c.909-5323G>A" "INTRON3" "Unknown significance" "rs557269548" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308468 "chr12:80857165:T>C" "PTPRQ" "NM_001145026:c.909-5322T>C" "INTRON3" "Unknown significance" "rs575642845" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308469 "chr12:80857174:T>A" "PTPRQ" "NM_001145026:c.909-5313T>A" "INTRON3" "Unknown significance" "rs545865929" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308470 "chr12:80857178:C>G" "PTPRQ" "NM_001145026:c.909-5309C>G" "INTRON3" "Unknown significance" "rs564548375" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308471 "chr12:80857179:C>G" "PTPRQ" "NM_001145026:c.909-5308C>G" "INTRON3" "Benign" "rs145624611" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 10 1322 0.0076 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 11 5008 0.00219649
308472 "chr12:80857193:G>A" "PTPRQ" "NM_001145026:c.909-5294G>A" "INTRON3" "Unknown significance" "rs138132610" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 1 1008 0.001 0 978 0 2 5008 0.000399361
308473 "chr12:80857197:A>G" "PTPRQ" "NM_001145026:c.909-5290A>G" "INTRON3" "Benign" "rs7316607" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 480 1322 0.3631 302 1006 0.3002 156 694 0.2248 3 1008 0.003 150 978 0.1534 1091 5008 0.217851
308474 "chr12:80857215:A>T" "PTPRQ" "NM_001145026:c.909-5272A>T" "INTRON3" "Unknown significance" "rs556299924" "This variant is a VUS because it does not have enough information."
308475 "chr12:80857248:C>A" "PTPRQ" "NM_001145026:c.909-5239C>A" "INTRON3" "Unknown significance" "rs774898652" "This variant is a VUS because it does not have enough information."
308476 "chr12:80857254:T>C" "PTPRQ" "NM_001145026:c.909-5233T>C" "INTRON3" "Unknown significance" "rs201003624" "This variant is a VUS because it does not have enough information."
308477 "chr12:80857266:C>T" "PTPRQ" "NM_001145026:c.909-5221C>T" "INTRON3" "Unknown significance" "rs202095802" "This variant is a VUS because it does not have enough information."
308478 "chr12:80857271:A>G" "PTPRQ" "NM_001145026:c.909-5216A>G" "INTRON3" "Unknown significance" "rs371679761" "This variant is a VUS because it does not have enough information."
308479 "chr12:80857308:A>T" "PTPRQ" "NM_001145026:c.909-5179A>T" "INTRON3" "Unknown significance" "rs529427141" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308480 "chr12:80857314:T>C" "PTPRQ" "NM_001145026:c.909-5173T>C" "INTRON3" "Benign" "rs550798172" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 228 1322 0.1725 0 1006 0 7 694 0.0101 1 1008 0.001 0 978 0 236 5008 0.0471246
308481 "chr12:80857320:G>T" "PTPRQ" "NM_001145026:c.909-5167G>T" "INTRON3" "Unknown significance" "rs562833439" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308482 "chr12:80857329:T>C" "PTPRQ" "NM_001145026:c.909-5158T>C" "INTRON3" "Unknown significance" "rs375309386" "This variant is a VUS because it does not have enough information."
308483 "chr12:80857366:G>A" "PTPRQ" "NM_001145026:c.909-5121G>A" "INTRON3" "Benign" "rs6539516" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
308484 "chr12:80857401:G>C" "PTPRQ" "NM_001145026:c.909-5086G>C" "INTRON3" "Benign" "rs551791311" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 0 1006 0 0 694 0 0 1008 0 0 978 0 14 5008 0.00279553
308485 "chr12:80857403:C>T" "PTPRQ" "NM_001145026:c.909-5084C>T" "INTRON3" "Unknown significance" "rs570387165" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308486 "chr12:80857413:A>T" "PTPRQ" "NM_001145026:c.909-5074A>T" "INTRON3" "Benign" "rs373226307" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 1 1006 0.001 0 694 0 25 1008 0.0248 0 978 0 26 5008 0.00519169
308487 "chr12:80857440:T>C" "PTPRQ" "NM_001145026:c.909-5047T>C" "INTRON3" "Unknown significance" "rs201614376" "This variant is a VUS because it does not have enough information."
308488 "chr12:80857450:G>A" "PTPRQ" "NM_001145026:c.909-5037G>A" "INTRON3" "Benign" "rs11503523" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 30 1322 0.0227 1 1006 0.001 0 694 0 0 1008 0 0 978 0 31 5008 0.0061901
308489 "chr12:80857459:C>T" "PTPRQ" "NM_001145026:c.909-5028C>T" "INTRON3" "Benign" "rs7486750" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1319 1322 0.9977 973 1006 0.9672 633 694 0.9121 783 1008 0.7768 938 978 0.9591 4646 5008 0.927716
308490 "chr12:80857463:G>C" "PTPRQ" "NM_001145026:c.909-5024G>C" "INTRON3" "Unknown significance" "rs369960760" "This variant is a VUS because it does not have enough information."
308491 "chr12:80857495:C>A" "PTPRQ" "NM_001145026:c.909-4992C>A" "INTRON3" "Benign" "rs57351588" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 93 1322 0.0703 82 1006 0.0815 42 694 0.0605 214 1008 0.2123 58 978 0.0593 489 5008 0.0976438
308492 "chr12:80857520:T>C" "PTPRQ" "NM_001145026:c.909-4967T>C" "INTRON3" "Benign" "rs57251896" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 334 1322 0.2526 82 1006 0.0815 51 694 0.0735 214 1008 0.2123 58 978 0.0593 739 5008 0.147564
308493 "chr12:80857548:G>A" "PTPRQ" "NM_001145026:c.909-4939G>A" "INTRON3" "Benign" "rs569168466" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 138 1322 0.1044 0 1006 0 8 694 0.0115 0 1008 0 0 978 0 146 5008 0.0291534
308494 "chr12:80857549:C>A" "PTPRQ" "NM_001145026:c.909-4938C>A" "INTRON3" "Unknown significance" "rs539681771" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308495 "chr12:80857551:T>A" "PTPRQ" "NM_001145026:c.909-4936T>A" "INTRON3" "Unknown significance" "rs370225950" "This variant is a VUS because it does not have enough information."
308496 "chr12:80857590:A>C" "PTPRQ" "NM_001145026:c.909-4897A>C" "INTRON3" "Unknown significance" "rs557785137" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308497 "chr12:80857669:C>A" "PTPRQ" "NM_001145026:c.909-4818C>A" "INTRON3" "Benign" "rs7486794" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1313 1322 0.9932 972 1006 0.9662 634 694 0.9135 778 1008 0.7718 936 978 0.9571 4633 5008 0.92512
308498 "chr12:80857671:G>A" "PTPRQ" "NM_001145026:c.909-4816G>A" "INTRON3" "Benign" "rs7486640" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1313 1322 0.9932 972 1006 0.9662 634 694 0.9135 778 1008 0.7718 936 978 0.9571 4633 5008 0.92512
308499 "chr12:80857700:A>T" "PTPRQ" "NM_001145026:c.909-4787A>T" "INTRON3" "Unknown significance" "rs555427632" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
308500 "chr12:80857711:A>G" "PTPRQ" "NM_001145026:c.909-4776A>G" "INTRON3" "Benign" "rs11522883" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 102 978 0.1043 616 5008 0.123003
308501 "chr12:80857714:G>A" "PTPRQ" "NM_001145026:c.909-4773G>A" "INTRON3" "Unknown significance" "rs544398933" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308502 "chr12:80857721:A>G" "PTPRQ" "NM_001145026:c.909-4766A>G" "INTRON3" "Benign" "rs28888790" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 102 1322 0.0772 86 1006 0.0855 42 694 0.0605 215 1008 0.2133 60 978 0.0613 505 5008 0.100839
308503 "chr12:80857742:C>T" "PTPRQ" "NM_001145026:c.909-4745C>T" "INTRON3" "Benign" "rs191137631" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489
308504 "chr12:80857770:C>A" "PTPRQ" "NM_001145026:c.909-4717C>A" "INTRON3" "Unknown significance" "rs28759776" "This variant is a VUS because it does not have enough information."
308505 "chr12:80857778:T>A" "PTPRQ" "NM_001145026:c.909-4709T>A" "INTRON3" "Unknown significance" "rs28793082" "This variant is a VUS because it does not have enough information."
308506 "chr12:80857790:C>T" "PTPRQ" "NM_001145026:c.909-4697C>T" "INTRON3" "Unknown significance" "rs540941473" "This variant is a VUS because it does not have enough information."
308507 "chr12:80857802:A>G" "PTPRQ" "NM_001145026:c.909-4685A>G" "INTRON3" "Unknown significance" "rs28853124" "This variant is a VUS because it does not have enough information."
308508 "chr12:80857810:A>C" "PTPRQ" "NM_001145026:c.909-4677A>C" "INTRON3" "Benign" "rs545648739" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 32 1322 0.0242 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 35 5008 0.00698882
308509 "chr12:80857816:A>G" "PTPRQ" "NM_001145026:c.909-4671A>G" "INTRON3" "Unknown significance" "rs560643385" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
308510 "chr12:80857833:A>G" "PTPRQ" "NM_001145026:c.909-4654A>G" "INTRON3" "Benign" "rs528065477" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 19 1322 0.0144 0 1006 0 0 694 0 0 1008 0 0 978 0 19 5008 0.00379393
308511 "chr12:80857852:C>G" "PTPRQ" "NM_001145026:c.909-4635C>G" "INTRON3" "Benign" "rs546650594" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 129 1322 0.0976 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 135 5008 0.0269569
308512 "chr12:80857858:A>G" "PTPRQ" "NM_001145026:c.909-4629A>G" "INTRON3" "Unknown significance" "rs28827895" "This variant is a VUS because it does not have enough information."
308513 "chr12:80857886:T>C" "PTPRQ" "NM_001145026:c.909-4601T>C" "INTRON3" "Unknown significance" "rs28790689" "This variant is a VUS because it does not have enough information."
308514 "chr12:80857900:C>A" "PTPRQ" "NM_001145026:c.909-4587C>A" "INTRON3" "Benign" "rs568149812" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 1 1008 0.001 0 978 0 238 5008 0.047524
308515 "chr12:80858035:T>C" "PTPRQ" "NM_001145026:c.909-4452T>C" "INTRON3" "Benign" "rs200663320" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 107 1322 0.0809 86 1006 0.0855 43 694 0.062 214 1008 0.2123 60 978 0.0613 510 5008 0.101837
308516 "chr12:80858039:A>G" "PTPRQ" "NM_001145026:c.909-4448A>G" "INTRON3" "Unknown significance" "rs550695545" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
308517 "chr12:80858040:A>G" "PTPRQ" "NM_001145026:c.909-4447A>G" "INTRON3" "Benign" "rs569042670" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 322 1322 0.2436 21 1006 0.0209 60 694 0.0865 37 1008 0.0367 101 978 0.1033 541 5008 0.108027
308518 "chr12:80858068:T>G" "PTPRQ" "NM_001145026:c.909-4419T>G" "INTRON3" "Benign" "rs539279349" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
308519 "chr12:80858095:T>C" "PTPRQ" "NM_001145026:c.909-4392T>C" "INTRON3" "Benign" "rs558012595" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 649 5008 0.129593
308520 "chr12:80858112:T>A" "PTPRQ" "NM_001145026:c.909-4375T>A" "INTRON3" "Benign" "rs566689702" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 271 1322 0.205 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 289 5008 0.0577077
308521 "chr12:80858133:C>T" "PTPRQ" "NM_001145026:c.909-4354C>T" "INTRON3" "Unknown significance" "rs534190246" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308522 "chr12:80858186:T>C" "PTPRQ" "NM_001145026:c.909-4301T>C" "INTRON3" "Unknown significance" "rs28841024" "This variant is a VUS because it does not have enough information."
308523 "chr12:80858228:->AGACAGATCAATG" "PTPRQ" "NM_001145026:c.909-4259_909-4258insAGACAGATCAATG" "INTRON3" "Unknown significance" "rs560586723" "This variant is a VUS because it does not have enough information."
308524 "chr12:80858235:->TC" "PTPRQ" "NM_001145026:c.909-4252_909-4251insTC" "INTRON3" "Unknown significance" "rs771871480" "This variant is a VUS because it does not have enough information."
308525 "chr12:80858236:->ATG" "PTPRQ" "NM_001145026:c.909-4251_909-4250insATG" "INTRON3" "Unknown significance" "rs761108220" "This variant is a VUS because it does not have enough information."
308526 "chr12:80858280:C>T" "PTPRQ" "NM_001145026:c.909-4207C>T" "INTRON3" "Unknown significance" "rs202002785" "This variant is a VUS because it does not have enough information."
308527 "chr12:80858300:G>A" "PTPRQ" "NM_001145026:c.909-4187G>A" "INTRON3" "Unknown significance" "rs200146351" "This variant is a VUS because it does not have enough information."
308528 "chr12:80858304:T>C" "PTPRQ" "NM_001145026:c.909-4183T>C" "INTRON3" "Unknown significance" "rs200492057" "This variant is a VUS because it does not have enough information."
308529 "chr12:80858308:C>-" "PTPRQ" "NM_001145026:c.909-4179delC" "INTRON3" "Unknown significance" "rs754221293" "This variant is a VUS because it does not have enough information."
308530 "chr12:80858432:G>A" "PTPRQ" "NM_001145026:c.909-4055G>A" "INTRON3" "Unknown significance" "rs201481089" "This variant is a VUS because it does not have enough information."
308531 "chr12:80858492:G>A" "PTPRQ" "NM_001145026:c.909-3995G>A" "INTRON3" "Unknown significance" "rs796856734" "This variant is a VUS because it does not have enough information."
308532 "chr12:80858622:G>A" "PTPRQ" "NM_001145026:c.909-3865G>A" "INTRON3" "Unknown significance" "rs182668315" "This variant is a VUS because it does not have enough information."
308533 "chr12:80858631:G>C" "PTPRQ" "NM_001145026:c.909-3856G>C" "INTRON3" "Unknown significance" "rs199957321" "This variant is a VUS because it does not have enough information."
308534 "chr12:80858645:G>A" "PTPRQ" "NM_001145026:c.909-3842G>A" "INTRON3" "Benign" "rs201232972" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 263 1322 0.1989 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 281 5008 0.0561102
308535 "chr12:80858731:A>G" "PTPRQ" "NM_001145026:c.909-3756A>G" "INTRON3" "Unknown significance" "rs575237504" "This variant is a VUS because it does not have enough information."
308536 "chr12:80858783:C>G" "PTPRQ" "NM_001145026:c.909-3704C>G" "INTRON3" "Unknown significance" "rs372241530" "This variant is a VUS because it does not have enough information."
308537 "chr12:80858807:G>A" "PTPRQ" "NM_001145026:c.909-3680G>A" "INTRON3" "Unknown significance" "rs56153918" "This variant is a VUS because it does not have enough information."
308538 "chr12:80858822:T>C" "PTPRQ" "NM_001145026:c.909-3665T>C" "INTRON3" "Unknown significance" "rs573702576" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308539 "chr12:80859036:G>T" "PTPRQ" "NM_001145026:c.909-3451G>T" "INTRON3" "Unknown significance" "rs544258636" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308540 "chr12:80859037:A>G" "PTPRQ" "NM_001145026:c.909-3450A>G" "INTRON3" "Unknown significance" "rs202140475" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361
308541 "chr12:80859053:C>T" "PTPRQ" "NM_001145026:c.909-3434C>T" "INTRON3" "Unknown significance" "rs578102539" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308542 "chr12:80859064:C>G" "PTPRQ" "NM_001145026:c.909-3423C>G" "INTRON3" "Unknown significance" "rs764557405" "This variant is a VUS because it does not have enough information."
308543 "chr12:80859068:C>T" "PTPRQ" "NM_001145026:c.909-3419C>T" "INTRON3" "Unknown significance" "rs545300632" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308544 "chr12:80859081:C>A" "PTPRQ" "NM_001145026:c.909-3406C>A" "INTRON3" "Benign" "rs529498362" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 7 1006 0.007 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744
308545 "chr12:80859093:G>T" "PTPRQ" "NM_001145026:c.909-3394G>T" "INTRON3" "Unknown significance" "rs528013329" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308546 "chr12:80859095:C>A" "PTPRQ" "NM_001145026:c.909-3392C>A" "INTRON3" "Unknown significance" "rs540228312" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 1 978 0.001 3 5008 0.000599042
308547 "chr12:80859108:C>T" "PTPRQ" "NM_001145026:c.909-3379C>T" "INTRON3" "Unknown significance" "rs561618080" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308548 "chr12:80859118:G>A" "PTPRQ" "NM_001145026:c.909-3369G>A" "INTRON3" "Unknown significance" "rs549119824" "This variant is a VUS because it does not have enough information."
308549 "chr12:80859139:G>T" "PTPRQ" "NM_001145026:c.909-3348G>T" "INTRON3" "Unknown significance" "rs376166058" "This variant is a VUS because it does not have enough information."
308550 "chr12:80859141:A>G" "PTPRQ" "NM_001145026:c.909-3346A>G" "INTRON3" "Benign" "rs187320063" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 304 1322 0.23 71 1006 0.0706 51 694 0.0735 2 1008 0.002 48 978 0.0491 476 5008 0.0950479
308551 "chr12:80859143:T>C" "PTPRQ" "NM_001145026:c.909-3344T>C" "INTRON3" "Unknown significance" "rs550670907" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308552 "chr12:80859150:C>A" "PTPRQ" "NM_001145026:c.909-3337C>A" "INTRON3" "Benign" "rs10862129" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 564 1006 0.5606 362 694 0.5216 531 1008 0.5268 628 978 0.6421 2166 5008 0.432508
308553 "chr12:80859176:T>C" "PTPRQ" "NM_001145026:c.909-3311T>C" "INTRON3" "Benign" "rs533136599" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 10 1008 0.0099 0 978 0 10 5008 0.00199681
308554 "chr12:80859283:A>G" "PTPRQ" "NM_001145026:c.909-3204A>G" "INTRON3" "Unknown significance" "rs551329014" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308555 "chr12:80859313:C>T" "PTPRQ" "NM_001145026:c.909-3174C>T" "INTRON3" "Unknown significance" "rs566757577" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308556 "chr12:80859322:A>T" "PTPRQ" "NM_001145026:c.909-3165A>T" "INTRON3" "Benign" "rs533791332" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521
308557 "chr12:80859324:A>T" "PTPRQ" "NM_001145026:c.909-3163A>T" "INTRON3" "Unknown significance" "rs201067645" "This variant is a VUS because it does not have enough information."
308558 "chr12:80859360:A>G" "PTPRQ" "NM_001145026:c.909-3127A>G" "INTRON3" "Unknown significance" "rs551391254" "This variant is a VUS because it does not have enough information."
308559 "chr12:80859368:C>T" "PTPRQ" "NM_001145026:c.909-3119C>T" "INTRON3" "Benign" "rs548876133" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 10 978 0.0102 10 5008 0.00199681
308560 "chr12:80859369:G>A" "PTPRQ" "NM_001145026:c.909-3118G>A" "INTRON3" "Benign" "rs371470429" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 10 1006 0.0099 2 694 0.0029 1 1008 0.001 33 978 0.0337 49 5008 0.00978435
308561 "chr12:80859385:G>A" "PTPRQ" "NM_001145026:c.909-3102G>A" "INTRON3" "Unknown significance" "rs191817561" "This variant is a VUS because it does not have enough information."
308562 "chr12:80859435:C>A" "PTPRQ" "NM_001145026:c.909-3052C>A" "INTRON3" "Unknown significance" "rs202127026" "This variant is a VUS because it does not have enough information."
308563 "chr12:80859437:T>C" "PTPRQ" "NM_001145026:c.909-3050T>C" "INTRON3" "Unknown significance" "rs375795281" "This variant is a VUS because it does not have enough information."
308564 "chr12:80859461:G>A" "PTPRQ" "NM_001145026:c.909-3026G>A" "INTRON3" "Benign" "rs12372781" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 51 1006 0.0507 30 694 0.0432 1 1008 0.001 8 978 0.0082 92 5008 0.0183706
308565 "chr12:80859465:C>A" "PTPRQ" "NM_001145026:c.909-3022C>A" "INTRON3" "Benign" "rs556215907" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 2 1006 0.002 0 694 0 18 1008 0.0179 0 978 0 20 5008 0.00399361
308566 "chr12:80859497:T>G" "PTPRQ" "NM_001145026:c.909-2990T>G" "INTRON3" "Unknown significance" "rs578061040" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308567 "chr12:80859499:T>G" "PTPRQ" "NM_001145026:c.909-2988T>G" "INTRON3" "Benign" "rs539210938" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 0 1006 0 0 694 0 0 1008 0 0 978 0 20 5008 0.00399361
308568 "chr12:80859522:A>G" "PTPRQ" "NM_001145026:c.909-2965A>G" "INTRON3" "Benign" "rs368133407" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 304 1322 0.23 71 1006 0.0706 51 694 0.0735 0 1008 0 48 978 0.0491 474 5008 0.0946486
308569 "chr12:80859533:C>T" "PTPRQ" "NM_001145026:c.909-2954C>T" "INTRON3" "Unknown significance" "rs369393162" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308570 "chr12:80859541:T>A" "PTPRQ" "NM_001145026:c.909-2946T>A" "INTRON3" "Unknown significance" "rs543300356" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308571 "chr12:80859559:AA>-" "PTPRQ" "NM_001145026:c.909-2928_909-2927delAA" "INTRON3" "Unknown significance" "rs779358992" "This variant is a VUS because it does not have enough information."
308572 "chr12:80859585:C>-" "PTPRQ" "NM_001145026:c.909-2902delC" "INTRON3" "Unknown significance" "rs540674095" "This variant is a VUS because it does not have enough information."
308573 "chr12:80859600:A>T" "PTPRQ" "NM_001145026:c.909-2887A>T" "INTRON3" "Benign" "rs12316759" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
308574 "chr12:80859602:C>T" "PTPRQ" "NM_001145026:c.909-2885C>T" "INTRON3" "Benign" "rs11114463" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 905 1322 0.6846 322 1006 0.3201 221 694 0.3184 40 1008 0.0397 250 978 0.2556 1738 5008 0.347045
308575 "chr12:80859608:T>A" "PTPRQ" "NM_001145026:c.909-2879T>A" "INTRON3" "Unknown significance" "rs544261752" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308576 "chr12:80859628:C>T" "PTPRQ" "NM_001145026:c.909-2859C>T" "INTRON3" "Benign" "rs11536120" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 565 1006 0.5616 362 694 0.5216 532 1008 0.5278 628 978 0.6421 2168 5008 0.432907
308577 "chr12:80859631:A>G" "PTPRQ" "NM_001145026:c.909-2856A>G" "INTRON3" "Benign" "rs113517580" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
308578 "chr12:80859642:A>T" "PTPRQ" "NM_001145026:c.909-2845A>T" "INTRON3" "Benign" "rs188750297" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 20 1008 0.0198 1 978 0.001 21 5008 0.00419329
308579 "chr12:80859677:C>A" "PTPRQ" "NM_001145026:c.909-2810C>A" "INTRON3" "Benign" "rs199751848" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 7 1008 0.0069 0 978 0 7 5008 0.00139776
308580 "chr12:80859697:T>C" "PTPRQ" "NM_001145026:c.909-2790T>C" "INTRON3" "Unknown significance" "rs527498766" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308581 "chr12:80859698:G>A" "PTPRQ" "NM_001145026:c.909-2789G>A" "INTRON3" "Unknown significance" "rs548837247" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308582 "chr12:80859702:G>A" "PTPRQ" "NM_001145026:c.909-2785G>A" "INTRON3" "Benign" "rs113043433" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 101 978 0.1033 615 5008 0.122804
308583 "chr12:80859728:A>T" "PTPRQ" "NM_001145026:c.909-2759A>T" "INTRON3" "Benign" "rs145171986" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 564 1006 0.5606 362 694 0.5216 532 1008 0.5278 628 978 0.6421 2167 5008 0.432708
308584 "chr12:80859780:G>C" "PTPRQ" "NM_001145026:c.909-2707G>C" "INTRON3" "Benign" "rs11503527" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 729 1322 0.5514 92 1006 0.0915 116 694 0.1671 37 1008 0.0367 149 978 0.1524 1123 5008 0.224241
308585 "chr12:80859780:G>T" "PTPRQ" "NM_001145026:c.909-2707G>T" "INTRON3" "Benign" "rs11503527" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 101 978 0.1033 615 5008 0.122804
308586 "chr12:80859807:G>A" "PTPRQ" "NM_001145026:c.909-2680G>A" "INTRON3" "Unknown significance" "rs538709783" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
308587 "chr12:80859813:G>A" "PTPRQ" "NM_001145026:c.909-2674G>A" "INTRON3" "Unknown significance" "rs554246103" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308588 "chr12:80859844:T>C" "PTPRQ" "NM_001145026:c.909-2643T>C" "INTRON3" "Benign" "rs150674450" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 304 1322 0.23 71 1006 0.0706 51 694 0.0735 0 1008 0 48 978 0.0491 474 5008 0.0946486
308589 "chr12:80859848:C>T" "PTPRQ" "NM_001145026:c.909-2639C>T" "INTRON3" "Unknown significance" "rs536877939" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308590 "chr12:80859860:C>T" "PTPRQ" "NM_001145026:c.909-2627C>T" "INTRON3" "Benign" "rs139868177" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 470 1322 0.3555 0 1006 0 25 694 0.036 0 1008 0 0 978 0 495 5008 0.0988419
308591 "chr12:80859861:G>A" "PTPRQ" "NM_001145026:c.909-2626G>A" "INTRON3" "Unknown significance" "rs576851131" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308592 "chr12:80859870:G>C" "PTPRQ" "NM_001145026:c.909-2617G>C" "INTRON3" "Unknown significance" "rs544224709" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308593 "chr12:80859890:C>T" "PTPRQ" "NM_001145026:c.909-2597C>T" "INTRON3" "Benign" "rs555841159" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 0 1006 0 0 694 0 0 1008 0 5 978 0.0051 25 5008 0.00499201
308594 "chr12:80859947:C>A" "PTPRQ" "NM_001145026:c.909-2540C>A" "INTRON3" "Unknown significance" "rs772886369" "This variant is a VUS because it does not have enough information."
308595 "chr12:80859952:T>C" "PTPRQ" "NM_001145026:c.909-2535T>C" "INTRON3" "Unknown significance" "rs372674748" "This variant is a VUS because it does not have enough information."
308596 "chr12:80859986:C>A" "PTPRQ" "NM_001145026:c.909-2501C>A" "INTRON3" "Unknown significance" "rs576241340" "This variant is a VUS because it does not have enough information."
308597 "chr12:80859989:C>T" "PTPRQ" "NM_001145026:c.909-2498C>T" "INTRON3" "Benign" "rs11114464" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 102 978 0.1043 651 5008 0.129992
308598 "chr12:80859996:C>G" "PTPRQ" "NM_001145026:c.909-2491C>G" "INTRON3" "Unknown significance" "rs544743997" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
308599 "chr12:80859997:A>C" "PTPRQ" "NM_001145026:c.909-2490A>C" "INTRON3" "Benign" "rs145774032" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 71 1006 0.0706 33 694 0.0476 0 1008 0 48 978 0.0491 186 5008 0.0371406
308600 "chr12:80860016:G>C" "PTPRQ" "NM_001145026:c.909-2471G>C" "INTRON3" "Unknown significance" "rs572019529" "This variant is a VUS because it does not have enough information."
308601 "chr12:80860035:G>A" "PTPRQ" "NM_001145026:c.909-2452G>A" "INTRON3" "Unknown significance" "rs201581029" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361
308602 "chr12:80860089:G>A" "PTPRQ" "NM_001145026:c.909-2398G>A" "INTRON3" "Unknown significance" "rs542446858" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
308603 "chr12:80860092:C>G" "PTPRQ" "NM_001145026:c.909-2395C>G" "INTRON3" "Benign" "rs12370027" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 471 1322 0.3563 302 1006 0.3002 156 694 0.2248 3 1008 0.003 149 978 0.1524 1081 5008 0.215855
308604 "chr12:80860113:C>T" "PTPRQ" "NM_001145026:c.909-2374C>T" "INTRON3" "Unknown significance" "rs531544600" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308605 "chr12:80860116:G>C" "PTPRQ" "NM_001145026:c.909-2371G>C" "INTRON3" "Unknown significance" "rs199517272" "This variant is a VUS because it does not have enough information."
308606 "chr12:80860143:A>G" "PTPRQ" "NM_001145026:c.909-2344A>G" "INTRON3" "Benign" "rs193036376" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 0 1006 0 0 694 0 0 1008 0 0 978 0 36 5008 0.0071885
308607 "chr12:80860150:G>C" "PTPRQ" "NM_001145026:c.909-2337G>C" "INTRON3" "Unknown significance" "rs571507482" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308608 "chr12:80860151:A>G" "PTPRQ" "NM_001145026:c.909-2336A>G" "INTRON3" "Benign" "rs10746168" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1216 1322 0.9198 887 1006 0.8817 590 694 0.8501 572 1008 0.5675 878 978 0.8978 4143 5008 0.827276
308609 "chr12:80860158:A>T" "PTPRQ" "NM_001145026:c.909-2329A>T" "INTRON3" "Unknown significance" "rs547554187" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 3 5008 0.000599042
308610 "chr12:80860207:T>C" "PTPRQ" "NM_001145026:c.909-2280T>C" "INTRON3" "Unknown significance" "rs566215816" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308611 "chr12:80860251:C>G" "PTPRQ" "NM_001145026:c.909-2236C>G" "INTRON3" "Benign" "rs144228083" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 38 1322 0.0287 7 1006 0.007 4 694 0.0058 0 1008 0 5 978 0.0051 54 5008 0.0107827
308612 "chr12:80860261:T>C" "PTPRQ" "NM_001145026:c.909-2226T>C" "INTRON3" "Unknown significance" "rs555251074" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308613 "chr12:80860263:T>C" "PTPRQ" "NM_001145026:c.909-2224T>C" "INTRON3" "Benign" "rs570268157" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 26 1322 0.0197 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 28 5008 0.00559105
308614 "chr12:80860309:A>C" "PTPRQ" "NM_001145026:c.909-2178A>C" "INTRON3" "Benign" "rs537308053" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 6 1006 0.006 3 694 0.0043 0 1008 0 4 978 0.0041 13 5008 0.00259585
308615 "chr12:80860311:G>A" "PTPRQ" "NM_001145026:c.909-2176G>A" "INTRON3" "Unknown significance" "rs377495528" "This variant is a VUS because it does not have enough information."
308616 "chr12:80860322:T>C" "PTPRQ" "NM_001145026:c.909-2165T>C" "INTRON3" "Unknown significance" "rs371019422" "This variant is a VUS because it does not have enough information."
308617 "chr12:80860331:A>T" "PTPRQ" "NM_001145026:c.909-2156A>T" "INTRON3" "Unknown significance" "rs375550129" "This variant is a VUS because it does not have enough information."
308618 "chr12:80860341:C>A" "PTPRQ" "NM_001145026:c.909-2146C>A" "INTRON3" "Benign" "rs10862130" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 13 1322 0.0098 0 1006 0 0 694 0 0 1008 0 0 978 0 13 5008 0.00259585
308619 "chr12:80860341:C>G" "PTPRQ" "NM_001145026:c.909-2146C>G" "INTRON3" "Benign" "rs10862130" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 467 1322 0.3533 302 1006 0.3002 156 694 0.2248 3 1008 0.003 149 978 0.1524 1077 5008 0.215056
308620 "chr12:80860358:A>G" "PTPRQ" "NM_001145026:c.909-2129A>G" "INTRON3" "Unknown significance" "rs545016357" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308621 "chr12:80860387:A>G" "PTPRQ" "NM_001145026:c.909-2100A>G" "INTRON3" "Unknown significance" "rs531762508" "This variant is a VUS because it does not have enough information."
308622 "chr12:80860391:C>T" "PTPRQ" "NM_001145026:c.909-2096C>T" "INTRON3" "Benign" "rs202014454" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 12 1322 0.0091 1 1006 0.001 0 694 0 0 1008 0 0 978 0 13 5008 0.00259585
308623 "chr12:80860414:A>C" "PTPRQ" "NM_001145026:c.909-2073A>C" "INTRON3" "Unknown significance" "rs371457968" "This variant is a VUS because it does not have enough information."
308624 "chr12:80860438:A>C" "PTPRQ" "NM_001145026:c.909-2049A>C" "INTRON3" "Unknown significance" "rs571848695" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308625 "chr12:80860440:A>G" "PTPRQ" "NM_001145026:c.909-2047A>G" "INTRON3" "Unknown significance" "rs542409921" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308626 "chr12:80860448:G>A" "PTPRQ" "NM_001145026:c.909-2039G>A" "INTRON3" "Unknown significance" "rs200174993" "This variant is a VUS because it does not have enough information."
308627 "chr12:80860477:C>T" "PTPRQ" "NM_001145026:c.909-2010C>T" "INTRON3" "Unknown significance" "rs560700022" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308628 "chr12:80860479:C>T" "PTPRQ" "NM_001145026:c.909-2008C>T" "INTRON3" "Benign" "rs28891836" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 389 1322 0.2943 21 1006 0.0209 62 694 0.0893 37 1008 0.0367 101 978 0.1033 610 5008 0.121805
308629 "chr12:80860516:A>T" "PTPRQ" "NM_001145026:c.909-1971A>T" "INTRON3" "Benign" "rs143175945" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 50 1322 0.0378 0 1006 0 0 694 0 0 1008 0 0 978 0 50 5008 0.00998403
308630 "chr12:80860527:C>G" "PTPRQ" "NM_001145026:c.909-1960C>G" "INTRON3" "Benign" "rs28863626" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
308631 "chr12:80860584:T>C" "PTPRQ" "NM_001145026:c.909-1903T>C" "INTRON3" "Unknown significance" "rs532388624" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308632 "chr12:80860642:A>G" "PTPRQ" "NM_001145026:c.909-1845A>G" "INTRON3" "Unknown significance" "rs10862131" "This variant is a VUS because it does not have enough information."
308633 "chr12:80860658:T>C" "PTPRQ" "NM_001145026:c.909-1829T>C" "INTRON3" "Unknown significance" "rs367688825" "This variant is a VUS because it does not have enough information."
308634 "chr12:80860749:C>G" "PTPRQ" "NM_001145026:c.909-1738C>G" "INTRON3" "Unknown significance" "rs547813544" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308635 "chr12:80860758:G>A" "PTPRQ" "NM_001145026:c.909-1729G>A" "INTRON3" "Benign" "rs11114465" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 177 1322 0.1339 231 1006 0.2296 105 694 0.1513 3 1008 0.003 101 978 0.1033 617 5008 0.123203
308636 "chr12:80860794:A>G" "PTPRQ" "NM_001145026:c.909-1693A>G" "INTRON3" "Unknown significance" "rs530171924" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308637 "chr12:80860802:A>C" "PTPRQ" "NM_001145026:c.909-1685A>C" "INTRON3" "Unknown significance" "rs548711279" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308638 "chr12:80860824:G>C" "PTPRQ" "NM_001145026:c.909-1663G>C" "INTRON3" "Benign" "rs138021124" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 237 5008 0.0473243
308639 "chr12:80860831:C>-" "PTPRQ" "NM_001145026:c.909-1656delC" "INTRON3" "Benign" "rs199640163" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 43 1006 0.0427 16 694 0.0231 0 1008 0 30 978 0.0307 91 5008 0.0181709
308640 "chr12:80860837:G>A" "PTPRQ" "NM_001145026:c.909-1650G>A" "INTRON3" "Unknown significance" "rs537673692" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
308641 "chr12:80860848:C>G" "PTPRQ" "NM_001145026:c.909-1639C>G" "INTRON3" "Benign" "rs558963540" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489
308642 "chr12:80860859:A>T" "PTPRQ" "NM_001145026:c.909-1628A>T" "INTRON3" "Unknown significance" "rs571156981" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308643 "chr12:80860863:G>A" "PTPRQ" "NM_001145026:c.909-1624G>A" "INTRON3" "Benign" "rs189094574" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
308644 "chr12:80860864:A>G" "PTPRQ" "NM_001145026:c.909-1623A>G" "INTRON3" "Unknown significance" "rs192814097" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308645 "chr12:80860953:A>G" "PTPRQ" "NM_001145026:c.909-1534A>G" "INTRON3" "Unknown significance" "rs571708452" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308646 "chr12:80860970:G>A" "PTPRQ" "NM_001145026:c.909-1517G>A" "INTRON3" "Benign" "rs183969157" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 32 1322 0.0242 0 1006 0 0 694 0 0 1008 0 0 978 0 32 5008 0.00638978
308647 "chr12:80860971:C>T" "PTPRQ" "NM_001145026:c.909-1516C>T" "INTRON3" "Benign" "rs10862132" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 80 1322 0.0605 564 1006 0.5606 362 694 0.5216 530 1008 0.5258 628 978 0.6421 2164 5008 0.432109
308648 "chr12:80860972:G>A" "PTPRQ" "NM_001145026:c.909-1515G>A" "INTRON3" "Benign" "rs188350350" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 83 1322 0.0628 58 1006 0.0577 40 694 0.0576 1 1008 0.001 9 978 0.0092 191 5008 0.038139
308649 "chr12:80860978:C>A" "PTPRQ" "NM_001145026:c.909-1509C>A" "INTRON3" "Unknown significance" "rs543638711" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308650 "chr12:80860995:C>A" "PTPRQ" "NM_001145026:c.909-1492C>A" "INTRON3" "Unknown significance" "rs565027404" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308651 "chr12:80861018:A>C" "PTPRQ" "NM_001145026:c.909-1469A>C" "INTRON3" "Benign" "rs181259804" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 105 694 0.1513 3 1008 0.003 101 978 0.1033 615 5008 0.122804
308652 "chr12:80861031:A>G" "PTPRQ" "NM_001145026:c.909-1456A>G" "INTRON3" "Benign" "rs540972739" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
308653 "chr12:80861059:A>G" "PTPRQ" "NM_001145026:c.909-1428A>G" "INTRON3" "Unknown significance" "rs185721878" "This variant is a VUS because it does not have enough information."
308654 "chr12:80861060:T>G" "PTPRQ" "NM_001145026:c.909-1427T>G" "INTRON3" "Benign" "rs10862133" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 381 1322 0.2882 635 1006 0.6312 410 694 0.5908 509 1008 0.505 672 978 0.6871 2607 5008 0.520567
308655 "chr12:80861162:A>G" "PTPRQ" "NM_001145026:c.909-1325A>G" "INTRON3" "Unknown significance" "rs371978438" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308656 "chr12:80861228:C>T" "PTPRQ" "NM_001145026:c.909-1259C>T" "INTRON3" "Benign" "rs548674765" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 23 1322 0.0174 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 25 5008 0.00499201
308657 "chr12:80861230:A>G" "PTPRQ" "NM_001145026:c.909-1257A>G" "INTRON3" "Benign" "rs563801515" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 37 5008 0.00738818
308658 "chr12:80861284:G>A" "PTPRQ" "NM_001145026:c.909-1203G>A" "INTRON3" "Unknown significance" "rs558625383" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 1 694 0.0014 0 1008 0 1 978 0.001 5 5008 0.000998403
308659 "chr12:80861286:G>A" "PTPRQ" "NM_001145026:c.909-1201G>A" "INTRON3" "Benign" "rs552777667" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 8 5008 0.00159744
308660 "chr12:80861314:C>G" "PTPRQ" "NM_001145026:c.909-1173C>G" "INTRON3" "Unknown significance" "rs571051875" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308661 "chr12:80861354:T>C" "PTPRQ" "NM_001145026:c.909-1133T>C" "INTRON3" "Unknown significance" "rs201066307" "This variant is a VUS because it does not have enough information."
308662 "chr12:80861366:G>A" "PTPRQ" "NM_001145026:c.909-1121G>A" "INTRON3" "Unknown significance" "rs182002305" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308663 "chr12:80861372:A>T" "PTPRQ" "NM_001145026:c.909-1115A>T" "INTRON3" "Unknown significance" "rs546896580" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308664 "chr12:80861377:C>A" "PTPRQ" "NM_001145026:c.909-1110C>A" "INTRON3" "Benign" "rs187662668" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 5 1006 0.005 7 694 0.0101 0 1008 0 3 978 0.0031 17 5008 0.00339457
308665 "chr12:80861407:C>T" "PTPRQ" "NM_001145026:c.909-1080C>T" "INTRON3" "Unknown significance" "rs535865577" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308666 "chr12:80861421:T>C" "PTPRQ" "NM_001145026:c.909-1066T>C" "INTRON3" "Benign" "rs10862134" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 564 1006 0.5606 363 694 0.5231 531 1008 0.5268 628 978 0.6421 2167 5008 0.432708
308667 "chr12:80861424:G>A" "PTPRQ" "NM_001145026:c.909-1063G>A" "INTRON3" "Unknown significance" "rs796990500" "This variant is a VUS because it does not have enough information."
308668 "chr12:80861481:T>C" "PTPRQ" "NM_001145026:c.909-1006T>C" "INTRON3" "Benign" "rs4397915" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 174 1322 0.1316 231 1006 0.2296 104 694 0.1499 3 1008 0.003 101 978 0.1033 613 5008 0.122404
308669 "chr12:80861496:T>C" "PTPRQ" "NM_001145026:c.909-991T>C" "INTRON3" "Unknown significance" "rs373909593" "This variant is a VUS because it does not have enough information."
308670 "chr12:80861501:T>C" "PTPRQ" "NM_001145026:c.909-986T>C" "INTRON3" "Benign" "rs71463877" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 104 1322 0.0787 86 1006 0.0855 43 694 0.062 214 1008 0.2123 60 978 0.0613 507 5008 0.101238
308671 "chr12:80861518:CA>-" "PTPRQ" "NM_001145026:c.909-969_909-968delCA" "INTRON3" "Unknown significance" "rs201418496" "This variant is a VUS because it does not have enough information."
308672 "chr12:80861527:A>T" "PTPRQ" "NM_001145026:c.909-960A>T" "INTRON3" "Benign" "rs201062741" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 389 1322 0.2943 21 1006 0.0209 62 694 0.0893 37 1008 0.0367 101 978 0.1033 610 5008 0.121805
308673 "chr12:80861605:G>T" "PTPRQ" "NM_001145026:c.909-882G>T" "INTRON3" "Benign" "rs576975495" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489
308674 "chr12:80861640:G>T" "PTPRQ" "NM_001145026:c.909-847G>T" "INTRON3" "Benign" "rs4600281" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 176 1322 0.1331 231 1006 0.2296 105 694 0.1513 3 1008 0.003 101 978 0.1033 616 5008 0.123003
308675 "chr12:80861653:G>A" "PTPRQ" "NM_001145026:c.909-834G>A" "INTRON3" "Unknown significance" "rs559707072" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
308676 "chr12:80861654:G>T" "PTPRQ" "NM_001145026:c.909-833G>T" "INTRON3" "Benign" "rs4444144" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 231 1006 0.2296 104 694 0.1499 3 1008 0.003 101 978 0.1033 614 5008 0.122604
308677 "chr12:80861657:G>T" "PTPRQ" "NM_001145026:c.909-830G>T" "INTRON3" "Unknown significance" "rs758937120" "This variant is a VUS because it does not have enough information."
308678 "chr12:80861658:T>G" "PTPRQ" "NM_001145026:c.909-829T>G" "INTRON3" "Benign" "rs61950910" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 102 978 0.1043 651 5008 0.129992
308679 "chr12:80861667:A>G" "PTPRQ" "NM_001145026:c.909-820A>G" "INTRON3" "Unknown significance" "rs61950911" "This variant is a VUS because it does not have enough information."
308680 "chr12:80861672:T>A" "PTPRQ" "NM_001145026:c.909-815T>A" "INTRON3" "Unknown significance" "rs61950912" "This variant is a VUS because it does not have enough information."
308681 "chr12:80861674:A>G" "PTPRQ" "NM_001145026:c.909-813A>G" "INTRON3" "Unknown significance" "rs556406511" "This variant is a VUS because it does not have enough information."
308682 "chr12:80861675:T>C" "PTPRQ" "NM_001145026:c.909-812T>C" "INTRON3" "Benign" "rs563762116" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 11 1322 0.0083 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 12 5008 0.00239617
308683 "chr12:80861684:C>-" "PTPRQ" "NM_001145026:c.909-803delC" "INTRON3" "Benign" "rs535654369" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 0 694 0 1 1008 0.001 0 978 0 16 5008 0.00319489
308684 "chr12:80861721:G>T" "PTPRQ" "NM_001145026:c.909-766G>T" "INTRON3" "Unknown significance" "rs531080732" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308685 "chr12:80861723:A>C" "PTPRQ" "NM_001145026:c.909-764A>C" "INTRON3" "Unknown significance" "rs552393817" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308686 "chr12:80861736:T>C" "PTPRQ" "NM_001145026:c.909-751T>C" "INTRON3" "Unknown significance" "rs564659056" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308687 "chr12:80861752:G>A" "PTPRQ" "NM_001145026:c.909-735G>A" "INTRON3" "Unknown significance" "rs752683435" "This variant is a VUS because it does not have enough information."
308688 "chr12:80861785:A>G" "PTPRQ" "NM_001145026:c.909-702A>G" "INTRON3" "Benign" "rs144400747" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 40 5008 0.00798722
308689 "chr12:80861802:A>G" "PTPRQ" "NM_001145026:c.909-685A>G" "INTRON3" "Unknown significance" "rs576238046" "This variant is a VUS because it does not have enough information."
308690 "chr12:80861833:->T" "PTPRQ" "NM_001145026:c.909-654_909-653insT" "INTRON3" "Benign" "rs140536566" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792
308691 "chr12:80861857:G>-" "PTPRQ" "NM_001145026:c.909-630delG" "INTRON3" "Unknown significance" "rs371589450" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 1 978 0.001 4 5008 0.000798722
308692 "chr12:80861893:A>C" "PTPRQ" "NM_001145026:c.909-594A>C" "INTRON3" "Unknown significance" "rs182122869" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308693 "chr12:80861917:TAGAG>-" "PTPRQ" "NM_001145026:c.909-570_909-566delTAGAG" "INTRON3" "Unknown significance" "rs777906640" "This variant is a VUS because it does not have enough information."
308694 "chr12:80861984:G>A" "PTPRQ" "NM_001145026:c.909-503G>A" "INTRON3" "Unknown significance" "rs749501463" "This variant is a VUS because it does not have enough information."
308695 "chr12:80862006:T>C" "PTPRQ" "NM_001145026:c.909-481T>C" "INTRON3" "Benign" "rs12296663" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 423 1322 0.32 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 647 5008 0.129193
308696 "chr12:80862006:T>G" "PTPRQ" "NM_001145026:c.909-481T>G" "INTRON3" "Unknown significance" "rs12296663" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308697 "chr12:80862024:C>T" "PTPRQ" "NM_001145026:c.909-463C>T" "INTRON3" "Unknown significance" "rs547830700" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308698 "chr12:80862031:T>C" "PTPRQ" "NM_001145026:c.909-456T>C" "INTRON3" "Unknown significance" "rs569556501" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308699 "chr12:80862064:T>A" "PTPRQ" "NM_001145026:c.909-423T>A" "INTRON3" "Benign" "rs185325409" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 18 1006 0.0179 2 694 0.0029 0 1008 0 2 978 0.002 23 5008 0.00459265
308700 "chr12:80862082:T>A" "PTPRQ" "NM_001145026:c.909-405T>A" "INTRON3" "Unknown significance" "rs558385392" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308701 "chr12:80862087:T>G" "PTPRQ" "NM_001145026:c.909-400T>G" "INTRON3" "Unknown significance" "rs746386046" "This variant is a VUS because it does not have enough information."
308702 "chr12:80862184:G>A" "PTPRQ" "NM_001145026:c.909-303G>A" "INTRON3" "Unknown significance" "rs570597901" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308703 "chr12:80862226:G>A" "PTPRQ" "NM_001145026:c.909-261G>A" "INTRON3" "Unknown significance" "rs541451877" "This variant is a VUS because it does not have enough information."
308704 "chr12:80862234:C>A" "PTPRQ" "NM_001145026:c.909-253C>A" "INTRON3" "Unknown significance" "rs555109756" "This variant is a VUS because it does not have enough information."
308705 "chr12:80862238:C>T" "PTPRQ" "NM_001145026:c.909-249C>T" "INTRON3" "Unknown significance" "rs543044745" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
308706 "chr12:80862239:G>A" "PTPRQ" "NM_001145026:c.909-248G>A" "INTRON3" "Benign" "rs75832109" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 71 1006 0.0706 36 694 0.0519 0 1008 0 48 978 0.0491 189 5008 0.0377396
308707 "chr12:80862241:A>C" "PTPRQ" "NM_001145026:c.909-246A>C" "INTRON3" "Unknown significance" "rs574824512" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308708 "chr12:80862299:A>C" "PTPRQ" "NM_001145026:c.909-188A>C" "INTRON3" "Unknown significance" "rs542239915" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308709 "chr12:80862316:A>C" "PTPRQ" "NM_001145026:c.909-171A>C" "INTRON3" "Benign" "rs190135327" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 5 1008 0.005 1 978 0.001 6 5008 0.00119808
308710 "chr12:80862333:A>T" "PTPRQ" "NM_001145026:c.909-154A>T" "INTRON3" "Benign" "rs575557784" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489
308711 "chr12:80862359:A>T" "PTPRQ" "NM_001145026:c.909-128A>T" "INTRON3" "Benign" "rs182734094" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 39 5008 0.00778754
308712 "chr12:80862366:C>A" "PTPRQ" "NM_001145026:c.909-121C>A" "INTRON3" "Unknown significance" "rs188319910" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308713 "chr12:80862373:T>G" "PTPRQ" "NM_001145026:c.909-114T>G" "INTRON3" "Unknown significance" "rs528638622" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
308714 "chr12:80862379:C>T" "PTPRQ" "NM_001145026:c.909-108C>T" "INTRON3" "Unknown significance" "rs530086643" "This variant is a VUS because it does not have enough information."
308715 "chr12:80862380:G>A" "PTPRQ" "NM_001145026:c.909-107G>A" "INTRON3" "Unknown significance" "rs193184269" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308716 "chr12:80862381:C>T" "PTPRQ" "NM_001145026:c.909-106C>T" "INTRON3" "Unknown significance" "rs770498714" "This variant is a VUS because it does not have enough information."
308717 "chr12:80862388:T>G" "PTPRQ" "NM_001145026:c.909-99T>G" "INTRON3" "Unknown significance" "rs762686659" "This variant is a VUS because it does not have enough information."
308718 "chr12:80862405:C>T" "PTPRQ" "NM_001145026:c.909-82C>T" "INTRON3" "Unknown significance" "rs562043267" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308719 "chr12:80862409:G>T" "PTPRQ" "NM_001145026:c.909-78G>T" "INTRON3" "Unknown significance" "rs776523627" "This variant is a VUS because it does not have enough information."
308720 "chr12:80862438:C>T" "PTPRQ" "NM_001145026:c.909-49C>T" "INTRON3" "Unknown significance" "rs754178025" "This variant is a VUS because it does not have enough information." 0 1872 0 0 350 0 0 496 0 0 16 0 0 7272 0 0 172 0 1 7394 0.000135245 1 17572 0.0000569087
308721 "chr12:80862439:G>A" "PTPRQ" "NM_001145026:c.909-48G>A" "INTRON3" "Unknown significance" "rs529499242" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 1 1008 0.001 0 978 0 7 5008 0.00139776 4 1868 0.00214133 0 346 0 0 494 0 0 16 0 1 7314 0.000136724 0 174 0 0 7458 0 5 17670 0.000282965
308722 "chr12:80862464:T>C" "PTPRQ" "NM_001145026:c.909-23T>C" "INTRON3" "Benign" "rs12296942" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 21 1006 0.0209 65 694 0.0937 37 1008 0.0367 101 978 0.1033 650 5008 0.129792 567 1964 0.288697 34 374 0.0909091 24 528 0.0454545 2 18 0.111111 169 7618 0.0221843 13 178 0.0730337 703 7728 0.0909679 1512 18408 0.0821382
308723 "chr12:80862469:A>T" "PTPRQ" "NM_001145026:c.909-18A>T" "INTRON3" "Benign" "rs56105723" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 636 3180 0.2 210 1384 0.151734 846 4564 0.185364 173 1322 0.1309 223 1006 0.2217 104 694 0.1499 3 1008 0.003 98 978 0.1002 601 5008 0.120008 328 2018 0.162537 54 382 0.141361 2 548 0.00364964 6 26 0.230769 1669 7926 0.210573 32 184 0.173913 880 7830 0.112388 2971 18914 0.157079
308724 "chr12:80862475:T>A" "PTPRQ" "NM_001145026:c.909-12T>A" "INTRON3" "Unknown significance" "rs530446362" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308725 "chr12:80862476:A>G" "PTPRQ" "NM_001145026:c.909-11A>G" "INTRON3" "Unknown significance" "rs552229433" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2062 0 0 390 0 0 582 0 0 30 0 0 8048 0 0 186 0 1 7872 0.000127033 1 19170 0.0000521648
308726 "chr12:80862477:T>C" "PTPRQ" "NM_001145026:c.909-10T>C" "INTRON3" "Unknown significance" "rs775316850" "This variant is a VUS because it does not have enough information."
308727 "chr12:80862515:G>A" "PTPRQ" "NM_001145026:p.Val313Ile" "NM_001145026:c.937G>A" "EXON4" "Unknown significance" "rs370185461" "This variant is a VUS because it does not have enough information." 0.154 "N" "0.002" "B" 0.999971 "N" "-2.21" "N" 2 3182 0.000628536 0 1384 0 2 4566 0.00043802 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 0 2148 0 0 410 0 1 622 0.00160772 0 34 0 1 8490 0.000117786 0 190 0 2 7912 0.000252781 4 19806 0.000201959
308728 "chr12:80862519:C>T" "PTPRQ" "NM_001145026:p.Thr314Ile" "NM_001145026:c.941C>T" "EXON4" "Unknown significance" "rs534799489" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.01" "B" 0.998932 "N" "2.05" "C" 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308729 "chr12:80862522:G>A" "PTPRQ" "NM_001145026:p.Gly315Asp" "NM_001145026:c.944G>A" "EXON4" "Unknown significance" "rs751850575" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.695" "P" 0.955872 "N" "4.0" "C" 3 2148 0.00139665 0 410 0 0 622 0 0 34 0 0 8496 0 0 190 0 1 7912 0.00012639 4 19812 0.000201898
308730 "chr12:80862531:C>T" "PTPRQ" "NM_001145026:p.Thr318Ile" "NM_001145026:c.953C>T" "EXON4" "Unknown significance" "rs755136352" "This variant is a VUS because it does not have enough information." 0.935 "N" "1.0" "D" 0.999412 "D" "4.0" "C" 0 2148 0 0 410 0 0 622 0 0 34 0 1 8498 0.000117675 0 190 0 0 7912 0 1 19814 0.0000504694
308731 "chr12:80862533:G>A" "PTPRQ" "NM_001145026:p.Gly319Arg" "NM_001145026:c.955G>A" "EXON4" "Unknown significance" "rs772277829" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.947" "P" 0.991061 "N" "4.0" "C"
308732 "chr12:80862621:A>G" "PTPRQ" "NM_001145026:c.1039+4A>G" "INTRON4" "Unknown significance" "rs777737278" "This variant is a VUS because it does not have enough information." 0 2148 0 0 410 0 0 622 0 0 34 0 1 8492 0.000117758 0 190 0 0 7912 0 1 19808 0.0000504847
308733 "chr12:80862626:T>G" "PTPRQ" "NM_001145026:c.1039+9T>G" "INTRON4" "Unknown significance" "rs553249132" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 0 2148 0 0 410 0 1 622 0.00160772 0 34 0 0 8490 0 0 190 0 0 7912 0 1 19806 0.0000504898
308734 "chr12:80862644:C>A" "PTPRQ" "NM_001145026:c.1039+27C>A" "INTRON4" "Unknown significance" "rs770996910" "This variant is a VUS because it does not have enough information." 0 2146 0 0 410 0 0 622 0 0 34 0 0 8486 0 0 190 0 3 7912 0.000379171 3 19800 0.000151515
308735 "chr12:80862649:T>C" "PTPRQ" "NM_001145026:c.1039+32T>C" "INTRON4" "Unknown significance" "rs148790375" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722 2 2146 0.000931966 0 410 0 0 622 0 0 34 0 0 8482 0 0 190 0 0 7912 0 2 19796 0.000101031
308736 "chr12:80862653:G>A" "PTPRQ" "NM_001145026:c.1039+36G>A" "INTRON4" "Unknown significance" "rs745780253" "This variant is a VUS because it does not have enough information." 1 2144 0.000466418 0 410 0 0 622 0 0 34 0 0 8480 0 0 190 0 0 7912 0 1 19792 0.0000505255
308737 "chr12:80862676:C>G" "PTPRQ" "NM_001145026:c.1039+59C>G" "INTRON4" "Unknown significance" "rs535705989" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308738 "chr12:80862722:C>T" "PTPRQ" "NM_001145026:c.1039+105C>T" "INTRON4" "Benign" "rs11614073" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 6 1322 0.0045 98 1006 0.0974 119 694 0.1715 0 1008 0 30 978 0.0307 253 5008 0.0505192
308739 "chr12:80862743:G>A" "PTPRQ" "NM_001145026:c.1039+126G>A" "INTRON4" "Benign" "rs183872366" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 17 5008 0.00339457
308740 "chr12:80862751:A>G" "PTPRQ" "NM_001145026:c.1039+134A>G" "INTRON4" "Unknown significance" "rs767398097" "This variant is a VUS because it does not have enough information."
308741 "chr12:80862775:T>A" "PTPRQ" "NM_001145026:c.1039+158T>A" "INTRON4" "Unknown significance" "rs545904620" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
308742 "chr12:80862849:G>A" "PTPRQ" "NM_001145026:c.1039+232G>A" "INTRON4" "Unknown significance" "rs766606734" "This variant is a VUS because it does not have enough information."
308743 "chr12:80862860:G>A" "PTPRQ" "NM_001145026:c.1039+243G>A" "INTRON4" "Unknown significance" "rs565808652" "This variant is a VUS because it does not have enough information."
308744 "chr12:80862862:T>G" "PTPRQ" "NM_001145026:c.1039+245T>G" "INTRON4" "Benign" "rs7958020" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 426 1322 0.3222 22 1006 0.0219 65 694 0.0937 37 1008 0.0367 101 978 0.1033 651 5008 0.129992
308745 "chr12:80862872:A>G" "PTPRQ" "NM_001145026:c.1039+255A>G" "INTRON4" "Unknown significance" "rs756208394" "This variant is a VUS because it does not have enough information."
308746 "chr12:80862890:A>G" "PTPRQ" "NM_001145026:c.1039+273A>G" "INTRON4" "Unknown significance" "rs760068100" "This variant is a VUS because it does not have enough information."
308747 "chr12:80862897:C>T" "PTPRQ" "NM_001145026:c.1039+280C>T" "INTRON4" "Unknown significance" "rs765691628" "This variant is a VUS because it does not have enough information."
308748 "chr12:80862961:A>C" "PTPRQ" "NM_001145026:c.1039+344A>C" "INTRON4" "Benign" "rs141524310" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 37 5008 0.00738818
308749 "chr12:80862984:C>T" "PTPRQ" "NM_001145026:c.1039+367C>T" "INTRON4" "Unknown significance" "rs540334751" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308750 "chr12:80862994:C>A" "PTPRQ" "NM_001145026:c.1039+377C>A" "INTRON4" "Benign" "rs189231394" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 0 1006 0 0 694 0 22 1008 0.0218 3 978 0.0031 26 5008 0.00519169
308751 "chr12:80863009:T>C" "PTPRQ" "NM_001145026:c.1039+392T>C" "INTRON4" "Unknown significance" "rs758750273" "This variant is a VUS because it does not have enough information."
308752 "chr12:80863088:A>-" "PTPRQ" "NM_001145026:c.1039+471delA" "INTRON4" "Unknown significance" "rs556974835" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 4 1008 0.004 2 978 0.002 6 5008 0.00119808
308753 "chr12:80863089:A>G" "PTPRQ" "NM_001145026:c.1039+472A>G" "INTRON4" "Unknown significance" "rs529463872" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308754 "chr12:80863132:G>T" "PTPRQ" "NM_001145026:c.1039+515G>T" "INTRON4" "Unknown significance" "rs777481293" "This variant is a VUS because it does not have enough information."
308755 "chr12:80863152:A>C" "PTPRQ" "NM_001145026:c.1039+535A>C" "INTRON4" "Unknown significance" "rs150867577" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308756 "chr12:80863230:T>C" "PTPRQ" "NM_001145026:c.1039+613T>C" "INTRON4" "Benign" "rs563068577" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 9 1008 0.0089 0 978 0 9 5008 0.00179712
308757 "chr12:80863249:T>C" "PTPRQ" "NM_001145026:c.1039+632T>C" "INTRON4" "Unknown significance" "rs541975502" "This variant is a VUS because it does not have enough information."
308758 "chr12:80863271:T>C" "PTPRQ" "NM_001145026:c.1039+654T>C" "INTRON4" "Benign" "rs5028207" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 389 1322 0.2943 22 1006 0.0219 62 694 0.0893 37 1008 0.0367 101 978 0.1033 611 5008 0.122005
308759 "chr12:80863292:A>G" "PTPRQ" "NM_001145026:c.1039+675A>G" "INTRON4" "Benign" "rs7134423" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 299 1322 0.2262 0 1006 0 22 694 0.0317 0 1008 0 0 978 0 321 5008 0.0640974
308760 "chr12:80863298:G>T" "PTPRQ" "NM_001145026:c.1039+681G>T" "INTRON4" "Benign" "rs35555475" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 53 1322 0.0401 86 1006 0.0855 39 694 0.0562 214 1008 0.2123 60 978 0.0613 452 5008 0.0902556
308761 "chr12:80863317:G>A" "PTPRQ" "NM_001145026:c.1039+700G>A" "INTRON4" "Benign" "rs116174385" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 35 1322 0.0265 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 38 5008 0.00758786
308762 "chr12:80863319:T>C" "PTPRQ" "NM_001145026:c.1039+702T>C" "INTRON4" "Unknown significance" "rs546727902" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308763 "chr12:80863374:AC>-" "PTPRQ" "NM_001145026:c.1039+757_1039+758delAC" "INTRON4" "Benign" "rs141826413" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 388 1322 0.2935 22 1006 0.0219 62 694 0.0893 38 1008 0.0377 100 978 0.1022 610 5008 0.121805
308764 "chr12:80863375:C>T" "PTPRQ" "NM_001145026:c.1039+758C>T" "INTRON4" "Benign" "rs568226772" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 0 1006 0 0 694 0 0 1008 0 0 978 0 36 5008 0.0071885
308765 "chr12:80863382:C>G" "PTPRQ" "NM_001145026:c.1039+765C>G" "INTRON4" "Unknown significance" "rs535666089" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308766 "chr12:80863402:A>G" "PTPRQ" "NM_001145026:c.1039+785A>G" "INTRON4" "Unknown significance" "rs559314115" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
308767 "chr12:80863406:C>T" "PTPRQ" "NM_001145026:c.1039+789C>T" "INTRON4" "Unknown significance" "rs745414351" "This variant is a VUS because it does not have enough information."
308768 "chr12:80863429:C>T" "PTPRQ" "NM_001145026:c.1039+812C>T" "INTRON4" "Benign" "rs5028208" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 424 1322 0.3207 22 1006 0.0219 65 694 0.0937 37 1008 0.0367 101 978 0.1033 649 5008 0.129593
308769 "chr12:80863457:C>T" "PTPRQ" "NM_001145026:c.1039+840C>T" "INTRON4" "Unknown significance" "rs373644284" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
308770 "chr12:80863504:A>C" "PTPRQ" "NM_001145026:c.1039+887A>C" "INTRON4" "Unknown significance" "rs111796861" "This variant is a VUS because it does not have enough information."
308771 "chr12:80863509:G>A" "PTPRQ" "NM_001145026:c.1039+892G>A" "INTRON4" "Unknown significance" "rs557822045" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 1 978 0.001 2 5008 0.000399361
308772 "chr12:80863544:A>G" "PTPRQ" "NM_001145026:c.1039+927A>G" "INTRON4" "Unknown significance" "rs572912409" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
308773 "chr12:80863567:A>G" "PTPRQ" "NM_001145026:c.1039+950A>G" "INTRON4" "Benign" "rs73145121" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 173 1322 0.1309 223 1006 0.2217 104 694 0.1499 3 1008 0.003 98 978 0.1002 601 5008 0.120008
308774 "chr12:80863574:C>T" "PTPRQ" "NM_001145026:c.1039+957C>T" "INTRON4" "Unknown significance" "rs768401835" "This variant is a VUS because it does not have enough information."
308775 "chr12:80863604:G>A" "PTPRQ" "NM_001145026:c.1039+987G>A" "INTRON4" "Unknown significance" "rs555465324" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308776 "chr12:80863615:T>A" "PTPRQ" "NM_001145026:c.1039+998T>A" "INTRON4" "Unknown significance" "rs371572884" "This variant is a VUS because it does not have enough information."
308777 "chr12:80863620:T>G" "PTPRQ" "NM_001145026:c.1039+1003T>G" "INTRON4" "Benign" "rs74108665" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 231 1322 0.1747 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 238 5008 0.047524
308778 "chr12:80863626:G>T" "PTPRQ" "NM_001145026:c.1039+1009G>T" "INTRON4" "Benign" "rs7968678" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 312 1322 0.236 0 1006 0 22 694 0.0317 0 1008 0 0 978 0 334 5008 0.0666933
308779 "chr12:80863626:G>A" "PTPRQ" "NM_001145026:c.1039+1009G>A" "INTRON4" "Unknown significance" "rs7968678" "This variant is a VUS because it does not have enough information."
308780 "chr12:80863640:C>G" "PTPRQ" "NM_001145026:c.1039+1023C>G" "INTRON4" "Unknown significance" "rs771297172" "This variant is a VUS because it does not have enough information."
308781 "chr12:80863650:G>A" "PTPRQ" "NM_001145026:c.1039+1033G>A" "INTRON4" "Unknown significance" "rs192548034" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
308782 "chr12:80863679:T>C" "PTPRQ" "NM_001145026:c.1039+1062T>C" "INTRON4" "Benign" "rs6539518" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 300 1322 0.2269 0 1006 0 22 694 0.0317 0 1008 0 0 978 0 322 5008 0.0642971
308783 "chr12:80863711:A>C" "PTPRQ" "NM_001145026:c.1039+1094A>C" "INTRON4" "Benign" "rs114079609" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 33 1322 0.025 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 36 5008 0.0071885
308784 "chr12:80863717:G>T" "PTPRQ" "NM_001145026:c.1039+1100G>T" "INTRON4" "Unknown significance" "rs183517410" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308785 "chr12:80863736:A>G" "PTPRQ" "NM_001145026:c.1039+1119A>G" "INTRON4" "Unknown significance" "rs528107884" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308786 "chr12:80863777:G>C" "PTPRQ" "NM_001145026:c.1039+1160G>C" "INTRON4" "Benign" "rs74965530" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 33 1322 0.025 70 1006 0.0696 33 694 0.0476 0 1008 0 47 978 0.0481 183 5008 0.0365415
308787 "chr12:80863803:T>G" "PTPRQ" "NM_001145026:c.1039+1186T>G" "INTRON4" "Unknown significance" "rs139649017" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308788 "chr12:80863827:A>T" "PTPRQ" "NM_001145026:c.1039+1210A>T" "INTRON4" "Unknown significance" "rs188209068" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308789 "chr12:80863853:A>G" "PTPRQ" "NM_001145026:c.1039+1236A>G" "INTRON4" "Unknown significance" "rs534014814" "This variant is a VUS because it does not have enough information."
308790 "chr12:80863884:TGTT>-" "PTPRQ" "NM_001145026:c.1039+1267_1039+1270delTGTT" "INTRON4" "Unknown significance" "rs776936214" "This variant is a VUS because it does not have enough information."
308791 "chr12:80863885:G>A" "PTPRQ" "NM_001145026:c.1039+1268G>A" "INTRON4" "Unknown significance" "rs753213274" "This variant is a VUS because it does not have enough information."
308792 "chr12:80863904:T>C" "PTPRQ" "NM_001145026:c.1039+1287T>C" "INTRON4" "Unknown significance" "rs769252101" "This variant is a VUS because it does not have enough information."
308793 "chr12:80863936:G>A" "PTPRQ" "NM_001145026:c.1039+1319G>A" "INTRON4" "Unknown significance" "rs377182044" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
308794 "chr12:80863942:C>T" "PTPRQ" "NM_001145026:c.1039+1325C>T" "INTRON4" "Unknown significance" "rs569038035" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308795 "chr12:80863951:C>T" "PTPRQ" "NM_001145026:c.1039+1334C>T" "INTRON4" "Unknown significance" "rs539315870" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308796 "chr12:80863960:T>G" "PTPRQ" "NM_001145026:c.1039+1343T>G" "INTRON4" "Unknown significance" "rs763349096" "This variant is a VUS because it does not have enough information."
308797 "chr12:80864044:A>G" "PTPRQ" "NM_001145026:c.1039+1427A>G" "INTRON4" "Unknown significance" "rs551672167" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308798 "chr12:80864058:C>T" "PTPRQ" "NM_001145026:c.1039+1441C>T" "INTRON4" "Unknown significance" "rs572534327" "This variant is a VUS because it does not have enough information."
308799 "chr12:80864128:->GG" "PTPRQ" "NM_001145026:c.1039+1511_1039+1512insGG" "INTRON4" "Unknown significance" "rs762722607" "This variant is a VUS because it does not have enough information."
308800 "chr12:80864194:A>G" "PTPRQ" "NM_001145026:c.1039+1577A>G" "INTRON4" "Unknown significance" "rs566503680" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
308801 "chr12:80864203:G>C" "PTPRQ" "NM_001145026:c.1039+1586G>C" "INTRON4" "Unknown significance" "rs144268101" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308802 "chr12:80864205:G>A" "PTPRQ" "NM_001145026:c.1039+1588G>A" "INTRON4" "Unknown significance" "rs748972968" "This variant is a VUS because it does not have enough information."
308803 "chr12:80864264:C>A" "PTPRQ" "NM_001145026:c.1040-1620C>A" "INTRON4" "Unknown significance" "rs191609446" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308804 "chr12:80864349:G>A" "PTPRQ" "NM_001145026:c.1040-1535G>A" "INTRON4" "Unknown significance" "rs146557026" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308805 "chr12:80864349:G>C" "PTPRQ" "NM_001145026:c.1040-1535G>C" "INTRON4" "Unknown significance" "rs146557026" "This variant is a VUS because it does not have enough information."
308806 "chr12:80864365:C>T" "PTPRQ" "NM_001145026:c.1040-1519C>T" "INTRON4" "Unknown significance" "rs541191684" "This variant is a VUS because it does not have enough information."
308807 "chr12:80864383:T>G" "PTPRQ" "NM_001145026:c.1040-1501T>G" "INTRON4" "Unknown significance" "rs770671771" "This variant is a VUS because it does not have enough information."
308808 "chr12:80864384:G>A" "PTPRQ" "NM_001145026:c.1040-1500G>A" "INTRON4" "Unknown significance" "rs751944080" "This variant is a VUS because it does not have enough information."
308809 "chr12:80864403:C>T" "PTPRQ" "NM_001145026:c.1040-1481C>T" "INTRON4" "Unknown significance" "rs756864513" "This variant is a VUS because it does not have enough information."
308810 "chr12:80864405:A>G" "PTPRQ" "NM_001145026:c.1040-1479A>G" "INTRON4" "Unknown significance" "rs368882686" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
308811 "chr12:80864413:A>C" "PTPRQ" "NM_001145026:c.1040-1471A>C" "INTRON4" "Unknown significance" "rs561396000" "This variant is a VUS because it does not have enough information."
308812 "chr12:80864431:G>A" "PTPRQ" "NM_001145026:c.1040-1453G>A" "INTRON4" "Unknown significance" "rs556433095" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308813 "chr12:80864480:G>C" "PTPRQ" "NM_001145026:c.1040-1404G>C" "INTRON4" "Unknown significance" "rs578130207" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308814 "chr12:80864490:C>A" "PTPRQ" "NM_001145026:c.1040-1394C>A" "INTRON4" "Unknown significance" "rs780828495" "This variant is a VUS because it does not have enough information."
308815 "chr12:80864493:G>C" "PTPRQ" "NM_001145026:c.1040-1391G>C" "INTRON4" "Benign" "rs73345975" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 390 1322 0.295 22 1006 0.0219 61 694 0.0879 39 1008 0.0387 61 978 0.0624 573 5008 0.114417
308816 "chr12:80864520:A>G" "PTPRQ" "NM_001145026:c.1040-1364A>G" "INTRON4" "Unknown significance" "rs755635277" "This variant is a VUS because it does not have enough information."
308817 "chr12:80864543:C>T" "PTPRQ" "NM_001145026:c.1040-1341C>T" "INTRON4" "Unknown significance" "rs543791234" "This variant is a VUS because it does not have enough information."
308818 "chr12:80864548:G>A" "PTPRQ" "NM_001145026:c.1040-1336G>A" "INTRON4" "Benign" "rs78057177" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 14 1008 0.0139 0 978 0 14 5008 0.00279553
308819 "chr12:80864560:C>T" "PTPRQ" "NM_001145026:c.1040-1324C>T" "INTRON4" "Unknown significance" "rs759454270" "This variant is a VUS because it does not have enough information."
308820 "chr12:80864581:A>C" "PTPRQ" "NM_001145026:c.1040-1303A>C" "INTRON4" "Unknown significance" "rs572852185" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308821 "chr12:80864662:A>T" "PTPRQ" "NM_001145026:c.1040-1222A>T" "INTRON4" "Unknown significance" "rs771887532" "This variant is a VUS because it does not have enough information."
308822 "chr12:80864791:G>A" "PTPRQ" "NM_001145026:c.1040-1093G>A" "INTRON4" "Benign" "rs117984679" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 8 1008 0.0079 0 978 0 8 5008 0.00159744
308823 "chr12:80864794:C>G" "PTPRQ" "NM_001145026:c.1040-1090C>G" "INTRON4" "Unknown significance" "rs775358362" "This variant is a VUS because it does not have enough information."
308824 "chr12:80864831:T>C" "PTPRQ" "NM_001145026:c.1040-1053T>C" "INTRON4" "Benign" "rs11114466" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1009 1322 0.7632 355 1006 0.3529 246 694 0.3545 161 1008 0.1597 318 978 0.3252 2089 5008 0.417133
308825 "chr12:80864831:TGA>CGG" "PTPRQ" "Unknown significance" "rs386764637" "This variant is a VUS because it does not have enough information."
308826 "chr12:80864832:G>A" "PTPRQ" "NM_001145026:c.1040-1052G>A" "INTRON4" "Benign" "rs529023679" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 61 1006 0.0606 28 694 0.0403 2 1008 0.002 47 978 0.0481 141 5008 0.028155
308827 "chr12:80864833:A>G" "PTPRQ" "NM_001145026:c.1040-1051A>G" "INTRON4" "Benign" "rs73145124" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 385 1322 0.2912 243 1006 0.2416 137 694 0.1974 3 1008 0.003 124 978 0.1268 892 5008 0.178115
308828 "chr12:80864855:C>T" "PTPRQ" "NM_001145026:c.1040-1029C>T" "INTRON4" "Unknown significance" "rs528612199" "This variant is a VUS because it does not have enough information."
308829 "chr12:80864861:G>A" "PTPRQ" "NM_001145026:c.1040-1023G>A" "INTRON4" "Benign" "rs73345979" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 72 1322 0.0545 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 75 5008 0.014976
308830 "chr12:80864872:ACG>-" "PTPRQ" "NM_001145026:c.1040-1012_1040-1010delACG" "INTRON4" "Unknown significance" "rs753864041" "This variant is a VUS because it does not have enough information."
308831 "chr12:80864873:C>T" "PTPRQ" "NM_001145026:c.1040-1011C>T" "INTRON4" "Unknown significance" "rs533176390" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308832 "chr12:80864898:T>C" "PTPRQ" "NM_001145026:c.1040-986T>C" "INTRON4" "Unknown significance" "rs551242407" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308833 "chr12:80864906:G>A" "PTPRQ" "NM_001145026:c.1040-978G>A" "INTRON4" "Unknown significance" "rs552383243" "This variant is a VUS because it does not have enough information."
308834 "chr12:80864922:C>T" "PTPRQ" "NM_001145026:c.1040-962C>T" "INTRON4" "Unknown significance" "rs184991032" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308835 "chr12:80864934:A>G" "PTPRQ" "NM_001145026:c.1040-950A>G" "INTRON4" "Unknown significance" "rs765483453" "This variant is a VUS because it does not have enough information."
308836 "chr12:80864969:C>T" "PTPRQ" "NM_001145026:c.1040-915C>T" "INTRON4" "Unknown significance" "rs527670624" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308837 "chr12:80865005:G>T" "PTPRQ" "NM_001145026:c.1040-879G>T" "INTRON4" "Unknown significance" "rs376774168" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308838 "chr12:80865025:G>A" "PTPRQ" "NM_001145026:c.1040-859G>A" "INTRON4" "Unknown significance" "rs750619026" "This variant is a VUS because it does not have enough information."
308839 "chr12:80865080:T>C" "PTPRQ" "NM_001145026:c.1040-804T>C" "INTRON4" "Benign" "rs73345980" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 379 1322 0.2867 34 1006 0.0338 70 694 0.1009 84 1008 0.0833 83 978 0.0849 650 5008 0.129792
308840 "chr12:80865090:A>G" "PTPRQ" "NM_001145026:c.1040-794A>G" "INTRON4" "Unknown significance" "rs537912049" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308841 "chr12:80865099:G>A" "PTPRQ" "NM_001145026:c.1040-785G>A" "INTRON4" "Unknown significance" "rs189970219" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308842 "chr12:80865139:C>T" "PTPRQ" "NM_001145026:c.1040-745C>T" "INTRON4" "Benign" "rs10083168" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 367 1322 0.2776 33 1006 0.0328 60 694 0.0865 44 1008 0.0437 32 978 0.0327 536 5008 0.107029
308843 "chr12:80865141:A>C" "PTPRQ" "NM_001145026:c.1040-743A>C" "INTRON4" "Unknown significance" "rs539246528" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308844 "chr12:80865146:G>A" "PTPRQ" "NM_001145026:c.1040-738G>A" "INTRON4" "Unknown significance" "rs554487671" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308845 "chr12:80865207:A>-" "PTPRQ" "NM_001145026:c.1040-677delA" "INTRON4" "Benign" "rs34836157" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 195 1322 0.1475 184 1006 0.1829 94 694 0.1354 1 1008 0.001 91 978 0.093 565 5008 0.112819
308846 "chr12:80865207:->A" "PTPRQ" "NM_001145026:c.1040-677_1040-676insA" "INTRON4" "Unknown significance" "rs754627175" "This variant is a VUS because it does not have enough information."
308847 "chr12:80865207:A>T" "PTPRQ" "NM_001145026:c.1040-677A>T" "INTRON4" "Unknown significance" "rs201658308" "This variant is a VUS because it does not have enough information."
308848 "chr12:80865268:TTTA>-" "PTPRQ" "NM_001145026:c.1040-616_1040-613delTTTA" "INTRON4" "Unknown significance" "rs796990685" "This variant is a VUS because it does not have enough information."
308849 "chr12:80865271:A>-" "PTPRQ" "NM_001145026:c.1040-613delA" "INTRON4" "Unknown significance" "rs755466454" "This variant is a VUS because it does not have enough information."
308850 "chr12:80865271:A>T" "PTPRQ" "NM_001145026:c.1040-613A>T" "INTRON4" "Unknown significance" "rs4370992" "This variant is a VUS because it does not have enough information."
308851 "chr12:80865279:C>T" "PTPRQ" "NM_001145026:c.1040-605C>T" "INTRON4" "Unknown significance" "rs11114467" "This variant is a VUS because it does not have enough information."
308852 "chr12:80865280:A>G" "PTPRQ" "NM_001145026:c.1040-604A>G" "INTRON4" "Unknown significance" "rs4370993" "This variant is a VUS because it does not have enough information."
308853 "chr12:80865287:C>T" "PTPRQ" "NM_001145026:c.1040-597C>T" "INTRON4" "Benign" "rs10862135" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 634 1322 0.4796 633 1006 0.6292 457 694 0.6585 418 1008 0.4147 716 978 0.7321 2858 5008 0.570687
308854 "chr12:80865298:C>A" "PTPRQ" "NM_001145026:c.1040-586C>A" "INTRON4" "Unknown significance" "rs540228356" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308855 "chr12:80865311:C>T" "PTPRQ" "NM_001145026:c.1040-573C>T" "INTRON4" "Unknown significance" "rs555363372" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308856 "chr12:80865319:G>C" "PTPRQ" "NM_001145026:c.1040-565G>C" "INTRON4" "Benign" "rs4609663" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 713 1322 0.5393 287 1006 0.2853 159 694 0.2291 302 1008 0.2996 227 978 0.2321 1688 5008 0.337061
308857 "chr12:80865319:G>T" "PTPRQ" "NM_001145026:c.1040-565G>T" "INTRON4" "Unknown significance" "rs4609663" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308858 "chr12:80865349:C>T" "PTPRQ" "NM_001145026:c.1040-535C>T" "INTRON4" "Unknown significance" "rs538944976" "This variant is a VUS because it does not have enough information."
308859 "chr12:80865368:T>C" "PTPRQ" "NM_001145026:c.1040-516T>C" "INTRON4" "Unknown significance" "rs373735020" "This variant is a VUS because it does not have enough information."
308860 "chr12:80865382:A>G" "PTPRQ" "NM_001145026:c.1040-502A>G" "INTRON4" "Benign" "rs10862136" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 805 1322 0.6089 727 1006 0.7227 500 694 0.7205 686 1008 0.6806 766 978 0.7832 3484 5008 0.695687
308861 "chr12:80865386:A>C" "PTPRQ" "NM_001145026:c.1040-498A>C" "INTRON4" "Benign" "rs371231159" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 1 694 0.0014 30 1008 0.0298 1 978 0.001 32 5008 0.00638978
308862 "chr12:80865404:G>C" "PTPRQ" "NM_001145026:c.1040-480G>C" "INTRON4" "Benign" "rs4272839" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1318 1322 0.997 974 1006 0.9682 626 694 0.902 736 1008 0.7302 922 978 0.9427 4576 5008 0.913738
308863 "chr12:80865411:T>C" "PTPRQ" "NM_001145026:c.1040-473T>C" "INTRON4" "Benign" "rs560012671" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 33 1006 0.0328 15 694 0.0216 0 1008 0 2 978 0.002 57 5008 0.0113818
308864 "chr12:80865412:A>G" "PTPRQ" "NM_001145026:c.1040-472A>G" "INTRON4" "Benign" "rs527536898" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 33 1006 0.0328 15 694 0.0216 0 1008 0 2 978 0.002 51 5008 0.0101837
308865 "chr12:80865413:C>T" "PTPRQ" "NM_001145026:c.1040-471C>T" "INTRON4" "Unknown significance" "rs548874032" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308866 "chr12:80865418:G>C" "PTPRQ" "NM_001145026:c.1040-466G>C" "INTRON4" "Unknown significance" "rs368029778" "This variant is a VUS because it does not have enough information."
308867 "chr12:80865447:G>A" "PTPRQ" "NM_001145026:c.1040-437G>A" "INTRON4" "Unknown significance" "rs200910493" "This variant is a VUS because it does not have enough information."
308868 "chr12:80865460:T>G" "PTPRQ" "NM_001145026:c.1040-424T>G" "INTRON4" "Unknown significance" "rs567517561" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
308869 "chr12:80865499:G>A" "PTPRQ" "NM_001145026:c.1040-385G>A" "INTRON4" "Benign" "rs11114468" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 292 1322 0.2209 6 1006 0.006 46 694 0.0663 44 1008 0.0437 22 978 0.0225 410 5008 0.081869
308870 "chr12:80865507:C>T" "PTPRQ" "NM_001145026:c.1040-377C>T" "INTRON4" "Unknown significance" "rs190448094" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
308871 "chr12:80865522:A>G" "PTPRQ" "NM_001145026:c.1040-362A>G" "INTRON4" "Unknown significance" "rs535177686" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 1 1008 0.001 0 978 0 2 5008 0.000399361
308872 "chr12:80865548:G>C" "PTPRQ" "NM_001145026:c.1040-336G>C" "INTRON4" "Unknown significance" "rs539223502" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308873 "chr12:80865553:T>G" "PTPRQ" "NM_001145026:c.1040-331T>G" "INTRON4" "Unknown significance" "rs113966292" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308874 "chr12:80865566:C>T" "PTPRQ" "NM_001145026:c.1040-318C>T" "INTRON4" "Benign" "rs77573699" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 502 1322 0.3797 213 1006 0.2117 123 694 0.1772 0 1008 0 106 978 0.1084 944 5008 0.188498
308875 "chr12:80865581:A>G" "PTPRQ" "NM_001145026:c.1040-303A>G" "INTRON4" "Unknown significance" "rs12301250" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308876 "chr12:80865585:T>C" "PTPRQ" "NM_001145026:c.1040-299T>C" "INTRON4" "Benign" "rs12302642" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 565 1322 0.4274 213 1006 0.2117 127 694 0.183 0 1008 0 106 978 0.1084 1011 5008 0.201877
308877 "chr12:80865622:G>A" "PTPRQ" "NM_001145026:c.1040-262G>A" "INTRON4" "Unknown significance" "rs571833540" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
308878 "chr12:80865624:A>T" "PTPRQ" "NM_001145026:c.1040-260A>T" "INTRON4" "Benign" "rs551466120" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 56 978 0.0573 57 5008 0.0113818
308879 "chr12:80865723:C>T" "PTPRQ" "NM_001145026:c.1040-161C>T" "INTRON4" "Unknown significance" "rs555976241" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308880 "chr12:80865745:A>G" "PTPRQ" "NM_001145026:c.1040-139A>G" "INTRON4" "Benign" "rs12301344" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 191 1322 0.1445 0 1006 0 8 694 0.0115 0 1008 0 0 978 0 199 5008 0.0397364
308881 "chr12:80865748:C>A" "PTPRQ" "NM_001145026:c.1040-136C>A" "INTRON4" "Unknown significance" "rs544708436" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308882 "chr12:80865761:A>G" "PTPRQ" "NM_001145026:c.1040-123A>G" "INTRON4" "Unknown significance" "rs778766545" "This variant is a VUS because it does not have enough information."
308883 "chr12:80865762:T>C" "PTPRQ" "NM_001145026:c.1040-122T>C" "INTRON4" "Unknown significance" "rs745531004" "This variant is a VUS because it does not have enough information."
308884 "chr12:80865813:C>T" "PTPRQ" "NM_001145026:c.1040-71C>T" "INTRON4" "Unknown significance" "rs142094595" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
308885 "chr12:80865840:C>T" "PTPRQ" "NM_001145026:c.1040-44C>T" "INTRON4" "Benign" "rs73345986" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 3182 0.000314268 50 1384 0.0361272 51 4566 0.0111695 0 400 0 0 320 0 1 320 0.003125 0 400 0 0 360 0 0 200 0 1 2000 0.0005 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792 95 2084 0.0455854 4 384 0.0104167 0 616 0 0 32 0 1 8192 0.00012207 0 184 0 2 7684 0.000260281 102 19176 0.00531915
308886 "chr12:80865848:A>C" "PTPRQ" "NM_001145026:c.1040-36A>C" "INTRON4" "Unknown significance" "rs774830176" "This variant is a VUS because it does not have enough information." 0 2088 0 0 384 0 0 616 0 0 32 0 1 8226 0.000121566 0 184 0 0 7752 0 1 19282 0.0000518618
308887 "chr12:80865857:T>C" "PTPRQ" "NM_001145026:c.1040-27T>C" "INTRON4" "Unknown significance" "rs760423207" "This variant is a VUS because it does not have enough information." 0 2084 0 0 388 0 0 618 0 0 34 0 1 8266 0.000120977 0 184 0 0 7808 0 1 19382 0.0000515943
308888 "chr12:80865860:A>G" "PTPRQ" "NM_001145026:c.1040-24A>G" "INTRON4" "Benign" "rs768247368" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 400 0.005 0 320 0 0 320 0 0 400 0 0 360 0 1 200 0.005 3 2000 0.0015 0 2092 0 1 388 0.00257732 0 620 0 0 34 0 9 8286 0.00108617 0 186 0 5 7842 0.000637592 15 19448 0.000771288
308889 "chr12:80865871:C>T" "PTPRQ" "NM_001145026:c.1040-13C>T" "INTRON4" "Unknown significance" "rs542485573" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361 2 2098 0.000953289 1 392 0.00255102 0 620 0 0 34 0 0 8342 0 0 186 0 0 7896 0 3 19568 0.000153312
308890 "chr12:80865886:C>T" "PTPRQ" "NM_001145026:p.Arg348Cys" "NM_001145026:c.1042C>T" "EXON5" "Unknown significance" "rs112718610" "This variant is a VUS because it does not have enough information." 0.02 "N" "0.951" "P" 1 "N" "0.497" "C"
308891 "chr12:80865887:G>T" "PTPRQ" "NM_001145026:p.Arg348Leu" "NM_001145026:c.1043G>T" "EXON5" "Unknown significance" "rs775296221" "This variant is a VUS because it does not have enough information." -0.231 "N" "0.0" "B" 1 "N" "-0.791" "N" 0 2114 0 0 394 0 0 620 0 0 34 0 0 8412 0 0 186 0 2 7908 0.000252908 2 19668 0.000101688
308892 "chr12:80865887:G>A" "PTPRQ" "NM_001145026:p.Arg348His" "NM_001145026:c.1043G>A" "EXON5" "Unknown significance" "rs775296221" "This variant is a VUS because it does not have enough information." -0.231 "N" "0.001" "B" 1 "N" "-0.791" "N"
308893 "chr12:80865889:A>-" "PTPRQ" "NM_001145026:c.1045delA" "EXON5" "Unknown significance" "rs763138435" "This variant is a VUS because it does not have enough information." 0 2118 0 0 394 0 0 620 0 0 34 0 0 8416 0 0 186 0 1 7910 0.000126422 1 19678 0.0000508182
308894 "chr12:80865906:AA>-" "PTPRQ" "NM_001145026:c.1062_1063delAA" "EXON5" "Unknown significance" "rs766596311" "This variant is a VUS because it does not have enough information."
308895 "chr12:80865948:A>G" "PTPRQ" "NM_001145026:p.Thr368Thr" "NM_001145026:c.1104A>G" "EXON5" "Benign" "rs61729291" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 168 3182 0.052797 15 1384 0.0108382 183 4566 0.0400788 15 400 0.0375 13 320 0.040625 13 320 0.040625 0 400 0 11 360 0.0305556 7 200 0.035 59 2000 0.0295 5 1322 0.0038 65 1006 0.0646 38 694 0.0548 0 1008 0 7 978 0.0072 115 5008 0.0229633 25 2130 0.0117371 24 404 0.0594059 0 620 0 1 36 0.0277778 480 8466 0.0566974 9 188 0.0478723 111 7910 0.0140329 650 19754 0.0329047
308896 "chr12:80865948:A>T" "PTPRQ" "NM_001145026:p.Thr368Thr" "NM_001145026:c.1104A>T" "EXON5" "Unknown significance" "rs61729291" "This variant is a VUS because it does not have enough information." 0 2130 0 0 404 0 0 620 0 0 36 0 0 8466 0 0 188 0 3 7910 0.000379267 3 19754 0.000151868
308897 "chr12:80865950:T>A" "PTPRQ" "NM_001145026:p.Met369Lys" "NM_001145026:c.1106T>A" "EXON5" "Unknown significance" "rs531589536" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.03" "B" 1 "N" "2.98" "C" 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2130 0 0 404 0 0 620 0 0 34 0 0 8460 0 0 188 0 1 7908 0.000126454 1 19744 0.0000506483
308898 "chr12:80865968:C>T" "PTPRQ" "NM_001145026:p.Ala375Val" "NM_001145026:c.1124C>T" "EXON5" "Unknown significance" "rs746899906" "This variant is a VUS because it does not have enough information." 0.852 "N" "0.966" "D" 1 "N" "3.47" "C"
308899 "chr12:80865979:A>C" "PTPRQ" "NM_001145026:p.Ser379Arg" "NM_001145026:c.1135A>C" "EXON5" "Pathogenic" "Non-syndromic deafness, autosomal recessive, DFNB84A" "26969326" "rs145855772" 1.088 "C" "0.998" "D" 0.934774 "D" "5.44" "C" 0 3182 0 4 1384 0.00289017 4 4566 0.00087604 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403 4 2114 0.00189215 0 400 0 0 618 0 0 34 0 0 8430 0 0 186 0 0 7902 0 4 19684 0.000203211
308900 "chr12:80865981:T>G" "PTPRQ" "NM_001145026:p.Ser379Arg" "NM_001145026:c.1137T>G" "EXON5" "Unknown significance" "rs751548081" "This variant is a VUS because it does not have enough information." 0.082 "N" "0.998" "D" 0.718059 "D" "3.03" "C" 0 2106 0 0 400 0 0 618 0 0 34 0 0 8426 0 0 186 0 1 7902 0.00012655 1 19672 0.0000508337
308901 "chr12:80865982:G>A" "PTPRQ" "NM_001145026:p.Ala380Thr" "NM_001145026:c.1138G>A" "EXON5" "Unknown significance" "rs755263966" "This variant is a VUS because it does not have enough information." 0.953 "C" "0.835" "P" 0.900828 "D" "5.44" "C" 0 2104 0 0 398 0 0 618 0 0 34 0 1 8422 0.000118737 0 186 0 0 7902 0 1 19664 0.0000508544
308902 "chr12:80865989:C>G" "PTPRQ" "NM_001145026:p.Thr382Ser" "NM_001145026:c.1145C>G" "EXON5" "Benign" "rs61729290" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.057 "N" "0.059" "B" 1 "N" "2.95" "C" 0 3182 0 31 1384 0.0223988 31 4566 0.00678931 0 400 0 0 320 0 1 320 0.003125 0 400 0 0 360 0 0 200 0 1 2000 0.0005 26 1322 0.0197 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 28 5008 0.00559105 47 2108 0.022296 0 396 0 0 618 0 0 34 0 1 8408 0.000118934 0 186 0 0 7904 0 48 19654 0.00244225
308903 "chr12:80866003:A>G" "PTPRQ" "NM_001145026:p.Asn387Asp" "NM_001145026:c.1159A>G" "EXON5" "Unknown significance" "rs76334533" "This variant is a VUS because it does not have enough information." 1.088 "C" "0.968" "D" 0.704318 "N" "4.29" "C"
308904 "chr12:80866031:G>C" "PTPRQ" "NM_001145026:c.1186+1G>C" "INTRON5" "Unknown significance" "rs753703537" "This variant is a VUS because it does not have enough information." 1.048 "C" 1 "D" "5.62" "C" 0 2064 0 0 378 0 0 608 0 0 34 0 0 8284 0 0 184 0 1 7880 0.000126904 1 19432 0.0000514615
308905 "chr12:80866041:A>C" "PTPRQ" "NM_001145026:c.1186+11A>C" "INTRON5" "Unknown significance" "rs757179903" "This variant is a VUS because it does not have enough information." 0 2036 0 0 376 0 0 606 0 0 34 0 0 8262 0 0 184 0 4 7878 0.000507743 4 19376 0.000206441
308906 "chr12:80866048:G>-" "PTPRQ" "NM_001145026:c.1186+18delG" "INTRON5" "Benign" "rs562118304" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521 19 2034 0.0093412 0 372 0 0 608 0 0 34 0 0 8238 0 0 184 0 0 7878 0 19 19348 0.000982014
308907 "chr12:80866055:A>G" "PTPRQ" "NM_001145026:c.1186+25A>G" "INTRON5" "Unknown significance" "rs774632983" "This variant is a VUS because it does not have enough information."
308908 "chr12:80866094:A>T" "PTPRQ" "NM_001145026:c.1186+64A>T" "INTRON5" "Benign" "rs189988624" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 9 1008 0.0089 0 978 0 9 5008 0.00179712
308909 "chr12:80866105:G>C" "PTPRQ" "NM_001145026:c.1186+75G>C" "INTRON5" "Unknown significance" "rs547929732" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308910 "chr12:80866186:C>T" "PTPRQ" "NM_001145026:c.1186+156C>T" "INTRON5" "Unknown significance" "rs566250522" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308911 "chr12:80866206:C>A" "PTPRQ" "NM_001145026:c.1186+176C>A" "INTRON5" "Unknown significance" "rs141163682" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308912 "chr12:80866242:G>A" "PTPRQ" "NM_001145026:c.1186+212G>A" "INTRON5" "Unknown significance" "rs182601293" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308913 "chr12:80866273:G>A" "PTPRQ" "NM_001145026:c.1186+243G>A" "INTRON5" "Unknown significance" "rs74853570" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 4 978 0.0041 7 5008 0.00139776
308914 "chr12:80866295:T>C" "PTPRQ" "NM_001145026:c.1186+265T>C" "INTRON5" "Unknown significance" "rs537440586" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308915 "chr12:80866362:G>A" "PTPRQ" "NM_001145026:c.1186+332G>A" "INTRON5" "Unknown significance" "rs762180914" "This variant is a VUS because it does not have enough information."
308916 "chr12:80866395:T>G" "PTPRQ" "NM_001145026:c.1186+365T>G" "INTRON5" "Benign" "rs186759955" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 0 1006 0 18 694 0.0259 0 1008 0 0 978 0 19 5008 0.00379393
308917 "chr12:80866471:T>C" "PTPRQ" "NM_001145026:c.1186+441T>C" "INTRON5" "Unknown significance" "rs577229587" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308918 "chr12:80866480:G>T" "PTPRQ" "NM_001145026:c.1186+450G>T" "INTRON5" "Unknown significance" "rs538310573" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308919 "chr12:80866483:G>T" "PTPRQ" "NM_001145026:c.1186+453G>T" "INTRON5" "Unknown significance" "rs553472509" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
308920 "chr12:80866483:G>A" "PTPRQ" "NM_001145026:c.1186+453G>A" "INTRON5" "Unknown significance" "rs553472509" "This variant is a VUS because it does not have enough information."
308921 "chr12:80866487:G>C" "PTPRQ" "NM_001145026:c.1186+457G>C" "INTRON5" "Unknown significance" "rs768540055" "This variant is a VUS because it does not have enough information."
308922 "chr12:80866511:G>C" "PTPRQ" "NM_001145026:c.1186+481G>C" "INTRON5" "Unknown significance" "rs750141306" "This variant is a VUS because it does not have enough information."
308923 "chr12:80866527:T>C" "PTPRQ" "NM_001145026:c.1186+497T>C" "INTRON5" "Unknown significance" "rs755618167" "This variant is a VUS because it does not have enough information."
308924 "chr12:80866529:T>A" "PTPRQ" "NM_001145026:c.1186+499T>A" "INTRON5" "Unknown significance" "rs577574452" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
308925 "chr12:80866600:G>A" "PTPRQ" "NM_001145026:c.1186+570G>A" "INTRON5" "Benign" "rs7980649" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 231 1322 0.1747 215 1006 0.2137 111 694 0.1599 0 1008 0 106 978 0.1084 663 5008 0.132388
308926 "chr12:80866601:A>C" "PTPRQ" "NM_001145026:c.1186+571A>C" "INTRON5" "Benign" "rs191552066" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 22 1322 0.0166 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 24 5008 0.00479233
308927 "chr12:80866625:A>G" "PTPRQ" "NM_001145026:c.1186+595A>G" "INTRON5" "Unknown significance" "rs576330743" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308928 "chr12:80866768:T>G" "PTPRQ" "NM_001145026:c.1186+738T>G" "INTRON5" "Benign" "rs150285391" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 5 1008 0.005 0 978 0 5 5008 0.000998403
308929 "chr12:80866799:T>G" "PTPRQ" "NM_001145026:c.1186+769T>G" "INTRON5" "Unknown significance" "rs565240754" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308930 "chr12:80866802:->AC" "PTPRQ" "NM_001145026:c.1186+772_1186+773insAC" "INTRON5" "Unknown significance" "rs765517847" "This variant is a VUS because it does not have enough information."
308931 "chr12:80866802:AC>-" "PTPRQ" "NM_001145026:c.1186+772_1186+773delAC" "INTRON5" "Unknown significance" "rs371484292" "This variant is a VUS because it does not have enough information."
308932 "chr12:80866815:CT>-" "PTPRQ" "NM_001145026:c.1186+785_1186+786delCT" "INTRON5" "Unknown significance" "rs747694708" "This variant is a VUS because it does not have enough information."
308933 "chr12:80866816:T>A" "PTPRQ" "NM_001145026:c.1186+786T>A" "INTRON5" "Benign" "rs4417374" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 821 1322 0.621 270 1006 0.2684 194 694 0.2795 52 1008 0.0516 174 978 0.1779 1511 5008 0.301717
308934 "chr12:80866816:T>G" "PTPRQ" "NM_001145026:c.1186+786T>G" "INTRON5" "Unknown significance" "rs4417374" "This variant is a VUS because it does not have enough information."
308935 "chr12:80866820:A>G" "PTPRQ" "NM_001145026:c.1186+790A>G" "INTRON5" "Benign" "rs547892971" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 27 1322 0.0204 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 31 5008 0.0061901
308936 "chr12:80866825:->CG" "PTPRQ" "NM_001145026:c.1186+795_1186+796insCG" "INTRON5" "Unknown significance" "rs10641262" "This variant is a VUS because it does not have enough information."
308937 "chr12:80866825:CG>-" "PTPRQ" "NM_001145026:c.1186+795_1186+796delCG" "INTRON5" "Unknown significance" "rs752222560" "This variant is a VUS because it does not have enough information."
308938 "chr12:80866826:G>A" "PTPRQ" "NM_001145026:c.1186+796G>A" "INTRON5" "Unknown significance" "rs56742420" "This variant is a VUS because it does not have enough information."
308939 "chr12:80866827:CA>-" "PTPRQ" "NM_001145026:c.1186+797_1186+798delCA" "INTRON5" "Benign" "rs34054644" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 68 1322 0.0514 761 1006 0.7565 437 694 0.6297 359 1008 0.3562 730 978 0.7464 2355 5008 0.470248
308940 "chr12:80866827:CACA>-" "PTPRQ" "NM_001145026:c.1186+797_1186+800delCACA" "INTRON5" "Unknown significance" "rs760118144" "This variant is a VUS because it does not have enough information."
308941 "chr12:80866828:A>G" "PTPRQ" "NM_001145026:c.1186+798A>G" "INTRON5" "Unknown significance" "rs6539519" "This variant is a VUS because it does not have enough information."
308942 "chr12:80866830:A>G" "PTPRQ" "NM_001145026:c.1186+800A>G" "INTRON5" "Benign" "rs201141360" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 68 1322 0.0514 761 1006 0.7565 437 694 0.6297 359 1008 0.3562 730 978 0.7464 2355 5008 0.470248
308943 "chr12:80866832:A>G" "PTPRQ" "NM_001145026:c.1186+802A>G" "INTRON5" "Benign" "rs61950913" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 83 1322 0.0628 102 1006 0.1014 57 694 0.0821 37 1008 0.0367 115 978 0.1176 394 5008 0.0786741
308944 "chr12:80866856:AG>-" "PTPRQ" "NM_001145026:c.1186+826_1186+827delAG" "INTRON5" "Unknown significance" "rs56668325" "This variant is a VUS because it does not have enough information."
308945 "chr12:80866857:G>C" "PTPRQ" "NM_001145026:c.1186+827G>C" "INTRON5" "Benign" "rs61950914" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 51 1006 0.0507 24 694 0.0346 11 1008 0.0109 58 978 0.0593 178 5008 0.0355431
308946 "chr12:80866924:C>T" "PTPRQ" "NM_001145026:c.1186+894C>T" "INTRON5" "Unknown significance" "rs183506817" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308947 "chr12:80866925:T>G" "PTPRQ" "NM_001145026:c.1186+895T>G" "INTRON5" "Unknown significance" "rs537710797" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
308948 "chr12:80866926:C>A" "PTPRQ" "NM_001145026:c.1186+896C>A" "INTRON5" "Benign" "rs7135559" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 79 1322 0.0598 633 1006 0.6292 382 694 0.5504 368 1008 0.3651 653 978 0.6677 2115 5008 0.422324
308949 "chr12:80866975:T>C" "PTPRQ" "NM_001145026:c.1186+945T>C" "INTRON5" "Unknown significance" "rs746127353" "This variant is a VUS because it does not have enough information."
308950 "chr12:80866995:T>C" "PTPRQ" "NM_001145026:c.1186+965T>C" "INTRON5" "Unknown significance" "rs770078383" "This variant is a VUS because it does not have enough information."
308951 "chr12:80867055:A>T" "PTPRQ" "NM_001145026:c.1186+1025A>T" "INTRON5" "Unknown significance" "rs775397019" "This variant is a VUS because it does not have enough information."
308952 "chr12:80867165:T>C" "PTPRQ" "NM_001145026:c.1186+1135T>C" "INTRON5" "Unknown significance" "rs570881845" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308953 "chr12:80867234:C>A" "PTPRQ" "NM_001145026:c.1186+1204C>A" "INTRON5" "Unknown significance" "rs367961844" "This variant is a VUS because it does not have enough information."
308954 "chr12:80867244:G>C" "PTPRQ" "NM_001145026:c.1186+1214G>C" "INTRON5" "Benign" "rs17006812" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 340 1322 0.2572 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 463 5008 0.0924521
308955 "chr12:80867247:C>T" "PTPRQ" "NM_001145026:c.1186+1217C>T" "INTRON5" "Unknown significance" "rs553435758" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308956 "chr12:80867266:C>T" "PTPRQ" "NM_001145026:c.1186+1236C>T" "INTRON5" "Unknown significance" "rs769096182" "This variant is a VUS because it does not have enough information."
308957 "chr12:80867274:A>G" "PTPRQ" "NM_001145026:c.1186+1244A>G" "INTRON5" "Unknown significance" "rs138950529" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308958 "chr12:80867390:A>G" "PTPRQ" "NM_001145026:c.1186+1360A>G" "INTRON5" "Unknown significance" "rs188450673" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308959 "chr12:80867419:G>T" "PTPRQ" "NM_001145026:c.1186+1389G>T" "INTRON5" "Benign" "rs4343087" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 79 1322 0.0598 633 1006 0.6292 382 694 0.5504 367 1008 0.3641 652 978 0.6667 2113 5008 0.421925
308960 "chr12:80867457:T>A" "PTPRQ" "NM_001145026:c.1186+1427T>A" "INTRON5" "Unknown significance" "rs190746755" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
308961 "chr12:80867514:T>C" "PTPRQ" "NM_001145026:c.1186+1484T>C" "INTRON5" "Unknown significance" "rs372720960" "This variant is a VUS because it does not have enough information."
308962 "chr12:80867560:T>A" "PTPRQ" "NM_001145026:c.1186+1530T>A" "INTRON5" "Unknown significance" "rs112656311" "This variant is a VUS because it does not have enough information."
308963 "chr12:80867682:C>T" "PTPRQ" "NM_001145026:c.1186+1652C>T" "INTRON5" "Unknown significance" "rs543675431" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308964 "chr12:80867685:T>G" "PTPRQ" "NM_001145026:c.1186+1655T>G" "INTRON5" "Unknown significance" "rs565208048" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308965 "chr12:80867698:G>C" "PTPRQ" "NM_001145026:c.1186+1668G>C" "INTRON5" "Unknown significance" "rs577297887" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
308966 "chr12:80867760:T>G" "PTPRQ" "NM_001145026:c.1186+1730T>G" "INTRON5" "Unknown significance" "rs751915929" "This variant is a VUS because it does not have enough information."
308967 "chr12:80867773:A>T" "PTPRQ" "NM_001145026:c.1186+1743A>T" "INTRON5" "Unknown significance" "rs183398009" "This variant is a VUS because it does not have enough information."
308968 "chr12:80867780:C>A" "PTPRQ" "NM_001145026:c.1186+1750C>A" "INTRON5" "Unknown significance" "rs541481499" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308969 "chr12:80867794:G>A" "PTPRQ" "NM_001145026:c.1186+1764G>A" "INTRON5" "Unknown significance" "rs559883278" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308970 "chr12:80867819:G>A" "PTPRQ" "NM_001145026:c.1186+1789G>A" "INTRON5" "Benign" "rs61530056" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 24 1006 0.0239 6 694 0.0086 9 1008 0.0089 49 978 0.0501 122 5008 0.024361
308971 "chr12:80867831:A>G" "PTPRQ" "NM_001145026:c.1186+1801A>G" "INTRON5" "Unknown significance" "rs541968972" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308972 "chr12:80867879:C>A" "PTPRQ" "NM_001145026:c.1186+1849C>A" "INTRON5" "Unknown significance" "rs563873486" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308973 "chr12:80867907:->A" "PTPRQ" "NM_001145026:c.1186+1877_1186+1878insA" "INTRON5" "Unknown significance" "rs35096303" "This variant is a VUS because it does not have enough information."
308974 "chr12:80867917:A>C" "PTPRQ" "NM_001145026:c.1186+1887A>C" "INTRON5" "Unknown significance" "rs149429577" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308975 "chr12:80867943:A>T" "PTPRQ" "NM_001145026:c.1186+1913A>T" "INTRON5" "Unknown significance" "rs528257064" "This variant is a VUS because it does not have enough information."
308976 "chr12:80867957:C>T" "PTPRQ" "NM_001145026:c.1186+1927C>T" "INTRON5" "Unknown significance" "rs772894905" "This variant is a VUS because it does not have enough information."
308977 "chr12:80867964:G>A" "PTPRQ" "NM_001145026:c.1186+1934G>A" "INTRON5" "Unknown significance" "rs760193080" "This variant is a VUS because it does not have enough information."
308978 "chr12:80868022:C>G" "PTPRQ" "NM_001145026:c.1186+1992C>G" "INTRON5" "Unknown significance" "rs781777973" "This variant is a VUS because it does not have enough information."
308979 "chr12:80868086:A>G" "PTPRQ" "NM_001145026:c.1186+2056A>G" "INTRON5" "Unknown significance" "rs61511492" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308980 "chr12:80868124:G>A" "PTPRQ" "NM_001145026:c.1186+2094G>A" "INTRON5" "Unknown significance" "rs570841989" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
308981 "chr12:80868152:T>C" "PTPRQ" "NM_001145026:c.1186+2122T>C" "INTRON5" "Unknown significance" "rs146371989" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
308982 "chr12:80868171:C>G" "PTPRQ" "NM_001145026:c.1186+2141C>G" "INTRON5" "Benign" "rs117662453" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 17 1008 0.0169 1 978 0.001 18 5008 0.00359425
308983 "chr12:80868177:A>T" "PTPRQ" "NM_001145026:c.1186+2147A>T" "INTRON5" "Unknown significance" "rs186576815" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
308984 "chr12:80868204:C>T" "PTPRQ" "NM_001145026:c.1186+2174C>T" "INTRON5" "Unknown significance" "rs536303994" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308985 "chr12:80868208:T>C" "PTPRQ" "NM_001145026:c.1186+2178T>C" "INTRON5" "Unknown significance" "rs554381841" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308986 "chr12:80868243:T>C" "PTPRQ" "NM_001145026:c.1186+2213T>C" "INTRON5" "Unknown significance" "rs569812443" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308987 "chr12:80868290:A>C" "PTPRQ" "NM_001145026:c.1186+2260A>C" "INTRON5" "Benign" "rs12296741" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
308988 "chr12:80868305:C>T" "PTPRQ" "NM_001145026:c.1186+2275C>T" "INTRON5" "Unknown significance" "rs139674786" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 3 5008 0.000599042
308989 "chr12:80868328:T>C" "PTPRQ" "NM_001145026:c.1186+2298T>C" "INTRON5" "Unknown significance" "rs191461976" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308990 "chr12:80868348:T>C" "PTPRQ" "NM_001145026:c.1186+2318T>C" "INTRON5" "Unknown significance" "rs541338685" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308991 "chr12:80868353:C>T" "PTPRQ" "NM_001145026:c.1186+2323C>T" "INTRON5" "Benign" "rs12316755" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 298 1322 0.2254 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 421 5008 0.0840655
308992 "chr12:80868367:A>G" "PTPRQ" "NM_001145026:c.1186+2337A>G" "INTRON5" "Benign" "rs142918083" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
308993 "chr12:80868376:T>G" "PTPRQ" "NM_001145026:c.1186+2346T>G" "INTRON5" "Unknown significance" "rs754529197" "This variant is a VUS because it does not have enough information."
308994 "chr12:80868472:T>A" "PTPRQ" "NM_001145026:c.1186+2442T>A" "INTRON5" "Unknown significance" "rs542283649" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
308995 "chr12:80868522:G>A" "PTPRQ" "NM_001145026:c.1186+2492G>A" "INTRON5" "Unknown significance" "rs550190674" "This variant is a VUS because it does not have enough information."
308996 "chr12:80868527:A>G" "PTPRQ" "NM_001145026:c.1186+2497A>G" "INTRON5" "Unknown significance" "rs570137978" "This variant is a VUS because it does not have enough information."
308997 "chr12:80868534:A>G" "PTPRQ" "NM_001145026:c.1186+2504A>G" "INTRON5" "Unknown significance" "rs765251492" "This variant is a VUS because it does not have enough information."
308998 "chr12:80868544:T>C" "PTPRQ" "NM_001145026:c.1186+2514T>C" "INTRON5" "Unknown significance" "rs564999675" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
308999 "chr12:80868582:G>A" "PTPRQ" "NM_001145026:c.1186+2552G>A" "INTRON5" "Benign" "rs60443777" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
309000 "chr12:80868591:G>A" "PTPRQ" "NM_001145026:c.1186+2561G>A" "INTRON5" "Unknown significance" "rs546118071" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
309001 "chr12:80868605:T>C" "PTPRQ" "NM_001145026:c.1186+2575T>C" "INTRON5" "Benign" "rs12099476" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 302 1322 0.2284 218 1006 0.2167 113 694 0.1628 0 1008 0 106 978 0.1084 739 5008 0.147564
309002 "chr12:80868615:C>T" "PTPRQ" "NM_001145026:c.1186+2585C>T" "INTRON5" "Unknown significance" "rs758246933" "This variant is a VUS because it does not have enough information."
309003 "chr12:80868628:T>C" "PTPRQ" "NM_001145026:c.1186+2598T>C" "INTRON5" "Benign" "rs12099478" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 302 1322 0.2284 218 1006 0.2167 113 694 0.1628 0 1008 0 106 978 0.1084 739 5008 0.147564
309004 "chr12:80868638:C>T" "PTPRQ" "NM_001145026:c.1186+2608C>T" "INTRON5" "Unknown significance" "rs199507554" "This variant is a VUS because it does not have enough information."
309005 "chr12:80868647:AAAC>-" "PTPRQ" "NM_001145026:c.1186+2617_1186+2620delAAAC" "INTRON5" "Benign" "rs532982488" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 21 1322 0.0159 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 23 5008 0.00459265
309006 "chr12:80868648:A>G" "PTPRQ" "NM_001145026:c.1186+2618A>G" "INTRON5" "Benign" "rs546898522" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 9 5008 0.00179712
309007 "chr12:80868708:A>G" "PTPRQ" "NM_001145026:c.1186+2678A>G" "INTRON5" "Benign" "rs12099453" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 217 1006 0.2157 111 694 0.1599 0 1008 0 106 978 0.1084 664 5008 0.132588
309008 "chr12:80868812:T>G" "PTPRQ" "NM_001145026:c.1186+2782T>G" "INTRON5" "Benign" "rs146098157" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 0 1006 0 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744
309009 "chr12:80868878:A>G" "PTPRQ" "NM_001145026:c.1186+2848A>G" "INTRON5" "Unknown significance" "rs548252943" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 1 694 0.0014 2 1008 0.002 0 978 0 4 5008 0.000798722
309010 "chr12:80868934:T>C" "PTPRQ" "NM_001145026:c.1186+2904T>C" "INTRON5" "Unknown significance" "rs569691903" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309011 "chr12:80868947:A>G" "PTPRQ" "NM_001145026:c.1186+2917A>G" "INTRON5" "Unknown significance" "rs756228748" "This variant is a VUS because it does not have enough information."
309012 "chr12:80868961:T>C" "PTPRQ" "NM_001145026:c.1186+2931T>C" "INTRON5" "Unknown significance" "rs75657080" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 4 1006 0.004 1 694 0.0014 0 1008 0 3 978 0.0031 9 5008 0.00179712
309013 "chr12:80868997:T>C" "PTPRQ" "NM_001145026:c.1186+2967T>C" "INTRON5" "Unknown significance" "rs142277163" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309014 "chr12:80869011:C>T" "PTPRQ" "NM_001145026:c.1186+2981C>T" "INTRON5" "Unknown significance" "rs570672014" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309015 "chr12:80869035:T>A" "PTPRQ" "NM_001145026:c.1186+3005T>A" "INTRON5" "Unknown significance" "rs376183279" "This variant is a VUS because it does not have enough information."
309016 "chr12:80869082:A>T" "PTPRQ" "NM_001145026:c.1186+3052A>T" "INTRON5" "Unknown significance" "rs117640149" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309017 "chr12:80869090:A>G" "PTPRQ" "NM_001145026:c.1186+3060A>G" "INTRON5" "Unknown significance" "rs553328409" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309018 "chr12:80869097:A>G" "PTPRQ" "NM_001145026:c.1186+3067A>G" "INTRON5" "Benign" "rs114367101" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 13 1322 0.0098 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 14 5008 0.00279553
309019 "chr12:80869109:G>T" "PTPRQ" "NM_001145026:c.1186+3079G>T" "INTRON5" "Unknown significance" "rs541891211" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361
309020 "chr12:80869116:G>T" "PTPRQ" "NM_001145026:c.1186+3086G>T" "INTRON5" "Unknown significance" "rs557415557" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309021 "chr12:80869133:G>A" "PTPRQ" "NM_001145026:c.1186+3103G>A" "INTRON5" "Unknown significance" "rs575692708" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309022 "chr12:80869134:T>C" "PTPRQ" "NM_001145026:c.1186+3104T>C" "INTRON5" "Unknown significance" "rs779358531" "This variant is a VUS because it does not have enough information."
309023 "chr12:80869135:A>G" "PTPRQ" "NM_001145026:c.1186+3105A>G" "INTRON5" "Unknown significance" "rs748699840" "This variant is a VUS because it does not have enough information."
309024 "chr12:80869159:C>A" "PTPRQ" "NM_001145026:c.1186+3129C>A" "INTRON5" "Unknown significance" "rs150821871" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
309025 "chr12:80869197:T>G" "PTPRQ" "NM_001145026:c.1186+3167T>G" "INTRON5" "Unknown significance" "rs374038333" "This variant is a VUS because it does not have enough information."
309026 "chr12:80869213:T>A" "PTPRQ" "NM_001145026:c.1186+3183T>A" "INTRON5" "Unknown significance" "rs564299214" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309027 "chr12:80869243:C>A" "PTPRQ" "NM_001145026:c.1186+3213C>A" "INTRON5" "Unknown significance" "rs536241622" "This variant is a VUS because it does not have enough information."
309028 "chr12:80869243:C>G" "PTPRQ" "NM_001145026:c.1186+3213C>G" "INTRON5" "Unknown significance" "rs536241622" "This variant is a VUS because it does not have enough information."
309029 "chr12:80869245:T>C" "PTPRQ" "NM_001145026:c.1186+3215T>C" "INTRON5" "Benign" "rs12300046" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309030 "chr12:80869261:T>C" "PTPRQ" "NM_001145026:c.1186+3231T>C" "INTRON5" "Benign" "rs77610329" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 97 1322 0.0734 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 102 5008 0.0203674
309031 "chr12:80869272:G>C" "PTPRQ" "NM_001145026:c.1186+3242G>C" "INTRON5" "Benign" "rs75042181" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309032 "chr12:80869294:A>G" "PTPRQ" "NM_001145026:c.1186+3264A>G" "INTRON5" "Unknown significance" "rs773404653" "This variant is a VUS because it does not have enough information."
309033 "chr12:80869318:A>G" "PTPRQ" "NM_001145026:c.1186+3288A>G" "INTRON5" "Unknown significance" "rs529684132" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309034 "chr12:80869331:T>C" "PTPRQ" "NM_001145026:c.1186+3301T>C" "INTRON5" "Unknown significance" "rs149952069" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309035 "chr12:80869377:->TT" "PTPRQ" "NM_001145026:c.1186+3347_1186+3348insTT" "INTRON5" "Benign" "rs560228586" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 31 1322 0.0234 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 34 5008 0.00678914
309036 "chr12:80869383:A>C" "PTPRQ" "NM_001145026:c.1186+3353A>C" "INTRON5" "Unknown significance" "rs761105782" "This variant is a VUS because it does not have enough information."
309037 "chr12:80869392:T>C" "PTPRQ" "NM_001145026:c.1186+3362T>C" "INTRON5" "Unknown significance" "rs770431694" "This variant is a VUS because it does not have enough information."
309038 "chr12:80869398:G>T" "PTPRQ" "NM_001145026:c.1186+3368G>T" "INTRON5" "Unknown significance" "rs369958945" "This variant is a VUS because it does not have enough information."
309039 "chr12:80869417:T>C" "PTPRQ" "NM_001145026:c.1186+3387T>C" "INTRON5" "Unknown significance" "rs184707063" "This variant is a VUS because it does not have enough information."
309040 "chr12:80869444:A>G" "PTPRQ" "NM_001145026:c.1186+3414A>G" "INTRON5" "Unknown significance" "rs188098421" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309041 "chr12:80869446:A>G" "PTPRQ" "NM_001145026:c.1186+3416A>G" "INTRON5" "Unknown significance" "rs555610576" "This variant is a VUS because it does not have enough information."
309042 "chr12:80869516:C>T" "PTPRQ" "NM_001145026:c.1186+3486C>T" "INTRON5" "Unknown significance" "rs192713175" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309043 "chr12:80869522:C>T" "PTPRQ" "NM_001145026:c.1186+3492C>T" "INTRON5" "Benign" "rs7972276" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 797 1322 0.6029 247 1006 0.2455 177 694 0.255 52 1008 0.0516 180 978 0.184 1453 5008 0.290136
309044 "chr12:80869598:A>G" "PTPRQ" "NM_001145026:c.1186+3568A>G" "INTRON5" "Unknown significance" "rs759110198" "This variant is a VUS because it does not have enough information."
309045 "chr12:80869616:A>T" "PTPRQ" "NM_001145026:c.1186+3586A>T" "INTRON5" "Unknown significance" "rs185171746" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
309046 "chr12:80869638:C>G" "PTPRQ" "NM_001145026:c.1186+3608C>G" "INTRON5" "Unknown significance" "rs534843371" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309047 "chr12:80869673:G>T" "PTPRQ" "NM_001145026:c.1186+3643G>T" "INTRON5" "Unknown significance" "rs546899295" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309048 "chr12:80869674:A>G" "PTPRQ" "NM_001145026:c.1186+3644A>G" "INTRON5" "Benign" "rs376353167" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 17 978 0.0174 17 5008 0.00339457
309049 "chr12:80869682:A>G" "PTPRQ" "NM_001145026:c.1186+3652A>G" "INTRON5" "Benign" "rs11114469" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 302 1322 0.2284 217 1006 0.2157 113 694 0.1628 0 1008 0 106 978 0.1084 738 5008 0.147364
309050 "chr12:80869690:A>G" "PTPRQ" "NM_001145026:c.1186+3660A>G" "INTRON5" "Benign" "rs531025183" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 17 978 0.0174 17 5008 0.00339457
309051 "chr12:80869716:T>G" "PTPRQ" "NM_001145026:c.1186+3686T>G" "INTRON5" "Benign" "rs55774833" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 26 1322 0.0197 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 28 5008 0.00559105
309052 "chr12:80869724:A>G" "PTPRQ" "NM_001145026:c.1186+3694A>G" "INTRON5" "Unknown significance" "rs557462918" "This variant is a VUS because it does not have enough information."
309053 "chr12:80869742:G>A" "PTPRQ" "NM_001145026:c.1186+3712G>A" "INTRON5" "Unknown significance" "rs762944586" "This variant is a VUS because it does not have enough information."
309054 "chr12:80869769:T>C" "PTPRQ" "NM_001145026:c.1186+3739T>C" "INTRON5" "Benign" "rs189136304" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 17 1322 0.0129 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 19 5008 0.00379393
309055 "chr12:80869796:T>G" "PTPRQ" "NM_001145026:c.1186+3766T>G" "INTRON5" "Benign" "rs11114470" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 302 1322 0.2284 217 1006 0.2157 113 694 0.1628 0 1008 0 106 978 0.1084 738 5008 0.147364
309056 "chr12:80869825:TGTT>-" "PTPRQ" "NM_001145026:c.1186+3795_1186+3798delTGTT" "INTRON5" "Benign" "rs549208810" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 0 1006 0 21 694 0.0303 1 1008 0.001 1 978 0.001 24 5008 0.00479233
309057 "chr12:80869827:->T" "PTPRQ" "NM_001145026:c.1186+3797_1186+3798insT" "INTRON5" "Unknown significance" "rs796103071" "This variant is a VUS because it does not have enough information."
309058 "chr12:80869839:C>T" "PTPRQ" "NM_001145026:c.1186+3809C>T" "INTRON5" "Unknown significance" "rs78009864" "This variant is a VUS because it does not have enough information."
309059 "chr12:80869850:C>T" "PTPRQ" "NM_001145026:c.1186+3820C>T" "INTRON5" "Unknown significance" "rs573087018" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309060 "chr12:80869879:T>C" "PTPRQ" "NM_001145026:c.1186+3849T>C" "INTRON5" "Unknown significance" "rs540466834" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 2 5008 0.000399361
309061 "chr12:80869894:G>T" "PTPRQ" "NM_001145026:c.1186+3864G>T" "INTRON5" "Benign" "rs73145135" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 302 1322 0.2284 217 1006 0.2157 113 694 0.1628 0 1008 0 106 978 0.1084 738 5008 0.147364
309062 "chr12:80869908:A>T" "PTPRQ" "NM_001145026:c.1186+3878A>T" "INTRON5" "Unknown significance" "rs574205928" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309063 "chr12:80869926:G>T" "PTPRQ" "NM_001145026:c.1186+3896G>T" "INTRON5" "Unknown significance" "rs199906525" "This variant is a VUS because it does not have enough information."
309064 "chr12:80869927:T>C" "PTPRQ" "NM_001145026:c.1186+3897T>C" "INTRON5" "Unknown significance" "rs780137654" "This variant is a VUS because it does not have enough information."
309065 "chr12:80869945:A>G" "PTPRQ" "NM_001145026:c.1186+3915A>G" "INTRON5" "Unknown significance" "rs372380434" "This variant is a VUS because it does not have enough information."
309066 "chr12:80869953:T>C" "PTPRQ" "NM_001145026:c.1186+3923T>C" "INTRON5" "Benign" "rs75185824" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 39 5008 0.00778754
309067 "chr12:80869962:A>C" "PTPRQ" "NM_001145026:c.1186+3932A>C" "INTRON5" "Benign" "rs76825338" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 4 1006 0.004 8 694 0.0115 0 1008 0 0 978 0 12 5008 0.00239617
309068 "chr12:80869970:T>G" "PTPRQ" "NM_001145026:c.1186+3940T>G" "INTRON5" "Unknown significance" "rs530543877" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309069 "chr12:80869987:->A" "PTPRQ" "NM_001145026:c.1186+3957_1186+3958insA" "INTRON5" "Unknown significance" "rs35250993" "This variant is a VUS because it does not have enough information."
309070 "chr12:80869993:->C" "PTPRQ" "NM_001145026:c.1186+3963_1186+3964insC" "INTRON5" "Unknown significance" "rs34386103" "This variant is a VUS because it does not have enough information."
309071 "chr12:80869995:A>G" "PTPRQ" "NM_001145026:c.1186+3965A>G" "INTRON5" "Unknown significance" "rs755025585" "This variant is a VUS because it does not have enough information."
309072 "chr12:80870038:C>G" "PTPRQ" "NM_001145026:c.1186+4008C>G" "INTRON5" "Unknown significance" "rs778912126" "This variant is a VUS because it does not have enough information."
309073 "chr12:80870055:G>A" "PTPRQ" "NM_001145026:c.1186+4025G>A" "INTRON5" "Benign" "rs61950916" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 24 1006 0.0239 6 694 0.0086 9 1008 0.0089 49 978 0.0501 122 5008 0.024361
309074 "chr12:80870077:ATG>-" "PTPRQ" "NM_001145026:c.1186+4047_1186+4049delATG" "INTRON5" "Unknown significance" "rs537608532" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 1 694 0.0014 0 1008 0 0 978 0 4 5008 0.000798722
309075 "chr12:80870077:A>G" "PTPRQ" "NM_001145026:c.1186+4047A>G" "INTRON5" "Unknown significance" "rs564202594" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309076 "chr12:80870091:A>T" "PTPRQ" "NM_001145026:c.1186+4061A>T" "INTRON5" "Benign" "rs12300408" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 460 1322 0.348 217 1006 0.2157 122 694 0.1758 0 1008 0 106 978 0.1084 905 5008 0.180711
309077 "chr12:80870100:A>T" "PTPRQ" "NM_001145026:c.1186+4070A>T" "INTRON5" "Unknown significance" "rs546860530" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309078 "chr12:80870106:A>-" "PTPRQ" "NM_001145026:c.1186+4076delA" "INTRON5" "Unknown significance" "rs369174251" "This variant is a VUS because it does not have enough information."
309079 "chr12:80870115:T>C" "PTPRQ" "NM_001145026:c.1186+4085T>C" "INTRON5" "Benign" "rs112283650" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
309080 "chr12:80870118:T>G" "PTPRQ" "NM_001145026:c.1186+4088T>G" "INTRON5" "Unknown significance" "rs181882891" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309081 "chr12:80870132:T>G" "PTPRQ" "NM_001145026:c.1186+4102T>G" "INTRON5" "Unknown significance" "rs778357133" "This variant is a VUS because it does not have enough information."
309082 "chr12:80870187:C>G" "PTPRQ" "NM_001145026:c.1186+4157C>G" "INTRON5" "Benign" "rs368276480" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 6 1008 0.006 0 978 0 6 5008 0.00119808
309083 "chr12:80870217:A>G" "PTPRQ" "NM_001145026:c.1186+4187A>G" "INTRON5" "Unknown significance" "rs144384135" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309084 "chr12:80870227:T>G" "PTPRQ" "NM_001145026:c.1186+4197T>G" "INTRON5" "Benign" "rs147799375" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309085 "chr12:80870249:C>A" "PTPRQ" "NM_001145026:c.1186+4219C>A" "INTRON5" "Unknown significance" "rs747320706" "This variant is a VUS because it does not have enough information."
309086 "chr12:80870254:G>A" "PTPRQ" "NM_001145026:c.1186+4224G>A" "INTRON5" "Unknown significance" "rs375323693" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309087 "chr12:80870254:G>C" "PTPRQ" "NM_001145026:c.1186+4224G>C" "INTRON5" "Unknown significance" "rs375323693" "This variant is a VUS because it does not have enough information."
309088 "chr12:80870268:C>T" "PTPRQ" "NM_001145026:c.1186+4238C>T" "INTRON5" "Unknown significance" "rs185028396" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309089 "chr12:80870282:C>T" "PTPRQ" "NM_001145026:c.1186+4252C>T" "INTRON5" "Unknown significance" "rs188280818" "This variant is a VUS because it does not have enough information."
309090 "chr12:80870283:C>T" "PTPRQ" "NM_001145026:c.1186+4253C>T" "INTRON5" "Unknown significance" "rs148840381" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309091 "chr12:80870284:G>A" "PTPRQ" "NM_001145026:c.1186+4254G>A" "INTRON5" "Unknown significance" "rs555640145" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309092 "chr12:80870289:C>G" "PTPRQ" "NM_001145026:c.1186+4259C>G" "INTRON5" "Benign" "rs143468337" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 1 1006 0.001 5 694 0.0072 0 1008 0 2 978 0.002 8 5008 0.00159744
309093 "chr12:80870294:T>G" "PTPRQ" "NM_001145026:c.1186+4264T>G" "INTRON5" "Unknown significance" "rs12227943" "This variant is a VUS because it does not have enough information."
309094 "chr12:80870323:G>A" "PTPRQ" "NM_001145026:c.1186+4293G>A" "INTRON5" "Benign" "rs74626415" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309095 "chr12:80870331:A>G" "PTPRQ" "NM_001145026:c.1186+4301A>G" "INTRON5" "Unknown significance" "rs759217234" "This variant is a VUS because it does not have enough information."
309096 "chr12:80870353:A>G" "PTPRQ" "NM_001145026:c.1186+4323A>G" "INTRON5" "Unknown significance" "rs181061167" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309097 "chr12:80870382:G>T" "PTPRQ" "NM_001145026:c.1186+4352G>T" "INTRON5" "Unknown significance" "rs769602679" "This variant is a VUS because it does not have enough information."
309098 "chr12:80870398:A>G" "PTPRQ" "NM_001145026:c.1186+4368A>G" "INTRON5" "Unknown significance" "rs575297770" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309099 "chr12:80870440:G>A" "PTPRQ" "NM_001145026:c.1186+4410G>A" "INTRON5" "Unknown significance" "rs530594567" "This variant is a VUS because it does not have enough information."
309100 "chr12:80870445:A>-" "PTPRQ" "NM_001145026:c.1186+4415delA" "INTRON5" "Unknown significance" "rs753261631" "This variant is a VUS because it does not have enough information."
309101 "chr12:80870473:T>C" "PTPRQ" "NM_001145026:c.1186+4443T>C" "INTRON5" "Unknown significance" "rs775074060" "This variant is a VUS because it does not have enough information."
309102 "chr12:80870499:T>A" "PTPRQ" "NM_001145026:c.1186+4469T>A" "INTRON5" "Unknown significance" "rs545854140" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
309103 "chr12:80870527:C>T" "PTPRQ" "NM_001145026:c.1186+4497C>T" "INTRON5" "Unknown significance" "rs762570347" "This variant is a VUS because it does not have enough information."
309104 "chr12:80870528:G>A" "PTPRQ" "NM_001145026:c.1186+4498G>A" "INTRON5" "Benign" "rs147974864" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 9 978 0.0092 11 5008 0.00219649
309105 "chr12:80870539:G>A" "PTPRQ" "NM_001145026:c.1186+4509G>A" "INTRON5" "Unknown significance" "rs186003147" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309106 "chr12:80870584:G>A" "PTPRQ" "NM_001145026:c.1186+4554G>A" "INTRON5" "Unknown significance" "rs751584966" "This variant is a VUS because it does not have enough information."
309107 "chr12:80870601:C>T" "PTPRQ" "NM_001145026:c.1186+4571C>T" "INTRON5" "Benign" "rs11114471" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 298 1322 0.2254 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 421 5008 0.0840655
309108 "chr12:80870683:G>T" "PTPRQ" "NM_001145026:c.1186+4653G>T" "INTRON5" "Unknown significance" "rs191250916" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309109 "chr12:80870736:A>G" "PTPRQ" "NM_001145026:c.1186+4706A>G" "INTRON5" "Unknown significance" "rs543921476" "This variant is a VUS because it does not have enough information."
309110 "chr12:80870787:A>G" "PTPRQ" "NM_001145026:c.1186+4757A>G" "INTRON5" "Unknown significance" "rs764859480" "This variant is a VUS because it does not have enough information."
309111 "chr12:80870862:C>T" "PTPRQ" "NM_001145026:c.1186+4832C>T" "INTRON5" "Unknown significance" "rs181323477" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309112 "chr12:80870870:C>A" "PTPRQ" "NM_001145026:c.1186+4840C>A" "INTRON5" "Unknown significance" "rs767393068" "This variant is a VUS because it does not have enough information."
309113 "chr12:80870920:T>C" "PTPRQ" "NM_001145026:c.1186+4890T>C" "INTRON5" "Unknown significance" "rs750237539" "This variant is a VUS because it does not have enough information."
309114 "chr12:80870925:C>T" "PTPRQ" "NM_001145026:c.1186+4895C>T" "INTRON5" "Unknown significance" "rs550577922" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
309115 "chr12:80870949:G>A" "PTPRQ" "NM_001145026:c.1186+4919G>A" "INTRON5" "Unknown significance" "rs528278995" "This variant is a VUS because it does not have enough information."
309116 "chr12:80870962:T>A" "PTPRQ" "NM_001145026:c.1186+4932T>A" "INTRON5" "Unknown significance" "rs568854337" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
309117 "chr12:80870963:G>A" "PTPRQ" "NM_001145026:c.1186+4933G>A" "INTRON5" "Unknown significance" "rs533153282" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309118 "chr12:80870996:A>T" "PTPRQ" "NM_001145026:c.1186+4966A>T" "INTRON5" "Unknown significance" "rs551315817" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
309119 "chr12:80870998:C>A" "PTPRQ" "NM_001145026:c.1186+4968C>A" "INTRON5" "Unknown significance" "rs566536947" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309120 "chr12:80871001:A>-" "PTPRQ" "NM_001145026:c.1186+4971delA" "INTRON5" "Benign" "rs141249342" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 102 1322 0.0772 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 109 5008 0.0217652
309121 "chr12:80871003:A>G" "PTPRQ" "NM_001145026:c.1186+4973A>G" "INTRON5" "Benign" "rs186891690" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 11 1322 0.0083 0 1006 0 0 694 0 0 1008 0 0 978 0 11 5008 0.00219649
309122 "chr12:80871028:T>C" "PTPRQ" "NM_001145026:c.1186+4998T>C" "INTRON5" "Unknown significance" "rs190602143" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
309123 "chr12:80871064:T>G" "PTPRQ" "NM_001145026:c.1186+5034T>G" "INTRON5" "Benign" "rs183221594" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 12 1322 0.0091 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 13 5008 0.00259585
309124 "chr12:80871092:G>A" "PTPRQ" "NM_001145026:c.1186+5062G>A" "INTRON5" "Benign" "rs74110904" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 152 1322 0.115 0 1006 0 8 694 0.0115 0 1008 0 0 978 0 160 5008 0.0319489
309125 "chr12:80871117:TGT>-" "PTPRQ" "NM_001145026:c.1186+5087_1186+5089delTGT" "INTRON5" "Unknown significance" "rs757623772" "This variant is a VUS because it does not have enough information."
309126 "chr12:80871160:T>A" "PTPRQ" "NM_001145026:c.1186+5130T>A" "INTRON5" "Unknown significance" "rs140635123" "This variant is a VUS because it does not have enough information."
309127 "chr12:80871164:->T" "PTPRQ" "NM_001145026:c.1186+5134_1186+5135insT" "INTRON5" "Unknown significance" "rs571179918" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309128 "chr12:80871237:T>C" "PTPRQ" "NM_001145026:c.1186+5207T>C" "INTRON5" "Unknown significance" "rs187913607" "This variant is a VUS because it does not have enough information."
309129 "chr12:80871284:G>A" "PTPRQ" "NM_001145026:c.1186+5254G>A" "INTRON5" "Unknown significance" "rs556567904" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309130 "chr12:80871288:A>G" "PTPRQ" "NM_001145026:c.1186+5258A>G" "INTRON5" "Unknown significance" "rs190925725" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309131 "chr12:80871292:T>C" "PTPRQ" "NM_001145026:c.1186+5262T>C" "INTRON5" "Unknown significance" "rs532790157" "This variant is a VUS because it does not have enough information."
309132 "chr12:80871299:A>T" "PTPRQ" "NM_001145026:c.1186+5269A>T" "INTRON5" "Unknown significance" "rs567978886" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309133 "chr12:80871305:A>G" "PTPRQ" "NM_001145026:c.1186+5275A>G" "INTRON5" "Unknown significance" "rs375384838" "This variant is a VUS because it does not have enough information."
309134 "chr12:80871306:G>A" "PTPRQ" "NM_001145026:c.1186+5276G>A" "INTRON5" "Unknown significance" "rs34966193" "This variant is a VUS because it does not have enough information."
309135 "chr12:80871315:G>T" "PTPRQ" "NM_001145026:c.1186+5285G>T" "INTRON5" "Unknown significance" "rs546569882" "This variant is a VUS because it does not have enough information."
309136 "chr12:80871317:C>T" "PTPRQ" "NM_001145026:c.1186+5287C>T" "INTRON5" "Benign" "rs115017821" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 96 1322 0.0726 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 101 5008 0.0201677
309137 "chr12:80871351:G>A" "PTPRQ" "NM_001145026:c.1186+5321G>A" "INTRON5" "Unknown significance" "rs757814264" "This variant is a VUS because it does not have enough information."
309138 "chr12:80871356:C>T" "PTPRQ" "NM_001145026:c.1186+5326C>T" "INTRON5" "Unknown significance" "rs572891283" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309139 "chr12:80871360:G>A" "PTPRQ" "NM_001145026:c.1186+5330G>A" "INTRON5" "Unknown significance" "rs368441771" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309140 "chr12:80871365:A>G" "PTPRQ" "NM_001145026:c.1186+5335A>G" "INTRON5" "Unknown significance" "rs182614425" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309141 "chr12:80871369:G>A" "PTPRQ" "NM_001145026:c.1186+5339G>A" "INTRON5" "Unknown significance" "rs529061388" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309142 "chr12:80871371:G>T" "PTPRQ" "NM_001145026:c.1186+5341G>T" "INTRON5" "Unknown significance" "rs187669785" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309143 "chr12:80871371:G>C" "PTPRQ" "NM_001145026:c.1186+5341G>C" "INTRON5" "Unknown significance" "rs187669785" "This variant is a VUS because it does not have enough information."
309144 "chr12:80871374:A>G" "PTPRQ" "NM_001145026:c.1186+5344A>G" "INTRON5" "Unknown significance" "rs746623868" "This variant is a VUS because it does not have enough information."
309145 "chr12:80871394:G>A" "PTPRQ" "NM_001145026:c.1186+5364G>A" "INTRON5" "Unknown significance" "rs200591843" "This variant is a VUS because it does not have enough information."
309146 "chr12:80871410:C>A" "PTPRQ" "NM_001145026:c.1186+5380C>A" "INTRON5" "Unknown significance" "rs562347303" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309147 "chr12:80871416:G>T" "PTPRQ" "NM_001145026:c.1186+5386G>T" "INTRON5" "Unknown significance" "rs533017668" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
309148 "chr12:80871430:C>T" "PTPRQ" "NM_001145026:c.1186+5400C>T" "INTRON5" "Benign" "rs78539449" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 153 1322 0.1157 0 1006 0 8 694 0.0115 0 1008 0 0 978 0 161 5008 0.0321486
309149 "chr12:80871431:G>A" "PTPRQ" "NM_001145026:c.1186+5401G>A" "INTRON5" "Benign" "rs192845697" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
309150 "chr12:80871443:GTGTGCGCACC>-" "PTPRQ" "NM_001145026:c.1186+5413_1186+5423delGTGTGCGCACC" "INTRON5" "Unknown significance" "rs112512031" "This variant is a VUS because it does not have enough information."
309151 "chr12:80871448:C>T" "PTPRQ" "NM_001145026:c.1186+5418C>T" "INTRON5" "Unknown significance" "rs754830454" "This variant is a VUS because it does not have enough information."
309152 "chr12:80871453:C>T" "PTPRQ" "NM_001145026:c.1186+5423C>T" "INTRON5" "Unknown significance" "rs527716620" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309153 "chr12:80871454:G>A" "PTPRQ" "NM_001145026:c.1186+5424G>A" "INTRON5" "Unknown significance" "rs549195982" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309154 "chr12:80871457:T>C" "PTPRQ" "NM_001145026:c.1186+5427T>C" "INTRON5" "Unknown significance" "rs567789634" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309155 "chr12:80871460:G>C" "PTPRQ" "NM_001145026:c.1186+5430G>C" "INTRON5" "Unknown significance" "rs538050163" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309156 "chr12:80871462:G>A" "PTPRQ" "NM_001145026:c.1186+5432G>A" "INTRON5" "Unknown significance" "rs752715435" "This variant is a VUS because it does not have enough information."
309157 "chr12:80871465:G>C" "PTPRQ" "NM_001145026:c.1186+5435G>C" "INTRON5" "Benign" "rs566282102" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 17 5008 0.00339457
309158 "chr12:80871465:G>A" "PTPRQ" "NM_001145026:c.1186+5435G>A" "INTRON5" "Unknown significance" "rs566282102" "This variant is a VUS because it does not have enough information."
309159 "chr12:80871467:A>G" "PTPRQ" "NM_001145026:c.1186+5437A>G" "INTRON5" "Unknown significance" "rs571876075" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309160 "chr12:80871475:G>A" "PTPRQ" "NM_001145026:c.1186+5445G>A" "INTRON5" "Unknown significance" "rs539302583" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309161 "chr12:80871490:T>A" "PTPRQ" "NM_001145026:c.1186+5460T>A" "INTRON5" "Unknown significance" "rs780895817" "This variant is a VUS because it does not have enough information."
309162 "chr12:80871507:T>C" "PTPRQ" "NM_001145026:c.1186+5477T>C" "INTRON5" "Benign" "rs138461566" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309163 "chr12:80871523:C>A" "PTPRQ" "NM_001145026:c.1186+5493C>A" "INTRON5" "Unknown significance" "rs572852607" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
309164 "chr12:80871527:T>C" "PTPRQ" "NM_001145026:c.1186+5497T>C" "INTRON5" "Benign" "rs115727055" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 85 5008 0.0169728
309165 "chr12:80871531:C>T" "PTPRQ" "NM_001145026:c.1186+5501C>T" "INTRON5" "Unknown significance" "rs748088698" "This variant is a VUS because it does not have enough information."
309166 "chr12:80871550:C>T" "PTPRQ" "NM_001145026:c.1186+5520C>T" "INTRON5" "Unknown significance" "rs184915927" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309167 "chr12:80871551:G>A" "PTPRQ" "NM_001145026:c.1186+5521G>A" "INTRON5" "Unknown significance" "rs573635399" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 1 1008 0.001 0 978 0 2 5008 0.000399361
309168 "chr12:80871556:C>T" "PTPRQ" "NM_001145026:c.1186+5526C>T" "INTRON5" "Unknown significance" "rs769681572" "This variant is a VUS because it does not have enough information."
309169 "chr12:80871576:G>A" "PTPRQ" "NM_001145026:c.1186+5546G>A" "INTRON5" "Unknown significance" "rs543982299" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309170 "chr12:80871580:C>A" "PTPRQ" "NM_001145026:c.1186+5550C>A" "INTRON5" "Benign" "rs142960015" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 10 1006 0.0099 2 694 0.0029 0 1008 0 2 978 0.002 14 5008 0.00279553
309171 "chr12:80871580:C>T" "PTPRQ" "NM_001145026:c.1186+5550C>T" "INTRON5" "Unknown significance" "rs142960015" "This variant is a VUS because it does not have enough information."
309172 "chr12:80871600:C>T" "PTPRQ" "NM_001145026:c.1186+5570C>T" "INTRON5" "Unknown significance" "rs577439282" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309173 "chr12:80871606:T>G" "PTPRQ" "NM_001145026:c.1186+5576T>G" "INTRON5" "Unknown significance" "rs772995271" "This variant is a VUS because it does not have enough information."
309174 "chr12:80871617:G>C" "PTPRQ" "NM_001145026:c.1186+5587G>C" "INTRON5" "Benign" "rs7979591" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 104 1322 0.0787 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 111 5008 0.0221645
309175 "chr12:80871620:C>G" "PTPRQ" "NM_001145026:c.1186+5590C>G" "INTRON5" "Unknown significance" "rs560052341" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309176 "chr12:80871648:G>A" "PTPRQ" "NM_001145026:c.1186+5618G>A" "INTRON5" "Benign" "rs4589363" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 82 1322 0.062 673 1006 0.669 404 694 0.5821 365 1008 0.3621 668 978 0.683 2192 5008 0.4377
309177 "chr12:80871664:A>G" "PTPRQ" "NM_001145026:c.1186+5634A>G" "INTRON5" "Benign" "rs187450253" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309178 "chr12:80871674:G>A" "PTPRQ" "NM_001145026:c.1186+5644G>A" "INTRON5" "Benign" "rs192342867" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 1 1006 0.001 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521
309179 "chr12:80871702:C>A" "PTPRQ" "NM_001145026:c.1186+5672C>A" "INTRON5" "Benign" "rs11114472" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 303 1322 0.2292 217 1006 0.2157 113 694 0.1628 0 1008 0 106 978 0.1084 739 5008 0.147564
309180 "chr12:80871715:G>A" "PTPRQ" "NM_001145026:c.1186+5685G>A" "INTRON5" "Unknown significance" "rs550311577" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
309181 "chr12:80871721:G>A" "PTPRQ" "NM_001145026:c.1186+5691G>A" "INTRON5" "Unknown significance" "rs571841139" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309182 "chr12:80871742:G>C" "PTPRQ" "NM_001145026:c.1186+5712G>C" "INTRON5" "Unknown significance" "rs184886273" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309183 "chr12:80871747:T>A" "PTPRQ" "NM_001145026:c.1186+5717T>A" "INTRON5" "Benign" "rs61950917" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 24 1006 0.0239 6 694 0.0086 9 1008 0.0089 49 978 0.0501 122 5008 0.024361
309184 "chr12:80871754:G>T" "PTPRQ" "NM_001145026:c.1186+5724G>T" "INTRON5" "Unknown significance" "rs566402174" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309185 "chr12:80871779:T>A" "PTPRQ" "NM_001145026:c.1186+5749T>A" "INTRON5" "Benign" "rs4643133" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 232 1322 0.1755 6 1006 0.006 45 694 0.0648 43 1008 0.0427 25 978 0.0256 351 5008 0.0700879
309186 "chr12:80871785:C>T" "PTPRQ" "NM_001145026:c.1186+5755C>T" "INTRON5" "Unknown significance" "rs555303767" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
309187 "chr12:80871786:T>C" "PTPRQ" "NM_001145026:c.1186+5756T>C" "INTRON5" "Unknown significance" "rs573571817" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309188 "chr12:80871793:G>A" "PTPRQ" "NM_001145026:c.1186+5763G>A" "INTRON5" "Unknown significance" "rs759766100" "This variant is a VUS because it does not have enough information."
309189 "chr12:80871797:G>A" "PTPRQ" "NM_001145026:c.1186+5767G>A" "INTRON5" "Unknown significance" "rs768008528" "This variant is a VUS because it does not have enough information."
309190 "chr12:80871801:C>T" "PTPRQ" "NM_001145026:c.1186+5771C>T" "INTRON5" "Unknown significance" "rs796205845" "This variant is a VUS because it does not have enough information."
309191 "chr12:80871806:A>C" "PTPRQ" "NM_001145026:c.1186+5776A>C" "INTRON5" "Unknown significance" "rs775949604" "This variant is a VUS because it does not have enough information."
309192 "chr12:80871826:T>C" "PTPRQ" "NM_001145026:c.1186+5796T>C" "INTRON5" "Unknown significance" "rs369553586" "This variant is a VUS because it does not have enough information."
309193 "chr12:80871833:T>C" "PTPRQ" "NM_001145026:c.1186+5803T>C" "INTRON5" "Benign" "rs537919226" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 22 1322 0.0166 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 24 5008 0.00479233
309194 "chr12:80871834:G>C" "PTPRQ" "NM_001145026:c.1186+5804G>C" "INTRON5" "Unknown significance" "rs555870840" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309195 "chr12:80871835:T>A" "PTPRQ" "NM_001145026:c.1186+5805T>A" "INTRON5" "Unknown significance" "rs761293180" "This variant is a VUS because it does not have enough information."
309196 "chr12:80871898:T>C" "PTPRQ" "NM_001145026:c.1186+5868T>C" "INTRON5" "Benign" "rs577402817" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 16 1322 0.0121 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 18 5008 0.00359425
309197 "chr12:80871901:A>G" "PTPRQ" "NM_001145026:c.1186+5871A>G" "INTRON5" "Benign" "rs544845678" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 58 1322 0.0439 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 62 5008 0.0123802
309198 "chr12:80871903:G>A" "PTPRQ" "NM_001145026:c.1186+5873G>A" "INTRON5" "Unknown significance" "rs557494016" "This variant is a VUS because it does not have enough information."
309199 "chr12:80871911:C>A" "PTPRQ" "NM_001145026:c.1186+5881C>A" "INTRON5" "Benign" "rs560015003" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 8 5008 0.00159744
309200 "chr12:80871911:C>G" "PTPRQ" "NM_001145026:c.1186+5881C>G" "INTRON5" "Unknown significance" "rs560015003" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
309201 "chr12:80871924:G>A" "PTPRQ" "NM_001145026:c.1186+5894G>A" "INTRON5" "Unknown significance" "rs542565053" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361
309202 "chr12:80871942:C>A" "PTPRQ" "NM_001145026:c.1186+5912C>A" "INTRON5" "Unknown significance" "rs570921773" "This variant is a VUS because it does not have enough information."
309203 "chr12:80871948:G>A" "PTPRQ" "NM_001145026:c.1186+5918G>A" "INTRON5" "Unknown significance" "rs371668937" "This variant is a VUS because it does not have enough information."
309204 "chr12:80871967:A>C" "PTPRQ" "NM_001145026:c.1186+5937A>C" "INTRON5" "Benign" "rs12304050" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 705 1322 0.5333 222 1006 0.2207 145 694 0.2089 45 1008 0.0446 161 978 0.1646 1278 5008 0.255192
309205 "chr12:80871971:G>C" "PTPRQ" "NM_001145026:c.1186+5941G>C" "INTRON5" "Benign" "rs61950937" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 702 1322 0.531 222 1006 0.2207 145 694 0.2089 45 1008 0.0446 161 978 0.1646 1275 5008 0.254593
309206 "chr12:80871973:A>G" "PTPRQ" "NM_001145026:c.1186+5943A>G" "INTRON5" "Benign" "rs12304051" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 703 1322 0.5318 222 1006 0.2207 145 694 0.2089 45 1008 0.0446 161 978 0.1646 1276 5008 0.254792
309207 "chr12:80872010:C>T" "PTPRQ" "NM_001145026:c.1186+5980C>T" "INTRON5" "Unknown significance" "rs184292809" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 1 978 0.001 2 5008 0.000399361
309208 "chr12:80872015:A>T" "PTPRQ" "NM_001145026:c.1186+5985A>T" "INTRON5" "Unknown significance" "rs111909659" "This variant is a VUS because it does not have enough information."
309209 "chr12:80872029:G>A" "PTPRQ" "NM_001145026:c.1186+5999G>A" "INTRON5" "Benign" "rs12811974" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 221 1322 0.1672 673 1006 0.669 424 694 0.611 367 1008 0.3641 673 978 0.6881 2358 5008 0.470847
309210 "chr12:80872032:T>C" "PTPRQ" "NM_001145026:c.1186+6002T>C" "INTRON5" "Benign" "rs547966004" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 294 1322 0.2224 6 1006 0.006 41 694 0.0591 40 1008 0.0397 20 978 0.0204 401 5008 0.0800719
309211 "chr12:80872045:G>A" "PTPRQ" "NM_001145026:c.1186+6015G>A" "INTRON5" "Unknown significance" "rs757984314" "This variant is a VUS because it does not have enough information."
309212 "chr12:80872063:T>C" "PTPRQ" "NM_001145026:c.1186+6033T>C" "INTRON5" "Unknown significance" "rs566153505" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309213 "chr12:80872067:C>A" "PTPRQ" "NM_001145026:c.1186+6037C>A" "INTRON5" "Unknown significance" "rs530384416" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309214 "chr12:80872068:A>G" "PTPRQ" "NM_001145026:c.1186+6038A>G" "INTRON5" "Unknown significance" "rs548623090" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309215 "chr12:80872071:T>G" "PTPRQ" "NM_001145026:c.1186+6041T>G" "INTRON5" "Unknown significance" "rs567233679" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309216 "chr12:80872120:A>G" "PTPRQ" "NM_001145026:c.1186+6090A>G" "INTRON5" "Unknown significance" "rs537485244" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 2 5008 0.000399361
309217 "chr12:80872136:A>G" "PTPRQ" "NM_001145026:c.1187-6076A>G" "INTRON5" "Unknown significance" "rs555832211" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309218 "chr12:80872145:A>G" "PTPRQ" "NM_001145026:c.1187-6067A>G" "INTRON5" "Unknown significance" "rs571058362" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 2 1008 0.002 0 978 0 4 5008 0.000798722
309219 "chr12:80872190:A>-" "PTPRQ" "NM_001145026:c.1187-6022delA" "INTRON5" "Benign" "rs577699638" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 24 1006 0.0239 6 694 0.0086 9 1008 0.0089 49 978 0.0501 122 5008 0.024361
309220 "chr12:80872234:C>G" "PTPRQ" "NM_001145026:c.1187-5978C>G" "INTRON5" "Benign" "rs538347278" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309221 "chr12:80872249:C>T" "PTPRQ" "NM_001145026:c.1187-5963C>T" "INTRON5" "Benign" "rs369567327" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 298 1322 0.2254 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 421 5008 0.0840655
309222 "chr12:80872271:T>C" "PTPRQ" "NM_001145026:c.1187-5941T>C" "INTRON5" "Benign" "rs572160317" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 5 5008 0.000998403
309223 "chr12:80872276:T>C" "PTPRQ" "NM_001145026:c.1187-5936T>C" "INTRON5" "Unknown significance" "rs542877072" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309224 "chr12:80872289:A>G" "PTPRQ" "NM_001145026:c.1187-5923A>G" "INTRON5" "Unknown significance" "rs765798109" "This variant is a VUS because it does not have enough information."
309225 "chr12:80872290:T>C" "PTPRQ" "NM_001145026:c.1187-5922T>C" "INTRON5" "Unknown significance" "rs554594548" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309226 "chr12:80872292:G>A" "PTPRQ" "NM_001145026:c.1187-5920G>A" "INTRON5" "Unknown significance" "rs181203759" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309227 "chr12:80872306:G>A" "PTPRQ" "NM_001145026:c.1187-5906G>A" "INTRON5" "Unknown significance" "rs543877499" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309228 "chr12:80872315:C>T" "PTPRQ" "NM_001145026:c.1187-5897C>T" "INTRON5" "Benign" "rs145331674" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 152 1322 0.115 0 1006 0 9 694 0.013 0 1008 0 0 978 0 161 5008 0.0321486
309229 "chr12:80872321:C>T" "PTPRQ" "NM_001145026:c.1187-5891C>T" "INTRON5" "Unknown significance" "rs532612155" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309230 "chr12:80872322:G>A" "PTPRQ" "NM_001145026:c.1187-5890G>A" "INTRON5" "Unknown significance" "rs575108987" "This variant is a VUS because it does not have enough information."
309231 "chr12:80872324:G>A" "PTPRQ" "NM_001145026:c.1187-5888G>A" "INTRON5" "Unknown significance" "rs541555156" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309232 "chr12:80872340:G>T" "PTPRQ" "NM_001145026:c.1187-5872G>T" "INTRON5" "Unknown significance" "rs373036047" "This variant is a VUS because it does not have enough information."
309233 "chr12:80872356:T>C" "PTPRQ" "NM_001145026:c.1187-5856T>C" "INTRON5" "Unknown significance" "rs559869495" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309234 "chr12:80872363:C>T" "PTPRQ" "NM_001145026:c.1187-5849C>T" "INTRON5" "Unknown significance" "rs530260411" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309235 "chr12:80872364:A>G" "PTPRQ" "NM_001145026:c.1187-5848A>G" "INTRON5" "Benign" "rs4505124" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 801 1322 0.6059 223 1006 0.2217 171 694 0.2464 44 1008 0.0437 132 978 0.135 1371 5008 0.273762
309236 "chr12:80872376:A>C" "PTPRQ" "NM_001145026:c.1187-5836A>C" "INTRON5" "Unknown significance" "rs570296463" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309237 "chr12:80872385:G>C" "PTPRQ" "NM_001145026:c.1187-5827G>C" "INTRON5" "Unknown significance" "rs564070747" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 3 694 0.0043 0 1008 0 0 978 0 5 5008 0.000998403
309238 "chr12:80872401:C>A" "PTPRQ" "NM_001145026:c.1187-5811C>A" "INTRON5" "Benign" "rs549322228" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 1 1006 0.001 0 694 0 0 1008 0 0 978 0 15 5008 0.00299521
309239 "chr12:80872427:T>C" "PTPRQ" "NM_001145026:c.1187-5785T>C" "INTRON5" "Unknown significance" "rs369840246" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
309240 "chr12:80872432:A>C" "PTPRQ" "NM_001145026:c.1187-5780A>C" "INTRON5" "Benign" "rs147225426" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 46 1322 0.0348 0 1006 0 0 694 0 0 1008 0 0 978 0 46 5008 0.0091853
309241 "chr12:80872437:A>C" "PTPRQ" "NM_001145026:c.1187-5775A>C" "INTRON5" "Benign" "rs190457320" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 22 1008 0.0218 3 978 0.0031 25 5008 0.00499201
309242 "chr12:80872490:G>A" "PTPRQ" "NM_001145026:c.1187-5722G>A" "INTRON5" "Unknown significance" "rs565843580" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309243 "chr12:80872525:C>T" "PTPRQ" "NM_001145026:c.1187-5687C>T" "INTRON5" "Unknown significance" "rs533035375" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309244 "chr12:80872526:G>A" "PTPRQ" "NM_001145026:c.1187-5686G>A" "INTRON5" "Benign" "rs181376549" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 298 1322 0.2254 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 421 5008 0.0840655
309245 "chr12:80872528:T>A" "PTPRQ" "NM_001145026:c.1187-5684T>A" "INTRON5" "Unknown significance" "rs539879681" "This variant is a VUS because it does not have enough information."
309246 "chr12:80872530:C>T" "PTPRQ" "NM_001145026:c.1187-5682C>T" "INTRON5" "Unknown significance" "rs576450774" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309247 "chr12:80872556:C>A" "PTPRQ" "NM_001145026:c.1187-5656C>A" "INTRON5" "Benign" "rs74975030" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 24 1006 0.0239 6 694 0.0086 9 1008 0.0089 49 978 0.0501 122 5008 0.024361
309248 "chr12:80872557:A>T" "PTPRQ" "NM_001145026:c.1187-5655A>T" "INTRON5" "Unknown significance" "rs558958531" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309249 "chr12:80872570:G>A" "PTPRQ" "NM_001145026:c.1187-5642G>A" "INTRON5" "Unknown significance" "rs749182642" "This variant is a VUS because it does not have enough information."
309250 "chr12:80872571:T>G" "PTPRQ" "NM_001145026:c.1187-5641T>G" "INTRON5" "Benign" "rs144423382" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 4 694 0.0058 53 1008 0.0526 0 978 0 57 5008 0.0113818
309251 "chr12:80872579:A>G" "PTPRQ" "NM_001145026:c.1187-5633A>G" "INTRON5" "Benign" "rs147822126" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 72 1322 0.0545 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 75 5008 0.014976
309252 "chr12:80872581:G>A" "PTPRQ" "NM_001145026:c.1187-5631G>A" "INTRON5" "Unknown significance" "rs559627364" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309253 "chr12:80872596:G>T" "PTPRQ" "NM_001145026:c.1187-5616G>T" "INTRON5" "Unknown significance" "rs528853783" "This variant is a VUS because it does not have enough information."
309254 "chr12:80872609:T>A" "PTPRQ" "NM_001145026:c.1187-5603T>A" "INTRON5" "Unknown significance" "rs201723668" "This variant is a VUS because it does not have enough information."
309255 "chr12:80872635:C>T" "PTPRQ" "NM_001145026:c.1187-5577C>T" "INTRON5" "Benign" "rs185906211" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309256 "chr12:80872663:C>A" "PTPRQ" "NM_001145026:c.1187-5549C>A" "INTRON5" "Unknown significance" "rs542108110" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309257 "chr12:80872673:G>C" "PTPRQ" "NM_001145026:c.1187-5539G>C" "INTRON5" "Unknown significance" "rs563912529" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309258 "chr12:80872698:C>T" "PTPRQ" "NM_001145026:c.1187-5514C>T" "INTRON5" "Benign" "rs531067695" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 0 1006 0 1 694 0.0014 1 1008 0.001 0 978 0 10 5008 0.00199681
309259 "chr12:80872699:G>A" "PTPRQ" "NM_001145026:c.1187-5513G>A" "INTRON5" "Benign" "rs552464476" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 9 1006 0.0089 2 694 0.0029 0 1008 0 2 978 0.002 13 5008 0.00259585
309260 "chr12:80872709:C>G" "PTPRQ" "NM_001145026:c.1187-5503C>G" "INTRON5" "Unknown significance" "rs564509526" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 1 694 0.0014 2 1008 0.002 0 978 0 7 5008 0.00139776
309261 "chr12:80872743:C>G" "PTPRQ" "NM_001145026:c.1187-5469C>G" "INTRON5" "Unknown significance" "rs548915073" "This variant is a VUS because it does not have enough information."
309262 "chr12:80872780:G>A" "PTPRQ" "NM_001145026:c.1187-5432G>A" "INTRON5" "Benign" "rs371013885" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 35 1322 0.0265 24 1006 0.0239 6 694 0.0086 9 1008 0.0089 49 978 0.0501 123 5008 0.0245607
309263 "chr12:80872823:T>C" "PTPRQ" "NM_001145026:c.1187-5389T>C" "INTRON5" "Benign" "rs547452628" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 272 1322 0.2057 6 1006 0.006 47 694 0.0677 45 1008 0.0446 26 978 0.0266 396 5008 0.0790735
309264 "chr12:80872900:G>A" "PTPRQ" "NM_001145026:c.1187-5312G>A" "INTRON5" "Unknown significance" "rs565677799" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 1 978 0.001 6 5008 0.00119808
309265 "chr12:80872941:A>G" "PTPRQ" "NM_001145026:c.1187-5271A>G" "INTRON5" "Unknown significance" "rs536443245" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 2 978 0.002 4 5008 0.000798722
309266 "chr12:80873084:A>C" "PTPRQ" "NM_001145026:c.1187-5128A>C" "INTRON5" "Unknown significance" "rs7974002" "This variant is a VUS because it does not have enough information."
309267 "chr12:80873169:A>G" "PTPRQ" "NM_001145026:c.1187-5043A>G" "INTRON5" "Unknown significance" "rs61950940" "This variant is a VUS because it does not have enough information."
309268 "chr12:80873177:A>G" "PTPRQ" "NM_001145026:c.1187-5035A>G" "INTRON5" "Unknown significance" "rs7974128" "This variant is a VUS because it does not have enough information."
309269 "chr12:80873192:T>G" "PTPRQ" "NM_001145026:c.1187-5020T>G" "INTRON5" "Unknown significance" "rs541163888" "This variant is a VUS because it does not have enough information."
309270 "chr12:80873199:T>A" "PTPRQ" "NM_001145026:c.1187-5013T>A" "INTRON5" "Unknown significance" "rs563061965" "This variant is a VUS because it does not have enough information."
309271 "chr12:80873209:A>T" "PTPRQ" "NM_001145026:c.1187-5003A>T" "INTRON5" "Benign" "rs574806540" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 453 1322 0.3427 216 1006 0.2147 119 694 0.1715 0 1008 0 105 978 0.1074 893 5008 0.178315
309272 "chr12:80873222:C>T" "PTPRQ" "NM_001145026:c.1187-4990C>T" "INTRON5" "Unknown significance" "rs527668627" "This variant is a VUS because it does not have enough information."
309273 "chr12:80873418:G>A" "PTPRQ" "NM_001145026:c.1187-4794G>A" "INTRON5" "Unknown significance" "rs11519744" "This variant is a VUS because it does not have enough information."
309274 "chr12:80873479:G>A" "PTPRQ" "NM_001145026:c.1187-4733G>A" "INTRON5" "Unknown significance" "rs7959135" "This variant is a VUS because it does not have enough information."
309275 "chr12:80873545:A>G" "PTPRQ" "NM_001145026:c.1187-4667A>G" "INTRON5" "Unknown significance" "rs536528197" "This variant is a VUS because it does not have enough information."
309276 "chr12:80873558:A>C" "PTPRQ" "NM_001145026:c.1187-4654A>C" "INTRON5" "Unknown significance" "rs368604060" "This variant is a VUS because it does not have enough information."
309277 "chr12:80873605:G>T" "PTPRQ" "NM_001145026:c.1187-4607G>T" "INTRON5" "Unknown significance" "rs61950944" "This variant is a VUS because it does not have enough information."
309278 "chr12:80873627:T>C" "PTPRQ" "NM_001145026:c.1187-4585T>C" "INTRON5" "Unknown significance" "rs569882800" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309279 "chr12:80873628:A>G" "PTPRQ" "NM_001145026:c.1187-4584A>G" "INTRON5" "Unknown significance" "rs537313591" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
309280 "chr12:80873641:G>A" "PTPRQ" "NM_001145026:c.1187-4571G>A" "INTRON5" "Unknown significance" "rs11536121" "This variant is a VUS because it does not have enough information."
309281 "chr12:80873651:G>A" "PTPRQ" "NM_001145026:c.1187-4561G>A" "INTRON5" "Unknown significance" "rs61950945" "This variant is a VUS because it does not have enough information."
309282 "chr12:80873690:C>T" "PTPRQ" "NM_001145026:c.1187-4522C>T" "INTRON5" "Unknown significance" "rs766345811" "This variant is a VUS because it does not have enough information."
309283 "chr12:80873694:T>A" "PTPRQ" "NM_001145026:c.1187-4518T>A" "INTRON5" "Unknown significance" "rs753987787" "This variant is a VUS because it does not have enough information."
309284 "chr12:80873743:C>T" "PTPRQ" "NM_001145026:c.1187-4469C>T" "INTRON5" "Unknown significance" "rs558920571" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
309285 "chr12:80873744:A>G" "PTPRQ" "NM_001145026:c.1187-4468A>G" "INTRON5" "Unknown significance" "rs371041709" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
309286 "chr12:80873756:C>T" "PTPRQ" "NM_001145026:c.1187-4456C>T" "INTRON5" "Unknown significance" "rs543474210" "This variant is a VUS because it does not have enough information."
309287 "chr12:80873791:A>T" "PTPRQ" "NM_001145026:c.1187-4421A>T" "INTRON5" "Benign" "rs534752107" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 21 1322 0.0159 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 23 5008 0.00459265
309288 "chr12:80873799:G>A" "PTPRQ" "NM_001145026:c.1187-4413G>A" "INTRON5" "Unknown significance" "rs61950947" "This variant is a VUS because it does not have enough information."
309289 "chr12:80873828:C>G" "PTPRQ" "NM_001145026:c.1187-4384C>G" "INTRON5" "Benign" "rs9668331" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1204 1322 0.9107 918 1006 0.9125 601 694 0.866 413 1008 0.4097 848 978 0.8671 3984 5008 0.795527
309290 "chr12:80873849:A>T" "PTPRQ" "NM_001145026:c.1187-4363A>T" "INTRON5" "Benign" "rs574795768" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 7 1006 0.007 0 694 0 0 1008 0 1 978 0.001 8 5008 0.00159744
309291 "chr12:80873860:CACCA>-" "PTPRQ" "NM_001145026:c.1187-4352_1187-4348delCACCA" "INTRON5" "Unknown significance" "rs751474047" "This variant is a VUS because it does not have enough information."
309292 "chr12:80873867:C>G" "PTPRQ" "NM_001145026:c.1187-4345C>G" "INTRON5" "Unknown significance" "rs542320797" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309293 "chr12:80873872:C>T" "PTPRQ" "NM_001145026:c.1187-4340C>T" "INTRON5" "Benign" "rs563502754" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 9 1008 0.0089 0 978 0 9 5008 0.00179712
309294 "chr12:80873875:A>G" "PTPRQ" "NM_001145026:c.1187-4337A>G" "INTRON5" "Benign" "rs56850795" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 152 1322 0.115 0 1006 0 8 694 0.0115 0 1008 0 0 978 0 160 5008 0.0319489
309295 "chr12:80873876:T>C" "PTPRQ" "NM_001145026:c.1187-4336T>C" "INTRON5" "Unknown significance" "rs546063943" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
309296 "chr12:80873956:G>C" "PTPRQ" "NM_001145026:c.1187-4256G>C" "INTRON5" "Unknown significance" "rs11503530" "This variant is a VUS because it does not have enough information."
309297 "chr12:80873960:C>A" "PTPRQ" "NM_001145026:c.1187-4252C>A" "INTRON5" "Unknown significance" "rs564472900" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309298 "chr12:80873961:C>T" "PTPRQ" "NM_001145026:c.1187-4251C>T" "INTRON5" "Unknown significance" "rs531971236" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309299 "chr12:80873965:G>A" "PTPRQ" "NM_001145026:c.1187-4247G>A" "INTRON5" "Unknown significance" "rs190758780" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309300 "chr12:80874003:C>G" "PTPRQ" "NM_001145026:c.1187-4209C>G" "INTRON5" "Unknown significance" "rs559303385" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
309301 "chr12:80874011:C>T" "PTPRQ" "NM_001145026:c.1187-4201C>T" "INTRON5" "Unknown significance" "rs529721364" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309302 "chr12:80874016:C>A" "PTPRQ" "NM_001145026:c.1187-4196C>A" "INTRON5" "Unknown significance" "rs548288527" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309303 "chr12:80874025:A>G" "PTPRQ" "NM_001145026:c.1187-4187A>G" "INTRON5" "Unknown significance" "rs569846991" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309304 "chr12:80874065:T>A" "PTPRQ" "NM_001145026:c.1187-4147T>A" "INTRON5" "Benign" "rs537278960" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309305 "chr12:80874113:A>T" "PTPRQ" "NM_001145026:c.1187-4099A>T" "INTRON5" "Unknown significance" "rs552492314" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309306 "chr12:80874118:C>A" "PTPRQ" "NM_001145026:c.1187-4094C>A" "INTRON5" "Unknown significance" "rs570808463" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309307 "chr12:80874124:A>G" "PTPRQ" "NM_001145026:c.1187-4088A>G" "INTRON5" "Unknown significance" "rs534924343" "This variant is a VUS because it does not have enough information." 4 1322 0.003 2 1006 0.002 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
309308 "chr12:80874128:G>C" "PTPRQ" "NM_001145026:c.1187-4084G>C" "INTRON5" "Benign" "rs61333381" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 152 1322 0.115 0 1006 0 8 694 0.0115 0 1008 0 0 978 0 160 5008 0.0319489
309309 "chr12:80874140:C>T" "PTPRQ" "NM_001145026:c.1187-4072C>T" "INTRON5" "Benign" "rs142723923" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 64 1322 0.0484 70 1006 0.0696 25 694 0.036 292 1008 0.2897 75 978 0.0767 526 5008 0.105032
309310 "chr12:80874165:A>C" "PTPRQ" "NM_001145026:c.1187-4047A>C" "INTRON5" "Benign" "rs11114474" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 758 1322 0.5734 223 1006 0.2217 171 694 0.2464 43 1008 0.0427 131 978 0.1339 1326 5008 0.264776
309311 "chr12:80874247:A>C" "PTPRQ" "NM_001145026:c.1187-3965A>C" "INTRON5" "Benign" "rs557060240" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309312 "chr12:80874257:G>A" "PTPRQ" "NM_001145026:c.1187-3955G>A" "INTRON5" "Benign" "rs11835299" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 459 1322 0.3472 217 1006 0.2157 122 694 0.1758 0 1008 0 105 978 0.1074 903 5008 0.180312
309313 "chr12:80874270:A>T" "PTPRQ" "NM_001145026:c.1187-3942A>T" "INTRON5" "Unknown significance" "rs546027127" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 2 694 0.0029 0 1008 0 0 978 0 5 5008 0.000998403
309314 "chr12:80874280:G>A" "PTPRQ" "NM_001145026:c.1187-3932G>A" "INTRON5" "Unknown significance" "rs564435816" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309315 "chr12:80874316:A>T" "PTPRQ" "NM_001145026:c.1187-3896A>T" "INTRON5" "Benign" "rs4536294" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1210 1322 0.9153 920 1006 0.9145 600 694 0.8646 409 1008 0.4058 848 978 0.8671 3987 5008 0.796126
309316 "chr12:80874320:A>C" "PTPRQ" "NM_001145026:c.1187-3892A>C" "INTRON5" "Benign" "rs200961797" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1210 1322 0.9153 920 1006 0.9145 600 694 0.8646 409 1008 0.4058 848 978 0.8671 3987 5008 0.796126
309317 "chr12:80874322:C>T" "PTPRQ" "NM_001145026:c.1187-3890C>T" "INTRON5" "Benign" "rs201610961" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1210 1322 0.9153 920 1006 0.9145 600 694 0.8646 409 1008 0.4058 848 978 0.8671 3987 5008 0.796126
309318 "chr12:80874326:G>A" "PTPRQ" "NM_001145026:c.1187-3886G>A" "INTRON5" "Benign" "rs4625539" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1210 1322 0.9153 920 1006 0.9145 600 694 0.8646 409 1008 0.4058 848 978 0.8671 3987 5008 0.796126
309319 "chr12:80874338:C>A" "PTPRQ" "NM_001145026:c.1187-3874C>A" "INTRON5" "Benign" "rs541931844" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309320 "chr12:80874350:C>T" "PTPRQ" "NM_001145026:c.1187-3862C>T" "INTRON5" "Unknown significance" "rs4460868" "This variant is a VUS because it does not have enough information."
309321 "chr12:80874371:T>A" "PTPRQ" "NM_001145026:c.1187-3841T>A" "INTRON5" "Benign" "rs11833717" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 398 1322 0.3011 217 1006 0.2157 118 694 0.17 0 1008 0 105 978 0.1074 838 5008 0.167332
309322 "chr12:80874399:C>T" "PTPRQ" "NM_001145026:c.1187-3813C>T" "INTRON5" "Unknown significance" "rs376621463" "This variant is a VUS because it does not have enough information."
309323 "chr12:80874437:T>C" "PTPRQ" "NM_001145026:c.1187-3775T>C" "INTRON5" "Unknown significance" "rs530724123" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309324 "chr12:80874460:A>C" "PTPRQ" "NM_001145026:c.1187-3752A>C" "INTRON5" "Unknown significance" "rs190912306" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
309325 "chr12:80874461:T>A" "PTPRQ" "NM_001145026:c.1187-3751T>A" "INTRON5" "Unknown significance" "rs111776018" "This variant is a VUS because it does not have enough information."
309326 "chr12:80874480:G>A" "PTPRQ" "NM_001145026:c.1187-3732G>A" "INTRON5" "Unknown significance" "rs570672102" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309327 "chr12:80874529:A>G" "PTPRQ" "NM_001145026:c.1187-3683A>G" "INTRON5" "Benign" "rs61950948" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 24 1006 0.0239 6 694 0.0086 9 1008 0.0089 49 978 0.0501 122 5008 0.024361
309328 "chr12:80874575:C>T" "PTPRQ" "NM_001145026:c.1187-3637C>T" "INTRON5" "Benign" "rs145133332" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 72 1322 0.0545 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 75 5008 0.014976
309329 "chr12:80874598:A>G" "PTPRQ" "NM_001145026:c.1187-3614A>G" "INTRON5" "Benign" "rs148345506" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309330 "chr12:80874638:C>A" "PTPRQ" "NM_001145026:c.1187-3574C>A" "INTRON5" "Unknown significance" "rs535875415" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309331 "chr12:80874654:A>G" "PTPRQ" "NM_001145026:c.1187-3558A>G" "INTRON5" "Benign" "rs11114475" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 84 1322 0.0635 673 1006 0.669 406 694 0.585 364 1008 0.3611 669 978 0.684 2196 5008 0.438498
309332 "chr12:80874691:C>T" "PTPRQ" "NM_001145026:c.1187-3521C>T" "INTRON5" "Unknown significance" "rs569055693" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309333 "chr12:80874692:G>A" "PTPRQ" "NM_001145026:c.1187-3520G>A" "INTRON5" "Benign" "rs377584394" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 63 1322 0.0477 0 1006 0 4 694 0.0058 0 1008 0 20 978 0.0204 87 5008 0.0173722
309334 "chr12:80874756:C>T" "PTPRQ" "NM_001145026:c.1187-3456C>T" "INTRON5" "Benign" "rs370569948" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 459 1322 0.3472 217 1006 0.2157 122 694 0.1758 0 1008 0 105 978 0.1074 903 5008 0.180312
309335 "chr12:80874809:C>T" "PTPRQ" "NM_001145026:c.1187-3403C>T" "INTRON5" "Unknown significance" "rs573399746" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309336 "chr12:80874833:A>T" "PTPRQ" "NM_001145026:c.1187-3379A>T" "INTRON5" "Unknown significance" "rs374235182" "This variant is a VUS because it does not have enough information."
309337 "chr12:80874846:A>G" "PTPRQ" "NM_001145026:c.1187-3366A>G" "INTRON5" "Unknown significance" "rs540549426" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309338 "chr12:80874878:G>C" "PTPRQ" "NM_001145026:c.1187-3334G>C" "INTRON5" "Unknown significance" "rs376720285" "This variant is a VUS because it does not have enough information."
309339 "chr12:80874895:A>C" "PTPRQ" "NM_001145026:c.1187-3317A>C" "INTRON5" "Unknown significance" "rs556060981" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309340 "chr12:80874904:G>A" "PTPRQ" "NM_001145026:c.1187-3308G>A" "INTRON5" "Unknown significance" "rs371635965" "This variant is a VUS because it does not have enough information."
309341 "chr12:80874921:C>T" "PTPRQ" "NM_001145026:c.1187-3291C>T" "INTRON5" "Unknown significance" "rs574342581" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309342 "chr12:80874928:A>G" "PTPRQ" "NM_001145026:c.1187-3284A>G" "INTRON5" "Unknown significance" "rs535420605" "This variant is a VUS because it does not have enough information."
309343 "chr12:80874958:A>G" "PTPRQ" "NM_001145026:c.1187-3254A>G" "INTRON5" "Unknown significance" "rs778802212" "This variant is a VUS because it does not have enough information."
309344 "chr12:80874985:A>C" "PTPRQ" "NM_001145026:c.1187-3227A>C" "INTRON5" "Unknown significance" "rs555243298" "This variant is a VUS because it does not have enough information."
309345 "chr12:80874986:A>G" "PTPRQ" "NM_001145026:c.1187-3226A>G" "INTRON5" "Unknown significance" "rs575179377" "This variant is a VUS because it does not have enough information."
309346 "chr12:80874999:A>G" "PTPRQ" "NM_001145026:c.1187-3213A>G" "INTRON5" "Benign" "rs541895220" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 36 978 0.0368 37 5008 0.00738818
309347 "chr12:80875018:T>C" "PTPRQ" "NM_001145026:c.1187-3194T>C" "INTRON5" "Unknown significance" "rs563278195" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309348 "chr12:80875029:A>G" "PTPRQ" "NM_001145026:c.1187-3183A>G" "INTRON5" "Unknown significance" "rs530583088" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309349 "chr12:80875035:A>C" "PTPRQ" "NM_001145026:c.1187-3177A>C" "INTRON5" "Unknown significance" "rs537688837" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
309350 "chr12:80875037:A>G" "PTPRQ" "NM_001145026:c.1187-3175A>G" "INTRON5" "Unknown significance" "rs150855449" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
309351 "chr12:80875044:G>C" "PTPRQ" "NM_001145026:c.1187-3168G>C" "INTRON5" "Unknown significance" "rs528314473" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309352 "chr12:80875052:T>C" "PTPRQ" "NM_001145026:c.1187-3160T>C" "INTRON5" "Benign" "rs183231999" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 27 1006 0.0268 43 694 0.062 0 1008 0 18 978 0.0184 96 5008 0.0191693
309353 "chr12:80875063:T>G" "PTPRQ" "NM_001145026:c.1187-3149T>G" "INTRON5" "Unknown significance" "rs568382119" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
309354 "chr12:80875076:A>G" "PTPRQ" "NM_001145026:c.1187-3136A>G" "INTRON5" "Unknown significance" "rs529267371" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309355 "chr12:80875095:A>C" "PTPRQ" "NM_001145026:c.1187-3117A>C" "INTRON5" "Unknown significance" "rs550513838" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
309356 "chr12:80875113:C>T" "PTPRQ" "NM_001145026:c.1187-3099C>T" "INTRON5" "Unknown significance" "rs568920667" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309357 "chr12:80875135:G>T" "PTPRQ" "NM_001145026:c.1187-3077G>T" "INTRON5" "Unknown significance" "rs539511931" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309358 "chr12:80875139:T>C" "PTPRQ" "NM_001145026:c.1187-3073T>C" "INTRON5" "Unknown significance" "rs557859521" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 2 1008 0.002 0 978 0 3 5008 0.000599042
309359 "chr12:80875147:C>T" "PTPRQ" "NM_001145026:c.1187-3065C>T" "INTRON5" "Benign" "rs138195121" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 12 1008 0.0119 0 978 0 12 5008 0.00239617
309360 "chr12:80875168:C>T" "PTPRQ" "NM_001145026:c.1187-3044C>T" "INTRON5" "Unknown significance" "rs534446280" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309361 "chr12:80875169:C>T" "PTPRQ" "NM_001145026:c.1187-3043C>T" "INTRON5" "Benign" "rs555782617" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 10 1322 0.0076 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 11 5008 0.00219649
309362 "chr12:80875172:C>T" "PTPRQ" "NM_001145026:c.1187-3040C>T" "INTRON5" "Benign" "rs574230899" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 1322 0.0068 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 10 5008 0.00199681
309363 "chr12:80875173:C>T" "PTPRQ" "NM_001145026:c.1187-3039C>T" "INTRON5" "Benign" "rs544933198" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 1322 0.0068 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 10 5008 0.00199681
309364 "chr12:80875180:A>C" "PTPRQ" "NM_001145026:c.1187-3032A>C" "INTRON5" "Benign" "rs143838692" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 298 1322 0.2254 6 1006 0.006 49 694 0.0706 43 1008 0.0427 26 978 0.0266 422 5008 0.0842652
309365 "chr12:80875221:G>A" "PTPRQ" "NM_001145026:c.1187-2991G>A" "INTRON5" "Benign" "rs575335972" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309366 "chr12:80875243:C>T" "PTPRQ" "NM_001145026:c.1187-2969C>T" "INTRON5" "Unknown significance" "rs545890862" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309367 "chr12:80875248:C>G" "PTPRQ" "NM_001145026:c.1187-2964C>G" "INTRON5" "Unknown significance" "rs368732642" "This variant is a VUS because it does not have enough information."
309368 "chr12:80875251:G>C" "PTPRQ" "NM_001145026:c.1187-2961G>C" "INTRON5" "Unknown significance" "rs11519745" "This variant is a VUS because it does not have enough information."
309369 "chr12:80875274:A>G" "PTPRQ" "NM_001145026:c.1187-2938A>G" "INTRON5" "Benign" "rs12309989" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 296 1322 0.2239 6 1006 0.006 49 694 0.0706 43 1008 0.0427 26 978 0.0266 420 5008 0.0838658
309370 "chr12:80875299:C>T" "PTPRQ" "NM_001145026:c.1187-2913C>T" "INTRON5" "Benign" "rs11513781" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 788 1322 0.5961 247 1006 0.2455 176 694 0.2536 52 1008 0.0516 178 978 0.182 1441 5008 0.28774
309371 "chr12:80875306:C>T" "PTPRQ" "NM_001145026:c.1187-2906C>T" "INTRON5" "Benign" "rs540465363" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 4 1006 0.004 0 694 0 8 1008 0.0079 1 978 0.001 13 5008 0.00259585
309372 "chr12:80875313:G>C" "PTPRQ" "NM_001145026:c.1187-2899G>C" "INTRON5" "Unknown significance" "rs187333575" "This variant is a VUS because it does not have enough information."
309373 "chr12:80875344:G>A" "PTPRQ" "NM_001145026:c.1187-2868G>A" "INTRON5" "Unknown significance" "rs559958204" "This variant is a VUS because it does not have enough information."
309374 "chr12:80875362:T>A" "PTPRQ" "NM_001145026:c.1187-2850T>A" "INTRON5" "Unknown significance" "rs561736027" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
309375 "chr12:80875363:T>C" "PTPRQ" "NM_001145026:c.1187-2849T>C" "INTRON5" "Unknown significance" "rs529110447" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
309376 "chr12:80875371:C>T" "PTPRQ" "NM_001145026:c.1187-2841C>T" "INTRON5" "Benign" "rs10862137" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 789 1322 0.5968 247 1006 0.2455 177 694 0.255 52 1008 0.0516 180 978 0.184 1445 5008 0.288538
309377 "chr12:80875394:T>C" "PTPRQ" "NM_001145026:c.1187-2818T>C" "INTRON5" "Unknown significance" "rs562515658" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309378 "chr12:80875455:G>T" "PTPRQ" "NM_001145026:c.1187-2757G>T" "INTRON5" "Benign" "rs533189670" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 0 1006 0 0 694 0 0 1008 0 0 978 0 14 5008 0.00279553
309379 "chr12:80875463:A>T" "PTPRQ" "NM_001145026:c.1187-2749A>T" "INTRON5" "Benign" "rs551575604" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309380 "chr12:80875486:C>T" "PTPRQ" "NM_001145026:c.1187-2726C>T" "INTRON5" "Unknown significance" "rs201842169" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309381 "chr12:80875488:C>T" "PTPRQ" "NM_001145026:c.1187-2724C>T" "INTRON5" "Benign" "rs534040252" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 45 5008 0.00898562
309382 "chr12:80875490:A>G" "PTPRQ" "NM_001145026:c.1187-2722A>G" "INTRON5" "Benign" "rs549517443" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 16 1322 0.0121 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 18 5008 0.00359425
309383 "chr12:80875511:C>T" "PTPRQ" "NM_001145026:c.1187-2701C>T" "INTRON5" "Benign" "rs567781676" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 11 1008 0.0109 0 978 0 11 5008 0.00219649
309384 "chr12:80875522:A>G" "PTPRQ" "NM_001145026:c.1187-2690A>G" "INTRON5" "Unknown significance" "rs538515094" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309385 "chr12:80875602:G>A" "PTPRQ" "NM_001145026:c.1187-2610G>A" "INTRON5" "Benign" "rs191783751" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 0 1006 0 0 694 0 0 1008 0 0 978 0 14 5008 0.00279553
309386 "chr12:80875608:G>C" "PTPRQ" "NM_001145026:c.1187-2604G>C" "INTRON5" "Unknown significance" "rs575293632" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 1 694 0.0014 1 1008 0.001 0 978 0 3 5008 0.000599042
309387 "chr12:80875619:G>T" "PTPRQ" "NM_001145026:c.1187-2593G>T" "INTRON5" "Unknown significance" "rs539477700" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309388 "chr12:80875630:A>C" "PTPRQ" "NM_001145026:c.1187-2582A>C" "INTRON5" "Benign" "rs11114476" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 457 1322 0.3457 217 1006 0.2157 121 694 0.1744 0 1008 0 105 978 0.1074 900 5008 0.179712
309389 "chr12:80875633:C>T" "PTPRQ" "NM_001145026:c.1187-2579C>T" "INTRON5" "Unknown significance" "rs572847371" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
309390 "chr12:80875655:G>A" "PTPRQ" "NM_001145026:c.1187-2557G>A" "INTRON5" "Unknown significance" "rs539960063" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309391 "chr12:80875662:A>G" "PTPRQ" "NM_001145026:c.1187-2550A>G" "INTRON5" "Benign" "rs11114477" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 457 1322 0.3457 217 1006 0.2157 121 694 0.1744 0 1008 0 105 978 0.1074 900 5008 0.179712
309392 "chr12:80875691:G>T" "PTPRQ" "NM_001145026:c.1187-2521G>T" "INTRON5" "Unknown significance" "rs573522621" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309393 "chr12:80875776:C>A" "PTPRQ" "NM_001145026:c.1187-2436C>A" "INTRON5" "Unknown significance" "rs10862138" "This variant is a VUS because it does not have enough information."
309394 "chr12:80875830:A>G" "PTPRQ" "NM_001145026:c.1187-2382A>G" "INTRON5" "Unknown significance" "rs544086233" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309395 "chr12:80875836:C>T" "PTPRQ" "NM_001145026:c.1187-2376C>T" "INTRON5" "Unknown significance" "rs562484523" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309396 "chr12:80875837:G>T" "PTPRQ" "NM_001145026:c.1187-2375G>T" "INTRON5" "Unknown significance" "rs200808755" "This variant is a VUS because it does not have enough information."
309397 "chr12:80875841:C>T" "PTPRQ" "NM_001145026:c.1187-2371C>T" "INTRON5" "Benign" "rs182877154" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 240 1322 0.1815 222 1006 0.2207 118 694 0.17 16 1008 0.0159 121 978 0.1237 717 5008 0.143171
309398 "chr12:80875860:C>G" "PTPRQ" "NM_001145026:c.1187-2352C>G" "INTRON5" "Unknown significance" "rs551708120" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309399 "chr12:80875883:A>T" "PTPRQ" "NM_001145026:c.1187-2329A>T" "INTRON5" "Unknown significance" "rs560297073" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309400 "chr12:80875937:T>G" "PTPRQ" "NM_001145026:c.1187-2275T>G" "INTRON5" "Unknown significance" "rs527752783" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309401 "chr12:80875984:C>G" "PTPRQ" "NM_001145026:c.1187-2228C>G" "INTRON5" "Unknown significance" "rs61950950" "This variant is a VUS because it does not have enough information."
309402 "chr12:80875998:C>T" "PTPRQ" "NM_001145026:c.1187-2214C>T" "INTRON5" "Benign" "rs12304760" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 291 1322 0.2201 6 1006 0.006 49 694 0.0706 44 1008 0.0437 26 978 0.0266 416 5008 0.0830671
309403 "chr12:80876041:C>T" "PTPRQ" "NM_001145026:c.1187-2171C>T" "INTRON5" "Unknown significance" "rs113054662" "This variant is a VUS because it does not have enough information."
309404 "chr12:80876047:A>G" "PTPRQ" "NM_001145026:c.1187-2165A>G" "INTRON5" "Unknown significance" "rs774161915" "This variant is a VUS because it does not have enough information."
309405 "chr12:80876071:T>G" "PTPRQ" "NM_001145026:c.1187-2141T>G" "INTRON5" "Unknown significance" "rs112774137" "This variant is a VUS because it does not have enough information."
309406 "chr12:80876115:A>T" "PTPRQ" "NM_001145026:c.1187-2097A>T" "INTRON5" "Unknown significance" "rs567841476" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309407 "chr12:80876208:A>T" "PTPRQ" "NM_001145026:c.1187-2004A>T" "INTRON5" "Unknown significance" "rs538473146" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309408 "chr12:80876220:A>T" "PTPRQ" "NM_001145026:c.1187-1992A>T" "INTRON5" "Unknown significance" "rs550484238" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 2 978 0.002 3 5008 0.000599042
309409 "chr12:80876221:T>C" "PTPRQ" "NM_001145026:c.1187-1991T>C" "INTRON5" "Unknown significance" "rs572014613" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 2 978 0.002 3 5008 0.000599042
309410 "chr12:80876305:G>A" "PTPRQ" "NM_001145026:c.1187-1907G>A" "INTRON5" "Unknown significance" "rs538965388" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309411 "chr12:80876327:T>G" "PTPRQ" "NM_001145026:c.1187-1885T>G" "INTRON5" "Unknown significance" "rs557693327" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309412 "chr12:80876390:G>T" "PTPRQ" "NM_001145026:c.1187-1822G>T" "INTRON5" "Benign" "rs75533578" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1154 1322 0.8729 916 1006 0.9105 578 694 0.8329 375 1008 0.372 832 978 0.8507 3855 5008 0.769768
309413 "chr12:80876490:C>T" "PTPRQ" "NM_001145026:c.1187-1722C>T" "INTRON5" "Unknown significance" "rs762227079" "This variant is a VUS because it does not have enough information."
309414 "chr12:80876491:G>A" "PTPRQ" "NM_001145026:c.1187-1721G>A" "INTRON5" "Unknown significance" "rs370005606" "This variant is a VUS because it does not have enough information."
309415 "chr12:80876557:C>G" "PTPRQ" "NM_001145026:c.1187-1655C>G" "INTRON5" "Unknown significance" "rs61950952" "This variant is a VUS because it does not have enough information."
309416 "chr12:80876561:T>C" "PTPRQ" "NM_001145026:c.1187-1651T>C" "INTRON5" "Unknown significance" "rs61950953" "This variant is a VUS because it does not have enough information."
309417 "chr12:80876571:C>T" "PTPRQ" "NM_001145026:c.1187-1641C>T" "INTRON5" "Unknown significance" "rs61950954" "This variant is a VUS because it does not have enough information."
309418 "chr12:80876673:G>A" "PTPRQ" "NM_001145026:c.1187-1539G>A" "INTRON5" "Unknown significance" "rs373370439" "This variant is a VUS because it does not have enough information."
309419 "chr12:80876868:T>C" "PTPRQ" "NM_001145026:c.1187-1344T>C" "INTRON5" "Unknown significance" "rs113862228" "This variant is a VUS because it does not have enough information."
309420 "chr12:80876873:C>T" "PTPRQ" "NM_001145026:c.1187-1339C>T" "INTRON5" "Unknown significance" "rs772585561" "This variant is a VUS because it does not have enough information."
309421 "chr12:80876903:T>C" "PTPRQ" "NM_001145026:c.1187-1309T>C" "INTRON5" "Unknown significance" "rs376510551" "This variant is a VUS because it does not have enough information."
309422 "chr12:80877024:A>G" "PTPRQ" "NM_001145026:c.1187-1188A>G" "INTRON5" "Benign" "rs533855700" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489
309423 "chr12:80877030:T>G" "PTPRQ" "NM_001145026:c.1187-1182T>G" "INTRON5" "Benign" "rs61950955" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 689 1006 0.6849 416 694 0.5994 365 1008 0.3621 672 978 0.6871 2223 5008 0.44389
309424 "chr12:80877090:A>G" "PTPRQ" "NM_001145026:c.1187-1122A>G" "INTRON5" "Benign" "rs373729300" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 151 1322 0.1142 155 1006 0.1541 75 694 0.1081 0 1008 0 69 978 0.0706 450 5008 0.0898562
309425 "chr12:80877127:G>A" "PTPRQ" "NM_001145026:c.1187-1085G>A" "INTRON5" "Unknown significance" "rs544049331" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309426 "chr12:80877129:G>T" "PTPRQ" "NM_001145026:c.1187-1083G>T" "INTRON5" "Unknown significance" "rs555944520" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309427 "chr12:80877159:G>T" "PTPRQ" "NM_001145026:c.1187-1053G>T" "INTRON5" "Unknown significance" "rs549002112" "This variant is a VUS because it does not have enough information."
309428 "chr12:80877166:G>C" "PTPRQ" "NM_001145026:c.1187-1046G>C" "INTRON5" "Unknown significance" "rs377096799" "This variant is a VUS because it does not have enough information."
309429 "chr12:80877255:T>C" "PTPRQ" "NM_001145026:c.1187-957T>C" "INTRON5" "Unknown significance" "rs577476131" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309430 "chr12:80877265:C>A" "PTPRQ" "NM_001145026:c.1187-947C>A" "INTRON5" "Unknown significance" "rs544993135" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309431 "chr12:80877271:A>T" "PTPRQ" "NM_001145026:c.1187-941A>T" "INTRON5" "Benign" "rs560513625" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 18 1322 0.0136 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 20 5008 0.00399361
309432 "chr12:80877274:G>A" "PTPRQ" "NM_001145026:c.1187-938G>A" "INTRON5" "Unknown significance" "rs527715872" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309433 "chr12:80877281:T>G" "PTPRQ" "NM_001145026:c.1187-931T>G" "INTRON5" "Unknown significance" "rs112976021" "This variant is a VUS because it does not have enough information."
309434 "chr12:80877286:C>T" "PTPRQ" "NM_001145026:c.1187-926C>T" "INTRON5" "Unknown significance" "rs543089633" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309435 "chr12:80877304:A>T" "PTPRQ" "NM_001145026:c.1187-908A>T" "INTRON5" "Unknown significance" "rs561405165" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309436 "chr12:80877314:A>G" "PTPRQ" "NM_001145026:c.1187-898A>G" "INTRON5" "Benign" "rs12824443" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 673 1006 0.669 404 694 0.5821 365 1008 0.3621 669 978 0.684 2192 5008 0.4377
309437 "chr12:80877320:AAG>-" "PTPRQ" "NM_001145026:c.1187-892_1187-890delAAG" "INTRON5" "Benign" "rs555792198" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 21 1322 0.0159 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 23 5008 0.00459265
309438 "chr12:80877351:A>G" "PTPRQ" "NM_001145026:c.1187-861A>G" "INTRON5" "Benign" "rs143209309" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309439 "chr12:80877358:T>C" "PTPRQ" "NM_001145026:c.1187-854T>C" "INTRON5" "Unknown significance" "rs193234649" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
309440 "chr12:80877375:T>A" "PTPRQ" "NM_001145026:c.1187-837T>A" "INTRON5" "Benign" "rs532805292" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 7 978 0.0072 7 5008 0.00139776
309441 "chr12:80877411:C>T" "PTPRQ" "NM_001145026:c.1187-801C>T" "INTRON5" "Benign" "rs146664218" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 297 1322 0.2247 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 420 5008 0.0838658
309442 "chr12:80877417:G>A" "PTPRQ" "NM_001145026:c.1187-795G>A" "INTRON5" "Benign" "rs117369027" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 24 1006 0.0239 6 694 0.0086 9 1008 0.0089 49 978 0.0501 122 5008 0.024361
309443 "chr12:80877434:T>C" "PTPRQ" "NM_001145026:c.1187-778T>C" "INTRON5" "Unknown significance" "rs533592833" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309444 "chr12:80877449:G>T" "PTPRQ" "NM_001145026:c.1187-763G>T" "INTRON5" "Unknown significance" "rs777257621" "This variant is a VUS because it does not have enough information."
309445 "chr12:80877454:A>G" "PTPRQ" "NM_001145026:c.1187-758A>G" "INTRON5" "Benign" "rs4565968" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 834 1322 0.6309 247 1006 0.2455 177 694 0.255 52 1008 0.0516 179 978 0.183 1489 5008 0.297324
309446 "chr12:80877471:G>A" "PTPRQ" "NM_001145026:c.1187-741G>A" "INTRON5" "Unknown significance" "rs185699317" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
309447 "chr12:80877473:CATCTACATTAGGTA>-" "PTPRQ" "NM_001145026:c.1187-739_1187-725delCATCTACATTAGGTA" "INTRON5" "Benign" "rs11272985" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 297 1322 0.2247 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 420 5008 0.0838658
309448 "chr12:80877505:C>T" "PTPRQ" "NM_001145026:c.1187-707C>T" "INTRON5" "Unknown significance" "rs547082830" "This variant is a VUS because it does not have enough information."
309449 "chr12:80877517:C>A" "PTPRQ" "NM_001145026:c.1187-695C>A" "INTRON5" "Unknown significance" "rs537558854" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309450 "chr12:80877519:C>A" "PTPRQ" "NM_001145026:c.1187-693C>A" "INTRON5" "Benign" "rs141457282" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 85 5008 0.0169728
309451 "chr12:80877528:G>A" "PTPRQ" "NM_001145026:c.1187-684G>A" "INTRON5" "Unknown significance" "rs202234424" "This variant is a VUS because it does not have enough information."
309452 "chr12:80877529:A>T" "PTPRQ" "NM_001145026:c.1187-683A>T" "INTRON5" "Unknown significance" "rs577439220" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309453 "chr12:80877537:C>T" "PTPRQ" "NM_001145026:c.1187-675C>T" "INTRON5" "Unknown significance" "rs189427339" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
309454 "chr12:80877538:G>A" "PTPRQ" "NM_001145026:c.1187-674G>A" "INTRON5" "Benign" "rs145154886" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 52 1322 0.0393 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 54 5008 0.0107827
309455 "chr12:80877579:G>A" "PTPRQ" "NM_001145026:c.1187-633G>A" "INTRON5" "Benign" "rs145848246" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309456 "chr12:80877588:C>T" "PTPRQ" "NM_001145026:c.1187-624C>T" "INTRON5" "Benign" "rs148986942" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
309457 "chr12:80877596:G>A" "PTPRQ" "NM_001145026:c.1187-616G>A" "INTRON5" "Unknown significance" "rs561268826" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309458 "chr12:80877611:G>A" "PTPRQ" "NM_001145026:c.1187-601G>A" "INTRON5" "Benign" "rs143740260" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309459 "chr12:80877612:C>T" "PTPRQ" "NM_001145026:c.1187-600C>T" "INTRON5" "Benign" "rs4564397" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1059 1322 0.8011 920 1006 0.9145 593 694 0.8545 418 1008 0.4147 848 978 0.8671 3838 5008 0.766374
309460 "chr12:80877613:G>A" "PTPRQ" "NM_001145026:c.1187-599G>A" "INTRON5" "Benign" "rs565675610" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 5 978 0.0051 5 5008 0.000998403
309461 "chr12:80877618:G>T" "PTPRQ" "NM_001145026:c.1187-594G>T" "INTRON5" "Benign" "rs143909976" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 51 1006 0.0507 24 694 0.0346 9 1008 0.0089 58 978 0.0593 178 5008 0.0355431
309462 "chr12:80877644:G>A" "PTPRQ" "NM_001145026:c.1187-568G>A" "INTRON5" "Benign" "rs6539520" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 304 1322 0.23 8 1006 0.008 50 694 0.072 212 1008 0.2103 50 978 0.0511 624 5008 0.124601
309463 "chr12:80877671:T>C" "PTPRQ" "NM_001145026:c.1187-541T>C" "INTRON5" "Unknown significance" "rs113166740" "This variant is a VUS because it does not have enough information."
309464 "chr12:80877692:C>T" "PTPRQ" "NM_001145026:c.1187-520C>T" "INTRON5" "Unknown significance" "rs753827977" "This variant is a VUS because it does not have enough information."
309465 "chr12:80877704:T>A" "PTPRQ" "NM_001145026:c.1187-508T>A" "INTRON5" "Benign" "rs139018049" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309466 "chr12:80877705:T>A" "PTPRQ" "NM_001145026:c.1187-507T>A" "INTRON5" "Unknown significance" "rs192515493" "This variant is a VUS because it does not have enough information."
309467 "chr12:80877720:T>A" "PTPRQ" "NM_001145026:c.1187-492T>A" "INTRON5" "Unknown significance" "rs530426143" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309468 "chr12:80877726:C>G" "PTPRQ" "NM_001145026:c.1187-486C>G" "INTRON5" "Benign" "rs183635596" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 17 1322 0.0129 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 19 5008 0.00379393
309469 "chr12:80877733:A>C" "PTPRQ" "NM_001145026:c.1187-479A>C" "INTRON5" "Unknown significance" "rs566941431" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309470 "chr12:80877767:->TTTG" "PTPRQ" "NM_001145026:c.1187-445_1187-444insTTTG" "INTRON5" "Benign" "rs367970347" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 578 1322 0.4372 781 1006 0.7763 493 694 0.7104 362 1008 0.3591 643 978 0.6575 2857 5008 0.570487
309471 "chr12:80877767:TTTG>-" "PTPRQ" "NM_001145026:c.1187-445_1187-442delTTTG" "INTRON5" "Unknown significance" "rs143340032" "This variant is a VUS because it does not have enough information."
309472 "chr12:80877768:->TTTG" "PTPRQ" "NM_001145026:c.1187-444_1187-443insTTTG" "INTRON5" "Unknown significance" "rs72150554" "This variant is a VUS because it does not have enough information."
309473 "chr12:80877775:->GTTT" "PTPRQ" "NM_001145026:c.1187-437_1187-436insGTTT" "INTRON5" "Unknown significance" "rs386377127" "This variant is a VUS because it does not have enough information."
309474 "chr12:80877815:T>C" "PTPRQ" "NM_001145026:c.1187-397T>C" "INTRON5" "Benign" "rs5029106" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 800 1322 0.6051 223 1006 0.2217 171 694 0.2464 43 1008 0.0427 130 978 0.1329 1367 5008 0.272963
309475 "chr12:80877823:C>T" "PTPRQ" "NM_001145026:c.1187-389C>T" "INTRON5" "Unknown significance" "rs760475929" "This variant is a VUS because it does not have enough information."
309476 "chr12:80877847:C>T" "PTPRQ" "NM_001145026:c.1187-365C>T" "INTRON5" "Benign" "rs12578568" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 297 1322 0.2247 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 420 5008 0.0838658
309477 "chr12:80877869:C>T" "PTPRQ" "NM_001145026:c.1187-343C>T" "INTRON5" "Benign" "rs80255587" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 26 1322 0.0197 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 28 5008 0.00559105
309478 "chr12:80877870:C>T" "PTPRQ" "NM_001145026:c.1187-342C>T" "INTRON5" "Unknown significance" "rs538494804" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309479 "chr12:80877872:C>T" "PTPRQ" "NM_001145026:c.1187-340C>T" "INTRON5" "Unknown significance" "rs554029145" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309480 "chr12:80877878:G>A" "PTPRQ" "NM_001145026:c.1187-334G>A" "INTRON5" "Unknown significance" "rs188389571" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 0 978 0 0 5008 0
309481 "chr12:80877898:C>T" "PTPRQ" "NM_001145026:c.1187-314C>T" "INTRON5" "Unknown significance" "rs111385519" "This variant is a VUS because it does not have enough information."
309482 "chr12:80877925:C>T" "PTPRQ" "NM_001145026:c.1187-287C>T" "INTRON5" "Unknown significance" "rs752982901" "This variant is a VUS because it does not have enough information."
309483 "chr12:80877932:G>A" "PTPRQ" "NM_001145026:c.1187-280G>A" "INTRON5" "Unknown significance" "rs758376368" "This variant is a VUS because it does not have enough information."
309484 "chr12:80877950:T>A" "PTPRQ" "NM_001145026:c.1187-262T>A" "INTRON5" "Benign" "rs7311165" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 304 1322 0.23 6 1006 0.006 46 694 0.0663 43 1008 0.0427 25 978 0.0256 424 5008 0.0846645
309485 "chr12:80877967:G>A" "PTPRQ" "NM_001145026:c.1187-245G>A" "INTRON5" "Benign" "rs111712174" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 76 1322 0.0575 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 81 5008 0.0161741
309486 "chr12:80877988:G>A" "PTPRQ" "NM_001145026:c.1187-224G>A" "INTRON5" "Unknown significance" "rs144028198" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
309487 "chr12:80877988:G>T" "PTPRQ" "NM_001145026:c.1187-224G>T" "INTRON5" "Unknown significance" "rs144028198" "This variant is a VUS because it does not have enough information."
309488 "chr12:80878001:G>A" "PTPRQ" "NM_001145026:c.1187-211G>A" "INTRON5" "Unknown significance" "rs543912453" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309489 "chr12:80878019:C>T" "PTPRQ" "NM_001145026:c.1187-193C>T" "INTRON5" "Unknown significance" "rs757716555" "This variant is a VUS because it does not have enough information."
309490 "chr12:80878021:G>A" "PTPRQ" "NM_001145026:c.1187-191G>A" "INTRON5" "Unknown significance" "rs565412323" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309491 "chr12:80878038:G>T" "PTPRQ" "NM_001145026:c.1187-174G>T" "INTRON5" "Unknown significance" "rs577366360" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309492 "chr12:80878054:G>A" "PTPRQ" "NM_001145026:c.1187-158G>A" "INTRON5" "Benign" "rs139890327" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 96 1322 0.0726 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 101 5008 0.0201677
309493 "chr12:80878079:C>A" "PTPRQ" "NM_001145026:c.1187-133C>A" "INTRON5" "Unknown significance" "rs559908047" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
309494 "chr12:80878090:C>T" "PTPRQ" "NM_001145026:c.1187-122C>T" "INTRON5" "Unknown significance" "rs530297354" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309495 "chr12:80878099:A>G" "PTPRQ" "NM_001145026:c.1187-113A>G" "INTRON5" "Unknown significance" "rs181249926" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
309496 "chr12:80878143:G>A" "PTPRQ" "NM_001145026:c.1187-69G>A" "INTRON5" "Benign" "rs10862139" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 231 1322 0.1747 6 1006 0.006 44 694 0.0634 43 1008 0.0427 25 978 0.0256 349 5008 0.0696885
309497 "chr12:80878154:A>G" "PTPRQ" "NM_001145026:c.1187-58A>G" "INTRON5" "Unknown significance" "rs756616535" "This variant is a VUS because it does not have enough information."
309498 "chr12:80878169:T>C" "PTPRQ" "NM_001145026:c.1187-43T>C" "INTRON5" "Unknown significance" "rs531243671" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 514 0 0 66 0 0 278 0 0 0 0 0 1042 0 0 40 0 1 1630 0.000613497 1 3570 0.000280112
309499 "chr12:80878174:T>A" "PTPRQ" "NM_001145026:c.1187-38T>A" "INTRON5" "Benign" "rs7311413" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1059 1322 0.8011 920 1006 0.9145 593 694 0.8545 417 1008 0.4137 848 978 0.8671 3837 5008 0.766174 1327 1616 0.821163 265 298 0.889262 204 408 0.5 4 4 1 6891 7450 0.924966 155 176 0.880682 6918 7816 0.885107 15764 17768 0.887213
309500 "chr12:80878176:T>A" "PTPRQ" "NM_001145026:c.1187-36T>A" "INTRON5" "Unknown significance" "rs758243377" "This variant is a VUS because it does not have enough information."
309501 "chr12:80878181:C>T" "PTPRQ" "NM_001145026:c.1187-31C>T" "INTRON5" "Benign" "rs200831779" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 2 694 0.0029 2 1008 0.002 0 978 0 11 5008 0.00219649
309502 "chr12:80878182:->T" "PTPRQ" "NM_001145026:c.1187-30_1187-29insT" "INTRON5" "Benign" "rs56351124" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1047 1322 0.792 919 1006 0.9135 590 694 0.8501 416 1008 0.4127 847 978 0.8661 3819 5008 0.76258 1416 1724 0.821346 275 310 0.887097 210 424 0.495283 7 8 0.875 7149 7734 0.92436 160 184 0.869565 6893 7824 0.881007 16110 18208 0.884776
309503 "chr12:80878183:->TTTTC" "PTPRQ" "NM_001145026:c.1187-29_1187-28insTTTTC" "INTRON5" "Unknown significance" "rs546357099" "This variant is a VUS because it does not have enough information."
309504 "chr12:80878186:C>T" "PTPRQ" "NM_001145026:c.1187-26C>T" "INTRON5" "Unknown significance" "rs201715211" "This variant is a VUS because it does not have enough information."
309505 "chr12:80878186:CT>TCTTTTC" "PTPRQ" "Unknown significance" "rs796191517" "This variant is a VUS because it does not have enough information."
309506 "chr12:80878188:->TTTC" "PTPRQ" "NM_001145026:c.1187-24_1187-23insTTTC" "INTRON5" "Benign" "rs562555844" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 365 1322 0.2761 6 1006 0.006 49 694 0.0706 43 1008 0.0427 23 978 0.0235 486 5008 0.0970447
309507 "chr12:80878188:->TTTCTTTC" "PTPRQ" "NM_001145026:c.1187-24_1187-23insTTTCTTTC" "INTRON5" "Unknown significance" "rs562555844" "This variant is a VUS because it does not have enough information."
309508 "chr12:80878188:->TTTCTTTCTTTC" "PTPRQ" "NM_001145026:c.1187-24_1187-23insTTTCTTTCTTTC" "INTRON5" "Unknown significance" "rs562555844" "This variant is a VUS because it does not have enough information."
309509 "chr12:80878193:T>G" "PTPRQ" "NM_001145026:c.1187-19T>G" "INTRON5" "Unknown significance" "rs779634861" "This variant is a VUS because it does not have enough information." 0 1888 0 0 324 0 0 440 0 0 10 0 2 7932 0.000252143 0 188 0 0 7864 0 2 18646 0.000107262
309510 "chr12:80878201:T>C" "PTPRQ" "NM_001145026:c.1187-11T>C" "INTRON5" "Unknown significance" "rs749371481" "This variant is a VUS because it does not have enough information."
309511 "chr12:80878218:G>C" "PTPRQ" "NM_001145026:p.Gly398Ala" "NM_001145026:c.1193G>C" "EXON6" "Unknown significance" "rs746459141" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.033" "B" 0.960669 "D" "5.87" "C" 0 1964 0 0 338 0 0 486 0 0 14 0 0 8184 0 0 190 0 2 7874 0.000254001 2 19050 0.000104987
309512 "chr12:80878257:C>T" "PTPRQ" "NM_001145026:p.Thr411Met" "NM_001145026:c.1232C>T" "EXON6" "Unknown significance" "rs768302254" "This variant is a VUS because it does not have enough information." 0.935 "N" "1.0" "D" 0.992624 "D" "5.17" "C" 0 2104 0 0 392 0 0 570 0 0 28 0 1 8406 0.000118963 0 190 0 1 7904 0.000126518 2 19594 0.000102072
309513 "chr12:80878258:G>A" "PTPRQ" "NM_001145026:p.Thr411Thr" "NM_001145026:c.1233G>A" "EXON6" "Benign" "rs185755490" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 12 3182 0.00377121 0 1384 0 12 4566 0.00262812 3 400 0.0075 0 320 0 2 320 0.00625 0 400 0 3 360 0.00833333 2 200 0.01 10 2000 0.005 0 1322 0 10 1006 0.0099 2 694 0.0029 0 1008 0 2 978 0.002 14 5008 0.00279553 0 2104 0 0 392 0 1 570 0.00175439 1 30 0.0333333 40 8406 0.00475851 1 190 0.00526316 14 7904 0.00177126 57 19596 0.00290876
309514 "chr12:80878268:A>G" "PTPRQ" "NM_001145026:p.Ile415Val" "NM_001145026:c.1243A>G" "EXON6" "Unknown significance" "rs747783884" "This variant is a VUS because it does not have enough information." 0.237 "N" "0.0" "B" 0.994464 "N" "3.67" "C" 0 2116 0 0 398 0 0 590 0 0 30 0 1 8430 0.000118624 0 190 0 0 7904 0 1 19658 0.0000508699
309515 "chr12:80878271:->A" "PTPRQ" "NM_001145026:c.1246_1247insA" "EXON6" "Unknown significance" "rs778061943" "This variant is a VUS because it does not have enough information." 0 2122 0 0 398 0 0 590 0 0 30 0 1 8432 0.000118596 0 190 0 0 7904 0 1 19666 0.0000508492
309516 "chr12:80878272:C>A" "PTPRQ" "NM_001145026:p.Thr416Asn" "NM_001145026:c.1247C>A" "EXON6" "Unknown significance" "rs372238123" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.033" "B" 0.994009 "N" "6.06" "C" 1 3182 0.000314268 0 1384 0 1 4566 0.00021901 0 2124 0 0 398 0 0 590 0 0 30 0 1 8432 0.000118596 0 190 0 0 7904 0 1 19668 0.000050844
309517 "chr12:80878273:T>C" "PTPRQ" "NM_001145026:p.Thr416Thr" "NM_001145026:c.1248T>C" "EXON6" "Unknown significance" "rs773429164" "This variant is a VUS because it does not have enough information." 0 2128 0 0 398 0 0 590 0 0 30 0 1 8434 0.000118568 0 190 0 0 7904 0 1 19674 0.0000508285
309518 "chr12:80878276:G>A" "PTPRQ" "NM_001145026:p.Trp417Stop" "NM_001145026:c.1251G>A" "EXON6" "Unknown significance" "03/15/2017 -- Manually curated by the MORL." 1.048 "C" 1 "A" "6.06" "C"
309519 "chr12:80878279:G>A" "PTPRQ" "NM_001145026:p.Lys418Lys" "NM_001145026:c.1254G>A" "EXON6" "Unknown significance" "rs190098322" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 0 2132 0 0 398 0 0 596 0 0 32 0 1 8450 0.000118343 0 190 0 0 7906 0 1 19704 0.0000507511
309520 "chr12:80878290:A>G" "PTPRQ" "NM_001145026:p.Gln422Arg" "NM_001145026:c.1265A>G" "EXON6" "Unknown significance" "rs766757071" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.999" "D" 0.994074 "D" "6.06" "C" 0 2138 0 0 402 0 0 604 0 0 32 0 0 8466 0 0 190 0 9 7906 0.00113838 9 19738 0.000455973
309521 "chr12:80878299:G>A" "PTPRQ" "NM_001145026:p.Gly425Glu" "NM_001145026:c.1274G>A" "EXON6" "Unknown significance" "rs577783320" "This variant is a VUS because it does not have enough information." 1.048 "C" "1.0" "D" 0.999945 "D" "6.06" "C"
309522 "chr12:80878310:C>G" "PTPRQ" "NM_001145026:p.Gln429Glu" "NM_001145026:c.1285C>G" "EXON6" "Benign" "rs61729287" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.935 "N" "0.934" "P" 0.848855 "D" "6.06" "C" 89 3182 0.0279698 8 1384 0.00578035 97 4566 0.021244 7 400 0.0175 3 320 0.009375 9 320 0.028125 0 400 0 9 360 0.025 2 200 0.01 30 2000 0.015 0 1322 0 25 1006 0.0249 9 694 0.013 0 1008 0 14 978 0.0143 48 5008 0.00958466 7 2144 0.00326493 9 408 0.0220588 0 616 0 2 32 0.0625 160 8476 0.0188768 3 190 0.0157895 204 7912 0.0257836 385 19778 0.0194661
309523 "chr12:80878317:G>A" "PTPRQ" "NM_001145026:p.Arg431Gln" "NM_001145026:c.1292G>A" "EXON6" "Benign" "rs57971665" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1.048 "C" "1.0" "D" 0.00793348 "P" "6.06" "C" 3 3182 0.000942803 278 1384 0.200867 281 4566 0.0615418 0 400 0 33 320 0.103125 4 320 0.0125 32 400 0.08 1 360 0.00277778 0 200 0 70 2000 0.035 340 1322 0.2572 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 463 5008 0.0924521 473 2144 0.220616 28 408 0.0686275 24 618 0.038835 1 34 0.0294118 7 8472 0.000826251 5 190 0.0263158 145 7912 0.0183266 683 19778 0.0345333
309524 "chr12:80878327:G>A" "PTPRQ" "NM_001145026:p.Val434Val" "NM_001145026:c.1302G>A" "EXON6" "Unknown significance" "rs767695379" "This variant is a VUS because it does not have enough information." 0 2140 0 0 406 0 0 616 0 0 34 0 3 8472 0.000354108 0 190 0 0 7910 0 3 19768 0.00015176
309525 "chr12:80878363:T>G" "PTPRQ" "NM_001145026:p.Thr446Thr" "NM_001145026:c.1338T>G" "EXON6" "Unknown significance" "rs753038688" "This variant is a VUS because it does not have enough information."
309526 "chr12:80878366:G>C" "PTPRQ" "NM_001145026:p.Leu447Phe" "NM_001145026:c.1341G>C" "EXON6" "Benign" "rs773869003" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1.048 "C" "0.948" "P" 0.881501 "N" "5.13" "C" 2 400 0.005 0 320 0 1 320 0.003125 0 400 0 0 360 0 0 200 0 3 2000 0.0015 0 2076 0 0 384 0 0 608 0 0 34 0 23 8318 0.00276509 0 190 0 0 7890 0 23 19500 0.00117949
309527 "chr12:80878371:C>T" "PTPRQ" "NM_001145026:p.Thr449Ile" "NM_001145026:c.1346C>T" "EXON6" "Unknown significance" "rs747612931" "This variant is a VUS because it does not have enough information." -0.326 "N" "0.0" "B" 0.999676 "N" "1.21" "C"
309528 "chr12:80878386:T>C" "PTPRQ" "NM_001145026:c.1359+2T>C" "INTRON6" "Pathogenic" "Non-syndromic deafness, autosomal recessive, DFNB84A" "26969326" "rs377572771" 1.061 "C" 1 "D" "6.06" "C" 0 3182 0 1 1384 0.000722543 1 4566 0.00021901 1 2006 0.000498504 0 370 0 0 586 0 0 32 0 0 8170 0 0 188 0 0 7870 0 1 19222 0.0000520237
309529 "chr12:80878393:->T" "PTPRQ" "NM_001145026:c.1359+9_1359+10insT" "INTRON6" "Unknown significance" "rs768790872" "This variant is a VUS because it does not have enough information."
309530 "chr12:80878403:A>T" "PTPRQ" "NM_001145026:c.1359+19A>T" "INTRON6" "Unknown significance" "rs554930585" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309531 "chr12:80878405:T>G" "PTPRQ" "NM_001145026:c.1359+21T>G" "INTRON6" "Unknown significance" "rs534550525" "This variant is a VUS because it does not have enough information."
309532 "chr12:80878407:A>G" "PTPRQ" "NM_001145026:c.1359+23A>G" "INTRON6" "Unknown significance" "rs750132916" "This variant is a VUS because it does not have enough information." 0 1972 0 0 364 0 0 568 0 0 32 0 0 8034 0 0 188 0 1 7848 0.000127421 1 19006 0.000052615
309533 "chr12:80878413:G>A" "PTPRQ" "NM_001145026:c.1359+29G>A" "INTRON6" "Unknown significance" "rs576490030" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 1958 0 0 358 0 0 564 0 0 32 0 0 8014 0 0 188 0 25 7830 0.00319285 25 18944 0.00131968
309534 "chr12:80878418:C>T" "PTPRQ" "NM_001145026:c.1359+34C>T" "INTRON6" "Unknown significance" "rs779784942" "This variant is a VUS because it does not have enough information." 0 1952 0 0 350 0 0 562 0 0 32 0 0 7962 0 0 188 0 1 7826 0.000127779 1 18872 0.0000529886
309535 "chr12:80878422:C>G" "PTPRQ" "NM_001145026:c.1359+38C>G" "INTRON6" "Unknown significance" "rs771983585" "This variant is a VUS because it does not have enough information." 0 1916 0 1 334 0.00299401 0 562 0 0 32 0 0 7888 0 0 188 0 0 7810 0 1 18730 0.0000533903
309536 "chr12:80878422:C>T" "PTPRQ" "NM_001145026:c.1359+38C>T" "INTRON6" "Unknown significance" "rs771983585" "This variant is a VUS because it does not have enough information." 0 1916 0 0 334 0 0 562 0 0 32 0 1 7888 0.000126775 0 188 0 0 7810 0 1 18730 0.0000533903
309537 "chr12:80878497:C>A" "PTPRQ" "NM_001145026:c.1359+113C>A" "INTRON6" "Unknown significance" "rs537482636" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309538 "chr12:80878507:T>C" "PTPRQ" "NM_001145026:c.1359+123T>C" "INTRON6" "Unknown significance" "rs773190810" "This variant is a VUS because it does not have enough information."
309539 "chr12:80878509:A>C" "PTPRQ" "NM_001145026:c.1359+125A>C" "INTRON6" "Unknown significance" "rs770157919" "This variant is a VUS because it does not have enough information."
309540 "chr12:80878521:G>A" "PTPRQ" "NM_001145026:c.1359+137G>A" "INTRON6" "Unknown significance" "rs558914781" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309541 "chr12:80878530:C>T" "PTPRQ" "NM_001145026:c.1359+146C>T" "INTRON6" "Unknown significance" "rs182319420" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309542 "chr12:80878568:A>G" "PTPRQ" "NM_001145026:c.1359+184A>G" "INTRON6" "Unknown significance" "rs376694776" "This variant is a VUS because it does not have enough information."
309543 "chr12:80878617:A>T" "PTPRQ" "NM_001145026:c.1359+233A>T" "INTRON6" "Benign" "rs187379441" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 16 1322 0.0121 0 1006 0 0 694 0 0 1008 0 0 978 0 16 5008 0.00319489
309544 "chr12:80878618:A>C" "PTPRQ" "NM_001145026:c.1359+234A>C" "INTRON6" "Unknown significance" "rs559661800" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309545 "chr12:80878652:T>G" "PTPRQ" "NM_001145026:c.1359+268T>G" "INTRON6" "Unknown significance" "rs575003251" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309546 "chr12:80878667:T>G" "PTPRQ" "NM_001145026:c.1359+283T>G" "INTRON6" "Benign" "rs60419022" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
309547 "chr12:80878675:T>C" "PTPRQ" "NM_001145026:c.1359+291T>C" "INTRON6" "Unknown significance" "rs760457605" "This variant is a VUS because it does not have enough information."
309548 "chr12:80878685:G>A" "PTPRQ" "NM_001145026:c.1359+301G>A" "INTRON6" "Unknown significance" "rs766200295" "This variant is a VUS because it does not have enough information."
309549 "chr12:80878726:G>A" "PTPRQ" "NM_001145026:c.1359+342G>A" "INTRON6" "Unknown significance" "rs775665805" "This variant is a VUS because it does not have enough information."
309550 "chr12:80878736:T>G" "PTPRQ" "NM_001145026:c.1359+352T>G" "INTRON6" "Unknown significance" "rs563676789" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309551 "chr12:80878776:T>G" "PTPRQ" "NM_001145026:c.1359+392T>G" "INTRON6" "Unknown significance" "rs531207349" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309552 "chr12:80878805:G>A" "PTPRQ" "NM_001145026:c.1359+421G>A" "INTRON6" "Unknown significance" "rs573085467" "This variant is a VUS because it does not have enough information."
309553 "chr12:80878837:T>C" "PTPRQ" "NM_001145026:c.1359+453T>C" "INTRON6" "Unknown significance" "rs549322315" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309554 "chr12:80878839:T>-" "PTPRQ" "NM_001145026:c.1359+455delT" "INTRON6" "Unknown significance" "rs553833685" "This variant is a VUS because it does not have enough information."
309555 "chr12:80878839:T>C" "PTPRQ" "NM_001145026:c.1359+455T>C" "INTRON6" "Unknown significance" "rs79792821" "This variant is a VUS because it does not have enough information."
309556 "chr12:80878862:G>T" "PTPRQ" "NM_001145026:c.1359+478G>T" "INTRON6" "Unknown significance" "rs763196329" "This variant is a VUS because it does not have enough information."
309557 "chr12:80878864:T>C" "PTPRQ" "NM_001145026:c.1359+480T>C" "INTRON6" "Unknown significance" "rs375024238" "This variant is a VUS because it does not have enough information."
309558 "chr12:80878900:C>T" "PTPRQ" "NM_001145026:c.1359+516C>T" "INTRON6" "Benign" "rs61950956" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 51 1006 0.0507 24 694 0.0346 9 1008 0.0089 58 978 0.0593 178 5008 0.0355431
309559 "chr12:80878901:G>A" "PTPRQ" "NM_001145026:c.1359+517G>A" "INTRON6" "Unknown significance" "rs532077544" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309560 "chr12:80878942:A>C" "PTPRQ" "NM_001145026:c.1359+558A>C" "INTRON6" "Benign" "rs139111378" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 16 1006 0.0159 9 694 0.013 0 1008 0 3 978 0.0031 28 5008 0.00559105
309561 "chr12:80878943:T>G" "PTPRQ" "NM_001145026:c.1359+559T>G" "INTRON6" "Unknown significance" "rs562447519" "This variant is a VUS because it does not have enough information."
309562 "chr12:80878956:A>G" "PTPRQ" "NM_001145026:c.1359+572A>G" "INTRON6" "Unknown significance" "rs565716745" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 0 978 0 0 5008 0
309563 "chr12:80878972:TT>-" "PTPRQ" "NM_001145026:c.1359+588_1359+589delTT" "INTRON6" "Unknown significance" "rs748378283" "This variant is a VUS because it does not have enough information."
309564 "chr12:80879033:T>C" "PTPRQ" "NM_001145026:c.1359+649T>C" "INTRON6" "Unknown significance" "rs191010261" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
309565 "chr12:80879040:T>C" "PTPRQ" "NM_001145026:c.1359+656T>C" "INTRON6" "Benign" "rs77325543" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 159 1322 0.1203 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 164 5008 0.0327476
309566 "chr12:80879052:A>T" "PTPRQ" "NM_001145026:c.1359+668A>T" "INTRON6" "Unknown significance" "rs569919150" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309567 "chr12:80879089:G>T" "PTPRQ" "NM_001145026:c.1359+705G>T" "INTRON6" "Unknown significance" "rs537352576" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309568 "chr12:80879119:C>T" "PTPRQ" "NM_001145026:c.1359+735C>T" "INTRON6" "Unknown significance" "rs768137309" "This variant is a VUS because it does not have enough information."
309569 "chr12:80879120:G>A" "PTPRQ" "NM_001145026:c.1359+736G>A" "INTRON6" "Unknown significance" "rs751011581" "This variant is a VUS because it does not have enough information."
309570 "chr12:80879129:A>G" "PTPRQ" "NM_001145026:c.1359+745A>G" "INTRON6" "Unknown significance" "rs558644224" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309571 "chr12:80879138:A>C" "PTPRQ" "NM_001145026:c.1359+754A>C" "INTRON6" "Unknown significance" "rs570844917" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309572 "chr12:80879140:T>A" "PTPRQ" "NM_001145026:c.1359+756T>A" "INTRON6" "Benign" "rs6539521" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 800 1322 0.6051 223 1006 0.2217 172 694 0.2478 43 1008 0.0427 132 978 0.135 1370 5008 0.273562
309573 "chr12:80879168:G>A" "PTPRQ" "NM_001145026:c.1359+784G>A" "INTRON6" "Benign" "rs117139925" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 29 1006 0.0288 17 694 0.0245 2 1008 0.002 37 978 0.0378 87 5008 0.0173722
309574 "chr12:80879179:C>A" "PTPRQ" "NM_001145026:c.1359+795C>A" "INTRON6" "Unknown significance" "rs754183046" "This variant is a VUS because it does not have enough information."
309575 "chr12:80879186:G>C" "PTPRQ" "NM_001145026:c.1359+802G>C" "INTRON6" "Unknown significance" "rs574680693" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309576 "chr12:80879229:TGC>-" "PTPRQ" "NM_001145026:c.1359+845_1359+847delTGC" "INTRON6" "Unknown significance" "rs770671002" "This variant is a VUS because it does not have enough information."
309577 "chr12:80879243:C>T" "PTPRQ" "NM_001145026:c.1359+859C>T" "INTRON6" "Unknown significance" "rs763975592" "This variant is a VUS because it does not have enough information."
309578 "chr12:80879277:T>G" "PTPRQ" "NM_001145026:c.1359+893T>G" "INTRON6" "Unknown significance" "rs754588631" "This variant is a VUS because it does not have enough information."
309579 "chr12:80879348:C>T" "PTPRQ" "NM_001145026:c.1359+964C>T" "INTRON6" "Unknown significance" "rs142495574" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309580 "chr12:80879358:T>C" "PTPRQ" "NM_001145026:c.1359+974T>C" "INTRON6" "Unknown significance" "rs182096481" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309581 "chr12:80879368:C>G" "PTPRQ" "NM_001145026:c.1359+984C>G" "INTRON6" "Unknown significance" "rs753539952" "This variant is a VUS because it does not have enough information."
309582 "chr12:80879389:G>A" "PTPRQ" "NM_001145026:c.1359+1005G>A" "INTRON6" "Unknown significance" "rs778440506" "This variant is a VUS because it does not have enough information."
309583 "chr12:80879436:C>A" "PTPRQ" "NM_001145026:c.1359+1052C>A" "INTRON6" "Unknown significance" "rs185340088" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
309584 "chr12:80879494:C>T" "PTPRQ" "NM_001145026:c.1359+1110C>T" "INTRON6" "Unknown significance" "rs546493953" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309585 "chr12:80879504:G>A" "PTPRQ" "NM_001145026:c.1359+1120G>A" "INTRON6" "Unknown significance" "rs747681206" "This variant is a VUS because it does not have enough information."
309586 "chr12:80879510:G>-" "PTPRQ" "NM_001145026:c.1359+1126delG" "INTRON6" "Unknown significance" "rs373087280" "This variant is a VUS because it does not have enough information."
309587 "chr12:80879510:G>A" "PTPRQ" "NM_001145026:c.1359+1126G>A" "INTRON6" "Unknown significance" "rs771637111" "This variant is a VUS because it does not have enough information."
309588 "chr12:80879517:C>T" "PTPRQ" "NM_001145026:c.1359+1133C>T" "INTRON6" "Unknown significance" "rs564699909" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309589 "chr12:80879580:T>-" "PTPRQ" "NM_001145026:c.1359+1196delT" "INTRON6" "Unknown significance" "rs142464349" "This variant is a VUS because it does not have enough information."
309590 "chr12:80879587:C>A" "PTPRQ" "NM_001145026:c.1359+1203C>A" "INTRON6" "Benign" "rs151327028" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 25 1322 0.0189 0 1006 0 0 694 0 0 1008 0 0 978 0 25 5008 0.00499201
309591 "chr12:80879589:T>A" "PTPRQ" "NM_001145026:c.1359+1205T>A" "INTRON6" "Unknown significance" "rs190097759" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309592 "chr12:80879607:T>G" "PTPRQ" "NM_001145026:c.1359+1223T>G" "INTRON6" "Unknown significance" "rs746996663" "This variant is a VUS because it does not have enough information."
309593 "chr12:80879612:G>-" "PTPRQ" "NM_001145026:c.1359+1228delG" "INTRON6" "Unknown significance" "rs757047295" "This variant is a VUS because it does not have enough information."
309594 "chr12:80879658:G>A" "PTPRQ" "NM_001145026:c.1359+1274G>A" "INTRON6" "Unknown significance" "rs770887216" "This variant is a VUS because it does not have enough information."
309595 "chr12:80879659:C>T" "PTPRQ" "NM_001145026:c.1359+1275C>T" "INTRON6" "Unknown significance" "rs79005877" "This variant is a VUS because it does not have enough information."
309596 "chr12:80879660:->T" "PTPRQ" "NM_001145026:c.1359+1276_1359+1277insT" "INTRON6" "Unknown significance" "rs371659111" "This variant is a VUS because it does not have enough information."
309597 "chr12:80879660:T>C" "PTPRQ" "NM_001145026:c.1359+1276T>C" "INTRON6" "Unknown significance" "rs79990046" "This variant is a VUS because it does not have enough information."
309598 "chr12:80879677:G>A" "PTPRQ" "NM_001145026:c.1359+1293G>A" "INTRON6" "Unknown significance" "rs564586128" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042
309599 "chr12:80879701:G>A" "PTPRQ" "NM_001145026:c.1359+1317G>A" "INTRON6" "Unknown significance" "rs759263293" "This variant is a VUS because it does not have enough information."
309600 "chr12:80879708:A>G" "PTPRQ" "NM_001145026:c.1359+1324A>G" "INTRON6" "Unknown significance" "rs768910539" "This variant is a VUS because it does not have enough information."
309601 "chr12:80879711:A>G" "PTPRQ" "NM_001145026:c.1359+1327A>G" "INTRON6" "Benign" "rs78954977" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 96 1322 0.0726 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 101 5008 0.0201677
309602 "chr12:80879712:G>T" "PTPRQ" "NM_001145026:c.1359+1328G>T" "INTRON6" "Unknown significance" "rs533578519" "This variant is a VUS because it does not have enough information."
309603 "chr12:80879734:C>T" "PTPRQ" "NM_001145026:c.1359+1350C>T" "INTRON6" "Unknown significance" "rs540463921" "This variant is a VUS because it does not have enough information."
309604 "chr12:80879764:G>T" "PTPRQ" "NM_001145026:c.1359+1380G>T" "INTRON6" "Unknown significance" "rs761925692" "This variant is a VUS because it does not have enough information."
309605 "chr12:80879773:T>C" "PTPRQ" "NM_001145026:c.1359+1389T>C" "INTRON6" "Unknown significance" "rs767756796" "This variant is a VUS because it does not have enough information."
309606 "chr12:80879777:C>T" "PTPRQ" "NM_001145026:c.1359+1393C>T" "INTRON6" "Unknown significance" "rs750368962" "This variant is a VUS because it does not have enough information."
309607 "chr12:80879780:T>C" "PTPRQ" "NM_001145026:c.1359+1396T>C" "INTRON6" "Unknown significance" "rs548364546" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309608 "chr12:80879785:C>T" "PTPRQ" "NM_001145026:c.1359+1401C>T" "INTRON6" "Unknown significance" "rs560252115" "This variant is a VUS because it does not have enough information."
309609 "chr12:80879796:G>A" "PTPRQ" "NM_001145026:c.1359+1412G>A" "INTRON6" "Unknown significance" "rs758614180" "This variant is a VUS because it does not have enough information."
309610 "chr12:80879804:A>T" "PTPRQ" "NM_001145026:c.1359+1420A>T" "INTRON6" "Unknown significance" "rs750556715" "This variant is a VUS because it does not have enough information."
309611 "chr12:80879808:G>C" "PTPRQ" "NM_001145026:c.1359+1424G>C" "INTRON6" "Benign" "rs77007035" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 96 1322 0.0726 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 101 5008 0.0201677
309612 "chr12:80879826:G>A" "PTPRQ" "NM_001145026:c.1359+1442G>A" "INTRON6" "Unknown significance" "rs529330082" "This variant is a VUS because it does not have enough information."
309613 "chr12:80879826:G>T" "PTPRQ" "NM_001145026:c.1359+1442G>T" "INTRON6" "Unknown significance" "rs529330082" "This variant is a VUS because it does not have enough information."
309614 "chr12:80879897:A>T" "PTPRQ" "NM_001145026:c.1359+1513A>T" "INTRON6" "Unknown significance" "rs557893758" "This variant is a VUS because it does not have enough information."
309615 "chr12:80879903:A>G" "PTPRQ" "NM_001145026:c.1359+1519A>G" "INTRON6" "Unknown significance" "rs530796212" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309616 "chr12:80879907:T>A" "PTPRQ" "NM_001145026:c.1359+1523T>A" "INTRON6" "Unknown significance" "rs113233082" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309617 "chr12:80879953:T>C" "PTPRQ" "NM_001145026:c.1359+1569T>C" "INTRON6" "Unknown significance" "rs570739468" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309618 "chr12:80879985:T>C" "PTPRQ" "NM_001145026:c.1359+1601T>C" "INTRON6" "Benign" "rs140584275" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309619 "chr12:80880006:T>C" "PTPRQ" "NM_001145026:c.1359+1622T>C" "INTRON6" "Unknown significance" "rs150467754" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309620 "chr12:80880028:T>C" "PTPRQ" "NM_001145026:c.1359+1644T>C" "INTRON6" "Unknown significance" "rs182789950" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309621 "chr12:80880068:A>G" "PTPRQ" "NM_001145026:c.1359+1684A>G" "INTRON6" "Benign" "rs187476772" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776
309622 "chr12:80880085:CT>-" "PTPRQ" "NM_001145026:c.1359+1701_1359+1702delCT" "INTRON6" "Benign" "rs201129116" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309623 "chr12:80880087:C>T" "PTPRQ" "NM_001145026:c.1359+1703C>T" "INTRON6" "Unknown significance" "rs557101257" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309624 "chr12:80880109:T>C" "PTPRQ" "NM_001145026:c.1359+1725T>C" "INTRON6" "Benign" "rs78320617" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 398 1322 0.3011 217 1006 0.2157 118 694 0.17 0 1008 0 105 978 0.1074 838 5008 0.167332
309625 "chr12:80880132:A>T" "PTPRQ" "NM_001145026:c.1359+1748A>T" "INTRON6" "Unknown significance" "rs373249398" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309626 "chr12:80880132:A>C" "PTPRQ" "NM_001145026:c.1359+1748A>C" "INTRON6" "Unknown significance" "rs373249398" "This variant is a VUS because it does not have enough information."
309627 "chr12:80880136:C>T" "PTPRQ" "NM_001145026:c.1359+1752C>T" "INTRON6" "Unknown significance" "rs368154336" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309628 "chr12:80880141:T>A" "PTPRQ" "NM_001145026:c.1359+1757T>A" "INTRON6" "Benign" "rs576754819" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 22 1322 0.0166 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 24 5008 0.00479233
309629 "chr12:80880144:A>G" "PTPRQ" "NM_001145026:c.1359+1760A>G" "INTRON6" "Unknown significance" "rs541068271" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
309630 "chr12:80880196:G>A" "PTPRQ" "NM_001145026:c.1359+1812G>A" "INTRON6" "Unknown significance" "rs377326669" "This variant is a VUS because it does not have enough information."
309631 "chr12:80880261:C>G" "PTPRQ" "NM_001145026:c.1359+1877C>G" "INTRON6" "Benign" "rs73145142" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 398 1322 0.3011 217 1006 0.2157 118 694 0.17 0 1008 0 105 978 0.1074 838 5008 0.167332
309632 "chr12:80880273:G>T" "PTPRQ" "NM_001145026:c.1359+1889G>T" "INTRON6" "Unknown significance" "rs796776311" "This variant is a VUS because it does not have enough information."
309633 "chr12:80880275:C>T" "PTPRQ" "NM_001145026:c.1359+1891C>T" "INTRON6" "Benign" "rs12184469" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 215 1322 0.1626 646 1006 0.6421 398 694 0.5735 360 1008 0.3571 660 978 0.6748 2279 5008 0.455072
309634 "chr12:80880285:C>T" "PTPRQ" "NM_001145026:c.1359+1901C>T" "INTRON6" "Benign" "rs116644931" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309635 "chr12:80880315:C>A" "PTPRQ" "NM_001145026:c.1359+1931C>A" "INTRON6" "Benign" "rs145347616" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 7 1008 0.0069 1 978 0.001 8 5008 0.00159744
309636 "chr12:80880344:A>T" "PTPRQ" "NM_001145026:c.1359+1960A>T" "INTRON6" "Unknown significance" "rs370198357" "This variant is a VUS because it does not have enough information."
309637 "chr12:80880391:C>A" "PTPRQ" "NM_001145026:c.1359+2007C>A" "INTRON6" "Unknown significance" "rs201805819" "This variant is a VUS because it does not have enough information."
309638 "chr12:80880421:T>C" "PTPRQ" "NM_001145026:c.1359+2037T>C" "INTRON6" "Unknown significance" "rs781050110" "This variant is a VUS because it does not have enough information."
309639 "chr12:80880443:T>A" "PTPRQ" "NM_001145026:c.1359+2059T>A" "INTRON6" "Unknown significance" "rs530765149" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
309640 "chr12:80880491:T>C" "PTPRQ" "NM_001145026:c.1359+2107T>C" "INTRON6" "Benign" "rs12369921" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 398 1322 0.3011 217 1006 0.2157 118 694 0.17 1 1008 0.001 105 978 0.1074 839 5008 0.167532
309641 "chr12:80880558:G>T" "PTPRQ" "NM_001145026:c.1359+2174G>T" "INTRON6" "Unknown significance" "rs570769177" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309642 "chr12:80880561:G>C" "PTPRQ" "NM_001145026:c.1359+2177G>C" "INTRON6" "Benign" "rs76403432" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 22 1322 0.0166 0 1006 0 0 694 0 0 1008 0 0 978 0 22 5008 0.00439297
309643 "chr12:80880581:T>A" "PTPRQ" "NM_001145026:c.1359+2197T>A" "INTRON6" "Unknown significance" "rs192988058" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 3 5008 0.000599042
309644 "chr12:80880585:C>T" "PTPRQ" "NM_001145026:c.1359+2201C>T" "INTRON6" "Benign" "rs117322823" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 8 1006 0.008 4 694 0.0058 1 1008 0.001 0 978 0 13 5008 0.00259585
309645 "chr12:80880586:A>G" "PTPRQ" "NM_001145026:c.1359+2202A>G" "INTRON6" "Unknown significance" "rs184047876" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 3 5008 0.000599042
309646 "chr12:80880590:C>G" "PTPRQ" "NM_001145026:c.1359+2206C>G" "INTRON6" "Unknown significance" "rs761895233" "This variant is a VUS because it does not have enough information."
309647 "chr12:80880604:T>A" "PTPRQ" "NM_001145026:c.1359+2220T>A" "INTRON6" "Benign" "rs142466337" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 25 1322 0.0189 0 1006 0 0 694 0 0 1008 0 0 978 0 25 5008 0.00499201
309648 "chr12:80880615:C>T" "PTPRQ" "NM_001145026:c.1359+2231C>T" "INTRON6" "Unknown significance" "rs376582031" "This variant is a VUS because it does not have enough information."
309649 "chr12:80880620:G>T" "PTPRQ" "NM_001145026:c.1359+2236G>T" "INTRON6" "Unknown significance" "rs577775755" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
309650 "chr12:80880657:C>A" "PTPRQ" "NM_001145026:c.1359+2273C>A" "INTRON6" "Benign" "rs115604438" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 72 1322 0.0545 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 75 5008 0.014976
309651 "chr12:80880678:A>G" "PTPRQ" "NM_001145026:c.1359+2294A>G" "INTRON6" "Benign" "rs12369581" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 399 1322 0.3018 217 1006 0.2157 118 694 0.17 0 1008 0 106 978 0.1084 840 5008 0.167732
309652 "chr12:80880754:A>G" "PTPRQ" "NM_001145026:c.1359+2370A>G" "INTRON6" "Unknown significance" "rs760846814" "This variant is a VUS because it does not have enough information."
309653 "chr12:80880772:C>G" "PTPRQ" "NM_001145026:c.1359+2388C>G" "INTRON6" "Benign" "rs146579262" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 8 1006 0.008 7 694 0.0101 0 1008 0 2 978 0.002 18 5008 0.00359425
309654 "chr12:80880791:T>C" "PTPRQ" "NM_001145026:c.1359+2407T>C" "INTRON6" "Unknown significance" "rs567398055" "This variant is a VUS because it does not have enough information."
309655 "chr12:80880796:G>A" "PTPRQ" "NM_001145026:c.1359+2412G>A" "INTRON6" "Benign" "rs12315860" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 340 1322 0.2572 6 1006 0.006 49 694 0.0706 53 1008 0.0526 25 978 0.0256 473 5008 0.0944489
309656 "chr12:80880853:C>T" "PTPRQ" "NM_001145026:c.1359+2469C>T" "INTRON6" "Unknown significance" "rs188595757" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309657 "chr12:80880860:T>G" "PTPRQ" "NM_001145026:c.1359+2476T>G" "INTRON6" "Unknown significance" "rs771588092" "This variant is a VUS because it does not have enough information."
309658 "chr12:80880865:A>G" "PTPRQ" "NM_001145026:c.1359+2481A>G" "INTRON6" "Unknown significance" "rs574511797" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309659 "chr12:80880884:C>G" "PTPRQ" "NM_001145026:c.1359+2500C>G" "INTRON6" "Unknown significance" "rs536376587" "This variant is a VUS because it does not have enough information."
309660 "chr12:80880927:C>T" "PTPRQ" "NM_001145026:c.1359+2543C>T" "INTRON6" "Unknown significance" "rs541929765" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309661 "chr12:80880928:G>A" "PTPRQ" "NM_001145026:c.1359+2544G>A" "INTRON6" "Unknown significance" "rs556261386" "This variant is a VUS because it does not have enough information."
309662 "chr12:80880935:ATTCCT>-" "PTPRQ" "NM_001145026:c.1359+2551_1359+2556delATTCCT" "INTRON6" "Benign" "rs201258851" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 64 1006 0.0636 20 694 0.0288 1 1008 0.001 9 978 0.0092 97 5008 0.019369
309663 "chr12:80880970:C>G" "PTPRQ" "NM_001145026:c.1359+2586C>G" "INTRON6" "Unknown significance" "rs765568363" "This variant is a VUS because it does not have enough information."
309664 "chr12:80881008:A>G" "PTPRQ" "NM_001145026:c.1359+2624A>G" "INTRON6" "Unknown significance" "rs139110325" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309665 "chr12:80881062:G>A" "PTPRQ" "NM_001145026:c.1359+2678G>A" "INTRON6" "Unknown significance" "rs544633668" "This variant is a VUS because it does not have enough information."
309666 "chr12:80881077:G>A" "PTPRQ" "NM_001145026:c.1359+2693G>A" "INTRON6" "Unknown significance" "rs193263572" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309667 "chr12:80881096:G>A" "PTPRQ" "NM_001145026:c.1359+2712G>A" "INTRON6" "Unknown significance" "rs753125861" "This variant is a VUS because it does not have enough information."
309668 "chr12:80881100:T>C" "PTPRQ" "NM_001145026:c.1359+2716T>C" "INTRON6" "Unknown significance" "rs757980615" "This variant is a VUS because it does not have enough information."
309669 "chr12:80881102:G>A" "PTPRQ" "NM_001145026:c.1359+2718G>A" "INTRON6" "Unknown significance" "rs763752151" "This variant is a VUS because it does not have enough information."
309670 "chr12:80881110:T>C" "PTPRQ" "NM_001145026:c.1359+2726T>C" "INTRON6" "Unknown significance" "rs142998628" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309671 "chr12:80881129:C>T" "PTPRQ" "NM_001145026:c.1359+2745C>T" "INTRON6" "Unknown significance" "rs370748328" "This variant is a VUS because it does not have enough information."
309672 "chr12:80881157:G>A" "PTPRQ" "NM_001145026:c.1359+2773G>A" "INTRON6" "Unknown significance" "rs564138753" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309673 "chr12:80881178:G>A" "PTPRQ" "NM_001145026:c.1359+2794G>A" "INTRON6" "Unknown significance" "rs528355684" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309674 "chr12:80881181:C>G" "PTPRQ" "NM_001145026:c.1359+2797C>G" "INTRON6" "Unknown significance" "rs372224126" "This variant is a VUS because it does not have enough information."
309675 "chr12:80881189:C>T" "PTPRQ" "NM_001145026:c.1359+2805C>T" "INTRON6" "Unknown significance" "rs546513151" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309676 "chr12:80881190:G>A" "PTPRQ" "NM_001145026:c.1359+2806G>A" "INTRON6" "Benign" "rs11114478" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 75 1006 0.0746 45 694 0.0648 0 1008 0 11 978 0.0112 135 5008 0.0269569
309677 "chr12:80881225:T>A" "PTPRQ" "NM_001145026:c.1359+2841T>A" "INTRON6" "Unknown significance" "rs763696351" "This variant is a VUS because it does not have enough information."
309678 "chr12:80881272:T>A" "PTPRQ" "NM_001145026:c.1359+2888T>A" "INTRON6" "Unknown significance" "rs529283743" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309679 "chr12:80881288:C>T" "PTPRQ" "NM_001145026:c.1359+2904C>T" "INTRON6" "Unknown significance" "rs61950957" "This variant is a VUS because it does not have enough information."
309680 "chr12:80881289:A>G" "PTPRQ" "NM_001145026:c.1359+2905A>G" "INTRON6" "Unknown significance" "rs550652849" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309681 "chr12:80881332:T>G" "PTPRQ" "NM_001145026:c.1359+2948T>G" "INTRON6" "Unknown significance" "rs569057582" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309682 "chr12:80881334:T>G" "PTPRQ" "NM_001145026:c.1359+2950T>G" "INTRON6" "Unknown significance" "rs539552832" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
309683 "chr12:80881396:C>T" "PTPRQ" "NM_001145026:c.1359+3012C>T" "INTRON6" "Unknown significance" "rs551916373" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 1 1008 0.001 0 978 0 2 5008 0.000399361
309684 "chr12:80881436:A>G" "PTPRQ" "NM_001145026:c.1359+3052A>G" "INTRON6" "Benign" "rs117556513" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 10 1006 0.0099 5 694 0.0072 0 1008 0 4 978 0.0041 22 5008 0.00439297
309685 "chr12:80881462:A>G" "PTPRQ" "NM_001145026:c.1359+3078A>G" "INTRON6" "Unknown significance" "rs534483177" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309686 "chr12:80881473:C>A" "PTPRQ" "NM_001145026:c.1359+3089C>A" "INTRON6" "Unknown significance" "rs183509035" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309687 "chr12:80881512:T>C" "PTPRQ" "NM_001145026:c.1359+3128T>C" "INTRON6" "Unknown significance" "rs761568347" "This variant is a VUS because it does not have enough information."
309688 "chr12:80881561:A>T" "PTPRQ" "NM_001145026:c.1359+3177A>T" "INTRON6" "Unknown significance" "rs574474653" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309689 "chr12:80881563:C>G" "PTPRQ" "NM_001145026:c.1359+3179C>G" "INTRON6" "Unknown significance" "rs557097773" "This variant is a VUS because it does not have enough information."
309690 "chr12:80881569:A>-" "PTPRQ" "NM_001145026:c.1359+3185delA" "INTRON6" "Benign" "rs571238848" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 0 1006 0 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744
309691 "chr12:80881589:C>T" "PTPRQ" "NM_001145026:c.1359+3205C>T" "INTRON6" "Unknown significance" "rs535487319" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309692 "chr12:80881633:C>T" "PTPRQ" "NM_001145026:c.1359+3249C>T" "INTRON6" "Unknown significance" "rs745845572" "This variant is a VUS because it does not have enough information."
309693 "chr12:80881634:G>A" "PTPRQ" "NM_001145026:c.1359+3250G>A" "INTRON6" "Benign" "rs148070964" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 1 1006 0.001 0 694 0 5 1008 0.005 0 978 0 9 5008 0.00179712
309694 "chr12:80881635:C>T" "PTPRQ" "NM_001145026:c.1359+3251C>T" "INTRON6" "Unknown significance" "rs373168430" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309695 "chr12:80881636:G>A" "PTPRQ" "NM_001145026:c.1359+3252G>A" "INTRON6" "Unknown significance" "rs758353084" "This variant is a VUS because it does not have enough information."
309696 "chr12:80881657:T>A" "PTPRQ" "NM_001145026:c.1359+3273T>A" "INTRON6" "Unknown significance" "rs545598453" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309697 "chr12:80881682:C>T" "PTPRQ" "NM_001145026:c.1359+3298C>T" "INTRON6" "Unknown significance" "rs564281292" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309698 "chr12:80881740:G>T" "PTPRQ" "NM_001145026:c.1359+3356G>T" "INTRON6" "Unknown significance" "rs552916071" "This variant is a VUS because it does not have enough information."
309699 "chr12:80881752:G>A" "PTPRQ" "NM_001145026:c.1359+3368G>A" "INTRON6" "Unknown significance" "rs188240854" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309700 "chr12:80881767:G>A" "PTPRQ" "NM_001145026:c.1359+3383G>A" "INTRON6" "Unknown significance" "rs540121579" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309701 "chr12:80881777:T>G" "PTPRQ" "NM_001145026:c.1359+3393T>G" "INTRON6" "Unknown significance" "rs561689984" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
309702 "chr12:80881807:G>A" "PTPRQ" "NM_001145026:c.1359+3423G>A" "INTRON6" "Unknown significance" "rs779676681" "This variant is a VUS because it does not have enough information."
309703 "chr12:80881815:A>G" "PTPRQ" "NM_001145026:c.1359+3431A>G" "INTRON6" "Unknown significance" "rs749096480" "This variant is a VUS because it does not have enough information."
309704 "chr12:80881822:G>T" "PTPRQ" "NM_001145026:c.1359+3438G>T" "INTRON6" "Unknown significance" "rs529248241" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309705 "chr12:80881823:C>T" "PTPRQ" "NM_001145026:c.1359+3439C>T" "INTRON6" "Unknown significance" "rs766588306" "This variant is a VUS because it does not have enough information."
309706 "chr12:80881824:C>A" "PTPRQ" "NM_001145026:c.1359+3440C>A" "INTRON6" "Unknown significance" "rs550515904" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309707 "chr12:80881845:G>-" "PTPRQ" "NM_001145026:c.1359+3461delG" "INTRON6" "Unknown significance" "rs751552136" "This variant is a VUS because it does not have enough information."
309708 "chr12:80881870:A>G" "PTPRQ" "NM_001145026:c.1359+3486A>G" "INTRON6" "Benign" "rs12313038" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309709 "chr12:80881873:G>A" "PTPRQ" "NM_001145026:c.1359+3489G>A" "INTRON6" "Unknown significance" "rs533437296" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309710 "chr12:80881877:->T" "PTPRQ" "NM_001145026:c.1359+3493_1359+3494insT" "INTRON6" "Benign" "rs562962306" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 348 1322 0.2632 221 1006 0.2197 120 694 0.1729 9 1008 0.0089 118 978 0.1207 816 5008 0.162939
309711 "chr12:80881886:T>A" "PTPRQ" "NM_001145026:c.1359+3502T>A" "INTRON6" "Unknown significance" "rs540853612" "This variant is a VUS because it does not have enough information."
309712 "chr12:80881901:T>-" "PTPRQ" "NM_001145026:c.1359+3517delT" "INTRON6" "Unknown significance" "rs35310369" "This variant is a VUS because it does not have enough information."
309713 "chr12:80881907:A>G" "PTPRQ" "NM_001145026:c.1359+3523A>G" "INTRON6" "Unknown significance" "rs551612154" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309714 "chr12:80881978:T>A" "PTPRQ" "NM_001145026:c.1359+3594T>A" "INTRON6" "Benign" "rs146220341" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 33 1322 0.025 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 36 5008 0.0071885
309715 "chr12:80882000:T>A" "PTPRQ" "NM_001145026:c.1359+3616T>A" "INTRON6" "Unknown significance" "rs527928621" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309716 "chr12:80882030:A>G" "PTPRQ" "NM_001145026:c.1359+3646A>G" "INTRON6" "Benign" "rs7294789" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 376 1322 0.2844 6 1006 0.006 49 694 0.0706 43 1008 0.0427 25 978 0.0256 499 5008 0.0996406
309717 "chr12:80882064:G>C" "PTPRQ" "NM_001145026:c.1359+3680G>C" "INTRON6" "Unknown significance" "rs545309314" "This variant is a VUS because it does not have enough information."
309718 "chr12:80882080:G>T" "PTPRQ" "NM_001145026:c.1359+3696G>T" "INTRON6" "Benign" "rs7973387" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 306 1322 0.2315 217 1006 0.2157 113 694 0.1628 0 1008 0 105 978 0.1074 741 5008 0.147963
309719 "chr12:80882093:G>C" "PTPRQ" "NM_001145026:c.1359+3709G>C" "INTRON6" "Unknown significance" "rs375811211" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
309720 "chr12:80882104:C>T" "PTPRQ" "NM_001145026:c.1359+3720C>T" "INTRON6" "Unknown significance" "rs556965328" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309721 "chr12:80882115:C>T" "PTPRQ" "NM_001145026:c.1359+3731C>T" "INTRON6" "Unknown significance" "rs369411013" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 3 978 0.0031 5 5008 0.000998403
309722 "chr12:80882221:G>A" "PTPRQ" "NM_001145026:c.1359+3837G>A" "INTRON6" "Unknown significance" "rs79202662" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309723 "chr12:80882225:G>A" "PTPRQ" "NM_001145026:c.1359+3841G>A" "INTRON6" "Benign" "rs557604721" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 12 1322 0.0091 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 13 5008 0.00259585
309724 "chr12:80882229:A>G" "PTPRQ" "NM_001145026:c.1359+3845A>G" "INTRON6" "Unknown significance" "rs139149226" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309725 "chr12:80882232:TG>-" "PTPRQ" "NM_001145026:c.1359+3848_1359+3849delTG" "INTRON6" "Unknown significance" "rs760242609" "This variant is a VUS because it does not have enough information."
309726 "chr12:80882260:G>T" "PTPRQ" "NM_001145026:c.1359+3876G>T" "INTRON6" "Benign" "rs4436607" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1211 1322 0.916 920 1006 0.9145 601 694 0.866 413 1008 0.4097 848 978 0.8671 3993 5008 0.797324
309727 "chr12:80882286:A>T" "PTPRQ" "NM_001145026:c.1359+3902A>T" "INTRON6" "Unknown significance" "rs555145482" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309728 "chr12:80882291:G>T" "PTPRQ" "NM_001145026:c.1359+3907G>T" "INTRON6" "Benign" "rs74110908" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 152 1322 0.115 0 1006 0 8 694 0.0115 0 1008 0 0 978 0 160 5008 0.0319489
309729 "chr12:80882331:T>C" "PTPRQ" "NM_001145026:c.1359+3947T>C" "INTRON6" "Unknown significance" "rs375126010" "This variant is a VUS because it does not have enough information."
309730 "chr12:80882336:G>T" "PTPRQ" "NM_001145026:c.1359+3952G>T" "INTRON6" "Unknown significance" "rs756476599" "This variant is a VUS because it does not have enough information."
309731 "chr12:80882361:G>C" "PTPRQ" "NM_001145026:c.1359+3977G>C" "INTRON6" "Unknown significance" "rs563487037" "This variant is a VUS because it does not have enough information."
309732 "chr12:80882368:T>C" "PTPRQ" "NM_001145026:c.1359+3984T>C" "INTRON6" "Unknown significance" "rs544121382" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309733 "chr12:80882403:A>G" "PTPRQ" "NM_001145026:c.1359+4019A>G" "INTRON6" "Unknown significance" "rs562878756" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309734 "chr12:80882409:T>C" "PTPRQ" "NM_001145026:c.1359+4025T>C" "INTRON6" "Unknown significance" "rs777173771" "This variant is a VUS because it does not have enough information."
309735 "chr12:80882431:A>G" "PTPRQ" "NM_001145026:c.1359+4047A>G" "INTRON6" "Unknown significance" "rs542727339" "This variant is a VUS because it does not have enough information."
309736 "chr12:80882451:->T" "PTPRQ" "NM_001145026:c.1359+4067_1359+4068insT" "INTRON6" "Unknown significance" "rs562601368" "This variant is a VUS because it does not have enough information."
309737 "chr12:80882461:G>C" "PTPRQ" "NM_001145026:c.1359+4077G>C" "INTRON6" "Unknown significance" "rs759909370" "This variant is a VUS because it does not have enough information."
309738 "chr12:80882481:T>C" "PTPRQ" "NM_001145026:c.1359+4097T>C" "INTRON6" "Unknown significance" "rs765803579" "This variant is a VUS because it does not have enough information."
309739 "chr12:80882523:T>G" "PTPRQ" "NM_001145026:c.1359+4139T>G" "INTRON6" "Unknown significance" "rs533204837" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309740 "chr12:80882526:A>G" "PTPRQ" "NM_001145026:c.1359+4142A>G" "INTRON6" "Unknown significance" "rs112467018" "This variant is a VUS because it does not have enough information."
309741 "chr12:80882534:A>G" "PTPRQ" "NM_001145026:c.1359+4150A>G" "INTRON6" "Unknown significance" "rs545473666" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309742 "chr12:80882543:G>C" "PTPRQ" "NM_001145026:c.1359+4159G>C" "INTRON6" "Unknown significance" "rs560426028" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361
309743 "chr12:80882585:T>A" "PTPRQ" "NM_001145026:c.1359+4201T>A" "INTRON6" "Unknown significance" "rs749821407" "This variant is a VUS because it does not have enough information."
309744 "chr12:80882615:A>G" "PTPRQ" "NM_001145026:c.1359+4231A>G" "INTRON6" "Unknown significance" "rs527788716" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309745 "chr12:80882663:A>G" "PTPRQ" "NM_001145026:c.1359+4279A>G" "INTRON6" "Unknown significance" "rs10128946" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309746 "chr12:80882673:T>C" "PTPRQ" "NM_001145026:c.1359+4289T>C" "INTRON6" "Unknown significance" "rs775660780" "This variant is a VUS because it does not have enough information."
309747 "chr12:80882705:C>T" "PTPRQ" "NM_001145026:c.1359+4321C>T" "INTRON6" "Unknown significance" "rs531733406" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309748 "chr12:80882749:A>T" "PTPRQ" "NM_001145026:c.1360-4305A>T" "INTRON6" "Unknown significance" "rs532017457" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309749 "chr12:80882793:T>C" "PTPRQ" "NM_001145026:c.1360-4261T>C" "INTRON6" "Unknown significance" "rs537270697" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722
309750 "chr12:80882843:A>G" "PTPRQ" "NM_001145026:c.1360-4211A>G" "INTRON6" "Unknown significance" "rs369569823" "This variant is a VUS because it does not have enough information."
309751 "chr12:80882880:G>A" "PTPRQ" "NM_001145026:c.1360-4174G>A" "INTRON6" "Unknown significance" "rs771391652" "This variant is a VUS because it does not have enough information."
309752 "chr12:80882886:A>G" "PTPRQ" "NM_001145026:c.1360-4168A>G" "INTRON6" "Unknown significance" "rs763367356" "This variant is a VUS because it does not have enough information."
309753 "chr12:80882938:C>T" "PTPRQ" "NM_001145026:c.1360-4116C>T" "INTRON6" "Unknown significance" "rs568821939" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
309754 "chr12:80882938:C>A" "PTPRQ" "NM_001145026:c.1360-4116C>A" "INTRON6" "Unknown significance" "rs568821939" "This variant is a VUS because it does not have enough information."
309755 "chr12:80882941:C>T" "PTPRQ" "NM_001145026:c.1360-4113C>T" "INTRON6" "Unknown significance" "rs751254648" "This variant is a VUS because it does not have enough information."
309756 "chr12:80882942:G>A" "PTPRQ" "NM_001145026:c.1360-4112G>A" "INTRON6" "Unknown significance" "rs551482209" "This variant is a VUS because it does not have enough information."
309757 "chr12:80882971:G>A" "PTPRQ" "NM_001145026:c.1360-4083G>A" "INTRON6" "Unknown significance" "rs539104422" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
309758 "chr12:80882985:A>G" "PTPRQ" "NM_001145026:c.1360-4069A>G" "INTRON6" "Unknown significance" "rs756741945" "This variant is a VUS because it does not have enough information."
309759 "chr12:80882993:G>A" "PTPRQ" "NM_001145026:c.1360-4061G>A" "INTRON6" "Unknown significance" "rs557831731" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309760 "chr12:80883033:T>C" "PTPRQ" "NM_001145026:c.1360-4021T>C" "INTRON6" "Unknown significance" "rs749983003" "This variant is a VUS because it does not have enough information."
309761 "chr12:80883039:T>G" "PTPRQ" "NM_001145026:c.1360-4015T>G" "INTRON6" "Unknown significance" "rs184110857" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309762 "chr12:80883064:A>T" "PTPRQ" "NM_001145026:c.1360-3990A>T" "INTRON6" "Unknown significance" "rs533650642" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309763 "chr12:80883068:G>T" "PTPRQ" "NM_001145026:c.1360-3986G>T" "INTRON6" "Unknown significance" "rs555108621" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309764 "chr12:80883143:T>A" "PTPRQ" "NM_001145026:c.1360-3911T>A" "INTRON6" "Unknown significance" "rs573527149" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 2 5008 0.000399361
309765 "chr12:80883149:T>-" "PTPRQ" "NM_001145026:c.1360-3905delT" "INTRON6" "Unknown significance" "rs200954486" "This variant is a VUS because it does not have enough information."
309766 "chr12:80883152:G>-" "PTPRQ" "NM_001145026:c.1360-3902delG" "INTRON6" "Benign" "rs11305655" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 989 1322 0.7481 916 1006 0.9105 589 694 0.8487 412 1008 0.4087 842 978 0.8609 3748 5008 0.748403
309767 "chr12:80883152:G>T" "PTPRQ" "NM_001145026:c.1360-3902G>T" "INTRON6" "Unknown significance" "rs113016194" "This variant is a VUS because it does not have enough information."
309768 "chr12:80883175:C>T" "PTPRQ" "NM_001145026:c.1360-3879C>T" "INTRON6" "Unknown significance" "rs780052117" "This variant is a VUS because it does not have enough information."
309769 "chr12:80883198:C>T" "PTPRQ" "NM_001145026:c.1360-3856C>T" "INTRON6" "Unknown significance" "rs527569892" "This variant is a VUS because it does not have enough information."
309770 "chr12:80883241:A>G" "PTPRQ" "NM_001145026:c.1360-3813A>G" "INTRON6" "Unknown significance" "rs544086121" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309771 "chr12:80883267:T>G" "PTPRQ" "NM_001145026:c.1360-3787T>G" "INTRON6" "Unknown significance" "rs556223533" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309772 "chr12:80883273:T>C" "PTPRQ" "NM_001145026:c.1360-3781T>C" "INTRON6" "Unknown significance" "rs746552173" "This variant is a VUS because it does not have enough information."
309773 "chr12:80883287:C>T" "PTPRQ" "NM_001145026:c.1360-3767C>T" "INTRON6" "Unknown significance" "rs749074760" "This variant is a VUS because it does not have enough information."
309774 "chr12:80883339:G>C" "PTPRQ" "NM_001145026:c.1360-3715G>C" "INTRON6" "Unknown significance" "rs754882708" "This variant is a VUS because it does not have enough information."
309775 "chr12:80883342:C>T" "PTPRQ" "NM_001145026:c.1360-3712C>T" "INTRON6" "Unknown significance" "rs778108668" "This variant is a VUS because it does not have enough information."
309776 "chr12:80883392:A>T" "PTPRQ" "NM_001145026:c.1360-3662A>T" "INTRON6" "Benign" "rs149881527" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 37 1322 0.028 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 38 5008 0.00758786
309777 "chr12:80883406:T>C" "PTPRQ" "NM_001145026:c.1360-3648T>C" "INTRON6" "Benign" "rs10862140" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 414 1008 0.4107 848 978 0.8671 3762 5008 0.751198
309778 "chr12:80883435:A>G" "PTPRQ" "NM_001145026:c.1360-3619A>G" "INTRON6" "Unknown significance" "rs771204872" "This variant is a VUS because it does not have enough information."
309779 "chr12:80883468:T>C" "PTPRQ" "NM_001145026:c.1360-3586T>C" "INTRON6" "Unknown significance" "rs776210927" "This variant is a VUS because it does not have enough information."
309780 "chr12:80883469:C>A" "PTPRQ" "NM_001145026:c.1360-3585C>A" "INTRON6" "Unknown significance" "rs567486362" "This variant is a VUS because it does not have enough information."
309781 "chr12:80883481:C>T" "PTPRQ" "NM_001145026:c.1360-3573C>T" "INTRON6" "Unknown significance" "rs375483940" "This variant is a VUS because it does not have enough information."
309782 "chr12:80883499:G>A" "PTPRQ" "NM_001145026:c.1360-3555G>A" "INTRON6" "Benign" "rs77762137" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 81 1322 0.0613 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 85 5008 0.0169728
309783 "chr12:80883506:->A" "PTPRQ" "NM_001145026:c.1360-3548_1360-3547insA" "INTRON6" "Unknown significance" "rs201163074" "This variant is a VUS because it does not have enough information."
309784 "chr12:80883562:C>T" "PTPRQ" "NM_001145026:c.1360-3492C>T" "INTRON6" "Benign" "rs190199793" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489
309785 "chr12:80883566:A>T" "PTPRQ" "NM_001145026:c.1360-3488A>T" "INTRON6" "Unknown significance" "rs776532354" "This variant is a VUS because it does not have enough information."
309786 "chr12:80883577:G>A" "PTPRQ" "NM_001145026:c.1360-3477G>A" "INTRON6" "Unknown significance" "rs543163171" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309787 "chr12:80883620:G>C" "PTPRQ" "NM_001145026:c.1360-3434G>C" "INTRON6" "Unknown significance" "rs181894781" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 2 5008 0.000399361
309788 "chr12:80883697:T>G" "PTPRQ" "NM_001145026:c.1360-3357T>G" "INTRON6" "Unknown significance" "rs536412734" "This variant is a VUS because it does not have enough information."
309789 "chr12:80883702:T>C" "PTPRQ" "NM_001145026:c.1360-3352T>C" "INTRON6" "Unknown significance" "rs556299914" "This variant is a VUS because it does not have enough information."
309790 "chr12:80883705:A>G" "PTPRQ" "NM_001145026:c.1360-3349A>G" "INTRON6" "Unknown significance" "rs531978913" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309791 "chr12:80883712:->T" "PTPRQ" "NM_001145026:c.1360-3342_1360-3341insT" "INTRON6" "Unknown significance" "rs35120668" "This variant is a VUS because it does not have enough information."
309792 "chr12:80883764:->AAGAAGA" "PTPRQ" "NM_001145026:c.1360-3290_1360-3289insAAGAAGA" "INTRON6" "Unknown significance" "rs775621269" "This variant is a VUS because it does not have enough information."
309793 "chr12:80883764:AAGAAGA>-" "PTPRQ" "NM_001145026:c.1360-3290_1360-3284delAAGAAGA" "INTRON6" "Unknown significance" "rs200859538" "This variant is a VUS because it does not have enough information."
309794 "chr12:80883767:->TCTTGTGCT" "PTPRQ" "NM_001145026:c.1360-3287_1360-3286insTCTTGTGCT" "INTRON6" "Unknown significance" "rs369862702" "This variant is a VUS because it does not have enough information."
309795 "chr12:80883767:A>T" "PTPRQ" "NM_001145026:c.1360-3287A>T" "INTRON6" "Unknown significance" "rs371321864" "This variant is a VUS because it does not have enough information."
309796 "chr12:80883767:AAGA>TCTTGTGCTAAGTCTTGTGCC" "PTPRQ" "Unknown significance" "rs386764638" "This variant is a VUS because it does not have enough information."
309797 "chr12:80883770:->TCTTGTGC" "PTPRQ" "NM_001145026:c.1360-3284_1360-3283insTCTTGTGC" "INTRON6" "Unknown significance" "rs369818726" "This variant is a VUS because it does not have enough information."
309798 "chr12:80883770:A>C" "PTPRQ" "NM_001145026:c.1360-3284A>C" "INTRON6" "Unknown significance" "rs759498081" "This variant is a VUS because it does not have enough information."
309799 "chr12:80883786:->TCTTGTGCCAA" "PTPRQ" "NM_001145026:c.1360-3268_1360-3267insTCTTGTGCCAA" "INTRON6" "Unknown significance" "rs372130233" "This variant is a VUS because it does not have enough information."
309800 "chr12:80883788:C>T" "PTPRQ" "NM_001145026:c.1360-3266C>T" "INTRON6" "Unknown significance" "rs199963842" "This variant is a VUS because it does not have enough information."
309801 "chr12:80883832:T>C" "PTPRQ" "NM_001145026:c.1360-3222T>C" "INTRON6" "Unknown significance" "rs186973717" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
309802 "chr12:80883875:A>G" "PTPRQ" "NM_001145026:c.1360-3179A>G" "INTRON6" "Unknown significance" "rs565487083" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309803 "chr12:80883877:G>A" "PTPRQ" "NM_001145026:c.1360-3177G>A" "INTRON6" "Unknown significance" "rs770190472" "This variant is a VUS because it does not have enough information."
309804 "chr12:80883886:C>T" "PTPRQ" "NM_001145026:c.1360-3168C>T" "INTRON6" "Unknown significance" "rs143869602" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309805 "chr12:80883887:G>A" "PTPRQ" "NM_001145026:c.1360-3167G>A" "INTRON6" "Unknown significance" "rs776043990" "This variant is a VUS because it does not have enough information."
309806 "chr12:80883888:G>A" "PTPRQ" "NM_001145026:c.1360-3166G>A" "INTRON6" "Unknown significance" "rs763273594" "This variant is a VUS because it does not have enough information."
309807 "chr12:80883906:C>T" "PTPRQ" "NM_001145026:c.1360-3148C>T" "INTRON6" "Benign" "rs7132716" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
309808 "chr12:80883932:G>A" "PTPRQ" "NM_001145026:c.1360-3122G>A" "INTRON6" "Unknown significance" "rs148598327" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309809 "chr12:80883946:C>T" "PTPRQ" "NM_001145026:c.1360-3108C>T" "INTRON6" "Benign" "rs7132809" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
309810 "chr12:80883969:A>C" "PTPRQ" "NM_001145026:c.1360-3085A>C" "INTRON6" "Unknown significance" "rs578216496" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309811 "chr12:80883969:A>T" "PTPRQ" "NM_001145026:c.1360-3085A>T" "INTRON6" "Unknown significance" "rs578216496" "This variant is a VUS because it does not have enough information."
309812 "chr12:80884080:T>A" "PTPRQ" "NM_001145026:c.1360-2974T>A" "INTRON6" "Unknown significance" "rs767207148" "This variant is a VUS because it does not have enough information."
309813 "chr12:80884083:A>G" "PTPRQ" "NM_001145026:c.1360-2971A>G" "INTRON6" "Unknown significance" "rs190215764" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309814 "chr12:80884104:C>T" "PTPRQ" "NM_001145026:c.1360-2950C>T" "INTRON6" "Unknown significance" "rs142964790" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309815 "chr12:80884128:T>-" "PTPRQ" "NM_001145026:c.1360-2926delT" "INTRON6" "Unknown significance" "rs761500273" "This variant is a VUS because it does not have enough information."
309816 "chr12:80884128:T>C" "PTPRQ" "NM_001145026:c.1360-2926T>C" "INTRON6" "Unknown significance" "rs556324981" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309817 "chr12:80884129:T>C" "PTPRQ" "NM_001145026:c.1360-2925T>C" "INTRON6" "Unknown significance" "rs147735830" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309818 "chr12:80884228:C>T" "PTPRQ" "NM_001145026:c.1360-2826C>T" "INTRON6" "Unknown significance" "rs759602573" "This variant is a VUS because it does not have enough information."
309819 "chr12:80884229:T>C" "PTPRQ" "NM_001145026:c.1360-2825T>C" "INTRON6" "Unknown significance" "rs538936407" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309820 "chr12:80884241:A>G" "PTPRQ" "NM_001145026:c.1360-2813A>G" "INTRON6" "Unknown significance" "rs553850678" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309821 "chr12:80884248:C>A" "PTPRQ" "NM_001145026:c.1360-2806C>A" "INTRON6" "Benign" "rs556853729" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 28 978 0.0286 28 5008 0.00559105
309822 "chr12:80884257:C>T" "PTPRQ" "NM_001145026:c.1360-2797C>T" "INTRON6" "Unknown significance" "rs543131168" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309823 "chr12:80884258:C>T" "PTPRQ" "NM_001145026:c.1360-2796C>T" "INTRON6" "Unknown significance" "rs561409322" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
309824 "chr12:80884277:C>T" "PTPRQ" "NM_001145026:c.1360-2777C>T" "INTRON6" "Benign" "rs142557724" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 41 1322 0.031 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 43 5008 0.00858626
309825 "chr12:80884284:T>C" "PTPRQ" "NM_001145026:c.1360-2770T>C" "INTRON6" "Unknown significance" "rs202232125" "This variant is a VUS because it does not have enough information."
309826 "chr12:80884318:T>G" "PTPRQ" "NM_001145026:c.1360-2736T>G" "INTRON6" "Unknown significance" "rs181961218" "This variant is a VUS because it does not have enough information."
309827 "chr12:80884353:AT>-" "PTPRQ" "NM_001145026:c.1360-2701_1360-2700delAT" "INTRON6" "Unknown significance" "rs566741049" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 7 5008 0.00139776
309828 "chr12:80884374:T>G" "PTPRQ" "NM_001145026:c.1360-2680T>G" "INTRON6" "Benign" "rs543606814" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 6 978 0.0061 6 5008 0.00119808
309829 "chr12:80884389:C>A" "PTPRQ" "NM_001145026:c.1360-2665C>A" "INTRON6" "Unknown significance" "rs540589984" "This variant is a VUS because it does not have enough information."
309830 "chr12:80884389:C>T" "PTPRQ" "NM_001145026:c.1360-2665C>T" "INTRON6" "Unknown significance" "rs540589984" "This variant is a VUS because it does not have enough information."
309831 "chr12:80884394:G>C" "PTPRQ" "NM_001145026:c.1360-2660G>C" "INTRON6" "Unknown significance" "rs185191047" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309832 "chr12:80884408:->G" "PTPRQ" "NM_001145026:c.1360-2646_1360-2645insG" "INTRON6" "Unknown significance" "rs34569680" "This variant is a VUS because it does not have enough information."
309833 "chr12:80884430:A>G" "PTPRQ" "NM_001145026:c.1360-2624A>G" "INTRON6" "Unknown significance" "rs75250769" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309834 "chr12:80884443:G>A" "PTPRQ" "NM_001145026:c.1360-2611G>A" "INTRON6" "Unknown significance" "rs548092031" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309835 "chr12:80884448:C>T" "PTPRQ" "NM_001145026:c.1360-2606C>T" "INTRON6" "Benign" "rs74110910" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 27 1322 0.0204 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 29 5008 0.00579073
309836 "chr12:80884490:G>A" "PTPRQ" "NM_001145026:c.1360-2564G>A" "INTRON6" "Unknown significance" "rs189996370" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 2 694 0.0029 0 1008 0 0 978 0 5 5008 0.000998403
309837 "chr12:80884518:G>C" "PTPRQ" "NM_001145026:c.1360-2536G>C" "INTRON6" "Unknown significance" "rs554008360" "This variant is a VUS because it does not have enough information."
309838 "chr12:80884522:C>T" "PTPRQ" "NM_001145026:c.1360-2532C>T" "INTRON6" "Benign" "rs115335848" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
309839 "chr12:80884523:G>A" "PTPRQ" "NM_001145026:c.1360-2531G>A" "INTRON6" "Benign" "rs12810534" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 77 1322 0.0582 647 1006 0.6431 388 694 0.5591 363 1008 0.3601 660 978 0.6748 2135 5008 0.426318
309840 "chr12:80884565:T>C" "PTPRQ" "NM_001145026:c.1360-2489T>C" "INTRON6" "Unknown significance" "rs537953998" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309841 "chr12:80884573:C>G" "PTPRQ" "NM_001145026:c.1360-2481C>G" "INTRON6" "Benign" "rs549673973" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 12 978 0.0123 12 5008 0.00239617
309842 "chr12:80884658:T>A" "PTPRQ" "NM_001145026:c.1360-2396T>A" "INTRON6" "Unknown significance" "rs181254050" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309843 "chr12:80884686:A>G" "PTPRQ" "NM_001145026:c.1360-2368A>G" "INTRON6" "Benign" "rs538532279" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 0 1006 0 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744
309844 "chr12:80884713:G>T" "PTPRQ" "NM_001145026:c.1360-2341G>T" "INTRON6" "Benign" "rs201039782" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 6 1008 0.006 0 978 0 6 5008 0.00119808
309845 "chr12:80884810:G>A" "PTPRQ" "NM_001145026:c.1360-2244G>A" "INTRON6" "Unknown significance" "rs571803746" "This variant is a VUS because it does not have enough information."
309846 "chr12:80884828:T>G" "PTPRQ" "NM_001145026:c.1360-2226T>G" "INTRON6" "Unknown significance" "rs12822883" "This variant is a VUS because it does not have enough information."
309847 "chr12:80884840:A>G" "PTPRQ" "NM_001145026:c.1360-2214A>G" "INTRON6" "Benign" "rs12318704" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1322 1322 1 997 1006 0.9911 694 694 1 1008 1008 1 965 978 0.9867 4986 5008 0.995607
309848 "chr12:80884867:C>T" "PTPRQ" "NM_001145026:c.1360-2187C>T" "INTRON6" "Unknown significance" "rs542766045" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309849 "chr12:80884888:A>T" "PTPRQ" "NM_001145026:c.1360-2166A>T" "INTRON6" "Benign" "rs12318716" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 579 1322 0.438 223 1006 0.2217 159 694 0.2291 43 1008 0.0427 131 978 0.1339 1135 5008 0.226637
309850 "chr12:80884909:T>A" "PTPRQ" "NM_001145026:c.1360-2145T>A" "INTRON6" "Unknown significance" "rs754796845" "This variant is a VUS because it does not have enough information."
309851 "chr12:80884929:T>A" "PTPRQ" "NM_001145026:c.1360-2125T>A" "INTRON6" "Unknown significance" "rs576419369" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
309852 "chr12:80884936:T>C" "PTPRQ" "NM_001145026:c.1360-2118T>C" "INTRON6" "Unknown significance" "rs186532752" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
309853 "chr12:80884960:G>T" "PTPRQ" "NM_001145026:c.1360-2094G>T" "INTRON6" "Unknown significance" "rs371013653" "This variant is a VUS because it does not have enough information."
309854 "chr12:80884968:T>A" "PTPRQ" "NM_001145026:c.1360-2086T>A" "INTRON6" "Unknown significance" "rs191440551" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309855 "chr12:80884979:A>C" "PTPRQ" "NM_001145026:c.1360-2075A>C" "INTRON6" "Unknown significance" "rs577400050" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309856 "chr12:80885002:C>T" "PTPRQ" "NM_001145026:c.1360-2052C>T" "INTRON6" "Unknown significance" "rs778801474" "This variant is a VUS because it does not have enough information."
309857 "chr12:80885012:G>A" "PTPRQ" "NM_001145026:c.1360-2042G>A" "INTRON6" "Unknown significance" "rs541350523" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309858 "chr12:80885020:T>G" "PTPRQ" "NM_001145026:c.1360-2034T>G" "INTRON6" "Unknown significance" "rs559665175" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309859 "chr12:80885056:G>C" "PTPRQ" "NM_001145026:c.1360-1998G>C" "INTRON6" "Benign" "rs61513652" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
309860 "chr12:80885057:C>G" "PTPRQ" "NM_001145026:c.1360-1997C>G" "INTRON6" "Unknown significance" "rs752570780" "This variant is a VUS because it does not have enough information."
309861 "chr12:80885092:T>G" "PTPRQ" "NM_001145026:c.1360-1962T>G" "INTRON6" "Unknown significance" "rs542173509" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309862 "chr12:80885114:G>A" "PTPRQ" "NM_001145026:c.1360-1940G>A" "INTRON6" "Unknown significance" "rs560564145" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309863 "chr12:80885161:T>C" "PTPRQ" "NM_001145026:c.1360-1893T>C" "INTRON6" "Benign" "rs117599050" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 6 1006 0.006 1 694 0.0014 0 1008 0 2 978 0.002 9 5008 0.00179712
309864 "chr12:80885163:->TGTT" "PTPRQ" "NM_001145026:c.1360-1891_1360-1890insTGTT" "INTRON6" "Unknown significance" "rs764759768" "This variant is a VUS because it does not have enough information."
309865 "chr12:80885182:C>G" "PTPRQ" "NM_001145026:c.1360-1872C>G" "INTRON6" "Unknown significance" "rs183260301" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309866 "chr12:80885261:T>C" "PTPRQ" "NM_001145026:c.1360-1793T>C" "INTRON6" "Unknown significance" "rs781536482" "This variant is a VUS because it does not have enough information."
309867 "chr12:80885292:A>G" "PTPRQ" "NM_001145026:c.1360-1762A>G" "INTRON6" "Unknown significance" "rs571340524" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309868 "chr12:80885293:T>C" "PTPRQ" "NM_001145026:c.1360-1761T>C" "INTRON6" "Unknown significance" "rs545413428" "This variant is a VUS because it does not have enough information."
309869 "chr12:80885355:G>A" "PTPRQ" "NM_001145026:c.1360-1699G>A" "INTRON6" "Unknown significance" "rs769958213" "This variant is a VUS because it does not have enough information."
309870 "chr12:80885369:A>G" "PTPRQ" "NM_001145026:c.1360-1685A>G" "INTRON6" "Unknown significance" "rs565159094" "This variant is a VUS because it does not have enough information."
309871 "chr12:80885373:T>G" "PTPRQ" "NM_001145026:c.1360-1681T>G" "INTRON6" "Unknown significance" "rs527652806" "This variant is a VUS because it does not have enough information."
309872 "chr12:80885398:T>C" "PTPRQ" "NM_001145026:c.1360-1656T>C" "INTRON6" "Unknown significance" "rs746379254" "This variant is a VUS because it does not have enough information."
309873 "chr12:80885401:T>C" "PTPRQ" "NM_001145026:c.1360-1653T>C" "INTRON6" "Unknown significance" "rs532379716" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309874 "chr12:80885402:G>T" "PTPRQ" "NM_001145026:c.1360-1652G>T" "INTRON6" "Unknown significance" "rs373591953" "This variant is a VUS because it does not have enough information."
309875 "chr12:80885418:A>C" "PTPRQ" "NM_001145026:c.1360-1636A>C" "INTRON6" "Benign" "rs10746169" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
309876 "chr12:80885433:C>T" "PTPRQ" "NM_001145026:c.1360-1621C>T" "INTRON6" "Unknown significance" "rs565935643" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309877 "chr12:80885446:T>C" "PTPRQ" "NM_001145026:c.1360-1608T>C" "INTRON6" "Unknown significance" "rs536561492" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309878 "chr12:80885475:A>C" "PTPRQ" "NM_001145026:c.1360-1579A>C" "INTRON6" "Unknown significance" "rs554969595" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309879 "chr12:80885532:G>A" "PTPRQ" "NM_001145026:c.1360-1522G>A" "INTRON6" "Benign" "rs11829873" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 96 1322 0.0726 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 101 5008 0.0201677
309880 "chr12:80885573:T>C" "PTPRQ" "NM_001145026:c.1360-1481T>C" "INTRON6" "Unknown significance" "rs780691137" "This variant is a VUS because it does not have enough information."
309881 "chr12:80885607:T>C" "PTPRQ" "NM_001145026:c.1360-1447T>C" "INTRON6" "Unknown significance" "rs188723810" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309882 "chr12:80885664:G>A" "PTPRQ" "NM_001145026:c.1360-1390G>A" "INTRON6" "Unknown significance" "rs769185611" "This variant is a VUS because it does not have enough information."
309883 "chr12:80885665:A>G" "PTPRQ" "NM_001145026:c.1360-1389A>G" "INTRON6" "Unknown significance" "rs774635225" "This variant is a VUS because it does not have enough information."
309884 "chr12:80885696:A>G" "PTPRQ" "NM_001145026:c.1360-1358A>G" "INTRON6" "Unknown significance" "rs762255973" "This variant is a VUS because it does not have enough information."
309885 "chr12:80885701:A>G" "PTPRQ" "NM_001145026:c.1360-1353A>G" "INTRON6" "Unknown significance" "rs561121963" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
309886 "chr12:80885712:T>G" "PTPRQ" "NM_001145026:c.1360-1342T>G" "INTRON6" "Unknown significance" "rs577361169" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309887 "chr12:80885738:A>G" "PTPRQ" "NM_001145026:c.1360-1316A>G" "INTRON6" "Unknown significance" "rs772981774" "This variant is a VUS because it does not have enough information."
309888 "chr12:80885753:G>T" "PTPRQ" "NM_001145026:c.1360-1301G>T" "INTRON6" "Unknown significance" "rs149120677" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309889 "chr12:80885763:A>T" "PTPRQ" "NM_001145026:c.1360-1291A>T" "INTRON6" "Unknown significance" "rs553159923" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 1 978 0.001 2 5008 0.000399361
309890 "chr12:80885773:GTTTTGGAGGTAA>-" "PTPRQ" "NM_001145026:c.1360-1281_1360-1269delGTTTTGGAGGTAA" "INTRON6" "Unknown significance" "rs769530786" "This variant is a VUS because it does not have enough information."
309891 "chr12:80885804:A>-" "PTPRQ" "NM_001145026:c.1360-1250delA" "INTRON6" "Unknown significance" "rs575774792" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 2 978 0.002 3 5008 0.000599042
309892 "chr12:80885819:AG>-" "PTPRQ" "NM_001145026:c.1360-1235_1360-1234delAG" "INTRON6" "Unknown significance" "rs758777909" "This variant is a VUS because it does not have enough information."
309893 "chr12:80885836:G>A" "PTPRQ" "NM_001145026:c.1360-1218G>A" "INTRON6" "Unknown significance" "rs372829504" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309894 "chr12:80885838:A>G" "PTPRQ" "NM_001145026:c.1360-1216A>G" "INTRON6" "Unknown significance" "rs529965311" "This variant is a VUS because it does not have enough information."
309895 "chr12:80885938:C>G" "PTPRQ" "NM_001145026:c.1360-1116C>G" "INTRON6" "Benign" "rs143193826" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
309896 "chr12:80885971:C>T" "PTPRQ" "NM_001145026:c.1360-1083C>T" "INTRON6" "Unknown significance" "rs75464770" "This variant is a VUS because it does not have enough information."
309897 "chr12:80885989:C>T" "PTPRQ" "NM_001145026:c.1360-1065C>T" "INTRON6" "Unknown significance" "rs560523658" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
309898 "chr12:80885990:A>G" "PTPRQ" "NM_001145026:c.1360-1064A>G" "INTRON6" "Unknown significance" "rs138744349" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
309899 "chr12:80886001:C>T" "PTPRQ" "NM_001145026:c.1360-1053C>T" "INTRON6" "Unknown significance" "rs543144502" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
309900 "chr12:80886040:C>A" "PTPRQ" "NM_001145026:c.1360-1014C>A" "INTRON6" "Unknown significance" "rs190783403" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309901 "chr12:80886042:A>G" "PTPRQ" "NM_001145026:c.1360-1012A>G" "INTRON6" "Unknown significance" "rs772966430" "This variant is a VUS because it does not have enough information."
309902 "chr12:80886045:G>T" "PTPRQ" "NM_001145026:c.1360-1009G>T" "INTRON6" "Unknown significance" "rs532113108" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309903 "chr12:80886052:C>T" "PTPRQ" "NM_001145026:c.1360-1002C>T" "INTRON6" "Unknown significance" "rs183384452" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309904 "chr12:80886053:C>T" "PTPRQ" "NM_001145026:c.1360-1001C>T" "INTRON6" "Unknown significance" "rs565898233" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309905 "chr12:80886118:T>C" "PTPRQ" "NM_001145026:c.1360-936T>C" "INTRON6" "Unknown significance" "rs753418675" "This variant is a VUS because it does not have enough information."
309906 "chr12:80886123:A>G" "PTPRQ" "NM_001145026:c.1360-931A>G" "INTRON6" "Unknown significance" "rs529990197" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
309907 "chr12:80886127:C>T" "PTPRQ" "NM_001145026:c.1360-927C>T" "INTRON6" "Unknown significance" "rs548532482" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
309908 "chr12:80886146:T>C" "PTPRQ" "NM_001145026:c.1360-908T>C" "INTRON6" "Unknown significance" "rs368625321" "This variant is a VUS because it does not have enough information."
309909 "chr12:80886234:C>A" "PTPRQ" "NM_001145026:c.1360-820C>A" "INTRON6" "Unknown significance" "rs569941049" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309910 "chr12:80886273:G>A" "PTPRQ" "NM_001145026:c.1360-781G>A" "INTRON6" "Unknown significance" "rs759507301" "This variant is a VUS because it does not have enough information."
309911 "chr12:80886307:A>G" "PTPRQ" "NM_001145026:c.1360-747A>G" "INTRON6" "Unknown significance" "rs765270007" "This variant is a VUS because it does not have enough information."
309912 "chr12:80886319:G>T" "PTPRQ" "NM_001145026:c.1360-735G>T" "INTRON6" "Unknown significance" "rs186605389" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309913 "chr12:80886352:A>G" "PTPRQ" "NM_001145026:c.1360-702A>G" "INTRON6" "Unknown significance" "rs558683152" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309914 "chr12:80886423:G>A" "PTPRQ" "NM_001145026:c.1360-631G>A" "INTRON6" "Benign" "rs191438082" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 7 1008 0.0069 0 978 0 7 5008 0.00139776
309915 "chr12:80886434:G>A" "PTPRQ" "NM_001145026:c.1360-620G>A" "INTRON6" "Unknown significance" "rs752527932" "This variant is a VUS because it does not have enough information."
309916 "chr12:80886480:A>G" "PTPRQ" "NM_001145026:c.1360-574A>G" "INTRON6" "Unknown significance" "rs534806308" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
309917 "chr12:80886485:C>A" "PTPRQ" "NM_001145026:c.1360-569C>A" "INTRON6" "Unknown significance" "rs758280683" "This variant is a VUS because it does not have enough information."
309918 "chr12:80886489:A>T" "PTPRQ" "NM_001145026:c.1360-565A>T" "INTRON6" "Unknown significance" "rs553120952" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309919 "chr12:80886492:T>C" "PTPRQ" "NM_001145026:c.1360-562T>C" "INTRON6" "Unknown significance" "rs574719395" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309920 "chr12:80886493:C>T" "PTPRQ" "NM_001145026:c.1360-561C>T" "INTRON6" "Unknown significance" "rs781242715" "This variant is a VUS because it does not have enough information."
309921 "chr12:80886558:T>G" "PTPRQ" "NM_001145026:c.1360-496T>G" "INTRON6" "Unknown significance" "rs750708914" "This variant is a VUS because it does not have enough information."
309922 "chr12:80886609:A>T" "PTPRQ" "NM_001145026:c.1360-445A>T" "INTRON6" "Unknown significance" "rs535729882" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309923 "chr12:80886611:G>A" "PTPRQ" "NM_001145026:c.1360-443G>A" "INTRON6" "Unknown significance" "rs183974016" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
309924 "chr12:80886612:C>A" "PTPRQ" "NM_001145026:c.1360-442C>A" "INTRON6" "Unknown significance" "rs780071507" "This variant is a VUS because it does not have enough information."
309925 "chr12:80886664:A>G" "PTPRQ" "NM_001145026:c.1360-390A>G" "INTRON6" "Benign" "rs10862141" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
309926 "chr12:80886666:A>C" "PTPRQ" "NM_001145026:c.1360-388A>C" "INTRON6" "Unknown significance" "rs543361797" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309927 "chr12:80886717:G>T" "PTPRQ" "NM_001145026:c.1360-337G>T" "INTRON6" "Unknown significance" "rs770847622" "This variant is a VUS because it does not have enough information."
309928 "chr12:80886763:G>A" "PTPRQ" "NM_001145026:c.1360-291G>A" "INTRON6" "Unknown significance" "rs187788744" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
309929 "chr12:80886776:A>G" "PTPRQ" "NM_001145026:c.1360-278A>G" "INTRON6" "Unknown significance" "rs769097841" "This variant is a VUS because it does not have enough information."
309930 "chr12:80886786:C>T" "PTPRQ" "NM_001145026:c.1360-268C>T" "INTRON6" "Benign" "rs10862142" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
309931 "chr12:80886791:C>G" "PTPRQ" "NM_001145026:c.1360-263C>G" "INTRON6" "Unknown significance" "rs541149479" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309932 "chr12:80886801:C>G" "PTPRQ" "NM_001145026:c.1360-253C>G" "INTRON6" "Unknown significance" "rs558815923" "This variant is a VUS because it does not have enough information."
309933 "chr12:80886817:C>T" "PTPRQ" "NM_001145026:c.1360-237C>T" "INTRON6" "Benign" "rs141750985" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 5 1322 0.0038 0 1006 0 1 694 0.0014 9 1008 0.0089 0 978 0 15 5008 0.00299521
309934 "chr12:80886830:T>C" "PTPRQ" "NM_001145026:c.1360-224T>C" "INTRON6" "Unknown significance" "rs748453030" "This variant is a VUS because it does not have enough information."
309935 "chr12:80886880:->T" "PTPRQ" "NM_001145026:c.1360-174_1360-173insT" "INTRON6" "Unknown significance" "rs780712616" "This variant is a VUS because it does not have enough information."
309936 "chr12:80886882:T>A" "PTPRQ" "NM_001145026:c.1360-172T>A" "INTRON6" "Unknown significance" "rs529949941" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309937 "chr12:80886891:G>A" "PTPRQ" "NM_001145026:c.1360-163G>A" "INTRON6" "Unknown significance" "rs548498372" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309938 "chr12:80886894:G>A" "PTPRQ" "NM_001145026:c.1360-160G>A" "INTRON6" "Unknown significance" "rs192927116" "This variant is a VUS because it does not have enough information."
309939 "chr12:80886905:T>G" "PTPRQ" "NM_001145026:c.1360-149T>G" "INTRON6" "Unknown significance" "rs563550989" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309940 "chr12:80886906:G>T" "PTPRQ" "NM_001145026:c.1360-148G>T" "INTRON6" "Unknown significance" "rs530723236" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309941 "chr12:80886929:A>G" "PTPRQ" "NM_001145026:c.1360-125A>G" "INTRON6" "Unknown significance" "rs772524631" "This variant is a VUS because it does not have enough information."
309942 "chr12:80886955:G>A" "PTPRQ" "NM_001145026:c.1360-99G>A" "INTRON6" "Unknown significance" "rs185025648" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 0 978 0 0 5008 0
309943 "chr12:80886958:T>A" "PTPRQ" "NM_001145026:c.1360-96T>A" "INTRON6" "Unknown significance" "rs538331242" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 1 1006 0.001 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
309944 "chr12:80886977:T>G" "PTPRQ" "NM_001145026:c.1360-77T>G" "INTRON6" "Benign" "rs78315832" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 96 1322 0.0726 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 101 5008 0.0201677
309945 "chr12:80887015:A>G" "PTPRQ" "NM_001145026:c.1360-39A>G" "INTRON6" "Unknown significance" "rs780675030" "This variant is a VUS because it does not have enough information." 0 1586 0 0 214 0 0 312 0 0 6 0 1 4764 0.000209908 0 82 0 0 1016 0 1 7980 0.000125313
309946 "chr12:80887017:T>A" "PTPRQ" "NM_001145026:c.1360-37T>A" "INTRON6" "Unknown significance" "rs747836640" "This variant is a VUS because it does not have enough information."
309947 "chr12:80887036:A>G" "PTPRQ" "NM_001145026:c.1360-18A>G" "INTRON6" "Unknown significance" "rs546721524" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309948 "chr12:80887070:T>C" "PTPRQ" "NM_001145026:p.Met459Thr" "NM_001145026:c.1376T>C" "EXON7" "Unknown significance" "rs769390111" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.0" "B" 1 "N" "4.57" "C" 0 2046 0 0 350 0 0 554 0 0 20 0 1 7058 0.000141683 0 144 0 0 5026 0 1 15198 0.0000657981
309949 "chr12:80887075:C>T" "PTPRQ" "NM_001145026:p.Pro461Ser" "NM_001145026:c.1381C>T" "EXON7" "Unknown significance" "rs568303563" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.008" "B" 0.521408 "D" "3.89" "C" 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2074 0 0 366 0 0 568 0 0 20 0 0 7314 0 0 156 0 3 5680 0.000528169 3 16178 0.000185437
309950 "chr12:80887091:T>C" "PTPRQ" "NM_001145026:p.Ile466Thr" "NM_001145026:c.1397T>C" "EXON7" "Unknown significance" "rs749549587" "This variant is a VUS because it does not have enough information." 0.113 "N" "0.0" "B" 1 "N" "0.531" "C" 0 2114 0 0 404 0 0 590 0 0 30 0 2 7894 0.000253357 0 176 0 0 6770 0 2 17978 0.000111247
309951 "chr12:80887104:G>A" "PTPRQ" "NM_001145026:p.Met470Ile" "NM_001145026:c.1410G>A" "EXON7" "Unknown significance" "rs369284820" "This variant is a VUS because it does not have enough information." 0.142 "N" "0.05" "B" 0.999571 "N" "3.91" "C" 0 2130 0 0 408 0 0 596 0 0 32 0 1 8184 0.00012219 0 186 0 0 7416 0 1 18952 0.0000527649
309952 "chr12:80887104:G>T" "PTPRQ" "NM_001145026:p.Met470Ile" "NM_001145026:c.1410G>T" "EXON7" "Unknown significance" "rs369284820" "This variant is a VUS because it does not have enough information." 0.142 "N" "0.05" "B" 0.999554 "N" "3.91" "C" 0 3180 0 1 1384 0.000722543 1 4564 0.000219106
309953 "chr12:80887109:G>T" "PTPRQ" "NM_001145026:p.Gly472Val" "NM_001145026:c.1415G>T" "EXON7" "Unknown significance" "rs535700232" "This variant is a VUS because it does not have enough information." 0.135 "N" "0.121" "B" 0.999649 "N" "-1.02" "N" 0 1322 0 0 1006 0 0 694 0 0 1008 0 3 978 0.0031 3 5008 0.000599042 0 2134 0 0 408 0 0 598 0 0 32 0 0 8268 0 0 188 0 3 7576 0.000395987 3 19204 0.000156217
309954 "chr12:80887114:T>A" "PTPRQ" "NM_001145026:p.Tyr474Asn" "NM_001145026:c.1420T>A" "EXON7" "Unknown significance" "rs760119330" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.856" "P" 0.710519 "N" "2.15" "C" 0 2134 0 1 408 0.00245098 0 604 0 0 34 0 0 8300 0 0 188 0 0 7674 0 1 19342 0.000051701
309955 "chr12:80887117:G>T" "PTPRQ" "NM_001145026:p.Glu475Stop" "NM_001145026:c.1423G>T" "EXON7" "Unknown significance" "rs557277948" "This variant is a VUS because it does not have enough information." 1.048 "C" 1 "A" "5.73" "C" 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 2134 0.000468604 0 408 0 0 608 0 0 34 0 0 8314 0 0 188 0 0 7706 0 1 19392 0.0000515677
309956 "chr12:80887136:C>T" "PTPRQ" "NM_001145026:p.Ser481Leu" "NM_001145026:c.1442C>T" "EXON7" "Unknown significance" "rs575857456" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.936" "P" 0.722346 "N" "4.74" "C" 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 2134 0.000468604 0 410 0 1 614 0.00162866 0 34 0 0 8368 0 0 188 0 0 7858 0 2 19606 0.00010201
309957 "chr12:80887137:G>A" "PTPRQ" "NM_001145026:p.Ser481Ser" "NM_001145026:c.1443G>A" "EXON7" "Benign" "rs373744641" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 3182 0 4 1384 0.00289017 4 4566 0.00087604 1 1322 0.0008 1 1006 0.001 0 694 0 0 1008 0 10 978 0.0102 12 5008 0.00239617 5 2134 0.00234302 0 410 0 0 614 0 0 34 0 0 8368 0 0 188 0 44 7862 0.00559654 49 19610 0.00249873
309958 "chr12:80887165:A>G" "PTPRQ" "NM_001145026:p.Ile491Val" "NM_001145026:c.1471A>G" "EXON7" "Unknown significance" "rs764179518" "This variant is a VUS because it does not have enough information." 0.203 "N" "0.0" "B" 1 "N" "0.802" "C" 0 2134 0 0 408 0 0 612 0 0 34 0 1 8392 0.000119161 0 188 0 0 7886 0 1 19654 0.0000508802
309959 "chr12:80887167:A>G" "PTPRQ" "NM_001145026:p.Ile491Met" "NM_001145026:c.1473A>G" "EXON7" "Unknown significance" "rs375501727" "This variant is a VUS because it does not have enough information." -1.121 "N" "0.004" "B" 1 "N" "-10.4" "N" 0 3182 0 1 1384 0.000722543 1 4566 0.00021901
309960 "chr12:80887194:T>A" "PTPRQ" "NM_001145026:p.Phe500Leu" "NM_001145026:c.1500T>A" "EXON7" "Unknown significance" "rs558498724" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.0" "B" 0.985838 "N" "4.59" "C" 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2112 0 0 400 0 0 602 0 0 32 0 0 8358 0 0 186 0 1 7844 0.000127486 1 19534 0.0000511928
309961 "chr12:80887204:A>G" "PTPRQ" "NM_001145026:p.Asn504Asp" "NM_001145026:c.1510A>G" "EXON7" "Unknown significance" "rs576943149" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.004" "B" 1 "N" "3.39" "C" 0 1322 0 0 1006 0 1 694 0.0014 1 1008 0.001 0 978 0 2 5008 0.000399361
309962 "chr12:80887227:A>G" "PTPRQ" "NM_001145026:p.Ser511Ser" "NM_001145026:c.1533A>G" "EXON7" "Unknown significance" "rs552219391" "This variant is a VUS because it does not have enough information."
309963 "chr12:80887228:C>T" "PTPRQ" "NM_001145026:p.Pro512Ser" "NM_001145026:c.1534C>T" "EXON7" "Unknown significance" "rs541112749" "This variant is a VUS because it does not have enough information." 0.038 "N" "0.0" "B" 1 "N" "-0.359" "N" 0 1322 0 0 1006 0 0 694 0 0 1008 0 4 978 0.0041 4 5008 0.000798722 0 2034 0 0 368 0 0 576 0 0 24 0 0 7850 0 0 172 0 23 7128 0.00322671 23 18152 0.00126708
309964 "chr12:80887245:T>G" "PTPRQ" "NM_001145026:c.1540+11T>G" "INTRON7" "Benign" "rs115616201" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 0 694 0 0 1008 0 0 978 0 7 5008 0.00139776 9 1988 0.00452716 0 334 0 0 538 0 0 20 0 0 7440 0 0 162 0 0 6430 0 9 16912 0.000532167
309965 "chr12:80887263:T>C" "PTPRQ" "NM_001145026:c.1540+29T>C" "INTRON7" "Unknown significance" "rs751563536" "This variant is a VUS because it does not have enough information."
309966 "chr12:80887274:C>T" "PTPRQ" "NM_001145026:c.1540+40C>T" "INTRON7" "Unknown significance" "rs190312978" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309967 "chr12:80887277:C>T" "PTPRQ" "NM_001145026:c.1540+43C>T" "INTRON7" "Unknown significance" "rs377491194" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 3 1896 0.00158228 0 296 0 0 466 0 0 14 0 0 6712 0 0 140 0 0 4922 0 3 14446 0.00020767
309968 "chr12:80887350:C>T" "PTPRQ" "NM_001145026:c.1540+116C>T" "INTRON7" "Unknown significance" "rs563352926" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309969 "chr12:80887356:T>C" "PTPRQ" "NM_001145026:c.1540+122T>C" "INTRON7" "Unknown significance" "rs181887691" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309970 "chr12:80887369:C>T" "PTPRQ" "NM_001145026:c.1540+135C>T" "INTRON7" "Unknown significance" "rs760324987" "This variant is a VUS because it does not have enough information."
309971 "chr12:80887377:C>T" "PTPRQ" "NM_001145026:c.1540+143C>T" "INTRON7" "Unknown significance" "rs552213943" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
309972 "chr12:80887397:G>A" "PTPRQ" "NM_001145026:c.1540+163G>A" "INTRON7" "Unknown significance" "rs770737117" "This variant is a VUS because it does not have enough information."
309973 "chr12:80887446:G>A" "PTPRQ" "NM_001145026:c.1540+212G>A" "INTRON7" "Unknown significance" "rs564122823" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
309974 "chr12:80887510:A>T" "PTPRQ" "NM_001145026:c.1540+276A>T" "INTRON7" "Benign" "rs79496234" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 9 5008 0.00179712
309975 "chr12:80887529:G>A" "PTPRQ" "NM_001145026:c.1540+295G>A" "INTRON7" "Unknown significance" "rs146231400" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
309976 "chr12:80887560:C>T" "PTPRQ" "NM_001145026:c.1540+326C>T" "INTRON7" "Unknown significance" "rs568171094" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
309977 "chr12:80887571:T>C" "PTPRQ" "NM_001145026:c.1540+337T>C" "INTRON7" "Unknown significance" "rs534278074" "This variant is a VUS because it does not have enough information."
309978 "chr12:80887591:T>C" "PTPRQ" "NM_001145026:c.1540+357T>C" "INTRON7" "Unknown significance" "rs554046928" "This variant is a VUS because it does not have enough information."
309979 "chr12:80887633:A>C" "PTPRQ" "NM_001145026:c.1540+399A>C" "INTRON7" "Benign" "rs185085208" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 5 1322 0.0038 0 1006 0 1 694 0.0014 9 1008 0.0089 0 978 0 15 5008 0.00299521
309980 "chr12:80887634:T>G" "PTPRQ" "NM_001145026:c.1540+400T>G" "INTRON7" "Benign" "rs78155497" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 6 1322 0.0045 94 1006 0.0934 38 694 0.0548 0 1008 0 64 978 0.0654 202 5008 0.0403355
309981 "chr12:80887658:G>C" "PTPRQ" "NM_001145026:c.1540+424G>C" "INTRON7" "Unknown significance" "rs569374387" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309982 "chr12:80887667:A>T" "PTPRQ" "NM_001145026:c.1540+433A>T" "INTRON7" "Unknown significance" "rs540104398" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309983 "chr12:80887696:->TA" "PTPRQ" "NM_001145026:c.1540+462_1540+463insTA" "INTRON7" "Unknown significance" "rs755155548" "This variant is a VUS because it does not have enough information."
309984 "chr12:80887729:C>T" "PTPRQ" "NM_001145026:c.1540+495C>T" "INTRON7" "Unknown significance" "rs762635029" "This variant is a VUS because it does not have enough information."
309985 "chr12:80887740:A>G" "PTPRQ" "NM_001145026:c.1540+506A>G" "INTRON7" "Benign" "rs137963176" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 5 1322 0.0038 0 1006 0 1 694 0.0014 9 1008 0.0089 0 978 0 15 5008 0.00299521
309986 "chr12:80887754:A>C" "PTPRQ" "NM_001145026:c.1540+520A>C" "INTRON7" "Benign" "rs6539522" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 416 1008 0.4127 848 978 0.8671 3764 5008 0.751597
309987 "chr12:80887781:C>T" "PTPRQ" "NM_001145026:c.1540+547C>T" "INTRON7" "Unknown significance" "rs751345688" "This variant is a VUS because it does not have enough information."
309988 "chr12:80887800:T>G" "PTPRQ" "NM_001145026:c.1540+566T>G" "INTRON7" "Unknown significance" "rs534550512" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309989 "chr12:80887817:T>C" "PTPRQ" "NM_001145026:c.1540+583T>C" "INTRON7" "Benign" "rs61950958" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 1322 0.0272 51 1006 0.0507 24 694 0.0346 0 1008 0 58 978 0.0593 169 5008 0.033746
309990 "chr12:80887879:G>T" "PTPRQ" "NM_001145026:c.1540+645G>T" "INTRON7" "Unknown significance" "rs574550500" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309991 "chr12:80887903:G>A" "PTPRQ" "NM_001145026:c.1540+669G>A" "INTRON7" "Unknown significance" "rs541581380" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309992 "chr12:80888004:G>A" "PTPRQ" "NM_001145026:c.1541-708G>A" "INTRON7" "Unknown significance" "rs188282600" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
309993 "chr12:80888015:T>G" "PTPRQ" "NM_001145026:c.1541-697T>G" "INTRON7" "Unknown significance" "rs575380730" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309994 "chr12:80888066:A>C" "PTPRQ" "NM_001145026:c.1541-646A>C" "INTRON7" "Unknown significance" "rs546067480" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
309995 "chr12:80888125:G>T" "PTPRQ" "NM_001145026:c.1541-587G>T" "INTRON7" "Unknown significance" "rs573195318" "This variant is a VUS because it does not have enough information."
309996 "chr12:80888142:G>A" "PTPRQ" "NM_001145026:c.1541-570G>A" "INTRON7" "Unknown significance" "rs564084246" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309997 "chr12:80888146:T>C" "PTPRQ" "NM_001145026:c.1541-566T>C" "INTRON7" "Unknown significance" "rs576552500" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309998 "chr12:80888174:T>G" "PTPRQ" "NM_001145026:c.1541-538T>G" "INTRON7" "Unknown significance" "rs540196011" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
309999 "chr12:80888198:A>G" "PTPRQ" "NM_001145026:c.1541-514A>G" "INTRON7" "Unknown significance" "rs755113564" "This variant is a VUS because it does not have enough information."
310000 "chr12:80888226:C>A" "PTPRQ" "NM_001145026:c.1541-486C>A" "INTRON7" "Unknown significance" "rs561765679" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310001 "chr12:80888239:A>T" "PTPRQ" "NM_001145026:c.1541-473A>T" "INTRON7" "Unknown significance" "rs529362482" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310002 "chr12:80888266:T>C" "PTPRQ" "NM_001145026:c.1541-446T>C" "INTRON7" "Unknown significance" "rs550824183" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310003 "chr12:80888286:A>G" "PTPRQ" "NM_001145026:c.1541-426A>G" "INTRON7" "Unknown significance" "rs569418712" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310004 "chr12:80888328:T>C" "PTPRQ" "NM_001145026:c.1541-384T>C" "INTRON7" "Unknown significance" "rs533402088" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310005 "chr12:80888397:->G" "PTPRQ" "NM_001145026:c.1541-315_1541-314insG" "INTRON7" "Unknown significance" "rs781389225" "This variant is a VUS because it does not have enough information."
310006 "chr12:80888398:T>A" "PTPRQ" "NM_001145026:c.1541-314T>A" "INTRON7" "Unknown significance" "rs180688089" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310007 "chr12:80888443:A>G" "PTPRQ" "NM_001145026:c.1541-269A>G" "INTRON7" "Unknown significance" "rs112120575" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310008 "chr12:80888447:C>T" "PTPRQ" "NM_001145026:c.1541-265C>T" "INTRON7" "Unknown significance" "rs545188368" "This variant is a VUS because it does not have enough information."
310009 "chr12:80888462:T>C" "PTPRQ" "NM_001145026:c.1541-250T>C" "INTRON7" "Unknown significance" "rs534511169" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310010 "chr12:80888483:G>A" "PTPRQ" "NM_001145026:c.1541-229G>A" "INTRON7" "Benign" "rs73347718" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
310011 "chr12:80888527:C>T" "PTPRQ" "NM_001145026:c.1541-185C>T" "INTRON7" "Unknown significance" "rs748735965" "This variant is a VUS because it does not have enough information."
310012 "chr12:80888531:C>T" "PTPRQ" "NM_001145026:c.1541-181C>T" "INTRON7" "Benign" "rs139455725" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 25 1322 0.0189 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 26 5008 0.00519169
310013 "chr12:80888552:G>C" "PTPRQ" "NM_001145026:c.1541-160G>C" "INTRON7" "Unknown significance" "rs186126906" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310014 "chr12:80888570:C>T" "PTPRQ" "NM_001145026:c.1541-142C>T" "INTRON7" "Benign" "rs4616108" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
310015 "chr12:80888573:A>G" "PTPRQ" "NM_001145026:c.1541-139A>G" "INTRON7" "Unknown significance" "rs778157177" "This variant is a VUS because it does not have enough information."
310016 "chr12:80888584:A>G" "PTPRQ" "NM_001145026:c.1541-128A>G" "INTRON7" "Unknown significance" "rs747339035" "This variant is a VUS because it does not have enough information."
310017 "chr12:80888599:G>A" "PTPRQ" "NM_001145026:c.1541-113G>A" "INTRON7" "Unknown significance" "rs371790118" "This variant is a VUS because it does not have enough information."
310018 "chr12:80888611:C>T" "PTPRQ" "NM_001145026:c.1541-101C>T" "INTRON7" "Benign" "rs191046921" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 5 1322 0.0038 0 1006 0 2 694 0.0029 9 1008 0.0089 0 978 0 16 5008 0.00319489
310019 "chr12:80888616:A>-" "PTPRQ" "NM_001145026:c.1541-96delA" "INTRON7" "Benign" "rs201853534" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
310020 "chr12:80888633:T>G" "PTPRQ" "NM_001145026:c.1541-79T>G" "INTRON7" "Benign" "rs181481824" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 5 1322 0.0038 0 1006 0 1 694 0.0014 9 1008 0.0089 0 978 0 15 5008 0.00299521
310021 "chr12:80888667:A>G" "PTPRQ" "NM_001145026:c.1541-45A>G" "INTRON7" "Benign" "rs11114479" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 3182 0.000942803 192 1384 0.138728 195 4566 0.042707 231 1322 0.1747 6 1006 0.006 44 694 0.0634 43 1008 0.0427 25 978 0.0256 349 5008 0.0696885 314 2008 0.156375 20 386 0.0518135 23 582 0.0395189 1 30 0.0333333 5 7612 0.000656858 4 150 0.0266667 128 6648 0.0192539 495 17416 0.0284221
310022 "chr12:80888677:CTTT>-" "PTPRQ" "NM_001145026:c.1541-35_1541-32delCTTT" "INTRON7" "Unknown significance" "rs756377711" "This variant is a VUS because it does not have enough information." 0 2036 0 0 388 0 0 596 0 0 32 0 0 7690 0 0 158 0 26 6840 0.00380117 26 17740 0.00146561
310023 "chr12:80888689:C>A" "PTPRQ" "NM_001145026:c.1541-23C>A" "INTRON7" "Unknown significance" "rs186668035" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042 3 2070 0.00144928 0 392 0 0 598 0 0 34 0 0 7882 0 0 166 0 1 7146 0.000139938 4 18288 0.000218723
310024 "chr12:80888701:A>G" "PTPRQ" "NM_001145026:c.1541-11A>G" "INTRON7" "Benign" "rs75959595" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 3182 0 95 1384 0.0686416 95 4566 0.020806 0 400 0 0 320 0 0 320 0 0 400 0 1 360 0.00277778 2 200 0.01 3 2000 0.0015 102 1322 0.0772 0 1006 0 7 694 0.0101 0 1008 0 0 978 0 109 5008 0.0217652 139 2108 0.0659393 2 400 0.005 0 614 0 0 34 0 6 8190 0.000732601 0 184 0 1 7702 0.000129836 148 19232 0.00769551
310025 "chr12:80888712:T>C" "PTPRQ" "NM_001145026:p.Val514Ala" "NM_001145026:c.1541T>C" "EXON8" "Unknown significance" "rs777233958" "This variant is a VUS because it does not have enough information." 0.113 "N" "0.0" "B" 0.888334 "N" "0.505" "C" 0 2134 0 0 404 0 0 620 0 0 34 0 0 8318 0 0 190 0 4 7820 0.000511509 4 19520 0.000204918
310026 "chr12:80888721:G>A" "PTPRQ" "NM_001145026:p.Arg517Lys" "NM_001145026:c.1550G>A" "EXON8" "Benign" "rs748960988" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1.048 "C" "0.001" "B" 0.999914 "N" "4.08" "C" 2 400 0.005 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 2 2000 0.001 0 2136 0 0 404 0 0 620 0 0 34 0 5 8374 0.000597086 0 190 0 0 7876 0 5 19634 0.00025466
310027 "chr12:80888742:T>C" "PTPRQ" "NM_001145026:p.Ile524Thr" "NM_001145026:c.1571T>C" "EXON8" "Unknown significance" "rs771269909" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.856" "P" 0.982296 "D" "5.89" "C" 0 2142 0 0 410 0 0 620 0 0 34 0 1 8440 0.000118483 0 190 0 0 7904 0 1 19740 0.0000506586
310028 "chr12:80888771:A>G" "PTPRQ" "NM_001145026:p.Arg534Gly" "NM_001145026:c.1600A>G" "EXON8" "Unknown significance" "rs779308648" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.349" "B" 0.762039 "N" "4.75" "C" 1 2148 0.000465549 0 410 0 0 620 0 0 34 0 0 8478 0 0 190 0 0 7912 0 1 19792 0.0000505255
310029 "chr12:80888784:C>T" "PTPRQ" "NM_001145026:p.Pro538Leu" "NM_001145026:c.1613C>T" "EXON8" "Unknown significance" "rs190634187" "This variant is a VUS because it does not have enough information." 0.935 "N" "1.0" "D" 1 "D" "5.89" "C" 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310030 "chr12:80888822:A>G" "PTPRQ" "NM_001145026:p.Ile551Val" "NM_001145026:c.1651A>G" "EXON8" "Unknown significance" "rs183202655" "This variant is a VUS because it does not have enough information." 0.237 "N" "0.001" "B" 0.999405 "N" "4.71" "C" 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 2150 0.000465116 0 410 0 0 620 0 0 34 0 0 8492 0 0 190 0 0 7914 0 1 19810 0.0000504796
310031 "chr12:80888826:T>A" "PTPRQ" "NM_001145026:p.Met552Lys" "NM_001145026:c.1655T>A" "EXON8" "Unknown significance" "rs772655161" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.389" "B" 0.989388 "D" "5.89" "C" 0 2150 0 0 410 0 0 620 0 0 34 0 0 8494 0 0 190 0 1 7914 0.000126358 1 19812 0.0000504745
310032 "chr12:80888827:G>T" "PTPRQ" "NM_001145026:p.Met552Ile" "NM_001145026:c.1656G>T" "EXON8" "Unknown significance" "rs775740717" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.001" "B" 0.689953 "D" "5.89" "C" 0 2150 0 0 410 0 0 620 0 0 34 0 0 8490 0 0 190 0 1 7914 0.000126358 1 19808 0.0000504847
310033 "chr12:80888836:A>G" "PTPRQ" "NM_001145026:p.Gly555Gly" "NM_001145026:c.1665A>G" "EXON8" "Unknown significance" "rs377698467" "This variant is a VUS because it does not have enough information." 0 3182 0 2 1384 0.00144509 2 4566 0.00043802 1 2150 0.000465116 0 410 0 0 620 0 0 34 0 0 8492 0 0 190 0 0 7914 0 1 19810 0.0000504796
310034 "chr12:80888864:C>T" "PTPRQ" "NM_001145026:p.Arg565Cys" "NM_001145026:c.1693C>T" "EXON8" "Unknown significance" "rs149658681" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.986" "D" 0.99994 "N" "3.88" "C" 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 2 978 0.002 3 5008 0.000599042 0 2150 0 0 410 0 0 620 0 0 34 0 0 8492 0 0 190 0 19 7914 0.00240081 19 19810 0.000959112
310035 "chr12:80888865:G>A" "PTPRQ" "NM_001145026:p.Arg565His" "NM_001145026:c.1694G>A" "EXON8" "Unknown significance" "rs745340134" "This variant is a VUS because it does not have enough information." -3.175 "N" "0.003" "B" 1 "N" "-10.1" "N" 1 2150 0.000465116 0 410 0 0 620 0 0 34 0 0 8492 0 0 190 0 0 7914 0 1 19810 0.0000504796
310036 "chr12:80888866:T>C" "PTPRQ" "NM_001145026:p.Arg565Arg" "NM_001145026:c.1695T>C" "EXON8" "Unknown significance" "rs147326297" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 2150 0.000465116 0 410 0 0 620 0 0 34 0 0 8492 0 0 190 0 2 7914 0.000252717 3 19810 0.000151439
310037 "chr12:80888877:A>T" "PTPRQ" "NM_001145026:c.1702+4A>T" "INTRON8" "Unknown significance" "rs370321499" "This variant is a VUS because it does not have enough information." 0 3182 0 1 1384 0.000722543 1 4566 0.00021901 1 2148 0.000465549 0 410 0 0 620 0 0 34 0 1 8490 0.000117786 0 190 0 2 7912 0.000252781 4 19804 0.000201979
310038 "chr12:80888880:A>T" "PTPRQ" "NM_001145026:c.1702+7A>T" "INTRON8" "Unknown significance" "rs751332334" "This variant is a VUS because it does not have enough information." 0 2146 0 0 410 0 0 620 0 0 34 0 1 8490 0.000117786 0 190 0 0 7914 0 1 19804 0.0000504948
310039 "chr12:80888898:A>G" "PTPRQ" "NM_001145026:c.1702+25A>G" "INTRON8" "Unknown significance" "rs759503051" "This variant is a VUS because it does not have enough information." 0 2146 0 0 410 0 0 622 0 0 34 0 1 8486 0.000117841 0 190 0 0 7914 0 1 19802 0.0000504999
310040 "chr12:80888935:T>-" "PTPRQ" "NM_001145026:c.1703-36delT" "INTRON8" "Unknown significance" "rs573558033" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 2 694 0.0029 1 1008 0.001 0 978 0 8 5008 0.00159744 7 2134 0.00328022 1 406 0.00246305 0 616 0 0 34 0 1 8428 0.000118652 0 190 0 1 7910 0.000126422 10 19718 0.000507151
310041 "chr12:80888957:T>C" "PTPRQ" "NM_001145026:c.1703-14T>C" "INTRON8" "Unknown significance" "rs767377843" "This variant is a VUS because it does not have enough information." 0 2104 0 0 410 0 0 614 0 0 34 0 0 8394 0 0 190 0 1 7912 0.00012639 1 19658 0.0000508699
310042 "chr12:80888972:G>T" "PTPRQ" "NM_001145026:p.Val568Val" "NM_001145026:c.1704G>T" "EXON9" "Unknown significance" "rs752218516" "This variant is a VUS because it does not have enough information." 0 2088 0 0 410 0 0 606 0 0 34 0 2 8346 0.000239636 0 190 0 0 7912 0 2 19586 0.000102114
310043 "chr12:80888978:C>T" "PTPRQ" "NM_001145026:p.Ser570Ser" "NM_001145026:c.1710C>T" "EXON9" "Benign" "rs140978858" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 4 1006 0.004 1 694 0.0014 0 1008 0 0 978 0 5 5008 0.000998403 1 2080 0.000480769 1 408 0.00245098 0 606 0 0 32 0 43 8300 0.00518072 3 190 0.0157895 9 7910 0.0011378 57 19526 0.00291918
310044 "chr12:80888990:T>C" "PTPRQ" "NM_001145026:p.Ile574Ile" "NM_001145026:c.1722T>C" "EXON9" "Unknown significance" "rs551968579" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2016 0 0 408 0 0 602 0 0 32 0 1 8142 0.00012282 0 186 0 1 7906 0.000126486 2 19292 0.00010367
310045 "chr12:80889020:T>G" "PTPRQ" "NM_001145026:p.Ser584Ser" "NM_001145026:c.1752T>G" "EXON9" "Unknown significance" "rs753476866" "This variant is a VUS because it does not have enough information." 0 2082 0 0 408 0 0 608 0 0 32 0 0 8236 0 0 188 0 1 7902 0.00012655 1 19456 0.000051398
310046 "chr12:80889052:C>T" "PTPRQ" "NM_001145026:p.Pro595Leu" "NM_001145026:c.1784C>T" "EXON9" "Unknown significance" "rs756914432" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.998" "D" 1 "D" "6.03" "C" 0 2138 0 0 410 0 0 620 0 0 34 0 0 8388 0 0 190 0 1 7898 0.000126614 1 19678 0.0000508182
310047 "chr12:80889055:A>G" "PTPRQ" "NM_001145026:p.Asn596Ser" "NM_001145026:c.1787A>G" "EXON9" "Unknown significance" "rs779445990" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.96" "D" 0.999989 "D" "6.03" "C" 0 2138 0 0 410 0 0 620 0 0 34 0 0 8394 0 0 190 0 1 7898 0.000126614 1 19684 0.0000508027
310048 "chr12:80889060:A>G" "PTPRQ" "NM_001145026:p.Lys598Glu" "NM_001145026:c.1792A>G" "EXON9" "Unknown significance" "rs542556695" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.04" "B" 0.598047 "D" "4.89" "C"
310049 "chr12:80889075:A>G" "PTPRQ" "NM_001145026:p.Thr603Ala" "NM_001145026:c.1807A>G" "EXON9" "Unknown significance" "rs746192915" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.483" "P" 0.998185 "D" "5.91" "C" 0 2138 0 0 410 0 0 620 0 0 34 0 0 8402 0 0 188 0 1 7888 0.000126775 1 19680 0.000050813
310050 "chr12:80889077:G>A" "PTPRQ" "NM_001145026:p.Thr603Thr" "NM_001145026:c.1809G>A" "EXON9" "Unknown significance" "rs567091002" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310051 "chr12:80889099:A>T" "PTPRQ" "NM_001145026:p.Thr611Ser" "NM_001145026:c.1831A>T" "EXON9" "Unknown significance" "rs762910769" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.181" "B" 0.884985 "D" "4.7" "C"
310052 "chr12:80889100:C>T" "PTPRQ" "NM_001145026:p.Thr611Ile" "NM_001145026:c.1832C>T" "EXON9" "Unknown significance" "rs780646915" "This variant is a VUS because it does not have enough information." 0.892 "N" "0.997" "D" 0.996899 "D" "5.91" "C" 0 2142 0 0 408 0 0 620 0 0 34 0 1 8366 0.000119531 0 188 0 0 7828 0 1 19586 0.0000510569
310053 "chr12:80889115:A>G" "PTPRQ" "NM_001145026:p.Gln616Arg" "NM_001145026:c.1847A>G" "EXON9" "Unknown significance" "rs527967292" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.009" "B" 0.95785 "N" "5.91" "C" 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 2142 0.000466853 0 408 0 0 618 0 0 34 0 0 8328 0 0 188 0 0 7760 0 1 19478 0.00005134
310054 "chr12:80889127:T>C" "PTPRQ" "NM_001145026:p.Ile620Thr" "NM_001145026:c.1859T>C" "EXON9" "Benign" "rs549729194" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." -0.282 "N" "0.0" "B" 0.999983 "N" "1.94" "C" 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2142 0 1 408 0.00245098 0 618 0 0 34 0 1 8290 0.000120627 1 184 0.00543478 16 7688 0.00208117 19 19364 0.000981202
310055 "chr12:80889130:A>G" "PTPRQ" "NM_001145026:p.Asp621Gly" "NM_001145026:c.1862A>G" "EXON9" "Unknown significance" "rs776739933" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.134" "B" 0.983077 "N" "4.75" "C" 0 2140 0 0 406 0 0 618 0 0 34 0 0 8296 0 0 184 0 3 7674 0.00039093 3 19352 0.000155023
310056 "chr12:80889131:T>C" "PTPRQ" "NM_001145026:p.Asp621Asp" "NM_001145026:c.1863T>C" "EXON9" "Unknown significance" "rs568035867" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2138 0 0 406 0 0 618 0 0 34 0 0 8290 0 0 184 0 9 7660 0.00117493 9 19330 0.000465598
310057 "chr12:80889137:C>T" "PTPRQ" "NM_001145026:p.Ser623Ser" "NM_001145026:c.1869C>T" "EXON9" "Unknown significance" "rs770019394" "This variant is a VUS because it does not have enough information." 2 2134 0.000937207 0 406 0 0 616 0 0 34 0 0 8254 0 0 182 0 0 7548 0 2 19174 0.000104308
310058 "chr12:80889143:C>T" "PTPRQ" "NM_001145026:p.Leu625Leu" "NM_001145026:c.1875C>T" "EXON9" "Unknown significance" "rs774137152" "This variant is a VUS because it does not have enough information." 1 2130 0.000469484 0 402 0 0 614 0 0 34 0 0 8198 0 0 184 0 0 7368 0 1 18930 0.0000528262
310059 "chr12:80889157:AAC>-" "PTPRQ" "NM_001145026:c.1882+7_1882+9delAAC" "INTRON9" "Unknown significance" "rs779751671" "This variant is a VUS because it does not have enough information." 0 2086 0 0 360 0 0 602 0 0 34 0 1 7402 0.000135099 0 160 0 0 5540 0 1 16184 0.0000617894
310060 "chr12:80889159:C>T" "PTPRQ" "NM_001145026:c.1882+9C>T" "INTRON9" "Benign" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 400 0.005 2 320 0.00625 1 320 0.003125 1 400 0.0025 8 360 0.0222222 0 200 0 14 2000 0.007
310061 "chr12:80889160:A>G" "PTPRQ" "NM_001145026:c.1882+10A>G" "INTRON9" "Benign" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 400 0.02 6 320 0.01875 2 320 0.00625 1 400 0.0025 9 360 0.025 0 200 0 26 2000 0.013
310062 "chr12:80889161:A>T" "PTPRQ" "NM_001145026:c.1882+11A>T" "INTRON9" "Benign" "rs367763079" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 10 400 0.025 8 320 0.025 3 320 0.009375 2 400 0.005 9 360 0.025 0 200 0 32 2000 0.016
310063 "chr12:80889163:G>T" "PTPRQ" "NM_001145026:c.1882+13G>T" "INTRON9" "Benign" "rs372690187" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 400 0.0375 8 320 0.025 8 320 0.025 6 400 0.015 15 360 0.0416667 4 200 0.02 56 2000 0.028 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310064 "chr12:80889165:T>G" "PTPRQ" "NM_001145026:c.1882+15T>G" "INTRON9" "Benign" "rs375938303" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 18 400 0.045 9 320 0.028125 9 320 0.028125 8 400 0.02 17 360 0.0472222 6 200 0.03 67 2000 0.0335
310065 "chr12:80889166:->TTG" "PTPRQ" "NM_001145026:c.1882+16_1882+17insTTG" "INTRON9" "Benign" "rs145970310" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 971 1322 0.7345 904 1006 0.8986 579 694 0.8343 401 1008 0.3978 834 978 0.8528 3689 5008 0.736621 1450 1914 0.757576 275 324 0.848765 251 566 0.443463 29 32 0.90625 5586 6108 0.914538 94 114 0.824561 1953 2352 0.830357 9638 11410 0.844698
310066 "chr12:80889166:->TTGTTG" "PTPRQ" "NM_001145026:c.1882+16_1882+17insTTGTTG" "INTRON9" "Benign" "rs145970310" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1914 0 0 324 0 0 566 0 0 32 0 22 6108 0.00360183 1 114 0.00877193 0 2352 0 23 11410 0.00201578
310067 "chr12:80889166:TTG>-" "PTPRQ" "NM_001145026:c.1882+16_1882+18delTTG" "INTRON9" "Unknown significance" "rs776710708" "This variant is a VUS because it does not have enough information." 0 1914 0 0 324 0 0 566 0 0 32 0 0 6108 0 0 114 0 0 2352 0 0 11410 0
310068 "chr12:80889167:->TTG" "PTPRQ" "NM_001145026:c.1882+17_1882+18insTTG" "INTRON9" "Unknown significance" "rs35659761" "This variant is a VUS because it does not have enough information."
310069 "chr12:80889180:G>A" "PTPRQ" "NM_001145026:c.1882+30G>A" "INTRON9" "Unknown significance" "rs550552307" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2018 0 0 354 0 0 570 0 0 32 0 0 6790 0 0 132 0 2 3564 0.000561167 2 13460 0.000148588
310070 "chr12:80889181:->TTGTTGTTT" "PTPRQ" "NM_001145026:c.1882+31_1882+32insTTGTTGTTT" "INTRON9" "Unknown significance" "rs748055008" "This variant is a VUS because it does not have enough information." 0 2018 0 0 354 0 0 570 0 0 32 0 0 6790 0 0 132 0 0 3564 0 0 13460 0
310071 "chr12:80889184:->GTT" "PTPRQ" "NM_001145026:c.1882+34_1882+35insGTT" "INTRON9" "Unknown significance" "rs386377128" "This variant is a VUS because it does not have enough information."
310072 "chr12:80889193:C>T" "PTPRQ" "NM_001145026:c.1882+43C>T" "INTRON9" "Unknown significance" "rs767286191" "This variant is a VUS because it does not have enough information." 0 1942 0 0 328 0 0 526 0 0 32 0 1 6148 0.000162655 0 98 0 1 1856 0.000538793 2 10930 0.000182983
310073 "chr12:80889245:A>C" "PTPRQ" "NM_001145026:c.1882+95A>C" "INTRON9" "Unknown significance" "rs763945843" "This variant is a VUS because it does not have enough information."
310074 "chr12:80889260:T>C" "PTPRQ" "NM_001145026:c.1882+110T>C" "INTRON9" "Unknown significance" "rs144863467" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310075 "chr12:80889268:T>C" "PTPRQ" "NM_001145026:c.1882+118T>C" "INTRON9" "Unknown significance" "rs561209944" "This variant is a VUS because it does not have enough information."
310076 "chr12:80889274:G>A" "PTPRQ" "NM_001145026:c.1882+124G>A" "INTRON9" "Unknown significance" "rs774142070" "This variant is a VUS because it does not have enough information."
310077 "chr12:80889285:T>A" "PTPRQ" "NM_001145026:c.1882+135T>A" "INTRON9" "Unknown significance" "rs566396959" "This variant is a VUS because it does not have enough information."
310078 "chr12:80889323:C>T" "PTPRQ" "NM_001145026:c.1882+173C>T" "INTRON9" "Benign" "rs12309616" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 231 1322 0.1747 6 1006 0.006 44 694 0.0634 43 1008 0.0427 25 978 0.0256 349 5008 0.0696885
310079 "chr12:80889377:C>T" "PTPRQ" "NM_001145026:c.1882+227C>T" "INTRON9" "Unknown significance" "rs557504489" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310080 "chr12:80889404:T>C" "PTPRQ" "NM_001145026:c.1882+254T>C" "INTRON9" "Unknown significance" "rs187937415" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 4 1008 0.004 0 978 0 4 5008 0.000798722
310081 "chr12:80889434:C>T" "PTPRQ" "NM_001145026:c.1882+284C>T" "INTRON9" "Unknown significance" "rs533821148" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310082 "chr12:80889439:T>C" "PTPRQ" "NM_001145026:c.1882+289T>C" "INTRON9" "Benign" "rs59090607" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 96 1322 0.0726 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 101 5008 0.0201677
310083 "chr12:80889481:G>C" "PTPRQ" "NM_001145026:c.1883-297G>C" "INTRON9" "Unknown significance" "rs777637279" "This variant is a VUS because it does not have enough information."
310084 "chr12:80889526:A>G" "PTPRQ" "NM_001145026:c.1883-252A>G" "INTRON9" "Unknown significance" "rs147929202" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310085 "chr12:80889530:C>T" "PTPRQ" "NM_001145026:c.1883-248C>T" "INTRON9" "Benign" "rs11114480" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 40 1322 0.0303 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 42 5008 0.00838658
310086 "chr12:80889533:G>T" "PTPRQ" "NM_001145026:c.1883-245G>T" "INTRON9" "Unknown significance" "rs562915963" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
310087 "chr12:80889533:G>A" "PTPRQ" "NM_001145026:c.1883-245G>A" "INTRON9" "Unknown significance" "rs562915963" "This variant is a VUS because it does not have enough information."
310088 "chr12:80889534:C>A" "PTPRQ" "NM_001145026:c.1883-244C>A" "INTRON9" "Unknown significance" "rs754095799" "This variant is a VUS because it does not have enough information."
310089 "chr12:80889612:G>A" "PTPRQ" "NM_001145026:c.1883-166G>A" "INTRON9" "Benign" "rs11114481" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 275 1322 0.208 646 1006 0.6421 400 694 0.5764 363 1008 0.3601 660 978 0.6748 2344 5008 0.468051
310090 "chr12:80889636:T>A" "PTPRQ" "NM_001145026:c.1883-142T>A" "INTRON9" "Unknown significance" "rs765308533" "This variant is a VUS because it does not have enough information."
310091 "chr12:80889663:G>A" "PTPRQ" "NM_001145026:c.1883-115G>A" "INTRON9" "Unknown significance" "rs545546257" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310092 "chr12:80889666:A>G" "PTPRQ" "NM_001145026:c.1883-112A>G" "INTRON9" "Unknown significance" "rs190899683" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310093 "chr12:80889679:C>T" "PTPRQ" "NM_001145026:c.1883-99C>T" "INTRON9" "Unknown significance" "rs752750837" "This variant is a VUS because it does not have enough information."
310094 "chr12:80889680:C>T" "PTPRQ" "NM_001145026:c.1883-98C>T" "INTRON9" "Unknown significance" "rs527926743" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310095 "chr12:80889683:C>T" "PTPRQ" "NM_001145026:c.1883-95C>T" "INTRON9" "Unknown significance" "rs182379249" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 1 1008 0.001 0 978 0 2 5008 0.000399361
310096 "chr12:80889698:T>C" "PTPRQ" "NM_001145026:c.1883-80T>C" "INTRON9" "Unknown significance" "rs561374399" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310097 "chr12:80889704:C>A" "PTPRQ" "NM_001145026:c.1883-74C>A" "INTRON9" "Unknown significance" "rs532043341" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361
310098 "chr12:80889727:C>T" "PTPRQ" "NM_001145026:c.1883-51C>T" "INTRON9" "Unknown significance" "rs550275750" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310099 "chr12:80889729:A>T" "PTPRQ" "NM_001145026:c.1883-49A>T" "INTRON9" "Unknown significance" "rs568859152" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361 0 2082 0 0 380 0 0 596 0 0 32 0 0 8300 0 0 186 0 12 7888 0.0015213 12 19464 0.000616523
310100 "chr12:80889730:A>C" "PTPRQ" "NM_001145026:c.1883-48A>C" "INTRON9" "Unknown significance" "rs539127982" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310101 "chr12:80889731:G>A" "PTPRQ" "NM_001145026:c.1883-47G>A" "INTRON9" "Unknown significance" "rs551096434" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310102 "chr12:80889755:C>A" "PTPRQ" "NM_001145026:c.1883-23C>A" "INTRON9" "Unknown significance" "rs760633710" "This variant is a VUS because it does not have enough information." 0 2094 0 0 382 0 0 606 0 0 32 0 0 8330 0 0 186 0 1 7898 0.000126614 1 19528 0.0000512085
310103 "chr12:80889817:C>G" "PTPRQ" "NM_001145026:p.Ala641Gly" "NM_001145026:c.1922C>G" "EXON10" "Unknown significance" "rs763564412" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.985" "D" 1 "D" "5.93" "C"
310104 "chr12:80889828:G>A" "PTPRQ" "NM_001145026:p.Val645Ile" "NM_001145026:c.1933G>A" "EXON10" "Unknown significance" "rs753342336" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.504" "P" 0.947084 "D" "5.93" "C" 0 2134 0 0 404 0 0 616 0 0 32 0 0 8452 0 0 188 0 1 7910 0.000126422 1 19736 0.0000506688
310105 "chr12:80889828:G>T" "PTPRQ" "NM_001145026:p.Val645Phe" "NM_001145026:c.1933G>T" "EXON10" "Unknown significance" "rs753342336" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.992" "D" 0.998487 "D" "5.93" "C" 0 2134 0 0 404 0 0 616 0 0 32 0 1 8452 0.000118315 0 188 0 0 7910 0 1 19736 0.0000506688
310106 "chr12:80889829:T>A" "PTPRQ" "NM_001145026:p.Val645Asp" "NM_001145026:c.1934T>A" "EXON10" "Benign" "rs10778752" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1.061 "C" "0.99" "D" 0.000000293172 "P" "5.93" "C" 2980 3182 0.936518 1065 1384 0.769509 4045 4566 0.885896 986 1322 0.7458 920 1006 0.9145 588 694 0.8473 415 1008 0.4117 848 978 0.8671 3757 5008 0.7502 1652 2144 0.770522 356 410 0.868293 287 618 0.464401 30 34 0.882353 7839 8476 0.924847 163 190 0.857895 6997 7914 0.884129 17324 19786 0.875569
310107 "chr12:80889840:T>A" "PTPRQ" "NM_001145026:p.Ser649Thr" "NM_001145026:c.1945T>A" "EXON10" "Unknown significance" "rs750826858" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.863" "P" 0.988779 "N" "3.59" "C" 0 2136 0 0 406 0 0 618 0 0 34 0 1 8450 0.000118343 0 188 0 0 7908 0 1 19740 0.0000506586
310108 "chr12:80889841:C>T" "PTPRQ" "NM_001145026:p.Ser649Phe" "NM_001145026:c.1946C>T" "EXON10" "Benign" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.935 "N" "0.993" "D" 0.590025 "D" "5.05" "C" 0 400 0 0 320 0 0 320 0 2 400 0.005 0 360 0 0 200 0 2 2000 0.001
310109 "chr12:80889863:C>A" "PTPRQ" "NM_001145026:p.Ile656Ile" "NM_001145026:c.1968C>A" "EXON10" "Benign" "rs370595432" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 400 0 0 320 0 1 320 0.003125 2 400 0.005 0 360 0 0 200 0 3 2000 0.0015 0 1322 0 0 1006 0 0 694 0 9 1008 0.0089 0 978 0 9 5008 0.00179712 0 2128 0 0 402 0 7 616 0.0113636 0 34 0 0 8438 0 0 188 0 19 7906 0.00240324 26 19712 0.00131899
310110 "chr12:80889867:G>T" "PTPRQ" "NM_001145026:p.Val658Leu" "NM_001145026:c.1972G>T" "EXON10" "Unknown significance" "rs555147236" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.206" "B" 0.999689 "D" "4.05" "C" 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310111 "chr12:80889904:G>T" "PTPRQ" "NM_001145026:c.1990+19G>T" "INTRON10" "Unknown significance" "rs563357119" "This variant is a VUS because it does not have enough information."
310112 "chr12:80889910:A>C" "PTPRQ" "NM_001145026:c.1990+25A>C" "INTRON10" "Unknown significance" "rs747510550" "This variant is a VUS because it does not have enough information." 0 2122 0 0 402 0 0 612 0 0 34 0 0 8394 0 0 188 0 1 7890 0.000126743 1 19642 0.0000509113
310113 "chr12:80889911:->T" "PTPRQ" "NM_001145026:c.1990+26_1990+27insT" "INTRON10" "Unknown significance" "rs769836663" "This variant is a VUS because it does not have enough information." 0 2122 0 0 402 0 0 612 0 0 34 0 1 8394 0.000119133 0 188 0 0 7890 0 1 19642 0.0000509113
310114 "chr12:80889917:T>A" "PTPRQ" "NM_001145026:c.1990+32T>A" "INTRON10" "Benign" "rs187920771" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489 18 2120 0.00849057 1 402 0.00248756 0 610 0 0 32 0 0 8384 0 1 184 0.00543478 0 7890 0 20 19622 0.00101926
310115 "chr12:80889918:A>C" "PTPRQ" "NM_001145026:c.1990+33A>C" "INTRON10" "Unknown significance" "rs781152378" "This variant is a VUS because it does not have enough information." 0 2122 0 0 402 0 1 610 0.00163934 0 32 0 0 8378 0 0 186 0 0 7888 0 1 19618 0.0000509736
310116 "chr12:80889918:A>T" "PTPRQ" "NM_001145026:c.1990+33A>T" "INTRON10" "Unknown significance" "rs781152378" "This variant is a VUS because it does not have enough information." 0 2122 0 0 402 0 0 610 0 0 32 0 1 8378 0.00011936 0 186 0 4 7888 0.000507099 5 19618 0.000254868
310117 "chr12:80889988:A>G" "PTPRQ" "NM_001145026:c.1991-41A>G" "INTRON10" "Unknown significance" "rs769923675" "This variant is a VUS because it does not have enough information." 1 2138 0.000467727 0 410 0 0 620 0 0 34 0 0 8394 0 0 190 0 0 7912 0 1 19698 0.0000507666
310118 "chr12:80889992:A>G" "PTPRQ" "NM_001145026:c.1991-37A>G" "INTRON10" "Unknown significance" "rs538162665" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2136 0 0 410 0 0 620 0 0 34 0 0 8396 0 0 190 0 3 7912 0.000379171 3 19698 0.0001523
310119 "chr12:80889998:A>G" "PTPRQ" "NM_001145026:c.1991-31A>G" "INTRON10" "Unknown significance" "rs749507912" "This variant is a VUS because it does not have enough information." 1 2138 0.000467727 0 408 0 0 618 0 0 34 0 0 8382 0 0 186 0 0 7908 0 1 19674 0.0000508285
310120 "chr12:80890000:G>T" "PTPRQ" "NM_001145026:c.1991-29G>T" "INTRON10" "Unknown significance" "rs556262144" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310121 "chr12:80890002:A>G" "PTPRQ" "NM_001145026:c.1991-27A>G" "INTRON10" "Unknown significance" "rs377245885" "This variant is a VUS because it does not have enough information." 1 3182 0.000314268 0 1384 0 1 4566 0.00021901
310122 "chr12:80890003:C>-" "PTPRQ" "NM_001145026:c.1991-26delC" "INTRON10" "Unknown significance" "rs772924066" "This variant is a VUS because it does not have enough information." 0 2136 0 0 406 0 0 620 0 0 34 0 0 8372 0 0 186 0 2 7904 0.000253036 2 19658 0.00010174
310123 "chr12:80890004:T>C" "PTPRQ" "NM_001145026:c.1991-25T>C" "INTRON10" "Unknown significance" "rs370469425" "This variant is a VUS because it does not have enough information." 0 3182 0 5 1384 0.00361272 5 4566 0.00109505 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808 8 2142 0.00373483 0 410 0 0 620 0 0 34 0 0 8418 0 0 190 0 0 7908 0 8 19722 0.000405638
310124 "chr12:80890009:->ATGTTCTT" "PTPRQ" "NM_001145026:c.1991-20_1991-19insATGTTCTT" "INTRON10" "Benign" "rs527618942" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 5 1006 0.005 2 694 0.0029 0 1008 0 0 978 0 7 5008 0.00139776 1 2140 0.00046729 3 410 0.00731707 0 620 0 0 34 0 38 8418 0.00451414 2 190 0.0105263 4 7912 0.000505561 48 19724 0.00243358
310125 "chr12:80890032:C>T" "PTPRQ" "NM_001145026:p.Pro665Leu" "NM_001145026:c.1994C>T" "EXON11" "Unknown significance" "rs775248167" "This variant is a VUS because it does not have enough information." 0.935 "N" "1.0" "D" 1 "D" "5.93" "C" 0 2148 0 0 410 0 0 620 0 0 34 0 0 8440 0 0 190 0 5 7912 0.000631951 5 19754 0.000253113
310126 "chr12:80890054:C>G" "PTPRQ" "NM_001145026:p.Val672Val" "NM_001145026:c.2016C>G" "EXON11" "Unknown significance" "rs760554958" "This variant is a VUS because it does not have enough information." 0 2148 0 0 410 0 0 622 0 0 34 0 0 8472 0 0 190 0 1 7914 0.000126358 1 19790 0.0000505306
310127 "chr12:80890055:G>A" "PTPRQ" "NM_001145026:p.Glu673Lys" "NM_001145026:c.2017G>A" "EXON11" "Unknown significance" "rs375302493" "This variant is a VUS because it does not have enough information." -0.213 "N" "0.006" "B" 1 "N" "1.95" "C" 1 3182 0.000314268 0 1384 0 1 4566 0.00021901 0 2148 0 0 410 0 0 622 0 0 34 0 1 8476 0.00011798 0 190 0 0 7914 0 1 19794 0.0000505204
310128 "chr12:80890071:C>A" "PTPRQ" "NM_001145026:p.Thr678Asn" "NM_001145026:c.2033C>A" "EXON11" "Unknown significance" "rs776006118" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.052" "B" 0.687564 "D" "5.83" "C" 0 2148 0 0 410 0 0 622 0 0 34 0 1 8482 0.000117897 0 190 0 0 7914 0 1 19800 0.0000505051
310129 "chr12:80890072:C>T" "PTPRQ" "NM_001145026:p.Thr678Thr" "NM_001145026:c.2034C>T" "EXON11" "Unknown significance" "rs545505456" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681 0 2148 0 0 410 0 0 622 0 0 34 0 1 8484 0.000117869 0 190 0 2 7914 0.000252717 3 19802 0.0001515
310130 "chr12:80890073:G>A" "PTPRQ" "NM_001145026:p.Ala679Thr" "NM_001145026:c.2035G>A" "EXON11" "Unknown significance" "rs745470985" "This variant is a VUS because it does not have enough information." -0.353 "N" "0.843" "P" 0.964055 "N" "1.42" "C"
310131 "chr12:80890091:A>G" "PTPRQ" "NM_001145026:p.Lys685Glu" "NM_001145026:c.2053A>G" "EXON11" "Unknown significance" "rs764822457" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.064" "B" 0.999805 "N" "4.67" "C" 0 2148 0 0 410 0 0 622 0 0 34 0 0 8486 0 0 190 0 1 7914 0.000126358 1 19804 0.0000504948
310132 "chr12:80890096:G>A" "PTPRQ" "NM_001145026:p.Trp686Stop" "NM_001145026:c.2058G>A" "EXON11" "Pathogenic" "Hearing loss, non-syndromic, autosomal recessive" "04/10/2015 -- Manually curated by the MORL." 1.048 "C" 1 "A" "5.83" "C"
310133 "chr12:80890105:C>T" "PTPRQ" "NM_001145026:p.Pro689Pro" "NM_001145026:c.2067C>T" "EXON11" "Unknown significance" "rs560612932" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 0 2148 0 0 410 0 1 622 0.00160772 0 34 0 0 8488 0 0 190 0 0 7914 0 1 19806 0.0000504898
310134 "chr12:80890119:G>T" "PTPRQ" "NM_001145026:p.Gly694Val" "NM_001145026:c.2081G>T" "EXON11" "Unknown significance" "rs538702836" "This variant is a VUS because it does not have enough information." 0.998 "C" "1.0" "D" 1 "D" "5.74" "C"
310135 "chr12:80890120:G>A" "PTPRQ" "NM_001145026:p.Gly694Gly" "NM_001145026:c.2082G>A" "EXON11" "Unknown significance" "rs758091640" "This variant is a VUS because it does not have enough information."
310136 "chr12:80890120:G>T" "PTPRQ" "NM_001145026:p.Gly694Gly" "NM_001145026:c.2082G>T" "EXON11" "Unknown significance" "rs758091640" "This variant is a VUS because it does not have enough information."
310137 "chr12:80890140:T>A" "PTPRQ" "NM_001145026:p.Val701Glu" "NM_001145026:c.2102T>A" "EXON11" "Unknown significance" "rs532297503" "This variant is a VUS because it does not have enough information." 1.011 "C" "1.0" "D" 0.999997 "D" "5.74" "C"
310138 "chr12:80890152:A>C" "PTPRQ" "NM_001145026:p.Asn705Thr" "NM_001145026:c.2114A>C" "EXON11" "Unknown significance" "rs769602893" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.998" "D" 0.875369 "N" "3.38" "C"
310139 "chr12:80890157:G>A" "PTPRQ" "NM_001145026:p.Asp707Asn" "NM_001145026:c.2119G>A" "EXON11" "Unknown significance" "rs759426858" "This variant is a VUS because it does not have enough information." 0.106 "N" "0.0" "B" 1 "N" "2.94" "C"
310140 "chr12:80890160:A>G" "PTPRQ" "NM_001145026:p.Thr708Ala" "NM_001145026:c.2122A>G" "EXON11" "Unknown significance" "rs751901816" "This variant is a VUS because it does not have enough information." -0.205 "N" "0.0" "B" 1 "N" "-11.5" "N" 0 2146 0 0 410 0 0 622 0 0 34 0 0 8454 0 0 190 0 1 7914 0.000126358 1 19770 0.0000505817
310141 "chr12:80890161:C>G" "PTPRQ" "NM_001145026:p.Thr708Ser" "NM_001145026:c.2123C>G" "EXON11" "Unknown significance" "rs572573735" "This variant is a VUS because it does not have enough information." 0.892 "N" "0.0" "B" 1 "N" "4.78" "C" 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2146 0 0 410 0 0 622 0 0 34 0 0 8454 0 0 190 0 1 7914 0.000126358 1 19770 0.0000505817
310142 "chr12:80890163:T>C" "PTPRQ" "NM_001145026:p.Leu709Leu" "NM_001145026:c.2125T>C" "EXON11" "Benign" "rs77699008" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 3182 0.000628536 2 1384 0.00144509 4 4566 0.00087604 0 400 0 31 320 0.096875 1 320 0.003125 35 400 0.0875 0 360 0 0 200 0 67 2000 0.0335 3 1322 0.0023 6 1006 0.006 35 694 0.0504 42 1008 0.0417 25 978 0.0256 111 5008 0.0221645 3 2148 0.00139665 17 410 0.0414634 23 622 0.0369775 1 34 0.0294118 2 8458 0.000236463 1 190 0.00526316 139 7914 0.0175638 186 19776 0.00940534
310143 "chr12:80890165:A>G" "PTPRQ" "NM_001145026:p.Leu709Leu" "NM_001145026:c.2127A>G" "EXON11" "Unknown significance" "rs561548972" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 2146 0.000465983 0 410 0 0 622 0 0 34 0 0 8460 0 0 190 0 0 7914 0 1 19776 0.0000505663
310144 "chr12:80890180:A>G" "PTPRQ" "NM_001145026:p.Thr714Thr" "NM_001145026:c.2142A>G" "EXON11" "Unknown significance" "rs756254141" "This variant is a VUS because it does not have enough information." 1 2148 0.000465549 0 410 0 0 622 0 0 34 0 0 8472 0 0 190 0 0 7914 0 1 19790 0.0000505306
310145 "chr12:80890183:A>G" "PTPRQ" "NM_001145026:p.Ser715Ser" "NM_001145026:c.2145A>G" "EXON11" "Unknown significance" "rs531885101" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2148 0 0 410 0 0 622 0 0 34 0 1 8474 0.000118008 0 190 0 0 7914 0 1 19792 0.0000505255
310146 "chr12:80890192:C>T" "PTPRQ" "NM_001145026:p.Asp718Asp" "NM_001145026:c.2154C>T" "EXON11" "Unknown significance" "rs749565156" "This variant is a VUS because it does not have enough information." 0 2148 0 0 410 0 0 622 0 0 34 0 0 8476 0 0 190 0 1 7914 0.000126358 1 19794 0.0000505204
310147 "chr12:80890229:A>G" "PTPRQ" "NM_001145026:p.Asn731Asp" "NM_001145026:c.2191A>G" "EXON11" "Unknown significance" "rs748763943" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.996" "D" 0.999996 "D" "5.74" "C"
310148 "chr12:80890238:G>A" "PTPRQ" "NM_001145026:p.Val734Ile" "NM_001145026:c.2200G>A" "EXON11" "Unknown significance" "rs764845488" "This variant is a VUS because it does not have enough information." 0.12 "N" "0.059" "B" 0.953379 "D" "1.81" "C"
310149 "chr12:80890262:C>T" "PTPRQ" "NM_001145026:p.His742Tyr" "NM_001145026:c.2224C>T" "EXON11" "Unknown significance" "rs550480842" "This variant is a VUS because it does not have enough information." 0.892 "N" "1.0" "D" 0.999991 "D" "5.74" "C" 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310150 "chr12:80890263:A>G" "PTPRQ" "NM_001145026:p.His742Arg" "NM_001145026:c.2225A>G" "EXON11" "Unknown significance" "rs562332341" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.999" "D" 0.999985 "D" "4.57" "C" 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722 2 2140 0.000934579 0 406 0 0 618 0 0 34 0 0 8486 0 0 190 0 0 7914 0 2 19788 0.000101071
310151 "chr12:80890277:T>G" "PTPRQ" "NM_001145026:p.Ser747Ala" "NM_001145026:c.2239T>G" "EXON11" "Unknown significance" "rs768630187" "This variant is a VUS because it does not have enough information." 1.011 "C" "0.987" "D" 0.999719 "D" "5.74" "C"
310152 "chr12:80890289:T>C" "PTPRQ" "NM_001145026:p.Ser751Pro" "NM_001145026:c.2251T>C" "EXON11" "Unknown significance" "rs779748179" "This variant is a VUS because it does not have enough information." 1.011 "C" "0.984" "D" 0.870345 "N" "4.6" "C" 0 2140 0 0 406 0 0 612 0 0 34 0 0 8476 0 0 190 0 1 7912 0.00012639 1 19770 0.0000505817
310153 "chr12:80890291:T>C" "PTPRQ" "NM_001145026:p.Ser751Ser" "NM_001145026:c.2253T>C" "EXON11" "Unknown significance" "rs192599195" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310154 "chr12:80890294:A>G" "PTPRQ" "NM_001145026:p.Val752Val" "NM_001145026:c.2256A>G" "EXON11" "Unknown significance" "rs551059621" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310155 "chr12:80890320:T>G" "PTPRQ" "NM_001145026:c.2272+10T>G" "INTRON11" "Benign" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 6 400 0.015 3 320 0.009375 9 320 0.028125 1 400 0.0025 6 360 0.0166667 4 200 0.02 29 2000 0.0145
310156 "chr12:80890321:G>T" "PTPRQ" "NM_001145026:c.2272+11G>T" "INTRON11" "Benign" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 400 0.0225 5 320 0.015625 10 320 0.03125 1 400 0.0025 8 360 0.0222222 4 200 0.02 37 2000 0.0185
310157 "chr12:80890325:T>G" "PTPRQ" "NM_001145026:c.2272+15T>G" "INTRON11" "Benign" "rs113908903" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 12 400 0.03 8 320 0.025 17 320 0.053125 10 400 0.025 13 360 0.0361111 13 200 0.065 73 2000 0.0365
310158 "chr12:80890326:->G" "PTPRQ" "NM_001145026:c.2272+16_2272+17insG" "INTRON11" "Benign" "rs56929349" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398 1620 2088 0.775862 332 384 0.864583 281 598 0.4699 29 32 0.90625 7694 8318 0.924982 161 188 0.856383 6980 7890 0.884664 17097 19498 0.876859
310159 "chr12:80890326:C>G" "PTPRQ" "NM_001145026:c.2272+16C>G" "INTRON11" "Benign" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 24 400 0.06 18 320 0.05625 21 320 0.065625 14 400 0.035 23 360 0.0638889 15 200 0.075 115 2000 0.0575
310160 "chr12:80890327:->G" "PTPRQ" "NM_001145026:c.2272+17_2272+18insG" "INTRON11" "Unknown significance" "rs66828510" "This variant is a VUS because it does not have enough information."
310161 "chr12:80890327:T>C" "PTPRQ" "NM_001145026:c.2272+17T>C" "INTRON11" "Benign" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 400 0.05 14 320 0.04375 15 320 0.046875 10 400 0.025 17 360 0.0472222 7 200 0.035 83 2000 0.0415
310162 "chr12:80890330:G>T" "PTPRQ" "NM_001145026:c.2272+20G>T" "INTRON11" "Unknown significance" "This variant is a VUS because it does not have enough information." 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
310163 "chr12:80890338:A>-" "PTPRQ" "NM_001145026:c.2272+28delA" "INTRON11" "Benign" "rs538342431" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 6 978 0.0061 6 5008 0.00119808
310164 "chr12:80890340:T>C" "PTPRQ" "NM_001145026:c.2272+30T>C" "INTRON11" "Unknown significance" "rs746749223" "This variant is a VUS because it does not have enough information." 0 1982 0 0 350 0 0 586 0 0 32 0 0 8092 0 0 190 0 1 7860 0.000127226 1 19092 0.000052378
310165 "chr12:80890352:A>C" "PTPRQ" "NM_001145026:c.2272+42A>C" "INTRON11" "Unknown significance" "rs761561310" "This variant is a VUS because it does not have enough information." 0 1972 0 0 346 0 0 588 0 0 32 0 0 8052 0 0 188 0 2 7854 0.000254647 2 19032 0.000105086
310166 "chr12:80890352:A>G" "PTPRQ" "NM_001145026:c.2272+42A>G" "INTRON11" "Unknown significance" "rs761561310" "This variant is a VUS because it does not have enough information."
310167 "chr12:80890354:A>G" "PTPRQ" "NM_001145026:c.2272+44A>G" "INTRON11" "Unknown significance" "rs776684720" "This variant is a VUS because it does not have enough information." 0 1972 0 0 346 0 0 588 0 0 32 0 1 8056 0.000124131 0 186 0 0 7856 0 1 19036 0.000052532
310168 "chr12:80890355:T>C" "PTPRQ" "NM_001145026:c.2272+45T>C" "INTRON11" "Unknown significance" "rs761648214" "This variant is a VUS because it does not have enough information."
310169 "chr12:80890375:C>T" "PTPRQ" "NM_001145026:c.2272+65C>T" "INTRON11" "Unknown significance" "rs142862117" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310170 "chr12:80890407:A>G" "PTPRQ" "NM_001145026:c.2272+97A>G" "INTRON11" "Benign" "rs79102190" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 2 1006 0.002 1 694 0.0014 173 1008 0.1716 25 978 0.0256 208 5008 0.0415335
310171 "chr12:80890427:A>G" "PTPRQ" "NM_001145026:c.2272+117A>G" "INTRON11" "Benign" "rs10778753" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
310172 "chr12:80890488:A>C" "PTPRQ" "NM_001145026:c.2272+178A>C" "INTRON11" "Unknown significance" "rs151053801" "This variant is a VUS because it does not have enough information."
310173 "chr12:80890491:T>A" "PTPRQ" "NM_001145026:c.2272+181T>A" "INTRON11" "Unknown significance" "rs567480820" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310174 "chr12:80890514:G>A" "PTPRQ" "NM_001145026:c.2272+204G>A" "INTRON11" "Unknown significance" "rs537734308" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310175 "chr12:80890559:A>G" "PTPRQ" "NM_001145026:c.2272+249A>G" "INTRON11" "Unknown significance" "rs372419247" "This variant is a VUS because it does not have enough information."
310176 "chr12:80890584:C>T" "PTPRQ" "NM_001145026:c.2272+274C>T" "INTRON11" "Unknown significance" "rs759713370" "This variant is a VUS because it does not have enough information."
310177 "chr12:80890603:A>G" "PTPRQ" "NM_001145026:c.2272+293A>G" "INTRON11" "Unknown significance" "rs556459818" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310178 "chr12:80890619:G>C" "PTPRQ" "NM_001145026:c.2272+309G>C" "INTRON11" "Unknown significance" "rs571662025" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310179 "chr12:80890630:A>G" "PTPRQ" "NM_001145026:c.2272+320A>G" "INTRON11" "Unknown significance" "rs553480529" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310180 "chr12:80890632:C>T" "PTPRQ" "NM_001145026:c.2272+322C>T" "INTRON11" "Benign" "rs75894254" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 42 1322 0.0318 0 1006 0 0 694 0 0 1008 0 0 978 0 42 5008 0.00838658
310181 "chr12:80890635:A>C" "PTPRQ" "NM_001145026:c.2272+325A>C" "INTRON11" "Unknown significance" "rs572539277" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310182 "chr12:80890682:A>C" "PTPRQ" "NM_001145026:c.2272+372A>C" "INTRON11" "Unknown significance" "rs765379596" "This variant is a VUS because it does not have enough information."
310183 "chr12:80890684:AGA>-" "PTPRQ" "NM_001145026:c.2272+374_2272+376delAGA" "INTRON11" "Unknown significance" "rs761180180" "This variant is a VUS because it does not have enough information."
310184 "chr12:80890692:A>G" "PTPRQ" "NM_001145026:c.2272+382A>G" "INTRON11" "Benign" "rs2400718" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
310185 "chr12:80890709:A>G" "PTPRQ" "NM_001145026:c.2272+399A>G" "INTRON11" "Benign" "rs2400719" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 986 1322 0.7458 920 1006 0.9145 588 694 0.8473 407 1008 0.4038 848 978 0.8671 3749 5008 0.748602
310186 "chr12:80890731:A>G" "PTPRQ" "NM_001145026:c.2272+421A>G" "INTRON11" "Unknown significance" "rs536569066" "This variant is a VUS because it does not have enough information."
310187 "chr12:80890824:G>T" "PTPRQ" "NM_001145026:c.2272+514G>T" "INTRON11" "Unknown significance" "rs565260399" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310188 "chr12:80890839:T>C" "PTPRQ" "NM_001145026:c.2272+529T>C" "INTRON11" "Unknown significance" "rs373007151" "This variant is a VUS because it does not have enough information."
310189 "chr12:80890850:C>A" "PTPRQ" "NM_001145026:c.2272+540C>A" "INTRON11" "Benign" "rs2895799" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 986 1322 0.7458 920 1006 0.9145 588 694 0.8473 416 1008 0.4127 848 978 0.8671 3758 5008 0.750399
310190 "chr12:80890863:C>T" "PTPRQ" "NM_001145026:c.2272+553C>T" "INTRON11" "Benign" "rs184986501" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 12 978 0.0123 13 5008 0.00259585
310191 "chr12:80890865:C>T" "PTPRQ" "NM_001145026:c.2272+555C>T" "INTRON11" "Benign" "rs140948955" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 14 1006 0.0139 9 694 0.013 0 1008 0 0 978 0 24 5008 0.00479233
310192 "chr12:80890869:G>A" "PTPRQ" "NM_001145026:c.2272+559G>A" "INTRON11" "Unknown significance" "rs757862801" "This variant is a VUS because it does not have enough information."
310193 "chr12:80890889:G>A" "PTPRQ" "NM_001145026:c.2272+579G>A" "INTRON11" "Unknown significance" "rs373664045" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310194 "chr12:80890893:G>T" "PTPRQ" "NM_001145026:c.2272+583G>T" "INTRON11" "Unknown significance" "rs559737533" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310195 "chr12:80890905:T>C" "PTPRQ" "NM_001145026:c.2272+595T>C" "INTRON11" "Unknown significance" "rs527363491" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310196 "chr12:80890913:C>T" "PTPRQ" "NM_001145026:c.2272+603C>T" "INTRON11" "Unknown significance" "rs781656824" "This variant is a VUS because it does not have enough information."
310197 "chr12:80890914:G>T" "PTPRQ" "NM_001145026:c.2272+604G>T" "INTRON11" "Benign" "rs539174091" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 10 1322 0.0076 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 11 5008 0.00219649
310198 "chr12:80890914:G>A" "PTPRQ" "NM_001145026:c.2272+604G>A" "INTRON11" "Unknown significance" "rs539174091" "This variant is a VUS because it does not have enough information."
310199 "chr12:80890919:G>A" "PTPRQ" "NM_001145026:c.2272+609G>A" "INTRON11" "Unknown significance" "rs188352924" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310200 "chr12:80890937:T>G" "PTPRQ" "NM_001145026:c.2272+627T>G" "INTRON11" "Unknown significance" "rs558829537" "This variant is a VUS because it does not have enough information."
310201 "chr12:80891035:A>G" "PTPRQ" "NM_001145026:c.2272+725A>G" "INTRON11" "Unknown significance" "rs144939446" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310202 "chr12:80891037:G>A" "PTPRQ" "NM_001145026:c.2272+727G>A" "INTRON11" "Unknown significance" "rs549710739" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310203 "chr12:80891052:G>A" "PTPRQ" "NM_001145026:c.2272+742G>A" "INTRON11" "Unknown significance" "rs755736776" "This variant is a VUS because it does not have enough information."
310204 "chr12:80891055:A>G" "PTPRQ" "NM_001145026:c.2272+745A>G" "INTRON11" "Unknown significance" "rs192344846" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
310205 "chr12:80891137:T>G" "PTPRQ" "NM_001145026:c.2272+827T>G" "INTRON11" "Unknown significance" "rs538949393" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310206 "chr12:80891140:A>G" "PTPRQ" "NM_001145026:c.2272+830A>G" "INTRON11" "Unknown significance" "rs184556265" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310207 "chr12:80891146:C>T" "PTPRQ" "NM_001145026:c.2272+836C>T" "INTRON11" "Benign" "rs566109805" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 1 1006 0.001 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744
310208 "chr12:80891147:G>A" "PTPRQ" "NM_001145026:c.2272+837G>A" "INTRON11" "Unknown significance" "rs572489798" "This variant is a VUS because it does not have enough information."
310209 "chr12:80891148:C>G" "PTPRQ" "NM_001145026:c.2272+838C>G" "INTRON11" "Benign" "rs536335442" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 17 1322 0.0129 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 19 5008 0.00379393
310210 "chr12:80891152:A>T" "PTPRQ" "NM_001145026:c.2272+842A>T" "INTRON11" "Benign" "rs5005026" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
310211 "chr12:80891153:A>G" "PTPRQ" "NM_001145026:c.2272+843A>G" "INTRON11" "Unknown significance" "rs546875480" "This variant is a VUS because it does not have enough information."
310212 "chr12:80891165:T>C" "PTPRQ" "NM_001145026:c.2272+855T>C" "INTRON11" "Unknown significance" "rs576558222" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310213 "chr12:80891198:G>A" "PTPRQ" "NM_001145026:c.2272+888G>A" "INTRON11" "Unknown significance" "rs138764656" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310214 "chr12:80891213:G>A" "PTPRQ" "NM_001145026:c.2272+903G>A" "INTRON11" "Unknown significance" "rs558736283" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310215 "chr12:80891227:->GGGG" "PTPRQ" "NM_001145026:c.2272+917_2272+918insGGGG" "INTRON11" "Unknown significance" "rs372586931" "This variant is a VUS because it does not have enough information."
310216 "chr12:80891234:C>A" "PTPRQ" "NM_001145026:c.2272+924C>A" "INTRON11" "Unknown significance" "rs554983351" "This variant is a VUS because it does not have enough information."
310217 "chr12:80891262:G>T" "PTPRQ" "NM_001145026:c.2272+952G>T" "INTRON11" "Unknown significance" "rs189313091" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310218 "chr12:80891268:C>T" "PTPRQ" "NM_001145026:c.2272+958C>T" "INTRON11" "Unknown significance" "rs181973926" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310219 "chr12:80891282:->C" "PTPRQ" "NM_001145026:c.2272+972_2272+973insC" "INTRON11" "Unknown significance" "rs34792347" "This variant is a VUS because it does not have enough information."
310220 "chr12:80891285:C>T" "PTPRQ" "NM_001145026:c.2272+975C>T" "INTRON11" "Benign" "rs4636733" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
310221 "chr12:80891302:G>A" "PTPRQ" "NM_001145026:c.2272+992G>A" "INTRON11" "Unknown significance" "rs527327162" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 1 978 0.001 2 5008 0.000399361
310222 "chr12:80891315:T>G" "PTPRQ" "NM_001145026:c.2272+1005T>G" "INTRON11" "Unknown significance" "rs184200771" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
310223 "chr12:80891350:G>T" "PTPRQ" "NM_001145026:c.2272+1040G>T" "INTRON11" "Unknown significance" "rs189570736" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310224 "chr12:80891362:C>T" "PTPRQ" "NM_001145026:c.2272+1052C>T" "INTRON11" "Unknown significance" "rs375263670" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
310225 "chr12:80891386:C>A" "PTPRQ" "NM_001145026:c.2272+1076C>A" "INTRON11" "Unknown significance" "rs748027300" "This variant is a VUS because it does not have enough information."
310226 "chr12:80891412:G>A" "PTPRQ" "NM_001145026:c.2272+1102G>A" "INTRON11" "Unknown significance" "rs181222485" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 4 1008 0.004 0 978 0 4 5008 0.000798722
310227 "chr12:80891455:T>A" "PTPRQ" "NM_001145026:c.2272+1145T>A" "INTRON11" "Unknown significance" "rs772025450" "This variant is a VUS because it does not have enough information."
310228 "chr12:80891477:A>G" "PTPRQ" "NM_001145026:c.2272+1167A>G" "INTRON11" "Unknown significance" "rs565099657" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310229 "chr12:80891479:A>C" "PTPRQ" "NM_001145026:c.2272+1169A>C" "INTRON11" "Unknown significance" "rs532428228" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310230 "chr12:80891563:C>T" "PTPRQ" "NM_001145026:c.2272+1253C>T" "INTRON11" "Unknown significance" "rs547750236" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310231 "chr12:80891564:G>A" "PTPRQ" "NM_001145026:c.2272+1254G>A" "INTRON11" "Unknown significance" "rs543756777" "This variant is a VUS because it does not have enough information."
310232 "chr12:80891595:->A" "PTPRQ" "NM_001145026:c.2272+1285_2272+1286insA" "INTRON11" "Unknown significance" "rs764956403" "This variant is a VUS because it does not have enough information."
310233 "chr12:80891605:C>T" "PTPRQ" "NM_001145026:c.2272+1295C>T" "INTRON11" "Unknown significance" "rs566073044" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
310234 "chr12:80891637:G>A" "PTPRQ" "NM_001145026:c.2272+1327G>A" "INTRON11" "Unknown significance" "rs536699919" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310235 "chr12:80891644:A>G" "PTPRQ" "NM_001145026:c.2272+1334A>G" "INTRON11" "Unknown significance" "rs772922948" "This variant is a VUS because it does not have enough information."
310236 "chr12:80891656:A>G" "PTPRQ" "NM_001145026:c.2272+1346A>G" "INTRON11" "Unknown significance" "rs760475725" "This variant is a VUS because it does not have enough information."
310237 "chr12:80891658:A>G" "PTPRQ" "NM_001145026:c.2272+1348A>G" "INTRON11" "Unknown significance" "rs770043749" "This variant is a VUS because it does not have enough information."
310238 "chr12:80891666:G>A" "PTPRQ" "NM_001145026:c.2272+1356G>A" "INTRON11" "Unknown significance" "rs775640492" "This variant is a VUS because it does not have enough information."
310239 "chr12:80891681:C>T" "PTPRQ" "NM_001145026:c.2272+1371C>T" "INTRON11" "Unknown significance" "rs763066223" "This variant is a VUS because it does not have enough information."
310240 "chr12:80891721:AAGTAGCT>-" "PTPRQ" "NM_001145026:c.2272+1411_2272+1418delAAGTAGCT" "INTRON11" "Unknown significance" "rs763479489" "This variant is a VUS because it does not have enough information."
310241 "chr12:80891737:T>C" "PTPRQ" "NM_001145026:c.2272+1427T>C" "INTRON11" "Unknown significance" "rs548298675" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310242 "chr12:80891745:G>T" "PTPRQ" "NM_001145026:c.2272+1435G>T" "INTRON11" "Benign" "rs4353336" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
310243 "chr12:80891798:C>A" "PTPRQ" "NM_001145026:c.2272+1488C>A" "INTRON11" "Unknown significance" "rs751721103" "This variant is a VUS because it does not have enough information."
310244 "chr12:80891817:G>T" "PTPRQ" "NM_001145026:c.2272+1507G>T" "INTRON11" "Unknown significance" "rs532211904" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310245 "chr12:80891844:T>A" "PTPRQ" "NM_001145026:c.2272+1534T>A" "INTRON11" "Benign" "rs186723974" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 0 1006 0 0 694 0 0 1008 0 0 978 0 8 5008 0.00159744
310246 "chr12:80891880:T>A" "PTPRQ" "NM_001145026:c.2272+1570T>A" "INTRON11" "Unknown significance" "rs376459944" "This variant is a VUS because it does not have enough information."
310247 "chr12:80891888:A>G" "PTPRQ" "NM_001145026:c.2272+1578A>G" "INTRON11" "Unknown significance" "rs748970842" "This variant is a VUS because it does not have enough information."
310248 "chr12:80891953:A>G" "PTPRQ" "NM_001145026:c.2272+1643A>G" "INTRON11" "Unknown significance" "rs577056168" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310249 "chr12:80891966:A>C" "PTPRQ" "NM_001145026:c.2272+1656A>C" "INTRON11" "Unknown significance" "rs534974099" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310250 "chr12:80892052:G>A" "PTPRQ" "NM_001145026:c.2272+1742G>A" "INTRON11" "Unknown significance" "rs115157870" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
310251 "chr12:80892057:C>T" "PTPRQ" "NM_001145026:c.2272+1747C>T" "INTRON11" "Unknown significance" "rs768153745" "This variant is a VUS because it does not have enough information."
310252 "chr12:80892128:C>T" "PTPRQ" "NM_001145026:c.2272+1818C>T" "INTRON11" "Benign" "rs1987344" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 579 1322 0.438 223 1006 0.2217 159 694 0.2291 43 1008 0.0427 130 978 0.1329 1134 5008 0.226438
310253 "chr12:80892145:C>T" "PTPRQ" "NM_001145026:c.2272+1835C>T" "INTRON11" "Benign" "rs4271444" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 416 1008 0.4127 848 978 0.8671 3764 5008 0.751597
310254 "chr12:80892162:G>A" "PTPRQ" "NM_001145026:c.2272+1852G>A" "INTRON11" "Unknown significance" "rs560736148" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310255 "chr12:80892166:G>A" "PTPRQ" "NM_001145026:c.2272+1856G>A" "INTRON11" "Unknown significance" "rs528157928" "This variant is a VUS because it does not have enough information."
310256 "chr12:80892173:T>C" "PTPRQ" "NM_001145026:c.2272+1863T>C" "INTRON11" "Unknown significance" "rs576058041" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310257 "chr12:80892205:T>C" "PTPRQ" "NM_001145026:c.2272+1895T>C" "INTRON11" "Benign" "rs4485172" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1211 1322 0.916 920 1006 0.9145 601 694 0.866 415 1008 0.4117 848 978 0.8671 3995 5008 0.797724
310258 "chr12:80892208:C>T" "PTPRQ" "NM_001145026:c.2272+1898C>T" "INTRON11" "Unknown significance" "rs753478653" "This variant is a VUS because it does not have enough information."
310259 "chr12:80892223:T>C" "PTPRQ" "NM_001145026:c.2272+1913T>C" "INTRON11" "Unknown significance" "rs565058303" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 0 978 0 0 5008 0
310260 "chr12:80892231:A>G" "PTPRQ" "NM_001145026:c.2272+1921A>G" "INTRON11" "Unknown significance" "rs532389330" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
310261 "chr12:80892265:T>C" "PTPRQ" "NM_001145026:c.2272+1955T>C" "INTRON11" "Unknown significance" "rs140396994" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
310262 "chr12:80892292:A>G" "PTPRQ" "NM_001145026:c.2272+1982A>G" "INTRON11" "Unknown significance" "rs754678388" "This variant is a VUS because it does not have enough information."
310263 "chr12:80892296:G>A" "PTPRQ" "NM_001145026:c.2272+1986G>A" "INTRON11" "Unknown significance" "rs145506966" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
310264 "chr12:80892394:G>A" "PTPRQ" "NM_001145026:c.2272+2084G>A" "INTRON11" "Unknown significance" "rs753614259" "This variant is a VUS because it does not have enough information."
310265 "chr12:80892414:T>C" "PTPRQ" "NM_001145026:c.2272+2104T>C" "INTRON11" "Unknown significance" "rs376542828" "This variant is a VUS because it does not have enough information."
310266 "chr12:80892428:T>C" "PTPRQ" "NM_001145026:c.2272+2118T>C" "INTRON11" "Unknown significance" "rs529957493" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310267 "chr12:80892446:T>A" "PTPRQ" "NM_001145026:c.2272+2136T>A" "INTRON11" "Unknown significance" "rs548530816" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310268 "chr12:80892447:C>T" "PTPRQ" "NM_001145026:c.2272+2137C>T" "INTRON11" "Unknown significance" "rs569974001" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310269 "chr12:80892466:T>A" "PTPRQ" "NM_001145026:c.2272+2156T>A" "INTRON11" "Unknown significance" "rs537535169" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310270 "chr12:80892484:C>T" "PTPRQ" "NM_001145026:c.2272+2174C>T" "INTRON11" "Unknown significance" "rs138023759" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
310271 "chr12:80892519:C>T" "PTPRQ" "NM_001145026:c.2272+2209C>T" "INTRON11" "Unknown significance" "rs570705190" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310272 "chr12:80892542:C>T" "PTPRQ" "NM_001145026:c.2272+2232C>T" "INTRON11" "Unknown significance" "rs2400720" "This variant is a VUS because it does not have enough information."
310273 "chr12:80892556:C>T" "PTPRQ" "NM_001145026:c.2272+2246C>T" "INTRON11" "Unknown significance" "rs771752359" "This variant is a VUS because it does not have enough information."
310274 "chr12:80892582:C>T" "PTPRQ" "NM_001145026:c.2272+2272C>T" "INTRON11" "Benign" "rs116142015" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 46 1322 0.0348 0 1006 0 0 694 0 0 1008 0 0 978 0 46 5008 0.0091853
310275 "chr12:80892598:C>-" "PTPRQ" "NM_001145026:c.2272+2288delC" "INTRON11" "Unknown significance" "rs567733144" "This variant is a VUS because it does not have enough information."
310276 "chr12:80892650:A>G" "PTPRQ" "NM_001145026:c.2272+2340A>G" "INTRON11" "Benign" "rs149493434" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 22 1322 0.0166 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 25 5008 0.00499201
310277 "chr12:80892667:C>-" "PTPRQ" "NM_001145026:c.2272+2357delC" "INTRON11" "Benign" "rs5799481" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 579 1322 0.438 223 1006 0.2217 158 694 0.2277 43 1008 0.0427 130 978 0.1329 1133 5008 0.226238
310278 "chr12:80892667:->C" "PTPRQ" "NM_001145026:c.2272+2357_2272+2358insC" "INTRON11" "Unknown significance" "rs774136992" "This variant is a VUS because it does not have enough information."
310279 "chr12:80892684:A>G" "PTPRQ" "NM_001145026:c.2272+2374A>G" "INTRON11" "Unknown significance" "rs575041644" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310280 "chr12:80892698:T>C" "PTPRQ" "NM_001145026:c.2272+2388T>C" "INTRON11" "Unknown significance" "rs535794087" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310281 "chr12:80892721:T>C" "PTPRQ" "NM_001145026:c.2272+2411T>C" "INTRON11" "Benign" "rs78393080" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 96 1322 0.0726 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 101 5008 0.0201677
310282 "chr12:80892757:A>C" "PTPRQ" "NM_001145026:c.2272+2447A>C" "INTRON11" "Unknown significance" "rs550208531" "This variant is a VUS because it does not have enough information."
310283 "chr12:80892765:G>C" "PTPRQ" "NM_001145026:c.2272+2455G>C" "INTRON11" "Unknown significance" "rs369404773" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310284 "chr12:80892771:G>C" "PTPRQ" "NM_001145026:c.2272+2461G>C" "INTRON11" "Unknown significance" "rs543534467" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310285 "chr12:80892778:A>G" "PTPRQ" "NM_001145026:c.2272+2468A>G" "INTRON11" "Benign" "rs188920578" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 5 1008 0.005 0 978 0 5 5008 0.000998403
310286 "chr12:80892800:G>T" "PTPRQ" "NM_001145026:c.2272+2490G>T" "INTRON11" "Unknown significance" "rs113605256" "This variant is a VUS because it does not have enough information."
310287 "chr12:80892810:A>G" "PTPRQ" "NM_001145026:c.2272+2500A>G" "INTRON11" "Unknown significance" "rs778351979" "This variant is a VUS because it does not have enough information."
310288 "chr12:80892870:C>T" "PTPRQ" "NM_001145026:c.2272+2560C>T" "INTRON11" "Unknown significance" "rs181368521" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310289 "chr12:80892896:->A" "PTPRQ" "NM_001145026:c.2272+2586_2272+2587insA" "INTRON11" "Unknown significance" "rs202232912" "This variant is a VUS because it does not have enough information."
310290 "chr12:80892898:A>G" "PTPRQ" "NM_001145026:c.2272+2588A>G" "INTRON11" "Unknown significance" "rs199918312" "This variant is a VUS because it does not have enough information."
310291 "chr12:80892899:->G" "PTPRQ" "NM_001145026:c.2272+2589_2272+2590insG" "INTRON11" "Benign" "rs71094984" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
310292 "chr12:80892899:T>G" "PTPRQ" "NM_001145026:c.2272+2589T>G" "INTRON11" "Unknown significance" "rs74779738" "This variant is a VUS because it does not have enough information."
310293 "chr12:80892900:->G" "PTPRQ" "NM_001145026:c.2272+2590_2272+2591insG" "INTRON11" "Unknown significance" "rs66691427" "This variant is a VUS because it does not have enough information."
310294 "chr12:80892900:T>G" "PTPRQ" "NM_001145026:c.2272+2590T>G" "INTRON11" "Unknown significance" "rs111685766" "This variant is a VUS because it does not have enough information."
310295 "chr12:80892901:G>T" "PTPRQ" "NM_001145026:c.2272+2591G>T" "INTRON11" "Unknown significance" "rs74822365" "This variant is a VUS because it does not have enough information."
310296 "chr12:80892942:A>G" "PTPRQ" "NM_001145026:c.2272+2632A>G" "INTRON11" "Benign" "rs4265648" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 988 1322 0.7474 920 1006 0.9145 589 694 0.8487 417 1008 0.4137 849 978 0.8681 3763 5008 0.751398
310297 "chr12:80892942:AC>GT" "PTPRQ" "Unknown significance" "rs71432127" "This variant is a VUS because it does not have enough information."
310298 "chr12:80892943:C>T" "PTPRQ" "NM_001145026:c.2272+2633C>T" "INTRON11" "Benign" "rs4414293" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 417 1008 0.4137 849 978 0.8681 3766 5008 0.751997
310299 "chr12:80892949:A>T" "PTPRQ" "NM_001145026:c.2272+2639A>T" "INTRON11" "Unknown significance" "rs566984810" "This variant is a VUS because it does not have enough information."
310300 "chr12:80892989:C>T" "PTPRQ" "NM_001145026:c.2272+2679C>T" "INTRON11" "Unknown significance" "rs529974588" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310301 "chr12:80892991:A>G" "PTPRQ" "NM_001145026:c.2272+2681A>G" "INTRON11" "Unknown significance" "rs777744335" "This variant is a VUS because it does not have enough information."
310302 "chr12:80893013:C>A" "PTPRQ" "NM_001145026:c.2272+2703C>A" "INTRON11" "Unknown significance" "rs541791272" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310303 "chr12:80893027:C>T" "PTPRQ" "NM_001145026:c.2272+2717C>T" "INTRON11" "Benign" "rs73145172" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 56 1322 0.0424 68 1006 0.0676 24 694 0.0346 125 1008 0.124 52 978 0.0532 325 5008 0.0648962
310304 "chr12:80893033:A>G" "PTPRQ" "NM_001145026:c.2272+2723A>G" "INTRON11" "Benign" "rs75080029" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 5 1008 0.005 0 978 0 5 5008 0.000998403
310305 "chr12:80893072:G>T" "PTPRQ" "NM_001145026:c.2272+2762G>T" "INTRON11" "Unknown significance" "rs552153320" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310306 "chr12:80893087:A>T" "PTPRQ" "NM_001145026:c.2272+2777A>T" "INTRON11" "Benign" "rs10778754" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
310307 "chr12:80893118:T>G" "PTPRQ" "NM_001145026:c.2272+2808T>G" "INTRON11" "Unknown significance" "rs763431223" "This variant is a VUS because it does not have enough information."
310308 "chr12:80893141:T>G" "PTPRQ" "NM_001145026:c.2272+2831T>G" "INTRON11" "Unknown significance" "rs185897184" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310309 "chr12:80893189:A>G" "PTPRQ" "NM_001145026:c.2272+2879A>G" "INTRON11" "Benign" "rs148207357" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 0 1006 0 0 694 0 0 1008 0 0 978 0 14 5008 0.00279553
310310 "chr12:80893254:C>A" "PTPRQ" "NM_001145026:c.2272+2944C>A" "INTRON11" "Unknown significance" "rs568587163" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
310311 "chr12:80893284:G>A" "PTPRQ" "NM_001145026:c.2272+2974G>A" "INTRON11" "Benign" "rs141153817" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 5 1006 0.005 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
310312 "chr12:80893294:C>T" "PTPRQ" "NM_001145026:c.2272+2984C>T" "INTRON11" "Benign" "rs7968957" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 991 1322 0.7496 920 1006 0.9145 589 694 0.8487 415 1008 0.4117 848 978 0.8671 3763 5008 0.751398
310313 "chr12:80893308:T>C" "PTPRQ" "NM_001145026:c.2272+2998T>C" "INTRON11" "Unknown significance" "rs569631044" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310314 "chr12:80893323:A>T" "PTPRQ" "NM_001145026:c.2272+3013A>T" "INTRON11" "Unknown significance" "rs190748724" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310315 "chr12:80893347:T>C" "PTPRQ" "NM_001145026:c.2272+3037T>C" "INTRON11" "Benign" "rs184121804" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 32 1322 0.0242 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 35 5008 0.00698882
310316 "chr12:80893366:A>G" "PTPRQ" "NM_001145026:c.2272+3056A>G" "INTRON11" "Benign" "rs185855775" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 4 5008 0.000798722
310317 "chr12:80893378:G>C" "PTPRQ" "NM_001145026:c.2272+3068G>C" "INTRON11" "Benign" "rs191200548" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 32 1322 0.0242 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 35 5008 0.00698882
310318 "chr12:80893398:C>T" "PTPRQ" "NM_001145026:c.2272+3088C>T" "INTRON11" "Unknown significance" "rs147349280" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
310319 "chr12:80893418:A>G" "PTPRQ" "NM_001145026:c.2272+3108A>G" "INTRON11" "Unknown significance" "rs543754177" "This variant is a VUS because it does not have enough information."
310320 "chr12:80893462:T>-" "PTPRQ" "NM_001145026:c.2272+3152delT" "INTRON11" "Unknown significance" "rs35320628" "This variant is a VUS because it does not have enough information."
310321 "chr12:80893514:T>C" "PTPRQ" "NM_001145026:c.2272+3204T>C" "INTRON11" "Benign" "rs56134442" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 149 1322 0.1127 0 1006 0 8 694 0.0115 0 1008 0 0 978 0 157 5008 0.0313498
310322 "chr12:80893519:C>T" "PTPRQ" "NM_001145026:c.2272+3209C>T" "INTRON11" "Unknown significance" "rs141067812" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310323 "chr12:80893546:->TG" "PTPRQ" "NM_001145026:c.2272+3236_2272+3237insTG" "INTRON11" "Unknown significance" "rs756905344" "This variant is a VUS because it does not have enough information."
310324 "chr12:80893546:TG>-" "PTPRQ" "NM_001145026:c.2272+3236_2272+3237delTG" "INTRON11" "Unknown significance" "rs150219133" "This variant is a VUS because it does not have enough information."
310325 "chr12:80893547:G>C" "PTPRQ" "NM_001145026:c.2272+3237G>C" "INTRON11" "Unknown significance" "rs557021299" "This variant is a VUS because it does not have enough information."
310326 "chr12:80893547:G>T" "PTPRQ" "NM_001145026:c.2272+3237G>T" "INTRON11" "Unknown significance" "rs557021299" "This variant is a VUS because it does not have enough information."
310327 "chr12:80893555:G>A" "PTPRQ" "NM_001145026:c.2272+3245G>A" "INTRON11" "Benign" "rs2400721" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 751 1322 0.5681 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1399 5008 0.279353
310328 "chr12:80893697:C>T" "PTPRQ" "NM_001145026:c.2272+3387C>T" "INTRON11" "Benign" "rs74922651" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
310329 "chr12:80893712:A>G" "PTPRQ" "NM_001145026:c.2272+3402A>G" "INTRON11" "Benign" "rs182997340" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 33 1322 0.025 0 1006 0 3 694 0.0043 2 1008 0.002 0 978 0 38 5008 0.00758786
310330 "chr12:80893717:T>C" "PTPRQ" "NM_001145026:c.2272+3407T>C" "INTRON11" "Unknown significance" "rs564159915" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310331 "chr12:80893723:C>T" "PTPRQ" "NM_001145026:c.2272+3413C>T" "INTRON11" "Benign" "rs74809786" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 45 1322 0.034 0 1006 0 0 694 0 0 1008 0 0 978 0 45 5008 0.00898562
310332 "chr12:80893741:A>-" "PTPRQ" "NM_001145026:c.2272+3431delA" "INTRON11" "Benign" "rs575778466" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 11 1008 0.0109 0 978 0 11 5008 0.00219649
310333 "chr12:80893743:C>T" "PTPRQ" "NM_001145026:c.2272+3433C>T" "INTRON11" "Unknown significance" "rs143294117" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
310334 "chr12:80893744:C>T" "PTPRQ" "NM_001145026:c.2272+3434C>T" "INTRON11" "Unknown significance" "rs568631013" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310335 "chr12:80893770:A>C" "PTPRQ" "NM_001145026:c.2272+3460A>C" "INTRON11" "Benign" "rs61951976" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 753 1322 0.5696 274 1006 0.2724 188 694 0.2709 52 1008 0.0516 188 978 0.1922 1455 5008 0.290535
310336 "chr12:80893774:C>T" "PTPRQ" "NM_001145026:c.2272+3464C>T" "INTRON11" "Benign" "rs114463882" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
310337 "chr12:80893825:C>T" "PTPRQ" "NM_001145026:c.2272+3515C>T" "INTRON11" "Unknown significance" "rs369992931" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
310338 "chr12:80893825:C>A" "PTPRQ" "NM_001145026:c.2272+3515C>A" "INTRON11" "Unknown significance" "rs369992931" "This variant is a VUS because it does not have enough information."
310339 "chr12:80893826:C>A" "PTPRQ" "NM_001145026:c.2272+3516C>A" "INTRON11" "Unknown significance" "rs113697348" "This variant is a VUS because it does not have enough information."
310340 "chr12:80893835:G>A" "PTPRQ" "NM_001145026:c.2272+3525G>A" "INTRON11" "Unknown significance" "rs186999036" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
310341 "chr12:80893842:C>A" "PTPRQ" "NM_001145026:c.2272+3532C>A" "INTRON11" "Unknown significance" "rs191820947" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310342 "chr12:80893899:A>G" "PTPRQ" "NM_001145026:c.2272+3589A>G" "INTRON11" "Unknown significance" "rs768137442" "This variant is a VUS because it does not have enough information."
310343 "chr12:80893912:C>T" "PTPRQ" "NM_001145026:c.2272+3602C>T" "INTRON11" "Unknown significance" "rs570491669" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310344 "chr12:80893930:G>A" "PTPRQ" "NM_001145026:c.2272+3620G>A" "INTRON11" "Unknown significance" "rs534696073" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
310345 "chr12:80893960:A>G" "PTPRQ" "NM_001145026:c.2272+3650A>G" "INTRON11" "Unknown significance" "rs552837500" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310346 "chr12:80893974:T>C" "PTPRQ" "NM_001145026:c.2272+3664T>C" "INTRON11" "Unknown significance" "rs761075147" "This variant is a VUS because it does not have enough information."
310347 "chr12:80894025:T>C" "PTPRQ" "NM_001145026:c.2272+3715T>C" "INTRON11" "Unknown significance" "rs574475502" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310348 "chr12:80894031:C>A" "PTPRQ" "NM_001145026:c.2272+3721C>A" "INTRON11" "Unknown significance" "rs753442935" "This variant is a VUS because it does not have enough information."
310349 "chr12:80894054:T>C" "PTPRQ" "NM_001145026:c.2272+3744T>C" "INTRON11" "Unknown significance" "rs766599887" "This variant is a VUS because it does not have enough information."
310350 "chr12:80894082:G>A" "PTPRQ" "NM_001145026:c.2272+3772G>A" "INTRON11" "Benign" "rs147518930" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 16 1008 0.0159 0 978 0 16 5008 0.00319489
310351 "chr12:80894116:C>T" "PTPRQ" "NM_001145026:c.2272+3806C>T" "INTRON11" "Unknown significance" "rs756704601" "This variant is a VUS because it does not have enough information."
310352 "chr12:80894117:G>A" "PTPRQ" "NM_001145026:c.2272+3807G>A" "INTRON11" "Unknown significance" "rs796188433" "This variant is a VUS because it does not have enough information."
310353 "chr12:80894128:T>C" "PTPRQ" "NM_001145026:c.2272+3818T>C" "INTRON11" "Unknown significance" "rs754257963" "This variant is a VUS because it does not have enough information."
310354 "chr12:80894135:C>T" "PTPRQ" "NM_001145026:c.2272+3825C>T" "INTRON11" "Unknown significance" "rs557135459" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310355 "chr12:80894145:T>C" "PTPRQ" "NM_001145026:c.2272+3835T>C" "INTRON11" "Benign" "rs182916678" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 0 1006 0 0 694 0 9 1008 0.0089 0 978 0 12 5008 0.00239617
310356 "chr12:80894148:A>G" "PTPRQ" "NM_001145026:c.2272+3838A>G" "INTRON11" "Unknown significance" "rs778688290" "This variant is a VUS because it does not have enough information."
310357 "chr12:80894186:G>T" "PTPRQ" "NM_001145026:c.2272+3876G>T" "INTRON11" "Unknown significance" "rs545719392" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310358 "chr12:80894223:A>G" "PTPRQ" "NM_001145026:c.2272+3913A>G" "INTRON11" "Unknown significance" "rs564122945" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310359 "chr12:80894225:A>G" "PTPRQ" "NM_001145026:c.2272+3915A>G" "INTRON11" "Unknown significance" "rs572943086" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
310360 "chr12:80894244:T>C" "PTPRQ" "NM_001145026:c.2272+3934T>C" "INTRON11" "Unknown significance" "rs540718747" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
310361 "chr12:80894272:T>-" "PTPRQ" "NM_001145026:c.2272+3962delT" "INTRON11" "Benign" "rs145904177" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 1 1006 0.001 0 694 0 16 1008 0.0159 1 978 0.001 18 5008 0.00359425
310362 "chr12:80894273:A>G" "PTPRQ" "NM_001145026:c.2272+3963A>G" "INTRON11" "Unknown significance" "rs559520566" "This variant is a VUS because it does not have enough information."
310363 "chr12:80894280:C>A" "PTPRQ" "NM_001145026:c.2272+3970C>A" "INTRON11" "Unknown significance" "rs528237294" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 1 1008 0.001 0 978 0 2 5008 0.000399361
310364 "chr12:80894297:C>T" "PTPRQ" "NM_001145026:c.2272+3987C>T" "INTRON11" "Unknown significance" "rs529398878" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310365 "chr12:80894303:T>C" "PTPRQ" "NM_001145026:c.2272+3993T>C" "INTRON11" "Benign" "rs139366736" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 0 1006 0 0 694 0 0 1008 0 0 978 0 14 5008 0.00279553
310366 "chr12:80894305:T>C" "PTPRQ" "NM_001145026:c.2272+3995T>C" "INTRON11" "Unknown significance" "rs779764918" "This variant is a VUS because it does not have enough information."
310367 "chr12:80894310:G>A" "PTPRQ" "NM_001145026:c.2272+4000G>A" "INTRON11" "Unknown significance" "rs563100774" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
310368 "chr12:80894337:C>T" "PTPRQ" "NM_001145026:c.2272+4027C>T" "INTRON11" "Unknown significance" "rs150028645" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310369 "chr12:80894338:G>A" "PTPRQ" "NM_001145026:c.2272+4028G>A" "INTRON11" "Unknown significance" "rs540855691" "This variant is a VUS because it does not have enough information."
310370 "chr12:80894351:C>T" "PTPRQ" "NM_001145026:c.2272+4041C>T" "INTRON11" "Benign" "rs77220833" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 96 1322 0.0726 0 1006 0 5 694 0.0072 0 1008 0 0 978 0 101 5008 0.0201677
310371 "chr12:80894359:G>A" "PTPRQ" "NM_001145026:c.2272+4049G>A" "INTRON11" "Unknown significance" "rs187596718" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310372 "chr12:80894401:C>G" "PTPRQ" "NM_001145026:c.2272+4091C>G" "INTRON11" "Benign" "rs7973132" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310373 "chr12:80894409:T>A" "PTPRQ" "NM_001145026:c.2272+4099T>A" "INTRON11" "Unknown significance" "rs777656167" "This variant is a VUS because it does not have enough information."
310374 "chr12:80894410:A>G" "PTPRQ" "NM_001145026:c.2272+4100A>G" "INTRON11" "Benign" "rs77777071" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 135 1322 0.1021 0 1006 0 10 694 0.0144 0 1008 0 0 978 0 145 5008 0.0289537
310375 "chr12:80894416:C>A" "PTPRQ" "NM_001145026:c.2272+4106C>A" "INTRON11" "Unknown significance" "rs746872868" "This variant is a VUS because it does not have enough information."
310376 "chr12:80894442:TT>-" "PTPRQ" "NM_001145026:c.2272+4132_2272+4133delTT" "INTRON11" "Benign" "rs76355618" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 24 1006 0.0239 6 694 0.0086 0 1008 0 49 978 0.0501 113 5008 0.0225639
310377 "chr12:80894456:T>A" "PTPRQ" "NM_001145026:c.2272+4146T>A" "INTRON11" "Unknown significance" "rs568028626" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310378 "chr12:80894488:C>T" "PTPRQ" "NM_001145026:c.2272+4178C>T" "INTRON11" "Benign" "rs7973256" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310379 "chr12:80894496:C>T" "PTPRQ" "NM_001145026:c.2272+4186C>T" "INTRON11" "Unknown significance" "rs556855468" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310380 "chr12:80894497:T>C" "PTPRQ" "NM_001145026:c.2272+4187T>C" "INTRON11" "Unknown significance" "rs575128993" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310381 "chr12:80894506:T>G" "PTPRQ" "NM_001145026:c.2272+4196T>G" "INTRON11" "Unknown significance" "rs539340049" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310382 "chr12:80894508:C>T" "PTPRQ" "NM_001145026:c.2272+4198C>T" "INTRON11" "Benign" "rs7973265" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310383 "chr12:80894525:A>G" "PTPRQ" "NM_001145026:c.2272+4215A>G" "INTRON11" "Unknown significance" "rs763028453" "This variant is a VUS because it does not have enough information."
310384 "chr12:80894534:G>A" "PTPRQ" "NM_001145026:c.2272+4224G>A" "INTRON11" "Benign" "rs73347733" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
310385 "chr12:80894542:A>G" "PTPRQ" "NM_001145026:c.2272+4232A>G" "INTRON11" "Unknown significance" "rs745690640" "This variant is a VUS because it does not have enough information."
310386 "chr12:80894586:A>C" "PTPRQ" "NM_001145026:c.2272+4276A>C" "INTRON11" "Unknown significance" "rs774816586" "This variant is a VUS because it does not have enough information."
310387 "chr12:80894595:C>A" "PTPRQ" "NM_001145026:c.2272+4285C>A" "INTRON11" "Benign" "rs116401092" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 72 1322 0.0545 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 75 5008 0.014976
310388 "chr12:80894621:G>A" "PTPRQ" "NM_001145026:c.2272+4311G>A" "INTRON11" "Unknown significance" "rs562131685" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310389 "chr12:80894631:C>T" "PTPRQ" "NM_001145026:c.2272+4321C>T" "INTRON11" "Unknown significance" "rs768989081" "This variant is a VUS because it does not have enough information."
310390 "chr12:80894638:C>G" "PTPRQ" "NM_001145026:c.2272+4328C>G" "INTRON11" "Unknown significance" "rs574025223" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310391 "chr12:80894650:T>G" "PTPRQ" "NM_001145026:c.2272+4340T>G" "INTRON11" "Unknown significance" "rs759949423" "This variant is a VUS because it does not have enough information."
310392 "chr12:80894716:G>T" "PTPRQ" "NM_001145026:c.2272+4406G>T" "INTRON11" "Unknown significance" "rs143633623" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310393 "chr12:80894730:G>A" "PTPRQ" "NM_001145026:c.2272+4420G>A" "INTRON11" "Benign" "rs146786585" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 7 1008 0.0069 0 978 0 7 5008 0.00139776
310394 "chr12:80894758:G>A" "PTPRQ" "NM_001145026:c.2272+4448G>A" "INTRON11" "Unknown significance" "rs193058796" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310395 "chr12:80894835:A>C" "PTPRQ" "NM_001145026:c.2272+4525A>C" "INTRON11" "Unknown significance" "rs570285366" "This variant is a VUS because it does not have enough information."
310396 "chr12:80894837:G>T" "PTPRQ" "NM_001145026:c.2272+4527G>T" "INTRON11" "Unknown significance" "rs552005192" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
310397 "chr12:80894840:C>T" "PTPRQ" "NM_001145026:c.2272+4530C>T" "INTRON11" "Benign" "rs7976516" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 169 694 0.2435 69 1008 0.0685 180 978 0.184 1417 5008 0.282947
310398 "chr12:80894843:C>T" "PTPRQ" "NM_001145026:c.2272+4533C>T" "INTRON11" "Unknown significance" "rs185825833" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 7 5008 0.00139776
310399 "chr12:80894852:A>G" "PTPRQ" "NM_001145026:c.2272+4542A>G" "INTRON11" "Unknown significance" "rs546250234" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310400 "chr12:80894853:C>A" "PTPRQ" "NM_001145026:c.2272+4543C>A" "INTRON11" "Benign" "rs73145185" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 216 1006 0.2147 110 694 0.1585 0 1008 0 105 978 0.1074 661 5008 0.131989
310401 "chr12:80894866:->A" "PTPRQ" "NM_001145026:c.2272+4556_2272+4557insA" "INTRON11" "Benign" "rs531997606" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 0 1008 0 9 978 0.0092 9 5008 0.00179712
310402 "chr12:80894866:A>-" "PTPRQ" "NM_001145026:c.2272+4556delA" "INTRON11" "Benign" "rs549159211" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 33 1322 0.025 1 1006 0.001 4 694 0.0058 0 1008 0 0 978 0 38 5008 0.00758786
310403 "chr12:80894920:G>A" "PTPRQ" "NM_001145026:c.2272+4610G>A" "INTRON11" "Unknown significance" "rs774340998" "This variant is a VUS because it does not have enough information."
310404 "chr12:80894922:->GT" "PTPRQ" "NM_001145026:c.2272+4612_2272+4613insGT" "INTRON11" "Unknown significance" "rs749468471" "This variant is a VUS because it does not have enough information."
310405 "chr12:80894949:C>T" "PTPRQ" "NM_001145026:c.2272+4639C>T" "INTRON11" "Unknown significance" "rs535184355" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310406 "chr12:80894966:T>C" "PTPRQ" "NM_001145026:c.2272+4656T>C" "INTRON11" "Unknown significance" "rs375410532" "This variant is a VUS because it does not have enough information."
310407 "chr12:80895030:G>A" "PTPRQ" "NM_001145026:c.2272+4720G>A" "INTRON11" "Unknown significance" "rs773443224" "This variant is a VUS because it does not have enough information."
310408 "chr12:80895081:T>A" "PTPRQ" "NM_001145026:c.2273-4722T>A" "INTRON11" "Unknown significance" "rs189132794" "This variant is a VUS because it does not have enough information."
310409 "chr12:80895081:T>C" "PTPRQ" "NM_001145026:c.2273-4722T>C" "INTRON11" "Unknown significance" "rs189132794" "This variant is a VUS because it does not have enough information."
310410 "chr12:80895106:G>A" "PTPRQ" "NM_001145026:c.2273-4697G>A" "INTRON11" "Unknown significance" "rs550300936" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
310411 "chr12:80895137:TGTC>-" "PTPRQ" "NM_001145026:c.2273-4666_2273-4663delTGTC" "INTRON11" "Benign" "rs534142602" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 1 1006 0.001 0 694 0 10 1008 0.0099 0 978 0 11 5008 0.00219649
310412 "chr12:80895144:G>A" "PTPRQ" "NM_001145026:c.2273-4659G>A" "INTRON11" "Unknown significance" "rs192808205" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310413 "chr12:80895155:A>G" "PTPRQ" "NM_001145026:c.2273-4648A>G" "INTRON11" "Unknown significance" "rs766910884" "This variant is a VUS because it does not have enough information."
310414 "chr12:80895162:G>A" "PTPRQ" "NM_001145026:c.2273-4641G>A" "INTRON11" "Unknown significance" "rs539201945" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
310415 "chr12:80895177:A>G" "PTPRQ" "NM_001145026:c.2273-4626A>G" "INTRON11" "Unknown significance" "rs776800315" "This variant is a VUS because it does not have enough information."
310416 "chr12:80895189:A>G" "PTPRQ" "NM_001145026:c.2273-4614A>G" "INTRON11" "Unknown significance" "rs760002015" "This variant is a VUS because it does not have enough information."
310417 "chr12:80895267:C>A" "PTPRQ" "NM_001145026:c.2273-4536C>A" "INTRON11" "Benign" "rs4312126" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 45 1322 0.034 668 1006 0.664 399 694 0.5749 360 1008 0.3571 666 978 0.681 2138 5008 0.426917
310418 "chr12:80895294:G>A" "PTPRQ" "NM_001145026:c.2273-4509G>A" "INTRON11" "Unknown significance" "rs757936700" "This variant is a VUS because it does not have enough information."
310419 "chr12:80895312:G>T" "PTPRQ" "NM_001145026:c.2273-4491G>T" "INTRON11" "Unknown significance" "rs184358043" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 1 694 0.0014 0 1008 0 4 978 0.0041 7 5008 0.00139776
310420 "chr12:80895338:A>C" "PTPRQ" "NM_001145026:c.2273-4465A>C" "INTRON11" "Unknown significance" "rs751392000" "This variant is a VUS because it does not have enough information."
310421 "chr12:80895370:A>G" "PTPRQ" "NM_001145026:c.2273-4433A>G" "INTRON11" "Unknown significance" "rs534118654" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310422 "chr12:80895394:G>A" "PTPRQ" "NM_001145026:c.2273-4409G>A" "INTRON11" "Unknown significance" "rs140436350" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
310423 "chr12:80895399:G>A" "PTPRQ" "NM_001145026:c.2273-4404G>A" "INTRON11" "Unknown significance" "rs376209837" "This variant is a VUS because it does not have enough information."
310424 "chr12:80895415:C>A" "PTPRQ" "NM_001145026:c.2273-4388C>A" "INTRON11" "Unknown significance" "rs555105796" "This variant is a VUS because it does not have enough information."
310425 "chr12:80895453:T>C" "PTPRQ" "NM_001145026:c.2273-4350T>C" "INTRON11" "Unknown significance" "rs145547549" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
310426 "chr12:80895502:A>T" "PTPRQ" "NM_001145026:c.2273-4301A>T" "INTRON11" "Unknown significance" "rs763556491" "This variant is a VUS because it does not have enough information."
310427 "chr12:80895595:A>G" "PTPRQ" "NM_001145026:c.2273-4208A>G" "INTRON11" "Unknown significance" "rs751085883" "This variant is a VUS because it does not have enough information."
310428 "chr12:80895609:T>C" "PTPRQ" "NM_001145026:c.2273-4194T>C" "INTRON11" "Unknown significance" "rs757086839" "This variant is a VUS because it does not have enough information."
310429 "chr12:80895650:A>T" "PTPRQ" "NM_001145026:c.2273-4153A>T" "INTRON11" "Unknown significance" "rs544372053" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
310430 "chr12:80895682:A>G" "PTPRQ" "NM_001145026:c.2273-4121A>G" "INTRON11" "Benign" "rs75755827" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 34 1322 0.0257 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 36 5008 0.0071885
310431 "chr12:80895706:->GT" "PTPRQ" "NM_001145026:c.2273-4097_2273-4096insGT" "INTRON11" "Unknown significance" "rs368355950" "This variant is a VUS because it does not have enough information."
310432 "chr12:80895722:->A" "PTPRQ" "NM_001145026:c.2273-4081_2273-4080insA" "INTRON11" "Unknown significance" "rs762872736" "This variant is a VUS because it does not have enough information."
310433 "chr12:80895722:->AA" "PTPRQ" "NM_001145026:c.2273-4081_2273-4080insAA" "INTRON11" "Unknown significance" "rs762872736" "This variant is a VUS because it does not have enough information."
310434 "chr12:80895722:->AAA" "PTPRQ" "NM_001145026:c.2273-4081_2273-4080insAAA" "INTRON11" "Unknown significance" "rs762872736" "This variant is a VUS because it does not have enough information."
310435 "chr12:80895722:->AAAA" "PTPRQ" "NM_001145026:c.2273-4081_2273-4080insAAAA" "INTRON11" "Unknown significance" "rs762872736" "This variant is a VUS because it does not have enough information."
310436 "chr12:80895722:->AAAAA" "PTPRQ" "NM_001145026:c.2273-4081_2273-4080insAAAAA" "INTRON11" "Unknown significance" "rs762872736" "This variant is a VUS because it does not have enough information."
310437 "chr12:80895726:A>C" "PTPRQ" "NM_001145026:c.2273-4077A>C" "INTRON11" "Unknown significance" "rs151001692" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310438 "chr12:80895814:G>A" "PTPRQ" "NM_001145026:c.2273-3989G>A" "INTRON11" "Benign" "rs188383285" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 33 1322 0.025 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 36 5008 0.0071885
310439 "chr12:80895861:A>T" "PTPRQ" "NM_001145026:c.2273-3942A>T" "INTRON11" "Unknown significance" "rs568565359" "This variant is a VUS because it does not have enough information."
310440 "chr12:80895913:G>T" "PTPRQ" "NM_001145026:c.2273-3890G>T" "INTRON11" "Unknown significance" "rs560688717" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
310441 "chr12:80895940:C>T" "PTPRQ" "NM_001145026:c.2273-3863C>T" "INTRON11" "Benign" "rs7980634" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 754 1322 0.5703 274 1006 0.2724 188 694 0.2709 52 1008 0.0516 188 978 0.1922 1456 5008 0.290735
310442 "chr12:80895963:G>A" "PTPRQ" "NM_001145026:c.2273-3840G>A" "INTRON11" "Unknown significance" "rs181242846" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310443 "chr12:80895967:G>C" "PTPRQ" "NM_001145026:c.2273-3836G>C" "INTRON11" "Unknown significance" "rs561516962" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310444 "chr12:80896206:G>A" "PTPRQ" "NM_001145026:c.2273-3597G>A" "INTRON11" "Unknown significance" "rs528930507" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310445 "chr12:80896211:G>A" "PTPRQ" "NM_001145026:c.2273-3592G>A" "INTRON11" "Unknown significance" "rs570566753" "This variant is a VUS because it does not have enough information."
310446 "chr12:80896249:G>A" "PTPRQ" "NM_001145026:c.2273-3554G>A" "INTRON11" "Unknown significance" "rs185748584" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310447 "chr12:80896250:G>T" "PTPRQ" "NM_001145026:c.2273-3553G>T" "INTRON11" "Unknown significance" "rs568571873" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 2 978 0.002 3 5008 0.000599042
310448 "chr12:80896267:T>G" "PTPRQ" "NM_001145026:c.2273-3536T>G" "INTRON11" "Unknown significance" "rs756016494" "This variant is a VUS because it does not have enough information."
310449 "chr12:80896273:C>G" "PTPRQ" "NM_001145026:c.2273-3530C>G" "INTRON11" "Unknown significance" "rs532879585" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
310450 "chr12:80896275:A>G" "PTPRQ" "NM_001145026:c.2273-3528A>G" "INTRON11" "Unknown significance" "rs779259280" "This variant is a VUS because it does not have enough information."
310451 "chr12:80896285:G>A" "PTPRQ" "NM_001145026:c.2273-3518G>A" "INTRON11" "Benign" "rs140830165" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 41 1322 0.031 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 43 5008 0.00858626
310452 "chr12:80896288:T>G" "PTPRQ" "NM_001145026:c.2273-3515T>G" "INTRON11" "Unknown significance" "rs566690248" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310453 "chr12:80896300:A>G" "PTPRQ" "NM_001145026:c.2273-3503A>G" "INTRON11" "Unknown significance" "rs373723429" "This variant is a VUS because it does not have enough information."
310454 "chr12:80896334:G>T" "PTPRQ" "NM_001145026:c.2273-3469G>T" "INTRON11" "Unknown significance" "rs533832253" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310455 "chr12:80896335:G>T" "PTPRQ" "NM_001145026:c.2273-3468G>T" "INTRON11" "Unknown significance" "rs748327004" "This variant is a VUS because it does not have enough information."
310456 "chr12:80896355:A>C" "PTPRQ" "NM_001145026:c.2273-3448A>C" "INTRON11" "Benign" "rs150128985" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 20 1322 0.0151 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 21 5008 0.00419329
310457 "chr12:80896355:A>G" "PTPRQ" "NM_001145026:c.2273-3448A>G" "INTRON11" "Unknown significance" "rs150128985" "This variant is a VUS because it does not have enough information."
310458 "chr12:80896359:C>A" "PTPRQ" "NM_001145026:c.2273-3444C>A" "INTRON11" "Benign" "rs10862143" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310459 "chr12:80896578:T>A" "PTPRQ" "NM_001145026:c.2273-3225T>A" "INTRON11" "Benign" "rs113079814" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 67 1006 0.0666 21 694 0.0303 1 1008 0.001 9 978 0.0092 102 5008 0.0203674
310460 "chr12:80896593:A>G" "PTPRQ" "NM_001145026:c.2273-3210A>G" "INTRON11" "Benign" "rs10862144" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310461 "chr12:80896601:C>T" "PTPRQ" "NM_001145026:c.2273-3202C>T" "INTRON11" "Unknown significance" "rs189035766" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 4 1008 0.004 0 978 0 4 5008 0.000798722
310462 "chr12:80896616:A>G" "PTPRQ" "NM_001145026:c.2273-3187A>G" "INTRON11" "Unknown significance" "rs545546066" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310463 "chr12:80896624:G>C" "PTPRQ" "NM_001145026:c.2273-3179G>C" "INTRON11" "Unknown significance" "rs554391401" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310464 "chr12:80896634:T>C" "PTPRQ" "NM_001145026:c.2273-3169T>C" "INTRON11" "Unknown significance" "rs182022094" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310465 "chr12:80896647:G>A" "PTPRQ" "NM_001145026:c.2273-3156G>A" "INTRON11" "Unknown significance" "rs542947243" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310466 "chr12:80896667:A>G" "PTPRQ" "NM_001145026:c.2273-3136A>G" "INTRON11" "Unknown significance" "rs759862655" "This variant is a VUS because it does not have enough information."
310467 "chr12:80896692:G>A" "PTPRQ" "NM_001145026:c.2273-3111G>A" "INTRON11" "Unknown significance" "rs561581968" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 2 5008 0.000399361
310468 "chr12:80896700:G>A" "PTPRQ" "NM_001145026:c.2273-3103G>A" "INTRON11" "Benign" "rs10862145" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310469 "chr12:80896723:A>C" "PTPRQ" "NM_001145026:c.2273-3080A>C" "INTRON11" "Unknown significance" "rs543771399" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310470 "chr12:80896741:T>C" "PTPRQ" "NM_001145026:c.2273-3062T>C" "INTRON11" "Unknown significance" "rs775864128" "This variant is a VUS because it does not have enough information."
310471 "chr12:80896788:T>A" "PTPRQ" "NM_001145026:c.2273-3015T>A" "INTRON11" "Benign" "rs73347742" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
310472 "chr12:80896796:A>G" "PTPRQ" "NM_001145026:c.2273-3007A>G" "INTRON11" "Unknown significance" "rs762526666" "This variant is a VUS because it does not have enough information."
310473 "chr12:80896802:G>T" "PTPRQ" "NM_001145026:c.2273-3001G>T" "INTRON11" "Unknown significance" "rs552805634" "This variant is a VUS because it does not have enough information."
310474 "chr12:80896819:A>G" "PTPRQ" "NM_001145026:c.2273-2984A>G" "INTRON11" "Unknown significance" "rs376349122" "This variant is a VUS because it does not have enough information."
310475 "chr12:80896842:G>A" "PTPRQ" "NM_001145026:c.2273-2961G>A" "INTRON11" "Benign" "rs116871461" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 22 1008 0.0218 1 978 0.001 23 5008 0.00459265
310476 "chr12:80896849:T>C" "PTPRQ" "NM_001145026:c.2273-2954T>C" "INTRON11" "Unknown significance" "rs749857088" "This variant is a VUS because it does not have enough information."
310477 "chr12:80896854:C>A" "PTPRQ" "NM_001145026:c.2273-2949C>A" "INTRON11" "Unknown significance" "rs541620869" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310478 "chr12:80896859:G>A" "PTPRQ" "NM_001145026:c.2273-2944G>A" "INTRON11" "Unknown significance" "rs761455520" "This variant is a VUS because it does not have enough information."
310479 "chr12:80896904:C>T" "PTPRQ" "NM_001145026:c.2273-2899C>T" "INTRON11" "Unknown significance" "rs138551316" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
310480 "chr12:80896906:A>G" "PTPRQ" "NM_001145026:c.2273-2897A>G" "INTRON11" "Unknown significance" "rs527529958" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310481 "chr12:80896909:G>A" "PTPRQ" "NM_001145026:c.2273-2894G>A" "INTRON11" "Unknown significance" "rs142749065" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310482 "chr12:80896914:T>G" "PTPRQ" "NM_001145026:c.2273-2889T>G" "INTRON11" "Unknown significance" "rs567515969" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
310483 "chr12:80896916:A>G" "PTPRQ" "NM_001145026:c.2273-2887A>G" "INTRON11" "Benign" "rs12304567" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310484 "chr12:80896938:A>G" "PTPRQ" "NM_001145026:c.2273-2865A>G" "INTRON11" "Unknown significance" "rs750428393" "This variant is a VUS because it does not have enough information."
310485 "chr12:80896951:G>A" "PTPRQ" "NM_001145026:c.2273-2852G>A" "INTRON11" "Unknown significance" "rs756148047" "This variant is a VUS because it does not have enough information."
310486 "chr12:80897001:C>G" "PTPRQ" "NM_001145026:c.2273-2802C>G" "INTRON11" "Unknown significance" "rs556573399" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310487 "chr12:80897038:G>C" "PTPRQ" "NM_001145026:c.2273-2765G>C" "INTRON11" "Unknown significance" "rs571703129" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310488 "chr12:80897044:C>T" "PTPRQ" "NM_001145026:c.2273-2759C>T" "INTRON11" "Benign" "rs12297821" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310489 "chr12:80897049:A>G" "PTPRQ" "NM_001145026:c.2273-2754A>G" "INTRON11" "Unknown significance" "rs79501230" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
310490 "chr12:80897051:G>A" "PTPRQ" "NM_001145026:c.2273-2752G>A" "INTRON11" "Benign" "rs111530404" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
310491 "chr12:80897058:G>A" "PTPRQ" "NM_001145026:c.2273-2745G>A" "INTRON11" "Benign" "rs12310771" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310492 "chr12:80897132:C>T" "PTPRQ" "NM_001145026:c.2273-2671C>T" "INTRON11" "Unknown significance" "rs554880146" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310493 "chr12:80897133:G>A" "PTPRQ" "NM_001145026:c.2273-2670G>A" "INTRON11" "Unknown significance" "rs576648976" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310494 "chr12:80897163:A>G" "PTPRQ" "NM_001145026:c.2273-2640A>G" "INTRON11" "Unknown significance" "rs76786942" "This variant is a VUS because it does not have enough information." 0 1322 0 4 1006 0.004 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
310495 "chr12:80897211:G>A" "PTPRQ" "NM_001145026:c.2273-2592G>A" "INTRON11" "Unknown significance" "rs562131188" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310496 "chr12:80897226:C>T" "PTPRQ" "NM_001145026:c.2273-2577C>T" "INTRON11" "Benign" "rs187672769" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 9 1008 0.0089 0 978 0 9 5008 0.00179712
310497 "chr12:80897264:T>G" "PTPRQ" "NM_001145026:c.2273-2539T>G" "INTRON11" "Unknown significance" "rs752704496" "This variant is a VUS because it does not have enough information."
310498 "chr12:80897335:A>T" "PTPRQ" "NM_001145026:c.2273-2468A>T" "INTRON11" "Unknown significance" "rs545986001" "This variant is a VUS because it does not have enough information."
310499 "chr12:80897348:->ATG" "PTPRQ" "NM_001145026:c.2273-2455_2273-2454insATG" "INTRON11" "Unknown significance" "rs200750798" "This variant is a VUS because it does not have enough information."
310500 "chr12:80897364:C>A" "PTPRQ" "NM_001145026:c.2273-2439C>A" "INTRON11" "Unknown significance" "rs755966973" "This variant is a VUS because it does not have enough information."
310501 "chr12:80897380:A>C" "PTPRQ" "NM_001145026:c.2273-2423A>C" "INTRON11" "Unknown significance" "rs35575563" "This variant is a VUS because it does not have enough information."
310502 "chr12:80897396:A>G" "PTPRQ" "NM_001145026:c.2273-2407A>G" "INTRON11" "Benign" "rs10862146" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 750 1322 0.5673 247 1006 0.2455 170 694 0.245 52 1008 0.0516 179 978 0.183 1398 5008 0.279153
310503 "chr12:80897410:->A" "PTPRQ" "NM_001145026:c.2273-2393_2273-2392insA" "INTRON11" "Unknown significance" "rs35896053" "This variant is a VUS because it does not have enough information."
310504 "chr12:80897474:C>T" "PTPRQ" "NM_001145026:c.2273-2329C>T" "INTRON11" "Benign" "rs191982920" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 17 1322 0.0129 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 19 5008 0.00379393
310505 "chr12:80897475:T>C" "PTPRQ" "NM_001145026:c.2273-2328T>C" "INTRON11" "Unknown significance" "rs527408335" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310506 "chr12:80897505:G>A" "PTPRQ" "NM_001145026:c.2273-2298G>A" "INTRON11" "Unknown significance" "rs552845461" "This variant is a VUS because it does not have enough information."
310507 "chr12:80897698:T>A" "PTPRQ" "NM_001145026:c.2273-2105T>A" "INTRON11" "Unknown significance" "rs549131082" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
310508 "chr12:80897703:T>C" "PTPRQ" "NM_001145026:c.2273-2100T>C" "INTRON11" "Unknown significance" "rs146938054" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
310509 "chr12:80897724:T>-" "PTPRQ" "NM_001145026:c.2273-2079delT" "INTRON11" "Benign" "rs371526078" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 750 1322 0.5673 247 1006 0.2455 171 694 0.2464 52 1008 0.0516 179 978 0.183 1399 5008 0.279353
310510 "chr12:80897724:T>A" "PTPRQ" "NM_001145026:c.2273-2079T>A" "INTRON11" "Unknown significance" "rs12306482" "This variant is a VUS because it does not have enough information."
310511 "chr12:80897725:TT>-" "PTPRQ" "NM_001145026:c.2273-2078_2273-2077delTT" "INTRON11" "Unknown significance" "rs796535127" "This variant is a VUS because it does not have enough information."
310512 "chr12:80897725:T>A" "PTPRQ" "NM_001145026:c.2273-2078T>A" "INTRON11" "Benign" "rs115723267" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 750 1322 0.5673 247 1006 0.2455 171 694 0.2464 52 1008 0.0516 179 978 0.183 1399 5008 0.279353
310513 "chr12:80897740:C>T" "PTPRQ" "NM_001145026:c.2273-2063C>T" "INTRON11" "Unknown significance" "rs550140299" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 3 1008 0.003 0 978 0 3 5008 0.000599042
310514 "chr12:80897787:T>C" "PTPRQ" "NM_001145026:c.2273-2016T>C" "INTRON11" "Unknown significance" "rs182651710" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310515 "chr12:80897855:G>A" "PTPRQ" "NM_001145026:c.2273-1948G>A" "INTRON11" "Benign" "rs12367802" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 231 1322 0.1747 216 1006 0.2147 111 694 0.1599 0 1008 0 105 978 0.1074 663 5008 0.132388
310516 "chr12:80897860:A>G" "PTPRQ" "NM_001145026:c.2273-1943A>G" "INTRON11" "Unknown significance" "rs547484491" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310517 "chr12:80897863:A>G" "PTPRQ" "NM_001145026:c.2273-1940A>G" "INTRON11" "Unknown significance" "rs376195038" "This variant is a VUS because it does not have enough information."
310518 "chr12:80897873:G>C" "PTPRQ" "NM_001145026:c.2273-1930G>C" "INTRON11" "Benign" "rs10862147" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 612 1322 0.4629 247 1006 0.2455 165 694 0.2378 52 1008 0.0516 179 978 0.183 1255 5008 0.250599
310519 "chr12:80897888:C>T" "PTPRQ" "NM_001145026:c.2273-1915C>T" "INTRON11" "Unknown significance" "rs536369505" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
310520 "chr12:80897914:A>C" "PTPRQ" "NM_001145026:c.2273-1889A>C" "INTRON11" "Benign" "rs11114482" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 21 1006 0.0209 10 694 0.0144 0 1008 0 8 978 0.0082 39 5008 0.00778754
310521 "chr12:80897993:C>T" "PTPRQ" "NM_001145026:c.2273-1810C>T" "INTRON11" "Benign" "rs114030146" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 43 1322 0.0325 0 1006 0 0 694 0 0 1008 0 0 978 0 43 5008 0.00858626
310522 "chr12:80898021:A>G" "PTPRQ" "NM_001145026:c.2273-1782A>G" "INTRON11" "Unknown significance" "rs111594452" "This variant is a VUS because it does not have enough information."
310523 "chr12:80898031:C>G" "PTPRQ" "NM_001145026:c.2273-1772C>G" "INTRON11" "Unknown significance" "rs185383655" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 1 694 0.0014 0 1008 0 0 978 0 4 5008 0.000798722
310524 "chr12:80898058:C>T" "PTPRQ" "NM_001145026:c.2273-1745C>T" "INTRON11" "Unknown significance" "rs746024098" "This variant is a VUS because it does not have enough information."
310525 "chr12:80898072:C>T" "PTPRQ" "NM_001145026:c.2273-1731C>T" "INTRON11" "Benign" "rs10862148" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 750 1322 0.5673 247 1006 0.2455 172 694 0.2478 52 1008 0.0516 179 978 0.183 1400 5008 0.279553
310526 "chr12:80898136:A>G" "PTPRQ" "NM_001145026:c.2273-1667A>G" "INTRON11" "Unknown significance" "rs374894174" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310527 "chr12:80898146:G>C" "PTPRQ" "NM_001145026:c.2273-1657G>C" "INTRON11" "Unknown significance" "rs190137162" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310528 "chr12:80898177:A>T" "PTPRQ" "NM_001145026:c.2273-1626A>T" "INTRON11" "Unknown significance" "rs182782015" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 3 1006 0.003 0 694 0 0 1008 0 4 978 0.0041 8 5008 0.00159744
310529 "chr12:80898271:A>G" "PTPRQ" "NM_001145026:c.2273-1532A>G" "INTRON11" "Benign" "rs10862149" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 753 1322 0.5696 274 1006 0.2724 190 694 0.2738 52 1008 0.0516 188 978 0.1922 1457 5008 0.290935
310530 "chr12:80898274:G>A" "PTPRQ" "NM_001145026:c.2273-1529G>A" "INTRON11" "Unknown significance" "rs542390493" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
310531 "chr12:80898319:C>T" "PTPRQ" "NM_001145026:c.2273-1484C>T" "INTRON11" "Benign" "rs561127413" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 14 1322 0.0106 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 15 5008 0.00299521
310532 "chr12:80898370:C>T" "PTPRQ" "NM_001145026:c.2273-1433C>T" "INTRON11" "Benign" "rs114170444" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 72 1322 0.0545 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 75 5008 0.014976
310533 "chr12:80898390:C>G" "PTPRQ" "NM_001145026:c.2273-1413C>G" "INTRON11" "Unknown significance" "rs550003853" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310534 "chr12:80898421:T>C" "PTPRQ" "NM_001145026:c.2273-1382T>C" "INTRON11" "Benign" "rs11114483" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 740 1322 0.5598 274 1006 0.2724 191 694 0.2752 52 1008 0.0516 189 978 0.1933 1446 5008 0.288738
310535 "chr12:80898421:T>G" "PTPRQ" "NM_001145026:c.2273-1382T>G" "INTRON11" "Benign" "rs11114483" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 11 1322 0.0083 0 1006 0 0 694 0 0 1008 0 0 978 0 11 5008 0.00219649
310536 "chr12:80898489:A>G" "PTPRQ" "NM_001145026:c.2273-1314A>G" "INTRON11" "Unknown significance" "rs777169861" "This variant is a VUS because it does not have enough information."
310537 "chr12:80898496:T>C" "PTPRQ" "NM_001145026:c.2273-1307T>C" "INTRON11" "Unknown significance" "rs547743004" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310538 "chr12:80898513:G>A" "PTPRQ" "NM_001145026:c.2273-1290G>A" "INTRON11" "Unknown significance" "rs375978234" "This variant is a VUS because it does not have enough information."
310539 "chr12:80898524:A>T" "PTPRQ" "NM_001145026:c.2273-1279A>T" "INTRON11" "Unknown significance" "rs137889713" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310540 "chr12:80898529:A>G" "PTPRQ" "NM_001145026:c.2273-1274A>G" "INTRON11" "Unknown significance" "rs530196812" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
310541 "chr12:80898535:A>T" "PTPRQ" "NM_001145026:c.2273-1268A>T" "INTRON11" "Unknown significance" "rs761210587" "This variant is a VUS because it does not have enough information."
310542 "chr12:80898570:A>G" "PTPRQ" "NM_001145026:c.2273-1233A>G" "INTRON11" "Unknown significance" "rs548435557" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310543 "chr12:80898595:A>G" "PTPRQ" "NM_001145026:c.2273-1208A>G" "INTRON11" "Benign" "rs117650373" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 7 1006 0.007 3 694 0.0043 0 1008 0 0 978 0 10 5008 0.00199681
310544 "chr12:80898598:T>A" "PTPRQ" "NM_001145026:c.2273-1205T>A" "INTRON11" "Benign" "rs11114484" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 274 1006 0.2724 190 694 0.2738 52 1008 0.0516 188 978 0.1922 1456 5008 0.290735
310545 "chr12:80898600:A>G" "PTPRQ" "NM_001145026:c.2273-1203A>G" "INTRON11" "Unknown significance" "rs376733521" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361
310546 "chr12:80898618:T>A" "PTPRQ" "NM_001145026:c.2273-1185T>A" "INTRON11" "Unknown significance" "rs555118726" "This variant is a VUS because it does not have enough information."
310547 "chr12:80898647:A>G" "PTPRQ" "NM_001145026:c.2273-1156A>G" "INTRON11" "Unknown significance" "rs187468688" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310548 "chr12:80898654:T>C" "PTPRQ" "NM_001145026:c.2273-1149T>C" "INTRON11" "Benign" "rs79661246" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 21 1008 0.0208 0 978 0 21 5008 0.00419329
310549 "chr12:80898668:C>G" "PTPRQ" "NM_001145026:c.2273-1135C>G" "INTRON11" "Unknown significance" "rs553710901" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310550 "chr12:80898674:A>C" "PTPRQ" "NM_001145026:c.2273-1129A>C" "INTRON11" "Unknown significance" "rs199528256" "This variant is a VUS because it does not have enough information."
310551 "chr12:80898677:G>A" "PTPRQ" "NM_001145026:c.2273-1126G>A" "INTRON11" "Unknown significance" "rs571985472" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310552 "chr12:80898752:A>G" "PTPRQ" "NM_001145026:c.2273-1051A>G" "INTRON11" "Unknown significance" "rs575314620" "This variant is a VUS because it does not have enough information."
310553 "chr12:80898765:G>A" "PTPRQ" "NM_001145026:c.2273-1038G>A" "INTRON11" "Unknown significance" "rs544313941" "This variant is a VUS because it does not have enough information."
310554 "chr12:80898841:G>A" "PTPRQ" "NM_001145026:c.2273-962G>A" "INTRON11" "Unknown significance" "rs542703302" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310555 "chr12:80898846:C>G" "PTPRQ" "NM_001145026:c.2273-957C>G" "INTRON11" "Unknown significance" "rs753675050" "This variant is a VUS because it does not have enough information."
310556 "chr12:80898853:T>G" "PTPRQ" "NM_001145026:c.2273-950T>G" "INTRON11" "Benign" "rs10862150" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 274 1006 0.2724 192 694 0.2767 56 1008 0.0556 191 978 0.1953 1465 5008 0.292532
310557 "chr12:80898857:G>T" "PTPRQ" "NM_001145026:c.2273-946G>T" "INTRON11" "Unknown significance" "rs576213514" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310558 "chr12:80898868:A>G" "PTPRQ" "NM_001145026:c.2273-935A>G" "INTRON11" "Benign" "rs10862151" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 274 1006 0.2724 192 694 0.2767 56 1008 0.0556 191 978 0.1953 1465 5008 0.292532
310559 "chr12:80898881:C>T" "PTPRQ" "NM_001145026:c.2273-922C>T" "INTRON11" "Benign" "rs10862152" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 274 1006 0.2724 192 694 0.2767 56 1008 0.0556 191 978 0.1953 1465 5008 0.292532
310560 "chr12:80898884:G>A" "PTPRQ" "NM_001145026:c.2273-919G>A" "INTRON11" "Unknown significance" "rs532428044" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310561 "chr12:80898887:C>T" "PTPRQ" "NM_001145026:c.2273-916C>T" "INTRON11" "Unknown significance" "rs193194523" "This variant is a VUS because it does not have enough information."
310562 "chr12:80898893:T>C" "PTPRQ" "NM_001145026:c.2273-910T>C" "INTRON11" "Benign" "rs10862153" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 757 1322 0.5726 274 1006 0.2724 193 694 0.2781 56 1008 0.0556 191 978 0.1953 1471 5008 0.29373
310563 "chr12:80898929:A>G" "PTPRQ" "NM_001145026:c.2273-874A>G" "INTRON11" "Unknown significance" "rs373162323" "This variant is a VUS because it does not have enough information."
310564 "chr12:80898948:A>G" "PTPRQ" "NM_001145026:c.2273-855A>G" "INTRON11" "Unknown significance" "rs369286438" "This variant is a VUS because it does not have enough information."
310565 "chr12:80898965:T>C" "PTPRQ" "NM_001145026:c.2273-838T>C" "INTRON11" "Unknown significance" "rs76342999" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
310566 "chr12:80898967:T>C" "PTPRQ" "NM_001145026:c.2273-836T>C" "INTRON11" "Unknown significance" "rs530087921" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310567 "chr12:80898988:A>G" "PTPRQ" "NM_001145026:c.2273-815A>G" "INTRON11" "Unknown significance" "rs528781484" "This variant is a VUS because it does not have enough information."
310568 "chr12:80899037:T>C" "PTPRQ" "NM_001145026:c.2273-766T>C" "INTRON11" "Unknown significance" "rs781265967" "This variant is a VUS because it does not have enough information."
310569 "chr12:80899082:A>G" "PTPRQ" "NM_001145026:c.2273-721A>G" "INTRON11" "Unknown significance" "rs183851846" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 1 1008 0.001 0 978 0 2 5008 0.000399361
310570 "chr12:80899096:A>T" "PTPRQ" "NM_001145026:c.2273-707A>T" "INTRON11" "Unknown significance" "rs745960247" "This variant is a VUS because it does not have enough information."
310571 "chr12:80899098:C>T" "PTPRQ" "NM_001145026:c.2273-705C>T" "INTRON11" "Benign" "rs188863813" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 18 5008 0.00359425
310572 "chr12:80899148:T>C" "PTPRQ" "NM_001145026:c.2273-655T>C" "INTRON11" "Unknown significance" "rs756599264" "This variant is a VUS because it does not have enough information."
310573 "chr12:80899151:T>G" "PTPRQ" "NM_001145026:c.2273-652T>G" "INTRON11" "Unknown significance" "rs530931451" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310574 "chr12:80899196:A>T" "PTPRQ" "NM_001145026:c.2273-607A>T" "INTRON11" "Unknown significance" "rs552327332" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310575 "chr12:80899199:->G" "PTPRQ" "NM_001145026:c.2273-604_2273-603insG" "INTRON11" "Unknown significance" "rs35622561" "This variant is a VUS because it does not have enough information."
310576 "chr12:80899205:A>G" "PTPRQ" "NM_001145026:c.2273-598A>G" "INTRON11" "Benign" "rs10862154" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 753 1322 0.5696 274 1006 0.2724 190 694 0.2738 53 1008 0.0526 188 978 0.1922 1458 5008 0.291134
310577 "chr12:80899336:A>G" "PTPRQ" "NM_001145026:c.2273-467A>G" "INTRON11" "Benign" "rs10778755" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 274 1006 0.2724 190 694 0.2738 52 1008 0.0516 188 978 0.1922 1456 5008 0.290735
310578 "chr12:80899356:T>A" "PTPRQ" "NM_001145026:c.2273-447T>A" "INTRON11" "Unknown significance" "rs769110707" "This variant is a VUS because it does not have enough information."
310579 "chr12:80899399:C>T" "PTPRQ" "NM_001145026:c.2273-404C>T" "INTRON11" "Benign" "rs10778756" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 274 1006 0.2724 190 694 0.2738 52 1008 0.0516 188 978 0.1922 1456 5008 0.290735
310580 "chr12:80899409:TG>-" "PTPRQ" "NM_001145026:c.2273-394_2273-393delTG" "INTRON11" "Unknown significance" "rs544577785" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
310581 "chr12:80899418:A>C" "PTPRQ" "NM_001145026:c.2273-385A>C" "INTRON11" "Unknown significance" "rs746112549" "This variant is a VUS because it does not have enough information."
310582 "chr12:80899443:A>C" "PTPRQ" "NM_001145026:c.2273-360A>C" "INTRON11" "Unknown significance" "rs572914147" "This variant is a VUS because it does not have enough information."
310583 "chr12:80899445:A>G" "PTPRQ" "NM_001145026:c.2273-358A>G" "INTRON11" "Unknown significance" "rs568738736" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310584 "chr12:80899485:T>C" "PTPRQ" "NM_001145026:c.2273-318T>C" "INTRON11" "Unknown significance" "rs535832341" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310585 "chr12:80899537:T>C" "PTPRQ" "NM_001145026:c.2273-266T>C" "INTRON11" "Benign" "rs193107035" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 0 694 0 9 1008 0.0089 0 978 0 9 5008 0.00179712
310586 "chr12:80899593:T>C" "PTPRQ" "NM_001145026:c.2273-210T>C" "INTRON11" "Unknown significance" "rs576178878" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403
310587 "chr12:80899608:T>A" "PTPRQ" "NM_001145026:c.2273-195T>A" "INTRON11" "Unknown significance" "rs541543820" "This variant is a VUS because it does not have enough information."
310588 "chr12:80899644:G>A" "PTPRQ" "NM_001145026:c.2273-159G>A" "INTRON11" "Benign" "rs10732674" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1320 1322 0.9985 990 1006 0.9841 626 694 0.902 709 1008 0.7034 925 978 0.9458 4570 5008 0.91254
310589 "chr12:80899658:C>T" "PTPRQ" "NM_001145026:c.2273-145C>T" "INTRON11" "Unknown significance" "rs571946577" "This variant is a VUS because it does not have enough information."
310590 "chr12:80899676:A>T" "PTPRQ" "NM_001145026:c.2273-127A>T" "INTRON11" "Unknown significance" "rs558771157" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310591 "chr12:80899685:G>A" "PTPRQ" "NM_001145026:c.2273-118G>A" "INTRON11" "Benign" "rs10778757" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 752 1322 0.5688 274 1006 0.2724 190 694 0.2738 52 1008 0.0516 188 978 0.1922 1456 5008 0.290735
310592 "chr12:80899692:T>C" "PTPRQ" "NM_001145026:c.2273-111T>C" "INTRON11" "Unknown significance" "rs747379796" "This variant is a VUS because it does not have enough information."
310593 "chr12:80899721:T>C" "PTPRQ" "NM_001145026:c.2273-82T>C" "INTRON11" "Benign" "rs11114485" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 231 1322 0.1747 6 1006 0.006 43 694 0.062 43 1008 0.0427 25 978 0.0256 348 5008 0.0694888
310594 "chr12:80899761:G>C" "PTPRQ" "NM_001145026:c.2273-42G>C" "INTRON11" "Unknown significance" "rs760321761" "This variant is a VUS because it does not have enough information."
310595 "chr12:80899782:C>A" "PTPRQ" "NM_001145026:c.2273-21C>A" "INTRON11" "Benign" "rs183499320" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 31 1322 0.0234 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 34 5008 0.00678914 39 1800 0.0216667 3 386 0.00777202 0 600 0 0 32 0 1 7478 0.000133726 0 180 0 0 7786 0 43 18262 0.00235462
310596 "chr12:80899806:C>T" "PTPRQ" "NM_001145026:p.Pro759Leu" "NM_001145026:c.2276C>T" "EXON12" "Unknown significance" "rs772826579" "This variant is a VUS because it does not have enough information." 0.892 "N" "1.0" "D" 1 "D" "5.82" "C" 0 1948 0 0 398 0 1 610 0.00163934 0 32 0 0 7974 0 0 182 0 0 7882 0 1 19026 0.0000525597
310597 "chr12:80899814:G>T" "PTPRQ" "NM_001145026:p.Ala762Ser" "NM_001145026:c.2284G>T" "EXON12" "Unknown significance" "This variant is a VUS because it does not have enough information." 0.998 "C" "0.052" "B" 0.53888 "N" "2.82" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
310598 "chr12:80899817:C>G" "PTPRQ" "NM_001145026:p.Pro763Ala" "NM_001145026:c.2287C>G" "EXON12" "Benign" "rs530013415" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.892 "N" "1.0" "D" 1 "D" "5.82" "C" 0 400 0 0 320 0 0 320 0 2 400 0.005 0 360 0 0 200 0 2 2000 0.001 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 0 2022 0 0 400 0 1 614 0.00162866 0 32 0 0 8136 0 0 184 0 0 7892 0 1 19280 0.0000518672
310599 "chr12:80899840:->AT" "PTPRQ" "NM_001145026:c.2310_2311insAT" "EXON12" "Unknown significance" "rs759619251" "This variant is a VUS because it does not have enough information." 0 2082 0 0 406 0 0 618 0 0 34 0 1 8286 0.000120685 0 186 0 0 7900 0 1 19512 0.0000512505
310600 "chr12:80899857:T>C" "PTPRQ" "NM_001145026:p.Ile776Thr" "NM_001145026:c.2327T>C" "EXON12" "Benign" "rs147541734" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1.011 "C" "0.931" "P" 0.987091 "D" "5.82" "C" 0 400 0 0 320 0 0 320 0 8 400 0.02 0 360 0 0 200 0 8 2000 0.004 0 1322 0 0 1006 0 0 694 0 16 1008 0.0159 0 978 0 16 5008 0.00319489 0 2114 0 0 406 0 6 622 0.0096463 0 34 0 0 8336 0 0 188 0 2 7900 0.000253165 8 19600 0.000408163
310601 "chr12:80899857:T>G" "PTPRQ" "NM_001145026:p.Ile776Ser" "NM_001145026:c.2327T>G" "EXON12" "Unknown significance" "rs147541734" "This variant is a VUS because it does not have enough information." 1.011 "C" "0.99" "D" 0.996326 "D" "5.82" "C" 0 2114 0 0 406 0 0 622 0 0 34 0 0 8336 0 0 188 0 1 7900 0.000126582 1 19600 0.0000510204
310602 "chr12:80899877:C>G" "PTPRQ" "NM_001145026:p.Pro783Ala" "NM_001145026:c.2347C>G" "EXON12" "Unknown significance" "rs760006052" "This variant is a VUS because it does not have enough information." 0.892 "N" "1.0" "D" 0.999999 "D" "5.87" "C" 0 2122 0 0 406 0 0 620 0 0 34 0 0 8364 0 0 190 0 2 7900 0.000253165 2 19636 0.000101854
310603 "chr12:80899879:A>G" "PTPRQ" "NM_001145026:p.Pro783Pro" "NM_001145026:c.2349A>G" "EXON12" "Unknown significance" "rs533247418" "This variant is a VUS because it does not have enough information."
310604 "chr12:80899886:C>A" "PTPRQ" "NM_001145026:p.Pro786Thr" "NM_001145026:c.2356C>A" "EXON12" "Unknown significance" "rs767769646" "This variant is a VUS because it does not have enough information." 0.892 "N" "1.0" "D" 0.999987 "D" "5.87" "C" 0 2124 0 0 406 0 0 620 0 0 34 0 0 8368 0 0 190 0 1 7900 0.000126582 1 19642 0.0000509113
310605 "chr12:80899892:G>T" "PTPRQ" "NM_001145026:p.Gly788Stop" "NM_001145026:c.2362G>T" "EXON12" "Unknown significance" "rs753288938" "This variant is a VUS because it does not have enough information." 0.998 "C" 1 "A" "5.87" "C"
310606 "chr12:80899901:C>A" "PTPRQ" "NM_001145026:p.Gln791Lys" "NM_001145026:c.2371C>A" "EXON12" "Benign" "rs11114486" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.892 "N" 0.951923 "P" "4.96" "C" 77 1322 0.0582 649 1006 0.6451 388 694 0.5591 363 1008 0.3601 660 978 0.6748 2137 5008 0.426717 322 2122 0.151744 247 408 0.605392 257 620 0.414516 26 32 0.8125 5386 8396 0.641496 114 190 0.6 5413 7906 0.68467 11765 19674 0.597997
310607 "chr12:80899907:T>A" "PTPRQ" "NM_001145026:p.Tyr793Asn" "NM_001145026:c.2377T>A" "EXON12" "Unknown significance" "rs777856567" "This variant is a VUS because it does not have enough information." 1.011 "C" "1.0" "D" 0.999998 "D" "5.87" "C" 0 2114 0 0 408 0 0 618 0 0 34 0 1 8326 0.000120106 0 188 0 0 7904 0 1 19592 0.0000510412
310608 "chr12:80899925:A>G" "PTPRQ" "NM_001145026:p.Arg799Gly" "NM_001145026:c.2395A>G" "EXON12" "Unknown significance" "rs753878138" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.121" "B" 0.999999 "N" "4.39" "C" 1 2104 0.000475285 0 408 0 0 618 0 0 34 0 0 8288 0 0 188 0 0 7904 0 1 19544 0.0000511666
310609 "chr12:80899928:A>G" "PTPRQ" "NM_001145026:p.Ser800Gly" "NM_001145026:c.2398A>G" "EXON12" "Unknown significance" "rs757477465" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.134" "B" 1 "N" "4.41" "C"
310610 "chr12:80899931:A>C" "PTPRQ" "NM_001145026:p.Asn801His" "NM_001145026:c.2401A>C" "EXON12" "Unknown significance" "rs530895245" "This variant is a VUS because it does not have enough information." 1.14 "C" "0.858" "P" 0.990368 "N" "1.89" "C" 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 2102 0.000475737 0 408 0 0 618 0 0 34 0 0 8272 0 0 188 0 0 7902 0 1 19524 0.000051219
310611 "chr12:80899944:A>G" "PTPRQ" "NM_001145026:p.Glu805Gly" "NM_001145026:c.2414A>G" "EXON12" "Unknown significance" "rs776751683" "This variant is a VUS because it does not have enough information." 0.116 "N" "0.282" "B" 0.917867 "N" "4.41" "C"
310612 "chr12:80899959:C>A" "PTPRQ" "NM_001145026:p.Thr810Lys" "NM_001145026:c.2429C>A" "EXON12" "Unknown significance" "rs552292154" "This variant is a VUS because it does not have enough information." 0.892 "N" "0.909" "P" 0.998184 "D" "5.57" "C" 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310613 "chr12:80899969:A>G" "PTPRQ" "NM_001145026:p.Leu813Leu" "NM_001145026:c.2439A>G" "EXON12" "Unknown significance" "rs564336138" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 2028 0 0 400 0 0 616 0 0 34 0 0 7948 0 0 186 0 1 7710 0.000129702 1 18922 0.0000528485
310614 "chr12:80899972:C>A" "PTPRQ" "NM_001145026:p.Thr814Thr" "NM_001145026:c.2442C>A" "EXON12" "Unknown significance" "rs528629575" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 2018 0.00049554 0 398 0 0 616 0 0 34 0 0 7904 0 0 186 0 0 7666 0 1 18822 0.0000531293
310615 "chr12:80899975:A>G" "PTPRQ" "NM_001145026:p.Gln815Gln" "NM_001145026:c.2445A>G" "EXON12" "Unknown significance" "rs780815237" "This variant is a VUS because it does not have enough information." 0 2012 0 0 398 0 0 616 0 0 34 0 2 7896 0.000253293 0 184 0 0 7610 0 2 18750 0.000106667
310616 "chr12:80899987:T>A" "PTPRQ" "NM_001145026:c.2455+2T>A" "INTRON12" "Unknown significance" "This variant is a VUS because it does not have enough information." 1.011 "C" 1 "D" "5.63" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
310617 "chr12:80900007:T>A" "PTPRQ" "NM_001145026:c.2455+22T>A" "INTRON12" "Unknown significance" "rs188234415" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
310618 "chr12:80900010:A>G" "PTPRQ" "NM_001145026:c.2455+25A>G" "INTRON12" "Unknown significance" "rs748144862" "This variant is a VUS because it does not have enough information." 0 1850 0 0 386 0 0 604 0 0 32 0 0 7242 0 0 166 0 1 6598 0.000151561 1 16878 0.0000592487
310619 "chr12:80900017:C>T" "PTPRQ" "NM_001145026:c.2455+32C>T" "INTRON12" "Unknown significance" "rs769805993" "This variant is a VUS because it does not have enough information." 0 1764 0 0 378 0 0 602 0 0 32 0 2 6966 0.000287109 0 158 0 0 6284 0 2 16184 0.000123579
310620 "chr12:80900033:G>T" "PTPRQ" "NM_001145026:c.2455+48G>T" "INTRON12" "Unknown significance" "rs772879628" "This variant is a VUS because it does not have enough information."
310621 "chr12:80900034:T>G" "PTPRQ" "NM_001145026:c.2455+49T>G" "INTRON12" "Unknown significance" "rs191578673" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681
310622 "chr12:80900058:T>C" "PTPRQ" "NM_001145026:c.2455+73T>C" "INTRON12" "Benign" "rs7964887" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 303 1322 0.2292 217 1006 0.2157 113 694 0.1628 0 1008 0 106 978 0.1084 739 5008 0.147564
310623 "chr12:80900068:A>G" "PTPRQ" "NM_001145026:c.2455+83A>G" "INTRON12" "Benign" "rs184106664" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 13 1006 0.0129 2 694 0.0029 0 1008 0 4 978 0.0041 19 5008 0.00379393
310624 "chr12:80900085:G>A" "PTPRQ" "NM_001145026:c.2455+100G>A" "INTRON12" "Unknown significance" "rs569704510" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
310625 "chr12:80900102:T>-" "PTPRQ" "NM_001145026:c.2455+117delT" "INTRON12" "Unknown significance" "rs34307617" "This variant is a VUS because it does not have enough information."
310626 "chr12:80900123:A>G" "PTPRQ" "NM_001145026:c.2455+138A>G" "INTRON12" "Unknown significance" "rs752438557" "This variant is a VUS because it does not have enough information."
310627 "chr12:80900201:A>T" "PTPRQ" "NM_001145026:c.2456-147A>T" "INTRON12" "Unknown significance" "rs535379683" "This variant is a VUS because it does not have enough information."
310628 "chr12:80900207:G>T" "PTPRQ" "NM_001145026:c.2456-141G>T" "INTRON12" "Unknown significance" "rs757442116" "This variant is a VUS because it does not have enough information."
310629 "chr12:80900222:G>T" "PTPRQ" "NM_001145026:c.2456-126G>T" "INTRON12" "Unknown significance" "rs537134697" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310630 "chr12:80900226:G>A" "PTPRQ" "NM_001145026:c.2456-122G>A" "INTRON12" "Unknown significance" "rs773812263" "This variant is a VUS because it does not have enough information."
310631 "chr12:80900272:A>T" "PTPRQ" "NM_001145026:c.2456-76A>T" "INTRON12" "Unknown significance" "rs370798822" "This variant is a VUS because it does not have enough information."
310632 "chr12:80900292:C>T" "PTPRQ" "NM_001145026:c.2456-56C>T" "INTRON12" "Benign" "rs56978316" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 65 5008 0.0129792
310633 "chr12:80900307:T>C" "PTPRQ" "NM_001145026:c.2456-41T>C" "INTRON12" "Unknown significance" "rs767688342" "This variant is a VUS because it does not have enough information." 0 1936 0 0 304 0 0 446 0 0 6 0 3 7740 0.000387597 0 182 0 0 7690 0 3 18304 0.000163899
310634 "chr12:80900313:G>C" "PTPRQ" "NM_001145026:c.2456-35G>C" "INTRON12" "Unknown significance" "rs576876628" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 3 5008 0.000599042 0 1934 0 1 304 0.00328947 0 444 0 0 6 0 0 7750 0 0 182 0 0 7686 0 1 18306 0.0000546269
310635 "chr12:80900321:C>T" "PTPRQ" "NM_001145026:c.2456-27C>T" "INTRON12" "Unknown significance" "rs774119779" "This variant is a VUS because it does not have enough information." 0 1938 0 0 310 0 0 456 0 0 8 0 0 7808 0 0 186 0 1 7728 0.0001294 1 18434 0.0000542476
310636 "chr12:80900330:T>A" "PTPRQ" "NM_001145026:c.2456-18T>A" "INTRON12" "Unknown significance" "rs759080786" "This variant is a VUS because it does not have enough information." 0 1954 0 0 316 0 0 476 0 0 8 0 0 7926 0 0 188 0 1 7800 0.000128205 1 18668 0.0000535676
310637 "chr12:80900335:G>T" "PTPRQ" "NM_001145026:c.2456-13G>T" "INTRON12" "Benign" "rs7975096" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 866 3178 0.272498 684 1384 0.49422 1550 4562 0.339763 752 1322 0.5688 274 1006 0.2724 190 694 0.2738 52 1008 0.0516 188 978 0.1922 1456 5008 0.290735 1060 2052 0.516569 93 342 0.27193 28 498 0.0562249 2 8 0.25 2331 8164 0.285522 49 188 0.260638 1568 7840 0.2 5131 19092 0.268751
310638 "chr12:80900346:A>G" "PTPRQ" "NM_001145026:c.2456-2A>G" "INTRON12" "Unknown significance" "rs752959544" "This variant is a VUS because it does not have enough information." 1.028 "C" 1 "D" "5.3" "C" 0 2078 0 0 360 0 0 536 0 0 12 0 1 8246 0.000121271 0 188 0 0 7866 0 1 19286 0.0000518511
310639 "chr12:80900348:T>G" "PTPRQ" "NM_001145026:p.Val819Gly" "NM_001145026:c.2456T>G" "EXON13" "Benign" "rs7965277" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.039 "N" "0.0" "B" 0.243108 "P" "4.41" "C" 868 3178 0.273128 696 1384 0.50289 1564 4562 0.342832 183 400 0.4575 132 320 0.4125 98 320 0.30625 30 400 0.075 136 360 0.377778 66 200 0.33 645 2000 0.3225 756 1322 0.5719 274 1006 0.2724 192 694 0.2767 52 1008 0.0516 188 978 0.1922 1462 5008 0.291933 1085 2086 0.520134 96 360 0.266667 29 538 0.0539033 2 14 0.142857 2361 8276 0.285283 49 188 0.260638 1571 7870 0.199619 5193 19332 0.268622
310640 "chr12:80900348:T>C" "PTPRQ" "NM_001145026:p.Val819Ala" "NM_001145026:c.2456T>C" "EXON13" "Unknown significance" "rs7965277" "This variant is a VUS because it does not have enough information." 0.039 "N" "0.008" "B" 0.999952 "P" "4.41" "C" 0 2086 0 0 360 0 0 538 0 0 14 0 0 8276 0 0 188 0 1 7870 0.000127065 1 19332 0.0000517277
310641 "chr12:80900361:T>C" "PTPRQ" "NM_001145026:p.Tyr823Tyr" "NM_001145026:c.2469T>C" "EXON13" "Unknown significance" "rs780513672" "This variant is a VUS because it does not have enough information." 0 2102 0 0 378 0 0 576 0 0 20 0 2 8362 0.000239177 0 190 0 0 7890 0 2 19518 0.00010247
310642 "chr12:80900365:C>A" "PTPRQ" "NM_001145026:p.Gln825Lys" "NM_001145026:c.2473C>A" "EXON13" "Unknown significance" "rs749369907" "This variant is a VUS because it does not have enough information." 0.807 "N" "0.0" "B" 1 "N" "3.44" "C"
310643 "chr12:80900381:T>C" "PTPRQ" "NM_001145026:p.Val830Ala" "NM_001145026:c.2489T>C" "EXON13" "Benign" "rs12579151" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.913 "N" "1.0" "D" 0.998682 "D" "5.3" "C" 2 3182 0.000628536 2 1384 0.00144509 4 4566 0.00087604 0 400 0 28 320 0.0875 0 320 0 28 400 0.07 0 360 0 0 200 0 56 2000 0.028 2 1322 0.0015 6 1006 0.006 35 694 0.0504 43 1008 0.0427 25 978 0.0256 111 5008 0.0221645 3 2122 0.00141376 17 402 0.0422886 23 608 0.0378289 1 32 0.03125 2 8418 0.000237586 1 190 0.00526316 139 7906 0.0175816 186 19678 0.00945218
310644 "chr12:80900389:A>G" "PTPRQ" "NM_001145026:p.Ser833Gly" "NM_001145026:c.2497A>G" "EXON13" "Unknown significance" "rs371461479" "This variant is a VUS because it does not have enough information." 1.028 "C" "0.938" "P" 0.980521 "D" "5.44" "C" 0 3182 0 1 1384 0.000722543 1 4566 0.00021901
310645 "chr12:80900396:T>C" "PTPRQ" "NM_001145026:p.Leu835Pro" "NM_001145026:c.2504T>C" "EXON13" "Unknown significance" "rs778849557" "This variant is a VUS because it does not have enough information." 0.913 "N" "0.403" "B" 0.999983 "N" "4.27" "C" 0 2126 0 0 406 0 0 616 0 0 32 0 0 8446 0 0 190 0 1 7906 0.000126486 1 19722 0.0000507048
310646 "chr12:80900397:C>G" "PTPRQ" "NM_001145026:p.Leu835Leu" "NM_001145026:c.2505C>G" "EXON13" "Benign" "rs12824064" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2115 3182 0.664676 377 1384 0.272399 2492 4566 0.545773 234 1322 0.177 649 1006 0.6451 400 694 0.5764 363 1008 0.3601 660 978 0.6748 2306 5008 0.460463 542 2126 0.254939 251 406 0.618227 256 620 0.412903 28 34 0.823529 5446 8458 0.643887 114 190 0.6 5417 7910 0.684829 12054 19744 0.610515
310647 "chr12:80900401:G>T" "PTPRQ" "NM_001145026:p.Gly837Cys" "NM_001145026:c.2509G>T" "EXON13" "Unknown significance" "rs779274263" "This variant is a VUS because it does not have enough information." 0.902 "N" "1.0" "D" 0.999997 "D" "5.44" "C"
310648 "chr12:80900414:G>A" "PTPRQ" "NM_001145026:p.Arg841Gln" "NM_001145026:c.2522G>A" "EXON13" "Unknown significance" "rs748192361" "This variant is a VUS because it does not have enough information." 0.902 "N" "0.989" "D" 0.732019 "N" "3.6" "C"
310649 "chr12:80900424:C>T" "PTPRQ" "NM_001145026:p.Pro844Pro" "NM_001145026:c.2532C>T" "EXON13" "Unknown significance" "rs758525879" "This variant is a VUS because it does not have enough information." 0 2120 0 0 396 0 0 616 0 0 34 0 1 8396 0.000119104 0 190 0 0 7906 0 1 19658 0.0000508699
310650 "chr12:80900439:G>A" "PTPRQ" "NM_001145026:p.Thr849Thr" "NM_001145026:c.2547G>A" "EXON13" "Unknown significance" "rs368115315" "This variant is a VUS because it does not have enough information." 0 3182 0 3 1384 0.00216763 3 4566 0.00065703 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 3 2114 0.00141911 0 390 0 0 608 0 0 32 0 0 8348 0 0 190 0 0 7900 0 3 19582 0.000153202
310651 "chr12:80900446:G>A" "PTPRQ" "NM_001145026:p.Asp852Asn" "NM_001145026:c.2554G>A" "EXON13" "Unknown significance" "rs747909518" "This variant is a VUS because it does not have enough information." 0.902 "N" "1.0" "D" 0.999459 "D" "5.44" "C" 0 2112 0 0 392 0 1 608 0.00164474 0 32 0 0 8342 0 0 190 0 0 7900 0 1 19576 0.000051083
310652 "chr12:80900471:G>A" "PTPRQ" "NM_001145026:c.2557+22G>A" "INTRON13" "Unknown significance" "rs756123850" "This variant is a VUS because it does not have enough information." 0 2088 0 0 390 0 0 602 0 0 32 0 1 8270 0.000120919 0 190 0 4 7890 0.000506971 5 19462 0.000256911
310653 "chr12:80900480:T>G" "PTPRQ" "NM_001145026:c.2557+31T>G" "INTRON13" "Unknown significance" "rs777917257" "This variant is a VUS because it does not have enough information." 0 2076 0 0 392 0 0 602 0 0 32 0 0 8268 0 0 190 0 1 7886 0.000126807 1 19446 0.0000514245
310654 "chr12:80900495:C>T" "PTPRQ" "NM_001145026:c.2557+46C>T" "INTRON13" "Benign" "rs7976085" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 858 3182 0.269642 677 1384 0.489162 1535 4566 0.33618 752 1322 0.5688 274 1006 0.2724 190 694 0.2738 52 1008 0.0516 188 978 0.1922 1456 5008 0.290735 1055 2052 0.514133 97 388 0.25 31 586 0.052901 3 28 0.107143 2319 8212 0.282392 49 190 0.257895 1569 7872 0.199314 5123 19328 0.265056
310655 "chr12:80900496:C>T" "PTPRQ" "NM_001145026:c.2557+47C>T" "INTRON13" "Unknown significance" "rs770515827" "This variant is a VUS because it does not have enough information." 0 2056 0 0 380 0 0 594 0 0 28 0 0 8214 0 0 190 0 2 7880 0.000253807 2 19342 0.000103402
310656 "chr12:80900502:AC>-" "PTPRQ" "NM_001145026:c.2557+53_2557+54delAC" "INTRON13" "Unknown significance" "rs202010992" "This variant is a VUS because it does not have enough information."
310657 "chr12:80900551:C>G" "PTPRQ" "NM_001145026:c.2557+102C>G" "INTRON13" "Unknown significance" "rs545795030" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808
310658 "chr12:80900557:T>C" "PTPRQ" "NM_001145026:c.2557+108T>C" "INTRON13" "Unknown significance" "rs771746330" "This variant is a VUS because it does not have enough information."
310659 "chr12:80900566:C>A" "PTPRQ" "NM_001145026:c.2557+117C>A" "INTRON13" "Unknown significance" "rs150664861" "This variant is a VUS because it does not have enough information." 6 1322 0.0045 0 1006 0 0 694 0 0 1008 0 0 978 0 6 5008 0.00119808
310660 "chr12:80900570:C>T" "PTPRQ" "NM_001145026:c.2557+121C>T" "INTRON13" "Benign" "rs139828341" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 31 1322 0.0234 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 34 5008 0.00678914
310661 "chr12:80900577:C>T" "PTPRQ" "NM_001145026:c.2557+128C>T" "INTRON13" "Unknown significance" "rs546851170" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310662 "chr12:80900596:G>A" "PTPRQ" "NM_001145026:c.2557+147G>A" "INTRON13" "Unknown significance" "rs188935605" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310663 "chr12:80900597:T>A" "PTPRQ" "NM_001145026:c.2557+148T>A" "INTRON13" "Benign" "rs114065774" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 39 1322 0.0295 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 41 5008 0.0081869
310664 "chr12:80900607:G>T" "PTPRQ" "NM_001145026:c.2557+158G>T" "INTRON13" "Unknown significance" "rs539769121" "This variant is a VUS because it does not have enough information."
310665 "chr12:80900608:C>G" "PTPRQ" "NM_001145026:c.2557+159C>G" "INTRON13" "Unknown significance" "rs551336965" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681
310666 "chr12:80900615:C>T" "PTPRQ" "NM_001145026:c.2557+166C>T" "INTRON13" "Benign" "rs181622349" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 18 5008 0.00359425
310667 "chr12:80900651:G>C" "PTPRQ" "NM_001145026:c.2557+202G>C" "INTRON13" "Unknown significance" "rs536999810" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
310668 "chr12:80900652:->T" "PTPRQ" "NM_001145026:c.2557+203_2557+204insT" "INTRON13" "Unknown significance" "rs34261153" "This variant is a VUS because it does not have enough information."
310669 "chr12:80900678:C>T" "PTPRQ" "NM_001145026:c.2557+229C>T" "INTRON13" "Benign" "rs185214870" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 4 5008 0.000798722
310670 "chr12:80900721:A>-" "PTPRQ" "NM_001145026:c.2557+272delA" "INTRON13" "Benign" "rs139543851" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 1322 0.0068 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 11 5008 0.00219649
310671 "chr12:80900724:G>A" "PTPRQ" "NM_001145026:c.2557+275G>A" "INTRON13" "Benign" "rs190507070" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 31 1322 0.0234 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 34 5008 0.00678914
310672 "chr12:80900740:G>C" "PTPRQ" "NM_001145026:c.2557+291G>C" "INTRON13" "Unknown significance" "rs534741562" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310673 "chr12:80900743:C>T" "PTPRQ" "NM_001145026:c.2557+294C>T" "INTRON13" "Unknown significance" "rs552874145" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
310674 "chr12:80900744:G>A" "PTPRQ" "NM_001145026:c.2557+295G>A" "INTRON13" "Unknown significance" "rs773068538" "This variant is a VUS because it does not have enough information."
310675 "chr12:80900784:C>T" "PTPRQ" "NM_001145026:c.2557+335C>T" "INTRON13" "Unknown significance" "rs574614239" "This variant is a VUS because it does not have enough information." 0 1322