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
491872 "chr21:37832927:A>C" "CLDN14" "NM_144492:c.*347T>G" "THREE_PRIME_EXON" "Benign" "rs201508874" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 10 1322 0.0076 47 1006 0.0467 42 694 0.0605 31 1008 0.0308 2 978 0.002 132 5008 0.0263578
491873 "chr21:37832928:->AAAACC" "CLDN14" "NM_144492:c.*346_*347insGGTTTT" "THREE_PRIME_EXON" "Unknown significance" "rs370594336" "This variant is a VUS because it does not have enough information."
491874 "chr21:37832939:G>T" "CLDN14" "NM_144492:c.*335C>A" "THREE_PRIME_EXON" "Unknown significance" "rs185515617" "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
491875 "chr21:37832940:C>T" "CLDN14" "NM_144492:c.*334G>A" "THREE_PRIME_EXON" "Unknown significance" "rs142629054" "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
491876 "chr21:37832970:C>G" "CLDN14" "NM_144492:c.*304G>C" "THREE_PRIME_EXON" "Unknown significance" "rs377710646" "This variant is a VUS because it does not have enough information."
491877 "chr21:37832977:C>G" "CLDN14" "NM_144492:c.*297G>C" "THREE_PRIME_EXON" "Unknown significance" "rs532695308" "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
491878 "chr21:37832977:C>T" "CLDN14" "NM_144492:c.*297G>A" "THREE_PRIME_EXON" "Unknown significance" "rs532695308" "This variant is a VUS because it does not have enough information."
491879 "chr21:37832997:A>G" "CLDN14" "NM_144492:c.*277T>C" "THREE_PRIME_EXON" "Unknown significance" "rs551351878" "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
491880 "chr21:37833005:C>G" "CLDN14" "NM_144492:c.*269G>C" "THREE_PRIME_EXON" "Unknown significance" "rs571301747" "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
491881 "chr21:37833023:A>T" "CLDN14" "NM_144492:c.*251T>A" "THREE_PRIME_EXON" "Benign" "rs746123433" "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 0 200 0 2 2000 0.001
491882 "chr21:37833040:A>G" "CLDN14" "NM_144492:c.*234T>C" "THREE_PRIME_EXON" "Unknown significance" "rs527363387" "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
491883 "chr21:37833044:A>G" "CLDN14" "NM_144492:c.*230T>C" "THREE_PRIME_EXON" "Unknown significance" "rs547541223" "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
491884 "chr21:37833060:->T" "CLDN14" "NM_144492:c.*214_*215insA" "THREE_PRIME_EXON" "Unknown significance" "rs547523762" "This variant is a VUS because it does not have enough information."
491885 "chr21:37833064:T>C" "CLDN14" "NM_144492:c.*210A>G" "THREE_PRIME_EXON" "Unknown significance" "rs567389844" "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
491886 "chr21:37833099:C>T" "CLDN14" "NM_144492:c.*175G>A" "THREE_PRIME_EXON" "Unknown significance" "rs565686905" "This variant is a VUS because it does not have enough information."
491887 "chr21:37833109:C>T" "CLDN14" "NM_144492:c.*165G>A" "THREE_PRIME_EXON" "Unknown significance" "rs150553857" "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
491888 "chr21:37833167:C>T" "CLDN14" "NM_144492:c.*107G>A" "THREE_PRIME_EXON" "Benign" "rs112112443" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 400 0.0175 0 320 0 0 320 0 0 400 0 2 360 0.00555556 1 200 0.005 10 2000 0.005 0 1322 0 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 3 5008 0.000599042
491889 "chr21:37833200:A>C" "CLDN14" "NM_144492:c.*74T>G" "THREE_PRIME_EXON" "Benign" "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 10 320 0.03125 0 400 0 0 360 0 10 200 0.05 20 2000 0.01
491890 "chr21:37833208:C>T" "CLDN14" "NM_144492:c.*66G>A" "THREE_PRIME_EXON" "Unknown significance" "rs369966830" "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
491891 "chr21:37833223:C>T" "CLDN14" "NM_144492:c.*51G>A" "THREE_PRIME_EXON" "Benign" "rs114551506" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 6 8576 0.000699627 435 4396 0.0989536 441 12972 0.0339963 6 400 0.015 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 6 2000 0.003 159 1322 0.1203 1 1006 0.001 14 694 0.0202 0 1008 0 0 978 0 174 5008 0.0347444 818 7552 0.108316 25 6980 0.00358166 0 6094 0 0 3828 0 34 48924 0.000694955 5 652 0.00766871 1 13752 0.0000727167 883 87782 0.010059
491892 "chr21:37833224:G>T" "CLDN14" "NM_144492:c.*50C>A" "THREE_PRIME_EXON" "Unknown significance" "rs765378283" "This variant is a VUS because it does not have enough information." 0 7628 0 0 7012 0 0 6120 0 0 3846 0 1 48882 0.0000204574 0 650 0 0 13712 0 1 87850 0.000011383
491893 "chr21:37833226:C>T" "CLDN14" "NM_144492:c.*48G>A" "THREE_PRIME_EXON" "Unknown significance" "rs199523516" "This variant is a VUS because it does not have enough information." 0 8584 0 11 4398 0.00250114 11 12982 0.000847327 5 1322 0.0038 0 1006 0 0 694 0 0 1008 0 0 978 0 5 5008 0.000998403 35 7642 0.00457995 18 7004 0.00256996 0 6104 0 0 3868 0 1 48946 0.0000204307 0 648 0 0 13736 0 54 87948 0.000613999
491894 "chr21:37833227:G>A" "CLDN14" "NM_144492:c.*47C>T" "THREE_PRIME_EXON" "Unknown significance" "rs758566130" "This variant is a VUS because it does not have enough information." 0 7644 0 1 7098 0.000140885 0 6140 0 0 3860 0 3 49092 0.0000611098 0 658 0 0 13750 0 4 88242 0.0000453299
491895 "chr21:37833230:G>A" "CLDN14" "NM_144492:c.*44C>T" "THREE_PRIME_EXON" "Unknown significance" "rs780070024" "This variant is a VUS because it does not have enough information." 0 7732 0 0 7176 0 2 6302 0.00031736 0 3890 0 0 49756 0 0 662 0 0 13852 0 2 89370 0.0000223789
491896 "chr21:37833239:C>T" "CLDN14" "NM_144492:c.*35G>A" "THREE_PRIME_EXON" "Unknown significance" "rs746997205" "This variant is a VUS because it does not have enough information." 0 7874 0 0 7438 0 0 6464 0 0 3976 0 0 50770 0 0 668 0 1 14028 0.000071286 1 91218 0.0000109627
491897 "chr21:37833241:C>T" "CLDN14" "NM_144492:c.*33G>A" "THREE_PRIME_EXON" "Unknown significance" "rs754677688" "This variant is a VUS because it does not have enough information." 0 7922 0 0 7474 0 0 6494 0 0 4026 0 1 50998 0.0000196086 0 676 0 0 14058 0 1 91648 0.0000109113
491898 "chr21:37833244:C>A" "CLDN14" "NM_144492:c.*30G>T" "THREE_PRIME_EXON" "Unknown significance" "rs781087324" "This variant is a VUS because it does not have enough information." 0 7984 0 0 7554 0 0 6574 0 0 4016 0 1 51376 0.0000194643 0 680 0 0 14102 0 1 92286 0.0000108359
491899 "chr21:37833251:G>T" "CLDN14" "NM_144492:c.*23C>A" "THREE_PRIME_EXON" "Unknown significance" "rs747720793" "This variant is a VUS because it does not have enough information." 0 8168 0 0 7980 0 0 6776 0 0 4188 0 1 53056 0.000018848 0 700 0 0 14324 0 1 95192 0.0000105051
491900 "chr21:37833252:G>A" "CLDN14" "NM_144492:c.*22C>T" "THREE_PRIME_EXON" "Unknown significance" "rs769498667" "This variant is a VUS because it does not have enough information." 0 8214 0 0 8058 0 0 6820 0 0 4216 0 1 53302 0.000018761 0 720 0 0 14358 0 1 95688 0.0000104506
491901 "chr21:37833263:G>A" "CLDN14" "NM_144492:c.*11C>T" "THREE_PRIME_EXON" "Unknown significance" "rs772699208" "This variant is a VUS because it does not have enough information." 0 8692 0 0 9020 0 1 7402 0.000135099 0 4494 0 0 57040 0 0 742 0 0 14832 0 1 102222 0.00000978263
491902 "chr21:37833264:C>G" "CLDN14" "NM_144492:c.*10G>C" "THREE_PRIME_EXON" "Benign" "rs139628442" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 36 8600 0.00418605 6 4406 0.00136178 42 13006 0.00322928 0 400 0 2 320 0.00625 0 320 0 0 400 0 2 360 0.00555556 0 200 0 4 2000 0.002 0 1322 0 5 1006 0.005 1 694 0.0014 0 1008 0 0 978 0 6 5008 0.00119808 7 8744 0.000800549 16 9092 0.00175979 0 7430 0 35 4524 0.00773652 258 57320 0.00450105 4 748 0.00534759 0 14882 0 320 102740 0.00311466
491903 "chr21:37833268:G>A" "CLDN14" "NM_144492:c.*6C>T" "THREE_PRIME_EXON" "Unknown significance" "rs770435259" "This variant is a VUS because it does not have enough information."
491904 "chr21:37833279:C>T" "CLDN14" "NM_144492:p.Val239Met" "NM_144492:c.715G>A" "EXON3" "Unknown significance" "rs201218449" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.0" "D" "0.714" "P" 0.000002 "D" 0.999948 "D" "5.51" "C" 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 0 9502 0 1 10488 0.0000953471 0 8196 0 0 4984 0 1 61988 0.0000161322 0 796 0 0 15630 0 2 111584 0.0000179237
491905 "chr21:37833280:G>T" "CLDN14" "NM_144492:p.Tyr238Stop" "NM_144492:c.714C>A" "EXON3" "Unknown significance" "rs761269316" "This variant is a VUS because it does not have enough information." -0.74 "N" 0.000054 "D" 0.882107 "D" "-5.5" "N" 1 9590 0.000104275 0 10638 0 0 8258 0 0 5034 0 0 62414 0 0 804 0 0 15776 0 1 112514 0.00000888778
491906 "chr21:37833285:C>T" "CLDN14" "NM_144492:p.Asp237Asn" "NM_144492:c.709G>A" "EXON3" "Unknown significance" "rs768382153" "This variant is a VUS because it does not have enough information." 0.066 "N" "0.13" "T" "0.952" "P" 0.000003 "D" 0.999993 "D" "5.51" "C" 0 9782 0 0 10916 0 0 8416 0 0 5168 0 3 63270 0.0000474158 0 834 0 0 15970 0 3 114356 0.0000262339
491907 "chr21:37833286:G>A" "CLDN14" "NM_144492:p.Asn236Asn" "NM_144492:c.708C>T" "EXON3" "Unknown significance" "rs774161015" "This variant is a VUS because it does not have enough information."
491908 "chr21:37833300:C>T" "CLDN14" "NM_144492:p.Gly232Arg" "NM_144492:c.694G>A" "EXON3" "Pathogenic" "Hearing loss, non-syndromic, autosomal recessive" "22246673" "rs786204841" "Pathogenicity is based on ClinVar submissions and the literature provided in PubMed." 0.935 "N" "0.003" "D" "1.0" "D" 0.000006 "D" 1 "D" "4.62" "C"
491909 "chr21:37833301:G>A" "CLDN14" "NM_144492:p.Ser231Ser" "NM_144492:c.693C>T" "EXON3" "Unknown significance" "rs554611270" "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 10130 0 0 11354 0 1 8600 0.000116279 0 5538 0 1 65070 0.0000153681 0 850 0 0 16388 0 2 117930 0.0000169592
491910 "chr21:37833304:G>A" "CLDN14" "NM_144492:p.His230His" "NM_144492:c.690C>T" "EXON3" "Benign" "rs149733854" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 8600 0.000813953 0 4406 0 7 13006 0.000538213 3 400 0.0075 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 3 2000 0.0015 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 0 10184 0 2 11408 0.000175316 0 8608 0 0 5586 0 77 65304 0.0011791 2 854 0.00234192 10 16418 0.000609088 91 118362 0.000768828
491911 "chr21:37833307:C>T" "CLDN14" "NM_144492:p.Thr229Thr" "NM_144492:c.687G>A" "EXON3" "Benign" "rs219780" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1807 8600 0.210116 1095 4406 0.248525 2902 13006 0.223128 76 400 0.19 48 320 0.15 86 320 0.26875 0 400 0 88 360 0.244444 24 200 0.12 322 2000 0.161 300 1322 0.2269 206 1006 0.2048 79 694 0.1138 2 1008 0.002 91 978 0.093 678 5008 0.135383 2532 10282 0.246256 1081 11428 0.0945922 6 8604 0.00069735 1217 5828 0.208819 13353 65594 0.20357 148 868 0.170507 1692 16446 0.102882 20029 119050 0.16824
491912 "chr21:37833308:G>A" "CLDN14" "NM_144492:p.Thr229Met" "NM_144492:c.686C>T" "EXON3" "Unknown significance" "rs750677498" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.008" "D" "0.521" "P" 0.011774 "N" 1 "N" "5.66" "C" 0 10292 0 0 11470 0 0 8610 0 0 5892 0 1 65730 0.0000152138 0 870 0 1 16460 0.0000607533 2 119324 0.0000167611
491913 "chr21:37833313:C>T" "CLDN14" "NM_144492:p.Ser227Ser" "NM_144492:c.681G>A" "EXON3" "Unknown significance" "rs763085148" "This variant is a VUS because it does not have enough information."
491914 "chr21:37833320:A>G" "CLDN14" "NM_144492:p.Val225Ala" "NM_144492:c.674T>C" "EXON3" "Likely benign" "rs766586533" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." -0.274 "N" "0.358" "T" "0.0" "B" 0.563201 "N" 0.999996 "N" "0.253" "C" 1 10330 0.0000968054 0 11504 0 0 8616 0 0 6014 0 0 65910 0 0 884 0 0 16486 0 1 119744 0.00000835115
491915 "chr21:37833329:G>A" "CLDN14" "NM_144492:p.Ala222Val" "NM_144492:c.665C>T" "EXON3" "Unknown significance" "rs751427421" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.269" "T" "0.012" "B" 0.000017 "D" 0.994468 "D" "4.77" "C" 0 10342 0 1 11516 0.0000868357 0 8620 0 0 6074 0 0 65996 0 0 886 0 0 16494 0 1 119928 0.00000833834
491916 "chr21:37833329:G>T" "CLDN14" "NM_144492:p.Ala222Asp" "NM_144492:c.665C>A" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.351" "T" "0.964" "D" 0.000017 "D" 0.998562 "D" "4.77" "C" 0 10342 0 0 11516 0 0 8620 0 0 6074 0 1 65996 0.0000151524 0 886 0 0 16494 0 1 119928 0.00000833834
491917 "chr21:37833330:->C" "CLDN14" "NM_144492:c.664_665insG" "EXON3" "Unknown significance" "rs761918152" "This variant is a VUS because it does not have enough information." 0 10342 0 0 11516 0 0 8620 0 0 6074 0 1 65996 0.0000151524 0 886 0 0 16494 0 1 119928 0.00000833834
491918 "chr21:37833330:C>-" "CLDN14" "NM_144492:c.664delG" "EXON3" "Unknown significance" "rs772380452" "This variant is a VUS because it does not have enough information." 0 10342 0 0 11516 0 0 8620 0 0 6074 0 1 65996 0.0000151524 0 886 0 0 16494 0 1 119928 0.00000833834
491919 "chr21:37833330:C>T" "CLDN14" "NM_144492:p.Ala222Thr" "NM_144492:c.664G>A" "EXON3" "Unknown significance" "rs138008896" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.371" "T" "0.106" "B" 0.000017 "D" 0.980069 "D" "5.66" "C" 1 8600 0.000116279 1 4406 0.000226963 2 13006 0.000153775 2 10338 0.000193461 0 11518 0 0 8620 0 0 6084 0 1 66008 0.0000151497 0 886 0 0 16492 0 3 119946 0.0000250113
491920 "chr21:37833330:C>A" "CLDN14" "NM_144492:p.Ala222Ser" "NM_144492:c.664G>T" "EXON3" "Unknown significance" "rs138008896" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.582" "T" "0.13" "B" 0.000017 "D" 0.953425 "D" "5.66" "C" 0 10338 0 1 11518 0.0000868206 0 8620 0 0 6084 0 0 66008 0 0 886 0 0 16492 0 1 119946 0.00000833709
491921 "chr21:37833331:C>T" "CLDN14" "NM_144492:p.Arg221Arg" "NM_144492:c.663G>A" "EXON3" "Unknown significance" "rs387907414" "Pathogenicity is based on ClinVar submissions. All submitters agree with this pathogenicity."
491922 "chr21:37833332:C>T" "CLDN14" "NM_144492:p.Arg221Gln" "NM_144492:c.662G>A" "EXON3" "Unknown significance" "rs752592093" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.357" "T" "0.824" "P" 0.002986 "N" 0.589693 "D" "4.77" "C" 0 10342 0 0 11522 0 0 8626 0 0 6104 0 4 66020 0.0000605877 0 890 0 0 16494 0 4 119998 0.0000333339
491923 "chr21:37833333:G>A" "CLDN14" "NM_144492:p.Arg221Trp" "NM_144492:c.661C>T" "EXON3" "Unknown significance" "rs548981290" "This variant is a VUS because it does not have enough information." 0.135 "N" "0.152" "T" "0.992" "D" 0.002986 "N" 0.882902 "D" "4.62" "C" 0 10344 0 0 11520 0 0 8626 0 0 6116 0 2 66032 0.0000302883 0 890 0 2 16494 0.000121256 4 120022 0.0000333272
491924 "chr21:37833333:G>C" "CLDN14" "NM_144492:p.Arg221Gly" "NM_144492:c.661C>G" "EXON3" "Unknown significance" "rs548981290" "This variant is a VUS because it does not have enough information." 0.135 "N" "0.241" "T" "0.811" "P" 0.002986 "N" 0.72955 "D" "4.62" "C" 0 10344 0 2 11520 0.000173611 0 8626 0 0 6116 0 0 66032 0 0 890 0 0 16494 0 2 120022 0.0000166636
491925 "chr21:37833333:G>T" "CLDN14" "NM_144492:p.Arg221Arg" "NM_144492:c.661C>A" "EXON3" "Unknown significance" "rs548981290" "This variant is a VUS because it does not have enough information."
491926 "chr21:37833337:G>A" "CLDN14" "NM_144492:p.Asp219Asp" "NM_144492:c.657C>T" "EXON3" "Unknown significance" "rs143566360" "This variant is a VUS because it does not have enough information." 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876
491927 "chr21:37833348:C>A" "CLDN14" "NM_144492:p.Ala216Ser" "NM_144492:c.646G>T" "EXON3" "Unknown significance" "rs748973638" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.069" "T" "0.441" "B" 0.000017 "D" 0.984687 "D" "4.78" "C" 0 10344 0 0 11538 0 1 8632 0.000115848 0 6246 0 0 66104 0 0 892 0 0 16496 0 1 120252 0.00000831587
491928 "chr21:37833353:G>A" "CLDN14" "NM_144492:p.Pro214Leu" "NM_144492:c.641C>T" "EXON3" "Unknown significance" "rs770382134" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.099" "T" "0.747" "P" 0.008432 "U" 0.994811 "D" "4.77" "C" 0 10348 0 0 11540 0 0 8634 0 0 6274 0 1 66126 0.0000151226 0 896 0 0 16498 0 1 120316 0.00000831145
491929 "chr21:37833361:G>A" "CLDN14" "NM_144492:p.Tyr211Tyr" "NM_144492:c.633C>T" "EXON3" "Benign" "rs61745291" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 8600 0.000232558 278 4406 0.0630958 280 13006 0.0215285 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 1 200 0.005 1 2000 0.0005 114 1322 0.0862 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 118 5008 0.0235623 688 10356 0.0664349 35 11542 0.0030324 0 8634 0 0 6306 0 25 66146 0.000377952 5 898 0.00556793 3 16498 0.00018184 756 120380 0.00628011
491930 "chr21:37833369:G>T" "CLDN14" "NM_144492:p.Pro209Thr" "NM_144492:c.625C>A" "EXON3" "Likely benign" "rs747443576" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 0.065 "N" "0.272" "T" "0.191" "B" 0.959876 "N" 0.999962 "D" "4.64" "C" 0 10360 0 0 11544 0 0 8636 0 0 6348 0 1 66176 0.0000151112 0 898 0 0 16506 0 1 120468 0.00000830096
491931 "chr21:37833370:T>G" "CLDN14" "NM_144492:p.Ala208Ala" "NM_144492:c.624A>C" "EXON3" "Unknown significance" "rs769272352" "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
491932 "chr21:37833372:C>T" "CLDN14" "NM_144492:p.Ala208Thr" "NM_144492:c.622G>A" "EXON3" "Unknown significance" "rs371297575" "This variant is a VUS because it does not have enough information." 0.876 "N" "0.069" "T" "0.989" "D" 0.004171 "U" 0.999678 "D" "4.51" "C" 1 8600 0.000116279 0 4406 0 1 13006 0.0000768876 0 10356 0 1 11542 0.0000866401 0 8638 0 0 6356 0 4 66184 0.0000604376 0 898 0 0 16506 0 5 120480 0.0000415007
491933 "chr21:37833373:G>A" "CLDN14" "NM_144492:p.Thr207Thr" "NM_144492:c.621C>T" "EXON3" "Benign" "rs139437157" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 8600 0.000116279 55 4406 0.012483 56 13006 0.00430571 16 1322 0.0121 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 17 5008 0.00339457 132 10360 0.0127413 5 11542 0.0004332 0 8638 0 0 6360 0 6 66206 0.0000906262 1 898 0.00111359 1 16506 0.000060584 145 120510 0.00120322
491934 "chr21:37833375:T>G" "CLDN14" "NM_144492:p.Thr207Pro" "NM_144492:c.619A>C" "EXON3" "Likely benign" "Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic." 0.071 "N" "0.284" "T" "0.023" "B" 0.115061 "N" 1 "N" "-2.83" "N" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
491935 "chr21:37833376:G>A" "CLDN14" "NM_144492:p.Asn206Asn" "NM_144492:c.618C>T" "EXON3" "Unknown significance" "rs184035890" "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 10360 0 1 11544 0.0000866251 0 8638 0 0 6378 0 0 66222 0 0 896 0 0 16506 0 1 120544 0.00000829573
491936 "chr21:37833380:G>A" "CLDN14" "NM_144492:p.Ala205Val" "NM_144492:c.614C>T" "EXON3" "Likely benign" "rs149671826" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." 0.065 "N" "0.429" "T" "0.084" "B" 0.290412 "N" 1 "N" "3.56" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 2 10356 0.000193125 1 11546 0.0000866101 0 8638 0 0 6394 0 1 66236 0.0000150975 0 896 0 0 16502 0 4 120568 0.0000331763
491937 "chr21:37833388:C>T" "CLDN14" "NM_144492:p.Thr202Thr" "NM_144492:c.606G>A" "EXON3" "Unknown significance" "rs763313658" "This variant is a VUS because it does not have enough information." 1 10362 0.0000965065 1 11546 0.0000866101 0 8634 0 0 6418 0 0 66248 0 0 896 0 2 16500 0.000121212 4 120604 0.0000331664
491938 "chr21:37833389:G>A" "CLDN14" "NM_144492:p.Thr202Met" "NM_144492:c.605C>T" "EXON3" "Likely benign" "rs564851292" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." 0.138 "N" "0.232" "T" "0.091" "B" 0.931852 "N" 1 "N" "3.71" "C" 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361 1 10362 0.0000965065 0 11540 0 0 8638 0 0 6424 0 0 66252 0 0 898 0 12 16500 0.000727273 13 120614 0.000107782
491939 "chr21:37833391:G>T" "CLDN14" "NM_144492:p.Thr201Thr" "NM_144492:c.603C>A" "EXON3" "Unknown significance" "rs760219487" "This variant is a VUS because it does not have enough information." 0 10364 0 1 11544 0.0000866251 0 8638 0 0 6430 0 2 66262 0.0000301832 0 898 0 0 16500 0 3 120636 0.0000248682
491940 "chr21:37833393:T>G" "CLDN14" "NM_144492:p.Thr201Pro" "NM_144492:c.601A>C" "EXON3" "Likely benign" "Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic." -0.705 "N" "0.313" "T" "0.0" "B" 0.498578 "N" 1 "N" "-1.34" "N" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
491941 "chr21:37833403:C>T" "CLDN14" "NM_144492:p.Pro197Pro" "NM_144492:c.591G>A" "EXON3" "Unknown significance" "rs374840285" "This variant is a VUS because it does not have enough information." 1 8600 0.000116279 0 4406 0 1 13006 0.0000768876 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 10360 0 0 11542 0 0 8640 0 0 6450 0 2 66248 0.0000301896 0 894 0 3 16502 0.000181796 5 120636 0.000041447
491942 "chr21:37833404:G>A" "CLDN14" "NM_144492:p.Pro197Leu" "NM_144492:c.590C>T" "EXON3" "Likely benign" "rs374682296" "Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic." -0.274 "N" "0.357" "T" "0.0" "B" 0.327765 "N" 1 "N" "-10.3" "N" 0 10358 0 0 11546 0 0 8640 0 0 6462 0 1 66262 0.0000150916 0 898 0 0 16502 0 1 120668 0.0000082872
491943 "chr21:37833406:G>T" "CLDN14" "NM_144492:p.Ala196Ala" "NM_144492:c.588C>A" "EXON3" "Unknown significance" "rs144371384" "This variant is a VUS because it does not have enough information." 3 8600 0.000348837 0 4406 0 3 13006 0.000230663 0 10362 0 0 11546 0 0 8640 0 0 6462 0 4 66258 0.0000603701 0 898 0 0 16502 0 4 120668 0.0000331488
491944 "chr21:37833406:G>C" "CLDN14" "NM_144492:p.Ala196Ala" "NM_144492:c.588C>G" "EXON3" "Unknown significance" "rs144371384" "This variant is a VUS because it does not have enough information." 0 10362 0 0 11546 0 0 8640 0 0 6462 0 0 66258 0 1 898 0.00111359 21 16502 0.00127257 22 120668 0.000182318
491945 "chr21:37833407:G>A" "CLDN14" "NM_144492:p.Ala196Val" "NM_144492:c.587C>T" "EXON3" "Likely benign" "rs200651246" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." 0.135 "N" "0.475" "T" "0.0" "B" 0.000009 "N" 1 "N" "2.64" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361 0 10362 0 0 11546 0 11 8642 0.00127285 0 6468 0 1 66258 0.0000150925 0 898 0 0 16500 0 12 120674 0.0000994415
491946 "chr21:37833413:T>G" "CLDN14" "NM_144492:p.Tyr194Ser" "NM_144492:c.581A>C" "EXON3" "Likely benign" "Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic." 0.114 "N" "0.113" "T" "0.0" "B" 0.007467 "N" 0.999695 "N" "-1.71" "N" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
491947 "chr21:37833414:A>G" "CLDN14" "NM_144492:p.Tyr194His" "NM_144492:c.580T>C" "EXON3" "Likely benign" "rs372105353" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." 0.23 "N" "0.263" "T" "0.0" "B" 0.007467 "N" 1 "N" "0.289" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 1 10360 0.0000965251 0 11552 0 0 8640 0 0 6486 0 0 66272 0 0 896 0 0 16500 0 1 120706 0.00000828459
491948 "chr21:37833422:T>C" "CLDN14" "NM_144492:p.Tyr191Cys" "NM_144492:c.572A>G" "EXON3" "Likely benign" "rs755393537" "Pathogenicity is based on prediction data only. 1 out of 5 predictions were pathogenic." 0.113 "N" "0.111" "T" "0.0" "B" 0.091728 "U" 1 "N" "0.71" "C" 0 10366 0 0 11548 0 0 8640 0 0 6502 0 4 66284 0.0000603464 0 898 0 0 16502 0 4 120740 0.000033129
491949 "chr21:37833426:G>A" "CLDN14" "NM_144492:p.Pro190Ser" "NM_144492:c.568C>T" "EXON3" "Unknown significance" "rs778283119" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.349" "T" "0.098" "B" 0.531497 "U" 0.99109 "D" "5.55" "C" 1 10362 0.0000965065 0 11550 0 0 8640 0 0 6510 0 0 66308 0 0 898 0 0 16502 0 1 120770 0.0000082802
491950 "chr21:37833427:T>G" "CLDN14" "NM_144492:p.Ala189Ala" "NM_144492:c.567A>C" "EXON3" "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
491951 "chr21:37833432:C>T" "CLDN14" "NM_144492:p.Glu188Lys" "NM_144492:c.562G>A" "EXON3" "Likely benign" "rs745441972" "Pathogenicity is based on prediction data only. 1 out of 5 predictions were pathogenic." 0.935 "N" "0.305" "T" "0.019" "B" 0.000933 "U" 0.906843 "N" "4.53" "C" 1 10360 0.0000965251 0 11554 0 0 8640 0 0 6524 0 0 66298 0 0 898 0 0 16500 0 1 120774 0.00000827993
491952 "chr21:37833433:G>T" "CLDN14" "NM_144492:p.Asp187Glu" "NM_144492:c.561C>A" "EXON3" "Likely benign" "rs771486433" "Pathogenicity is based on prediction data only. 0 out of 5 predictions were pathogenic." 0.138 "N" "1.0" "T" "0.0" "B" 0.024908 "U" 0.989809 "N" "-4.95" "N" 0 10364 0 2 11554 0.0001731 0 8640 0 0 6528 0 0 66290 0 0 898 0 0 16502 0 2 120776 0.0000165596
491953 "chr21:37833433:G>A" "CLDN14" "NM_144492:p.Asp187Asp" "NM_144492:c.561C>T" "EXON3" "Unknown significance" "rs771486433" "This variant is a VUS because it does not have enough information." 0 10364 0 0 11554 0 0 8640 0 0 6528 0 1 66290 0.0000150852 0 898 0 0 16502 0 1 120776 0.00000827979
491954 "chr21:37833435:C>A" "CLDN14" "NM_144492:p.Asp187Tyr" "NM_144492:c.559G>T" "EXON3" "Unknown significance" "rs375904468" "This variant is a VUS because it does not have enough information." 0.061 "N" "0.031" "D" "0.454" "P" 0.024908 "U" 0.895582 "D" "3.61" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 3 10364 0.000289464 1 11558 0.0000865202 0 8638 0 0 6528 0 0 66308 0 0 898 0 0 16498 0 4 120792 0.0000331148
491955 "chr21:37833438:G>C" "CLDN14" "NM_144492:p.Gln186Glu" "NM_144492:c.556C>G" "EXON3" "Unknown significance" "rs770259212" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.547" "T" "0.031" "B" 0.004519 "N" 0.999437 "D" "5.42" "C" 0 10360 0 0 11558 0 0 8642 0 0 6532 0 0 66314 0 0 898 0 1 16500 0.0000606061 1 120804 0.00000827787
491956 "chr21:37833443:G>A" "CLDN14" "NM_144492:p.Ser184Phe" "NM_144492:c.551C>T" "EXON3" "Unknown significance" "rs773749542" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.0" "D" "0.747" "P" 0.003714 "N" 0.999988 "D" "5.42" "C" 0 10360 0 0 11556 0 0 8642 0 0 6542 0 1 66326 0.000015077 0 898 0 0 16498 0 1 120822 0.00000827664
491957 "chr21:37833451:A>C" "CLDN14" "NM_144492:p.Leu181Leu" "NM_144492:c.543T>G" "EXON3" "Unknown significance" "rs749515217" "This variant is a VUS because it does not have enough information." 0 10364 0 0 11560 0 0 8644 0 0 6556 0 1 66338 0.0000150743 0 902 0 0 16500 0 1 120864 0.00000827376
491958 "chr21:37833454:C>T" "CLDN14" "NM_144492:p.Leu180Leu" "NM_144492:c.540G>A" "EXON3" "Unknown significance" "rs369688436" "This variant is a VUS because it does not have enough information." 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 1 10362 0.0000965065 0 11562 0 0 8644 0 0 6556 0 0 66350 0 0 902 0 0 16504 0 1 120880 0.00000827267
491959 "chr21:37833455:A>G" "CLDN14" "NM_144492:p.Leu180Pro" "NM_144492:c.539T>C" "EXON3" "Unknown significance" "rs774446882" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.041" "D" "0.997" "D" 0.009847 "N" 1 "D" "5.42" "C" 0 10362 0 0 11562 0 0 8644 0 0 6556 0 1 66368 0.0000150675 0 902 0 0 16506 0 1 120900 0.0000082713
491960 "chr21:37833459:T>C" "CLDN14" "NM_144492:p.Thr179Ala" "NM_144492:c.535A>G" "EXON3" "Likely benign" "rs759597838" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 1.061 "C" "0.577" "T" "0.002" "B" 0.001186 "N" 0.999992 "N" "5.42" "C" 0 10358 0 0 11564 0 0 8644 0 0 6556 0 1 66348 0.000015072 0 900 0 0 16502 0 1 120872 0.00000827321
491961 "chr21:37833459:T>G" "CLDN14" "NM_144492:p.Thr179Pro" "NM_144492:c.535A>C" "EXON3" "Benign" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1.061 "C" "0.21" "T" "0.927" "P" 0.001186 "N" 0.999958 "N" "5.42" "C" 0 400 0 0 320 0 1 320 0.003125 0 400 0 0 360 0 4 200 0.02 5 2000 0.0025
491962 "chr21:37833468:T>C" "CLDN14" "NM_144492:p.Ile176Val" "NM_144492:c.526A>G" "EXON3" "Unknown significance" "rs767528825" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.414" "T" "0.267" "B" 0.00186 "N" 0.938867 "D" "5.42" "C" 0 10354 0 0 11564 0 0 8644 0 0 6588 0 1 66402 0.0000150598 0 902 0 0 16506 0 1 120960 0.0000082672
491963 "chr21:37833469:G>A" "CLDN14" "NM_144492:p.Leu175Leu" "NM_144492:c.525C>T" "EXON3" "Unknown significance" "rs373226526" "This variant is a VUS because it does not have enough information." 1 8600 0.000116279 0 4406 0 1 13006 0.0000768876 0 10354 0 0 11564 0 0 8642 0 0 6588 0 2 66396 0.0000301223 0 902 0 0 16504 0 2 120950 0.0000165358
491964 "chr21:37833471:G>A" "CLDN14" "NM_144492:p.Leu175Phe" "NM_144492:c.523C>T" "EXON3" "Likely benign" "rs760657763" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 0.108 "N" "0.053" "T" "0.317" "B" 0.016314 "N" 0.965236 "D" "4.52" "C" 0 10352 0 0 11564 0 0 8644 0 0 6590 0 1 66402 0.0000150598 0 902 0 0 16504 0 1 120958 0.00000826733
491965 "chr21:37833472:C>T" "CLDN14" "NM_144492:p.Ser174Ser" "NM_144492:c.522G>A" "EXON3" "Unknown significance" "rs763846537" "This variant is a VUS because it does not have enough information." 0 10348 0 0 11564 0 0 8644 0 1 6590 0.000151745 20 66388 0.000301259 1 902 0.00110865 1 16500 0.0000606061 23 120936 0.000190183
491966 "chr21:37833473:G>A" "CLDN14" "NM_144492:p.Ser174Leu" "NM_144492:c.521C>T" "EXON3" "Unknown significance" "rs140196815" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.221" "T" "0.021" "B" 0.19547 "N" 0.994039 "D" "4.54" "C" 1 8600 0.000116279 0 4406 0 1 13006 0.0000768876 1 10350 0.0000966184 0 11566 0 0 8644 0 0 6592 0 3 66422 0.0000451658 0 902 0 0 16506 0 4 120982 0.0000330628
491967 "chr21:37833481:C>G" "CLDN14" "NM_144492:p.Ser171Ser" "NM_144492:c.513G>C" "EXON3" "Unknown significance" "rs756847536" "This variant is a VUS because it does not have enough information." 0 10342 0 0 11566 0 0 8644 0 0 6594 0 1 66434 0.0000150525 0 904 0 0 16504 0 1 120988 0.00000826528
491968 "chr21:37833481:C>T" "CLDN14" "NM_144492:p.Ser171Ser" "NM_144492:c.513G>A" "EXON3" "Unknown significance" "rs756847536" "This variant is a VUS because it does not have enough information." 0 10342 0 0 11566 0 0 8644 0 0 6594 0 0 66434 0 0 904 0 2 16504 0.000121183 2 120988 0.0000165306
491969 "chr21:37833482:G>A" "CLDN14" "NM_144492:p.Ser171Leu" "NM_144492:c.512C>T" "EXON3" "Unknown significance" "rs75617474" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.005" "D" "0.774" "P" 0.023186 "N" 0.993575 "D" "5.42" "C" 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681 0 10346 0 0 11566 0 0 8644 0 0 6594 0 1 66436 0.0000150521 0 904 0 0 16506 0 1 120996 0.00000826474
491970 "chr21:37833482:G>T" "CLDN14" "NM_144492:p.Ser171Stop" "NM_144492:c.512C>A" "EXON3" "Unknown significance" "rs75617474" "This variant is a VUS because it does not have enough information." 1.048 "C" 0.023186 "N" 1 "D" "5.42" "C"
491971 "chr21:37833495:C>T" "CLDN14" "NM_144492:p.Gly167Ser" "NM_144492:c.499G>A" "EXON3" "Unknown significance" "rs377158611" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.0" "D" "1.0" "D" 0 "D" 1 "D" "5.42" "C" 1 8600 0.000116279 0 4406 0 1 13006 0.0000768876
491972 "chr21:37833499:G>A" "CLDN14" "NM_144492:p.Tyr165Tyr" "NM_144492:c.495C>T" "EXON3" "Unknown significance" "rs373672296" "This variant is a VUS because it does not have enough information." 0 10318 0 0 11566 0 1 8642 0.000115714 0 6602 0 1 66410 0.000015058 0 904 0 3 16508 0.00018173 5 120950 0.0000413394
491973 "chr21:37833500:T>G" "CLDN14" "NM_144492:p.Tyr165Ser" "NM_144492:c.494A>C" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.001" "D" "1.0" "D" 0.000001 "D" 1 "D" "5.42" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
491974 "chr21:37833505:G>C" "CLDN14" "NM_144492:p.Ala163Ala" "NM_144492:c.489C>G" "EXON3" "Unknown significance" "rs779757519" "This variant is a VUS because it does not have enough information." 0 10312 0 0 11566 0 0 8638 0 0 6604 0 1 66376 0.0000150657 0 904 0 0 16504 0 1 120904 0.00000827102
491975 "chr21:37833506:G>A" "CLDN14" "NM_144492:p.Ala163Val" "NM_144492:c.488C>T" "EXON3" "Unknown significance" "rs143797113" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.005" "D" "1.0" "D" 0 "D" 0.999775 "D" "5.42" "C" 6 8600 0.000697674 0 4406 0 6 13006 0.000461326 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0 0 1322 0 2 1006 0.002 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 2 10314 0.000193911 0 11566 0 0 8638 0 0 6604 0 29 66382 0.000436865 0 904 0 0 16504 0 31 120912 0.000256385
491976 "chr21:37833515:A>G" "CLDN14" "NM_144492:p.Ile160Thr" "NM_144492:c.479T>C" "EXON3" "Unknown significance" "rs756749130" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.013" "D" "0.909" "P" 0.847952 "N" 0.999948 "D" "5.42" "C" 0 10306 0 0 11562 0 0 8634 0 0 6606 0 0 66370 0 0 904 0 1 16498 0.0000606134 1 120880 0.00000827267
491977 "chr21:37833523:C>T" "CLDN14" "NM_144492:p.Lys157Lys" "NM_144492:c.471G>A" "EXON3" "Likely benign" "24033266" "rs146860442" "Pathogenicity is based on ClinVar submissions. All submitters agree with this pathogenicity." 0 8600 0 5 4406 0.00113482 5 13006 0.000384438 14 10290 0.00136054 3 11558 0.00025956 0 8628 0 0 6608 0 0 66330 0 0 904 0 0 16488 0 17 120806 0.000140721
491978 "chr21:37833531:C>T" "CLDN14" "NM_144492:p.Gly155Ser" "NM_144492:c.463G>A" "EXON3" "Likely benign" "rs749603296" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." -0.338 "N" "1.0" "T" "0.53" "P" 0.001251 "N" 0.905886 "N" "-1.39" "N" 1 10280 0.0000972763 3 11556 0.000259605 0 8628 0 0 6608 0 2 66290 0.0000301705 0 904 0 0 16486 0 6 120752 0.0000496886
491979 "chr21:37833532:G>A" "CLDN14" "NM_144492:p.Ser154Ser" "NM_144492:c.462C>T" "EXON3" "Unknown significance" "rs771208295" "This variant is a VUS because it does not have enough information." 0 10278 0 0 11556 0 0 8626 0 1 6608 0.000151332 0 66280 0 0 904 0 0 16486 0 1 120738 0.0000082824
491980 "chr21:37833535:G>A" "CLDN14" "NM_144492:p.Pro153Pro" "NM_144492:c.459C>T" "EXON3" "Unknown significance" "rs774596862" "This variant is a VUS because it does not have enough information." 1 10260 0.0000974659 0 11552 0 0 8624 0 0 6608 0 0 66248 0 0 898 0 0 16486 0 1 120676 0.00000828665
491981 "chr21:37833544:C>A" "CLDN14" "NM_144492:p.Pro150Pro" "NM_144492:c.450G>T" "EXON3" "Unknown significance" "rs746102559" "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 0 10250 0 0 11550 0 0 8622 0 0 6610 0 9 66188 0.000135976 0 900 0 2 16484 0.00012133 11 120604 0.0000912076
491982 "chr21:37833544:C>T" "CLDN14" "NM_144492:p.Pro150Pro" "NM_144492:c.450G>A" "EXON3" "Unknown significance" "rs746102559" "This variant is a VUS because it does not have enough information." 1 10250 0.000097561 0 11550 0 2 8622 0.000231965 0 6610 0 3 66188 0.0000453254 0 900 0 0 16484 0 6 120604 0.0000497496
491983 "chr21:37833545:G>A" "CLDN14" "NM_144492:p.Pro150Leu" "NM_144492:c.449C>T" "EXON3" "Unknown significance" "rs775588286" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.062" "T" "1.0" "D" 0 "D" 1 "D" "5.42" "C" 0 10246 0 0 11550 0 0 8624 0 0 6610 0 1 66190 0.000015108 0 900 0 0 16486 0 1 120606 0.00000829146
491984 "chr21:37833550:G>A" "CLDN14" "NM_144492:p.Tyr148Tyr" "NM_144492:c.444C>T" "EXON3" "Unknown significance" "rs549938800" "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 10236 0 0 11550 0 0 8620 0 0 6610 0 1 66164 0.000015114 0 900 0 0 16482 0 1 120562 0.00000829449
491985 "chr21:37833564:C>T" "CLDN14" "NM_144492:p.Val144Met" "NM_144492:c.430G>A" "EXON3" "Unknown significance" "rs764077250" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.006" "D" "0.998" "D" 0.000085 "D" 0.999995 "D" "5.42" "C" 0 10208 0 0 11542 0 0 8616 0 0 6608 0 6 66052 0.0000908375 0 900 0 0 16480 0 6 120406 0.0000498314
491986 "chr21:37833567:C>G" "CLDN14" "NM_144492:p.Val143Leu" "NM_144492:c.427G>C" "EXON3" "Unknown significance" "rs776564488" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.013" "D" "0.997" "D" 0.000003 "D" 0.999974 "D" "5.42" "C" 0 10202 0 0 11538 0 0 8616 0 0 6608 0 1 66046 0.000015141 0 900 0 0 16480 0 1 120390 0.00000830634
491987 "chr21:37833567:C>T" "CLDN14" "NM_144492:p.Val143Met" "NM_144492:c.427G>A" "EXON3" "Unknown significance" "rs776564488" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.002" "D" "1.0" "D" 0.000003 "D" 0.99998 "D" "5.42" "C" 0 10202 0 0 11538 0 1 8616 0.000116063 0 6608 0 0 66046 0 0 900 0 0 16480 0 1 120390 0.00000830634
491988 "chr21:37833568:G>A" "CLDN14" "NM_144492:p.Asp142Asp" "NM_144492:c.426C>T" "EXON3" "Unknown significance" "rs140671150" "This variant is a VUS because it does not have enough information." 1 8600 0.000116279 0 4406 0 1 13006 0.0000768876 0 10200 0 0 11536 0 0 8614 0 0 6608 0 1 66028 0.0000151451 0 896 0 3 16480 0.000182039 4 120362 0.0000332331
491989 "chr21:37833570:C>T" "CLDN14" "NM_144492:p.Asp142Asn" "NM_144492:c.424G>A" "EXON3" "Unknown significance" "rs146755542" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.126" "T" "0.997" "D" 0 "D" 0.999997 "D" "5.42" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0 0 1322 0 0 1006 0 1 694 0.0014 2 1008 0.002 0 978 0 3 5008 0.000599042 0 10202 0 3 11538 0.00026001 3 8612 0.000348351 0 6608 0 0 66030 0 0 896 0 0 16480 0 6 120366 0.000049848
491990 "chr21:37833571:G>T" "CLDN14" "NM_144492:p.Asn141Lys" "NM_144492:c.423C>A" "EXON3" "Unknown significance" "rs758024791" "This variant is a VUS because it does not have enough information." -0.2 "N" "0.236" "T" "0.878" "P" 0.003624 "N" 0.999664 "D" "0.178" "C" 0 10198 0 0 11538 0 0 8614 0 0 6608 0 0 66028 0 0 898 0 6 16480 0.000364078 6 120364 0.0000498488
491991 "chr21:37833571:G>A" "CLDN14" "NM_144492:p.Asn141Asn" "NM_144492:c.423C>T" "EXON3" "Unknown significance" "rs758024791" "This variant is a VUS because it does not have enough information." 0 10198 0 0 11538 0 0 8614 0 0 6608 0 1 66028 0.0000151451 0 898 0 0 16480 0 1 120364 0.00000830813
491992 "chr21:37833572:T>G" "CLDN14" "NM_144492:p.Asn141Thr" "NM_144492:c.422A>C" "EXON3" "Unknown significance" "rs751170450" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.017" "D" "0.852" "P" 0.003624 "N" 0.999968 "D" "5.42" "C" 0 10202 0 0 11538 0 0 8610 0 0 6608 0 1 66028 0.0000151451 0 898 0 1 16480 0.0000606796 2 120364 0.0000166163
491993 "chr21:37833575:G>A" "CLDN14" "NM_144492:p.Thr140Ile" "NM_144492:c.419C>T" "EXON3" "Unknown significance" "rs754545220" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.482" "T" "0.22" "B" 0.000012 "D" 1 "D" "5.42" "C" 0 10196 0 0 11534 0 0 8606 0 0 6608 0 2 66002 0.0000303021 0 898 0 1 16480 0.0000606796 3 120324 0.0000249327
491994 "chr21:37833580:C>T" "CLDN14" "NM_144492:p.Trp138Stop" "NM_144492:c.414G>A" "EXON3" "Unknown significance" "rs142846225" "This variant is a VUS because it does not have enough information." 0.935 "N" 0 "D" 1 "D" "5.42" "C" 0 8600 0 2 4406 0.000453926 2 13006 0.000153775 1 10188 0.0000981547 0 11534 0 0 8598 0 0 6608 0 0 65964 0 0 898 0 0 16476 0 1 120266 0.0000083149
491995 "chr21:37833581:C>T" "CLDN14" "NM_144492:p.Trp138Stop" "NM_144492:c.413G>A" "EXON3" "Unknown significance" "rs151069240" "This variant is a VUS because it does not have enough information." 0.935 "N" 0 "D" 1 "D" "5.42" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876
491996 "chr21:37833588:C>T" "CLDN14" "NM_144492:p.Val136Ile" "NM_144492:c.406G>A" "EXON3" "Benign" "rs140918123" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.935 "N" "0.089" "T" "0.997" "D" 0.000003 "D" 1 "D" "5.42" "C" 0 8600 0 26 4406 0.00590104 26 13006 0.00199908 4 1322 0.003 0 1006 0 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722 49 10180 0.00481336 2 11530 0.000173461 0 8596 0 0 6602 0 3 65924 0.0000455069 0 898 0 1 16476 0.0000606943 55 120206 0.000457548
491997 "chr21:37833591:C>A" "CLDN14" "NM_144492:p.Ala135Ser" "NM_144492:c.403G>T" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.019" "D" "0.507" "P" 0.000591 "D" 0.996775 "D" "5.42" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
491998 "chr21:37833596:A>-" "CLDN14" "NM_144492:c.398delT" "EXON3" "Pathogenic" "Deafness, autosomal recessive" "11163249|3" "rs786200885" "Pathogenicity is based on ClinVar submissions and the literature provided in PubMed."
491999 "chr21:37833597:T>C" "CLDN14" "NM_144492:p.Met133Val" "NM_144492:c.397A>G" "EXON3" "Likely benign" "rs757597772" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 1.061 "C" "0.02" "D" "0.013" "B" 0.053717 "N" 0.844011 "N" "-2.21" "N" 0 10168 0 0 11526 0 0 8594 0 0 6600 0 1 65890 0.0000151768 0 898 0 0 16478 0 1 120154 0.00000832265
492000 "chr21:37833602:A>G" "CLDN14" "NM_144492:p.Leu131Pro" "NM_144492:c.392T>C" "EXON3" "Unknown significance" "rs373777126" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.003" "D" "0.999" "D" 0.028668 "N" 0.99742 "D" "5.42" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 1 10162 0.0000984058 0 11524 0 0 8592 0 0 6600 0 0 65860 0 0 898 0 0 16480 0 1 120116 0.00000832529
492001 "chr21:37833607:G>A" "CLDN14" "NM_144492:p.Gly129Gly" "NM_144492:c.387C>T" "EXON3" "Unknown significance" "rs558404405" "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 10154 0 0 11522 0 0 8590 0 0 6598 0 1 65832 0.0000151902 0 898 0 1 16480 0.0000606796 2 120074 0.0000166564
492002 "chr21:37833609:C>T" "CLDN14" "NM_144492:p.Gly129Ser" "NM_144492:c.385G>A" "EXON3" "Unknown significance" "rs772250957" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.006" "D" "1.0" "D" 0 "D" 1 "D" "5.42" "C" 0 10150 0 2 11522 0.000173581 0 8590 0 0 6596 0 0 65812 0 0 898 0 0 16480 0 2 120048 0.00001666
492003 "chr21:37833610:G>A" "CLDN14" "NM_144492:p.Ala128Ala" "NM_144492:c.384C>T" "EXON3" "Unknown significance" "rs780095902" "This variant is a VUS because it does not have enough information." 0 10144 0 2 11522 0.000173581 0 8586 0 0 6598 0 2 65802 0.0000303942 0 898 0 0 16478 0 4 120028 0.0000333256
492004 "chr21:37833615:G>A" "CLDN14" "NM_144492:p.Leu127Leu" "NM_144492:c.379C>T" "EXON3" "Unknown significance" "rs747033624" "This variant is a VUS because it does not have enough information." 0 10140 0 0 11512 0 0 8590 0 0 6598 0 0 65770 0 0 898 0 1 16478 0.000060687 1 119986 0.00000833431
492005 "chr21:37833619:G>A" "CLDN14" "NM_144492:p.Phe125Phe" "NM_144492:c.375C>T" "EXON3" "Unknown significance" "rs768728088" "This variant is a VUS because it does not have enough information." 0 10140 0 1 11512 0.0000868659 0 8588 0 0 6596 0 0 65758 0 0 898 0 0 16472 0 1 119964 0.00000833583
492006 "chr21:37833625:G>T" "CLDN14" "NM_144492:p.Thr123Thr" "NM_144492:c.369C>A" "EXON3" "Likely benign" "24033266" "rs727502938" "Pathogenicity is based on ClinVar submissions. All submitters agree with this pathogenicity." 1 10130 0.0000987167 1 11514 0.0000868508 0 8588 0 0 6596 0 3 65730 0.0000456413 0 898 0 0 16476 0 5 119932 0.0000416903
492007 "chr21:37833625:G>A" "CLDN14" "NM_144492:p.Thr123Thr" "NM_144492:c.369C>T" "EXON3" "Unknown significance" "rs727502938" "This variant is a VUS because it does not have enough information." 0 10130 0 0 11514 0 0 8588 0 0 6596 0 2 65730 0.0000304275 0 898 0 0 16476 0 2 119932 0.0000166761
492008 "chr21:37833627:T>G" "CLDN14" "NM_144492:p.Thr123Pro" "NM_144492:c.367A>C" "EXON3" "Likely benign" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." -0.336 "N" "0.055" "T" "0.125" "B" 0.870245 "N" 1 "N" "0.289" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
492009 "chr21:37833630:C>T" "CLDN14" "NM_144492:p.Gly122Ser" "NM_144492:c.364G>A" "EXON3" "Unknown significance" "rs769599110" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.006" "D" "1.0" "D" 0 "D" 1 "D" "5.42" "C" 0 10132 0 0 11516 0 1 8584 0.000116496 0 6592 0 6 65676 0.0000913576 0 898 0 0 16472 0 7 119870 0.0000583966
492010 "chr21:37833631:G>A" "CLDN14" "NM_144492:p.Gly121Gly" "NM_144492:c.363C>T" "EXON3" "Unknown significance" "rs763411863" "This variant is a VUS because it does not have enough information." 0 10128 0 0 11514 0 0 8584 0 0 6592 0 6 65636 0.0000914132 0 896 0 0 16474 0 6 119824 0.0000500734
492011 "chr21:37833633:C>T" "CLDN14" "NM_144492:p.Gly121Ser" "NM_144492:c.361G>A" "EXON3" "Unknown significance" "rs150201704" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.0" "D" "1.0" "D" 0 "D" 1 "D" "5.42" "C" 3 8600 0.000348837 0 4406 0 3 13006 0.000230663 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681 1 10124 0.0000987752 1 11516 0.0000868357 1 8582 0.000116523 0 6592 0 5 65658 0.0000761522 0 898 0 0 16472 0 8 119842 0.0000667546
492012 "chr21:37833642:C>G" "CLDN14" "NM_144492:p.Ala118Pro" "NM_144492:c.352G>C" "EXON3" "Unknown significance" "rs377333347" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.006" "D" "1.0" "D" 0.000296 "D" 1 "D" "5.42" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 3 10122 0.000296384 0 11514 0 0 8576 0 0 6588 0 0 65614 0 0 894 0 0 16476 0 3 119784 0.0000250451
492013 "chr21:37833642:C>T" "CLDN14" "NM_144492:p.Ala118Thr" "NM_144492:c.352G>A" "EXON3" "Unknown significance" "rs377333347" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.006" "D" "0.998" "D" 0.000296 "D" 1 "D" "5.42" "C" 0 10122 0 0 11514 0 0 8576 0 0 6588 0 0 65614 0 0 894 0 1 16476 0.0000606943 1 119784 0.00000834836
492014 "chr21:37833647:G>A" "CLDN14" "NM_144492:p.Thr116Ile" "NM_144492:c.347C>T" "EXON3" "Likely benign" "rs370342285" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." 0.135 "N" "0.206" "T" "0.024" "B" 0.607169 "N" 1 "N" "1.36" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876
492015 "chr21:37833647:G>T" "CLDN14" "NM_144492:p.Thr116Asn" "NM_144492:c.347C>A" "EXON3" "Likely benign" "rs370342285" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." 0.135 "N" "0.524" "T" "0.001" "B" 0.607169 "N" 1 "N" "1.36" "C" 0 10116 0 0 11518 0 0 8570 0 0 6584 0 1 65604 0.000015243 0 892 0 0 16476 0 1 119760 0.00000835003
492016 "chr21:37833648:T>G" "CLDN14" "NM_144492:p.Thr116Pro" "NM_144492:c.346A>C" "EXON3" "Likely benign" "Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic." 0.141 "N" "0.303" "T" "0.001" "B" 0.607169 "N" 1 "N" "-2.47" "N" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
492017 "chr21:37833652:C>A" "CLDN14" "NM_144492:p.Lys114Asn" "NM_144492:c.342G>T" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.002" "D" "1.0" "D" 0 "D" 0.999953 "D" "5.42" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
492018 "chr21:37833657:C>T" "CLDN14" "NM_144492:p.Ala113Thr" "NM_144492:c.337G>A" "EXON3" "Unknown significance" "rs138631461" "This variant is a VUS because it does not have enough information." 0.068 "N" "0.181" "T" "0.569" "P" 0.002918 "N" 0.952664 "D" "4.54" "C" 1 8600 0.000116279 0 4406 0 1 13006 0.0000768876 0 10078 0 0 11496 0 0 8562 0 0 6558 0 1 65450 0.0000152788 0 888 0 0 16466 0 1 119498 0.00000836834
492019 "chr21:37833657:C>G" "CLDN14" "NM_144492:p.Ala113Pro" "NM_144492:c.337G>C" "EXON3" "Unknown significance" "rs138631461" "This variant is a VUS because it does not have enough information." 0.068 "N" "0.02" "D" "0.991" "D" 0.002918 "N" 0.985994 "D" "4.54" "C" 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
492020 "chr21:37833658:G>A" "CLDN14" "NM_144492:p.Pro112Pro" "NM_144492:c.336C>T" "EXON3" "Unknown significance" "rs754350037" "This variant is a VUS because it does not have enough information." 0 10078 0 0 11500 0 0 8564 0 0 6562 0 2 65444 0.0000305605 0 888 0 1 16466 0.0000607312 3 119502 0.0000251042
492021 "chr21:37833658:G>C" "CLDN14" "NM_144492:p.Pro112Pro" "NM_144492:c.336C>G" "EXON3" "Unknown significance" "rs754350037" "This variant is a VUS because it does not have enough information." 0 10078 0 0 11500 0 0 8564 0 0 6562 0 1 65444 0.0000152802 0 888 0 0 16466 0 1 119502 0.00000836806
492022 "chr21:37833659:G>A" "CLDN14" "NM_144492:p.Pro112Leu" "NM_144492:c.335C>T" "EXON3" "Likely benign" "rs555911451" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 0.108 "N" "0.221" "T" "0.002" "B" 0.037876 "N" 0.996571 "D" "5.42" "C" 0 10084 0 0 11504 0 0 8562 0 0 6570 0 1 65460 0.0000152765 0 890 0 0 16462 0 1 119532 0.00000836596
492023 "chr21:37833659:G>T" "CLDN14" "NM_144492:p.Pro112His" "NM_144492:c.335C>A" "EXON3" "Likely benign" "rs555911451" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 0.108 "N" "0.146" "T" "0.675" "P" 0.037876 "N" 0.627567 "N" "5.42" "C" 0 10084 0 0 11504 0 0 8562 0 0 6570 0 1 65460 0.0000152765 0 890 0 0 16462 0 1 119532 0.00000836596
492024 "chr21:37833661:T>G" "CLDN14" "NM_144492:p.Thr111Thr" "NM_144492:c.333A>C" "EXON3" "Benign" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 400 0.0025 0 320 0 8 320 0.025 0 400 0 0 360 0 8 200 0.04 17 2000 0.0085
492025 "chr21:37833671:G>A" "CLDN14" "NM_144492:p.Ala108Val" "NM_144492:c.323C>T" "EXON3" "Unknown significance" "rs373823945" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.179" "T" "0.985" "D" 0 "D" 0.999931 "D" "5.42" "C" 1 8598 0.000116306 0 4406 0 1 13004 0.0000768994 0 10076 0 0 11492 0 0 8548 0 0 6552 0 1 65322 0.0000153088 0 886 0 0 16468 0 1 119344 0.00000837914
492026 "chr21:37833672:C>T" "CLDN14" "NM_144492:p.Ala108Thr" "NM_144492:c.322G>A" "EXON3" "Unknown significance" "rs377019596" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.14" "T" "0.997" "D" 0 "D" 0.999846 "D" "5.42" "C" 0 8598 0 1 4406 0.000226963 1 13004 0.0000768994
492027 "chr21:37833673:G>A" "CLDN14" "NM_144492:p.Cys107Cys" "NM_144492:c.321C>T" "EXON3" "Unknown significance" "rs764548516" "This variant is a VUS because it does not have enough information." 0 10062 0 0 11484 0 0 8546 0 0 6550 0 5 65316 0.0000765509 0 884 0 1 16472 0.0000607091 6 119314 0.0000502875
492028 "chr21:37833677:C>T" "CLDN14" "NM_144492:p.Arg106His" "NM_144492:c.317G>A" "EXON3" "Likely benign" "rs747254086" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 0.935 "N" "0.147" "T" "0.033" "B" 0.079007 "N" 0.790314 "D" "3.42" "C" 0 10076 0 0 11488 0 0 8544 0 0 6546 0 1 65314 0.0000153107 0 884 0 0 16472 0 1 119324 0.00000838054
492029 "chr21:37833678:G>A" "CLDN14" "NM_144492:p.Arg106Cys" "NM_144492:c.316C>T" "EXON3" "Unknown significance" "rs140257182" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.022" "D" "0.997" "D" 0.079007 "N" 0.99748 "D" "3.54" "C" 0 8598 0 6 4406 0.00136178 6 13004 0.000461396 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 9 10070 0.000893744 1 11486 0.0000870625 1 8544 0.000117041 0 6546 0 2 65296 0.0000306297 0 882 0 2 16474 0.000121403 15 119298 0.000125736
492030 "chr21:37833679:C>T" "CLDN14" "NM_144492:p.Thr105Thr" "NM_144492:c.315G>A" "EXON3" "Unknown significance" "rs781167430" "This variant is a VUS because it does not have enough information." 0 10076 0 0 11492 0 1 8542 0.000117069 0 6546 0 0 65310 0 0 884 0 1 16476 0.0000606943 2 119326 0.0000167608
492031 "chr21:37833679:C>A" "CLDN14" "NM_144492:p.Thr105Thr" "NM_144492:c.315G>T" "EXON3" "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
492032 "chr21:37833680:G>A" "CLDN14" "NM_144492:p.Thr105Met" "NM_144492:c.314C>T" "EXON3" "Unknown significance" "rs748110915" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.0" "D" "1.0" "D" 0 "D" 1 "D" "5.42" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0 0 10072 0 1 11492 0.0000870171 0 8544 0 0 6544 0 1 65300 0.0000153139 0 884 0 0 16474 0 2 119310 0.0000167631
492033 "chr21:37833693:C>T" "CLDN14" "NM_144492:p.Gly101Arg" "NM_144492:c.301G>A" "EXON3" "Pathogenic" "Deafness, autosomal recessive" "15880785" "rs74315438" "Pathogenicity is based on ClinVar submissions and the literature provided in PubMed." 0.935 "N" "0.0" "D" "1.0" "D" 0 "D" 1 "A" "5.42" "C" 0 10082 0 1 11488 0.0000870474 0 8542 0 0 6522 0 5 65252 0.000076626 0 878 0 0 16486 0 6 119250 0.0000503145
492034 "chr21:37833694:G>A" "CLDN14" "NM_144492:p.Ile100Ile" "NM_144492:c.300C>T" "EXON3" "Benign" "rs113350364" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 10 8598 0.00116306 10 4406 0.00226963 20 13004 0.00153799 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 1 200 0.005 1 2000 0.0005 1 1322 0.0008 1 1006 0.001 3 694 0.0043 1 1008 0.001 16 978 0.0164 22 5008 0.00439297 25 10090 0.0024777 29 11486 0.00252481 9 8542 0.00105362 0 6524 0 96 65262 0.00147099 6 876 0.00684932 267 16490 0.0161916 432 119270 0.00362203
492035 "chr21:37833695:A>G" "CLDN14" "NM_144492:p.Ile100Thr" "NM_144492:c.299T>C" "EXON3" "Unknown significance" "rs557513586" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.006" "D" "0.064" "B" 0.644497 "N" 1 "N" "4.28" "C" 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 10084 0 0 11488 0 0 8542 0 0 6528 0 0 65262 0 0 876 0 12 16492 0.000727626 12 119272 0.00010061
492036 "chr21:37833699:C>T" "CLDN14" "NM_144492:p.Val99Ile" "NM_144492:c.295G>A" "EXON3" "Unknown significance" "rs371106978" "This variant is a VUS because it does not have enough information." 0.071 "N" "0.087" "T" "0.975" "D" 0.000074 "D" 0.916509 "N" "4.54" "C" 1 8598 0.000116306 1 4406 0.000226963 2 13004 0.000153799 0 10082 0 0 11488 0 1 8544 0.000117041 0 6520 0 3 65250 0.000045977 0 880 0 0 16492 0 4 119256 0.0000335413
492037 "chr21:37833700:->GGCGCA" "CLDN14" "NM_144492:c.294_295insTGCGCC" "EXON3" "Unknown significance" "rs773126341" "This variant is a VUS because it does not have enough information." 0 10082 0 0 11488 0 1 8544 0.000117041 0 6520 0 0 65250 0 0 880 0 0 16492 0 1 119256 0.00000838532
492038 "chr21:37833700:G>A" "CLDN14" "NM_144492:p.Ala98Ala" "NM_144492:c.294C>T" "EXON3" "Unknown significance" "rs374400022" "This variant is a VUS because it does not have enough information." 1 8598 0.000116306 0 4406 0 1 13004 0.0000768994 0 10070 0 0 11492 0 0 8540 0 0 6516 0 15 65212 0.000230019 0 876 0 1 16492 0.0000606355 16 119198 0.00013423
492039 "chr21:37833702:C>T" "CLDN14" "NM_144492:p.Ala98Thr" "NM_144492:c.292G>A" "EXON3" "Unknown significance" "rs759313432" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.232" "T" "0.747" "P" 0.003519 "N" 0.971319 "D" "4.48" "C" 0 10086 0 1 11488 0.0000870474 0 8546 0 0 6516 0 2 65218 0.0000306664 2 876 0.00228311 4 16490 0.000242571 9 119220 0.0000754907
492040 "chr21:37833703:G>T" "CLDN14" "NM_144492:p.Cys97Stop" "NM_144492:c.291C>A" "EXON3" "Unknown significance" "rs767108790" "This variant is a VUS because it does not have enough information." -2.281 "N" 0.930749 "N" 1 "D" "-1.42" "N" 0 10092 0 0 11488 0 0 8544 0 0 6512 0 2 65204 0.000030673 0 876 0 0 16490 0 2 119206 0.0000167777
492041 "chr21:37833703:G>A" "CLDN14" "NM_144492:p.Cys97Cys" "NM_144492:c.291C>T" "EXON3" "Unknown significance" "rs767108790" "This variant is a VUS because it does not have enough information." 0 10092 0 0 11488 0 0 8544 0 0 6512 0 0 65204 0 0 876 0 2 16490 0.000121286 2 119206 0.0000167777
492042 "chr21:37833707:G>A" "CLDN14" "NM_144492:p.Ala96Val" "NM_144492:c.287C>T" "EXON3" "Likely benign" "rs762368755" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 1.048 "C" "1.0" "T" "0.001" "B" 0.227306 "N" 1 "N" "4.52" "C" 0 10088 0 0 11490 0 0 8544 0 0 6516 0 0 65232 0 0 874 0 1 16490 0.0000606428 1 119234 0.00000838687
492043 "chr21:37833708:C>T" "CLDN14" "NM_144492:p.Ala96Thr" "NM_144492:c.286G>A" "EXON3" "Likely benign" "rs765605373" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." 0.935 "N" "0.359" "T" "0.015" "B" 0.227306 "N" 1 "N" "3.34" "C" 0 10088 0 0 11492 0 1 8540 0.000117096 0 6518 0 1 65244 0.0000153271 0 874 0 1 16490 0.0000606428 3 119246 0.0000251581
492044 "chr21:37833709:G>A" "CLDN14" "NM_144492:p.Cys95Cys" "NM_144492:c.285C>T" "EXON3" "Unknown significance" "rs750946312" "This variant is a VUS because it does not have enough information." 0 10098 0 0 11492 0 1 8542 0.000117069 0 6518 0 0 65228 0 0 876 0 0 16488 0 1 119242 0.00000838631
492045 "chr21:37833713:G>A" "CLDN14" "NM_144492:p.Ala94Val" "NM_144492:c.281C>T" "EXON3" "Pathogenic" "Deafness, autosomal recessive" "23235333" "Pathogenicity is based on the literature provided in PubMed." 1.048 "C" "0.003" "D" "1.0" "D" 0 "D" 1 "D" "5.53" "C"
492046 "chr21:37833714:C>G" "CLDN14" "NM_144492:p.Ala94Pro" "NM_144492:c.280G>C" "EXON3" "Unknown significance" "rs758724049" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.005" "D" "1.0" "D" 0 "D" 1 "D" "5.53" "C"
492047 "chr21:37833717:T>A" "CLDN14" "NM_144492:p.Ile93Leu" "NM_144492:c.277A>T" "EXON3" "Likely benign" "rs780444223" "Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic." -0.91 "N" "1.0" "T" "0.0" "B" 0.47202 "N" 1 "N" "-8.11" "N" 0 10104 0 0 11498 0 0 8552 0 0 6504 0 1 65278 0.0000153191 0 876 0 0 16498 0 1 119310 0.00000838153
492048 "chr21:37833718:G>C" "CLDN14" "NM_144492:p.Gly92Gly" "NM_144492:c.276C>G" "EXON3" "Unknown significance" "rs751747842" "This variant is a VUS because it does not have enough information." 0 10098 0 0 11498 0 0 8554 0 0 6506 0 1 65248 0.0000153261 0 878 0 0 16498 0 1 119280 0.00000838364
492049 "chr21:37833721:C>T" "CLDN14" "NM_144492:p.Ser91Ser" "NM_144492:c.273G>A" "EXON3" "Unknown significance" "24033266" "rs577393948" "Pathogenicity is based on ClinVar submissions. All submitters agree with this pathogenicity." 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681 1 10092 0.0000990884 1 11498 0.0000869716 6 8554 0.000701426 0 6500 0 3 65246 0.0000459798 0 880 0 0 16498 0 11 119268 0.0000922293
492050 "chr21:37833726:G>C" "CLDN14" "NM_144492:p.Leu90Val" "NM_144492:c.268C>G" "EXON3" "Likely benign" "rs781318012" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 0.154 "N" "0.215" "T" "0.412" "B" 0.002373 "N" 0.998505 "D" "4.64" "C" 0 10104 0 0 11500 0 0 8554 0 0 6498 0 0 65250 0 0 882 0 1 16496 0.0000606208 1 119284 0.00000838335
492051 "chr21:37833727:C>A" "CLDN14" "NM_144492:p.Leu89Leu" "NM_144492:c.267G>T" "EXON3" "Unknown significance" "rs748115585" "This variant is a VUS because it does not have enough information." 0 10102 0 1 11500 0.0000869565 0 8556 0 0 6496 0 0 65262 0 0 882 0 0 16498 0 1 119296 0.00000838251
492052 "chr21:37833732:A>G" "CLDN14" "NM_144492:p.Cys88Arg" "NM_144492:c.262T>C" "EXON3" "Unknown significance" "rs756218341" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.004" "D" "0.999" "D" 0 "D" 1 "D" "5.53" "C" 0 10114 0 0 11498 0 0 8562 0 0 6500 0 1 65276 0.0000153196 0 882 0 0 16496 0 1 119328 0.00000838026
492053 "chr21:37833734:G>C" "CLDN14" "NM_144492:p.Ser87Cys" "NM_144492:c.260C>G" "EXON3" "Unknown significance" "rs777529810" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.001" "D" "1.0" "D" 0 "D" 1 "D" "5.53" "C" 0 10114 0 0 11494 0 0 8562 0 0 6496 0 1 65278 0.0000153191 0 880 0 0 16496 0 1 119320 0.00000838082
492054 "chr21:37833734:GA>AT" "CLDN14" "Pathogenic" "Deafness, autosomal recessive" "23235333" "Pathogenicity is based on the literature provided in PubMed."
492055 "chr21:37833740:A>T" "CLDN14" "NM_144492:p.Val85Asp" "NM_144492:c.254T>A" "EXON3" "Pathogenic" "Deafness, autosomal recessive" "22246673|11163249|15880785" "rs74315437" "Pathogenicity is based on ClinVar submissions and the literature provided in PubMed." 1.199 "C" "0.0" "D" "1.0" "D" 0.000084 "D" 1 "A" "5.53" "C" 0 10112 0 0 11492 0 0 8560 0 0 6492 0 0 65230 0 0 880 0 1 16498 0.0000606134 1 119264 0.00000838476
492056 "chr21:37833741:C>A" "CLDN14" "NM_144492:p.Val85Phe" "NM_144492:c.253G>T" "EXON3" "Unknown significance" "rs770829440" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.002" "D" "0.999" "D" 0.000084 "D" 1 "D" "5.53" "C" 0 10108 0 0 11494 0 0 8562 0 0 6484 0 1 65218 0.0000153332 0 882 0 0 16498 0 1 119246 0.00000838603
492057 "chr21:37833751:G>A" "CLDN14" "NM_144492:p.Arg81Arg" "NM_144492:c.243C>T" "EXON3" "Benign" "rs219779" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2213 8600 0.257326 1380 4406 0.313209 3593 13006 0.276257 99 400 0.2475 96 320 0.3 129 320 0.403125 1 400 0.0025 121 360 0.336111 48 200 0.24 494 2000 0.247 408 1322 0.3086 250 1006 0.2485 156 694 0.2248 6 1008 0.006 132 978 0.135 952 5008 0.190096 3098 10142 0.305462 2177 11482 0.189601 42 8566 0.00490311 1347 6448 0.208902 16318 65286 0.249946 198 878 0.225513 2600 16498 0.157595 25780 119300 0.216094
492058 "chr21:37833752:C>T" "CLDN14" "NM_144492:p.Arg81His" "NM_144492:c.242G>A" "EXON3" "Pathogenic" "Hearing loss, non-syndromic, autosomal recessive" "22246673" "rs368027306" "Pathogenicity is based on ClinVar submissions and the literature provided in PubMed." 0.935 "N" "0.004" "D" "1.0" "D" 0 "D" 0.999993 "D" "5.53" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 2 10074 0.000198531 0 11482 0 0 8568 0 0 6390 0 0 65022 0 0 874 0 0 16496 0 2 118906 0.00001682
492059 "chr21:37833753:G>A" "CLDN14" "NM_144492:p.Arg81Cys" "NM_144492:c.241C>T" "EXON3" "Unknown significance" "rs143628692" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.001" "D" "1.0" "D" 0 "D" 1 "D" "4.62" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 1 10082 0.0000991867 0 11478 0 0 8566 0 2 6386 0.000313185 1 64996 0.0000153856 0 870 0 1 16494 0.0000606281 5 118872 0.000042062
492060 "chr21:37833755:G>A" "CLDN14" "NM_144492:p.Ala80Val" "NM_144492:c.239C>T" "EXON3" "Unknown significance" "rs775222236" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.002" "D" "1.0" "D" 0.000015 "D" 1 "D" "5.53" "C" 0 10076 0 0 11474 0 0 8566 0 0 6384 0 1 65012 0.0000153818 0 872 0 0 16492 0 1 118876 0.00000841213
492061 "chr21:37833760:C>G" "CLDN14" "NM_144492:p.Gln78His" "NM_144492:c.234G>C" "EXON3" "Unknown significance" "rs760039736" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.002" "D" "1.0" "D" 0 "D" 0.999974 "D" "5.53" "C" 0 10060 0 0 11470 0 0 8562 0 0 6352 0 1 64964 0.0000153931 0 872 0 0 16494 0 1 118774 0.00000841935
492062 "chr21:37833766:G>A" "CLDN14" "NM_144492:p.Asp76Asp" "NM_144492:c.228C>T" "EXON3" "Unknown significance" "rs763692550" "This variant is a VUS because it does not have enough information."
492063 "chr21:37833767:T>G" "CLDN14" "NM_144492:p.Asp76Ala" "NM_144492:c.227A>C" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.05" "D" "0.524" "P" 0.000005 "D" 0.999988 "D" "4.31" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
492064 "chr21:37833771:G>A" "CLDN14" "NM_144492:p.Gln75Stop" "NM_144492:c.223C>T" "EXON3" "Unknown significance" "rs560052879" "This variant is a VUS because it does not have enough information." 1.048 "C" 0.007843 "N" 1 "D" "5.53" "C" 0 1322 0 0 1006 0 0 694 0 0 1008 0 1 978 0.001 1 5008 0.000199681 0 10028 0 0 11460 0 0 8550 0 0 6298 0 0 64818 0 0 870 0 1 16460 0.0000607533 1 118484 0.00000843996
492065 "chr21:37833776:A>T" "CLDN14" "NM_144492:p.Leu73Gln" "NM_144492:c.218T>A" "EXON3" "Unknown significance" "rs763489263" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.0" "D" "1.0" "D" 0.000012 "D" 0.999998 "D" "5.53" "C" 0 10010 0 0 11454 0 0 8544 0 0 6274 0 0 64740 0 0 868 0 1 16434 0.0000608495 1 118324 0.00000845137
492066 "chr21:37833778:C>T" "CLDN14" "NM_144492:p.Ala72Ala" "NM_144492:c.216G>A" "EXON3" "Unknown significance" "rs370315827" "This variant is a VUS because it does not have enough information." 1 8600 0.000116279 0 4406 0 1 13006 0.0000768876 0 10002 0 0 11444 0 0 8542 0 0 6254 0 4 64690 0.0000618334 0 864 0 0 16432 0 4 118228 0.0000338329
492067 "chr21:37833779:G>A" "CLDN14" "NM_144492:p.Ala72Val" "NM_144492:c.215C>T" "EXON3" "Unknown significance" "rs573588226" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.02" "D" "1.0" "D" 0 "D" 0.999999 "D" "5.53" "C" 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361 0 9986 0 0 11446 0 0 8542 0 0 6248 0 0 64670 0 0 868 0 1 16426 0.0000608791 1 118186 0.00000846124
492068 "chr21:37833783:G>A" "CLDN14" "NM_144492:p.Leu71Leu" "NM_144492:c.211C>T" "EXON3" "Unknown significance" "rs755346413" "This variant is a VUS because it does not have enough information." 0 9970 0 0 11432 0 0 8532 0 0 6238 0 1 64610 0.0000154775 0 864 0 0 16406 0 1 118052 0.00000847084
492069 "chr21:37833785:A>C" "CLDN14" "NM_144492:p.Leu70Arg" "NM_144492:c.209T>G" "EXON3" "Unknown significance" "rs767565332" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.003" "D" "0.959" "D" 0.004033 "N" 0.806573 "D" "5.38" "C" 0 9968 0 0 11402 0 0 8528 0 0 6218 0 0 64566 0 0 864 0 1 16394 0.0000609979 1 117940 0.00000847889
492070 "chr21:37833786:G>C" "CLDN14" "NM_144492:p.Leu70Val" "NM_144492:c.208C>G" "EXON3" "Unknown significance" "rs752992781" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.103" "T" "0.931" "P" 0.004033 "N" 0.752653 "N" "5.38" "C" 0 9962 0 0 11402 0 0 8528 0 0 6220 0 0 64566 0 0 864 0 2 16392 0.000122011 2 117934 0.0000169586
492071 "chr21:37833791:C>T" "CLDN14" "NM_144492:p.Arg68Gln" "NM_144492:c.203G>A" "EXON3" "Unknown significance" "rs756095919" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.324" "T" "0.798" "P" 0.000031 "D" 0.991588 "D" "5.38" "C" 0 9954 0 0 11386 0 0 8524 0 0 6210 0 1 64466 0.0000155121 0 866 0 0 16378 0 1 117784 0.00000849012
492072 "chr21:37833799:C>-" "CLDN14" "NM_144492:c.195delG" "EXON3" "Unknown significance" "rs760769965" "This variant is a VUS because it does not have enough information." 0 9934 0 0 11358 0 1 8516 0.000117426 0 6172 0 0 64388 0 0 858 0 0 16336 0 1 117562 0.00000850615
492073 "chr21:37833799:C>T" "CLDN14" "NM_144492:p.Gln65Gln" "NM_144492:c.195G>A" "EXON3" "Unknown significance" "rs777960789" "This variant is a VUS because it does not have enough information." 1 9936 0.000100644 0 11354 0 0 8512 0 0 6158 0 0 64356 0 0 858 0 0 16328 0 1 117502 0.00000851049
492074 "chr21:37833809:T>C" "CLDN14" "NM_144492:p.Tyr62Cys" "NM_144492:c.185A>G" "EXON3" "Unknown significance" "rs148223897" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.012" "D" "1.0" "D" 0.000001 "D" 0.99998 "D" "5.51" "C" 5 8600 0.000581395 1 4406 0.000226963 6 13006 0.000461326 0 1322 0 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 1 5008 0.000199681 0 9882 0 3 11294 0.000265628 0 8472 0 0 6078 0 48 64036 0.000749578 1 856 0.00116822 0 16232 0 52 116850 0.000445015
492075 "chr21:37833813:T>A" "CLDN14" "NM_144492:p.Ile61Phe" "NM_144492:c.181A>T" "EXON3" "Unknown significance" "rs757334760" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.009" "D" "0.922" "P" 0.001131 "N" 0.995172 "D" "4.37" "C" 0 9876 0 1 11268 0.0000887469 0 8462 0 0 6052 0 0 63952 0 0 854 0 0 16204 0 1 116668 0.00000857133
492076 "chr21:37833823:G>A" "CLDN14" "NM_144492:p.His57His" "NM_144492:c.171C>T" "EXON3" "Unknown significance" "rs778842030" "This variant is a VUS because it does not have enough information." 0 9844 0 3 11206 0.000267714 0 8428 0 0 5964 0 0 63570 0 0 852 0 0 16112 0 3 115976 0.0000258674
492077 "chr21:37833825:G>A" "CLDN14" "NM_144492:p.His57Tyr" "NM_144492:c.169C>T" "EXON3" "Unknown significance" "rs745601274" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.576" "T" "0.555" "P" 0.000004 "D" 0.999562 "D" "4.63" "C" 0 9824 0 0 11170 0 0 8418 0 0 5928 0 1 63486 0.0000157515 0 852 0 0 16090 0 1 115768 0.00000863797
492078 "chr21:37833826:CC>-" "CLDN14" "NM_144492:c.168_171delGG" "EXON3" "Unknown significance" "rs765103185" "This variant is a VUS because it does not have enough information." 0 9824 0 0 11170 0 1 8418 0.000118793 0 5928 0 0 63486 0 0 852 0 0 16090 0 1 115768 0.00000863797
492079 "chr21:37833827:C>T" "CLDN14" "NM_144492:p.Trp56Stop" "NM_144492:c.167G>A" "EXON3" "Pathogenic" "Hearing loss, non-syndromic, autosomal recessive" "22246673" "rs371100799" "Pathogenicity is based on ClinVar submissions and the literature provided in PubMed." 0.935 "N" 0 "D" 1 "D" "5.51" "C" 0 8600 0 1 4406 0.000226963 1 13006 0.0000768876 2 9806 0.000203957 0 11138 0 0 8390 0 0 5892 0 0 63354 0 0 852 0 0 16046 0 2 115478 0.0000173193
492080 "chr21:37833830:A>G" "CLDN14" "NM_144492:p.Val55Ala" "NM_144492:c.164T>C" "EXON3" "Unknown significance" "rs752960573" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.597" "T" "0.801" "P" 0.000002 "D" 0.999961 "D" "4.34" "C" 0 9796 0 0 11112 0 0 8378 0 1 5878 0.000170126 0 63282 0 0 846 0 0 16008 0 1 115300 0.00000867303
492081 "chr21:37833832:A>G" "CLDN14" "NM_144492:p.Cys54Cys" "NM_144492:c.162T>C" "EXON3" "Unknown significance" "rs746698259" "This variant is a VUS because it does not have enough information." 0 9770 0 0 11084 0 0 8356 0 0 5860 0 1 63138 0.0000158383 0 846 0 0 15978 0 1 115032 0.00000869323
492082 "chr21:37833835:C>T" "CLDN14" "NM_144492:p.Glu53Glu" "NM_144492:c.159G>A" "EXON3" "Unknown significance" "rs768019537" "This variant is a VUS because it does not have enough information."
492083 "chr21:37833844:G>T" "CLDN14" "NM_144492:p.Leu50Leu" "NM_144492:c.150C>A" "EXON3" "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
492084 "chr21:37833864:C>T" "CLDN14" "NM_144492:p.Val44Met" "NM_144492:c.130G>A" "EXON3" "Unknown significance" "rs141139613" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.003" "D" "1.0" "D" 0.000585 "D" 0.99762 "D" "5.54" "C" 2 8600 0.000232558 0 4406 0 2 13006 0.000153775 0 8952 0 0 9808 0 0 7612 0 0 4920 0 3 57656 0.0000520327 0 760 0 0 14782 0 3 104490 0.0000287109
492085 "chr21:37833865:G>A" "CLDN14" "NM_144492:p.Ala43Ala" "NM_144492:c.129C>T" "EXON3" "Unknown significance" "rs150731625" "This variant is a VUS because it does not have enough information." 4 8600 0.000465116 0 4406 0 4 13006 0.00030755 0 8914 0 0 9774 0 0 7556 0 0 4874 0 20 57392 0.000348481 0 748 0 13 14730 0.000882553 33 103988 0.000317344
492086 "chr21:37833868:C>T" "CLDN14" "NM_144492:p.Thr42Thr" "NM_144492:c.126G>A" "EXON3" "Unknown significance" "rs140177046" "This variant is a VUS because it does not have enough information." 1 8600 0.000116279 1 4406 0.000226963 2 13006 0.000153775 2 8814 0.000226912 0 9600 0 0 7456 0 0 4772 0 1 56558 0.000017681 0 748 0 0 14556 0 3 102504 0.0000292672
492087 "chr21:37833869:G>A" "CLDN14" "NM_144492:p.Thr42Met" "NM_144492:c.125C>T" "EXON3" "Unknown significance" "rs533194857" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.0" "D" "1.0" "D" 0 "D" 0.999996 "D" "4.66" "C" 0 8764 0 0 9498 0 0 7402 0 0 4726 0 1 56062 0.0000178374 0 744 0 0 14458 0 1 101654 0.00000983729
492088 "chr21:37833876:TGT>-" "CLDN14" "NM_144492:c.118_122delACA" "EXON3" "Unknown significance" "rs752639706" "This variant is a VUS because it does not have enough information."
492089 "chr21:37833885:C>T" "CLDN14" "NM_144492:p.Gly37Ser" "NM_144492:c.109G>A" "EXON3" "Unknown significance" "rs759850341" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.005" "D" "1.0" "D" 0 "D" 1 "D" "5.54" "C" 0 7622 0 0 7808 0 0 6212 0 0 3836 0 0 47894 0 0 650 0 1 13274 0.0000753352 1 87296 0.0000114553
492090 "chr21:37833888:C>T" "CLDN14" "NM_144492:p.Val36Met" "NM_144492:c.106G>A" "EXON3" "Unknown significance" "rs142205038" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.036" "D" "1.0" "D" 0.000169 "D" 0.994375 "D" "3.7" "C" 1 8600 0.000116279 0 4406 0 1 13006 0.0000768876 0 7258 0 5 7340 0.000681199 0 5904 0 0 3580 0 3 45502 0.0000659312 1 612 0.00163399 8 12948 0.000617856 17 83144 0.000204465
492091 "chr21:37833888:C>A" "CLDN14" "NM_144492:p.Val36Leu" "NM_144492:c.106G>T" "EXON3" "Unknown significance" "rs142205038" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.01" "D" "0.92" "P" 0.000169 "D" 0.993414 "D" "3.7" "C" 0 7258 0 0 7340 0 1 5904 0.000169377 0 3580 0 0 45502 0 0 612 0 0 12948 0 1 83144 0.0000120273
492092 "chr21:37833889:G>A" "CLDN14" "NM_144492:p.His35His" "NM_144492:c.105C>T" "EXON3" "Benign" "rs560763542" "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 1 978 0.001 1 5008 0.000199681 0 7260 0 0 7342 0 0 5894 0 0 3588 0 1 45482 0.0000219867 5 606 0.00825083 13 12920 0.00100619 19 83092 0.000228662
492093 "chr21:37833892:C>T" "CLDN14" "NM_144492:p.Ala34Ala" "NM_144492:c.102G>A" "EXON3" "Unknown significance" "rs146395322" "This variant is a VUS because it does not have enough information." 2 8600 0.000232558 1 4406 0.000226963 3 13006 0.000230663 1 1322 0.0008 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 3 5008 0.000599042 5 6806 0.000734646 3 6680 0.000449102 4 5424 0.000737463 0 3230 0 10 42120 0.000237417 0 570 0 5 12446 0.000401735 27 77276 0.000349397
492094 "chr21:37833893:G>T" "CLDN14" "NM_144492:p.Ala34Glu" "NM_144492:c.101C>A" "EXON3" "Unknown significance" "rs754032374" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.002" "D" "1.0" "D" 0 "D" 0.999999 "D" "4.65" "C" 0 6782 0 0 6632 0 0 5400 0 0 3208 0 1 41848 0.000023896 0 568 0 0 12396 0 1 76834 0.0000130151
492095 "chr21:37833903:G>A" "CLDN14" "NM_144492:p.Arg31Trp" "NM_144492:c.91C>T" "EXON3" "Unknown significance" "rs757426764" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.167" "T" "0.081" "B" 0.000506 "D" 0.8177 "D" "3.52" "C" 0 6044 0 0 5716 0 0 4658 0 0 2748 0 1 36994 0.0000270314 0 516 0 2 11700 0.00017094 3 68376 0.000043875
492096 "chr21:37833910:C>T" "CLDN14" "NM_144492:p.Pro28Pro" "NM_144492:c.84G>A" "EXON3" "Unknown significance" "rs778927942" "This variant is a VUS because it does not have enough information." 0 5514 0 0 5094 0 0 4132 0 0 2402 0 2 33562 0.0000595912 0 456 0 0 11296 0 2 62456 0.0000320225
492097 "chr21:37833911:G>A" "CLDN14" "NM_144492:p.Pro28Leu" "NM_144492:c.83C>T" "EXON3" "Unknown significance" "24033266" "rs727504989" "Pathogenicity is based on ClinVar submissions. All submitters agree with this pathogenicity." 1.048 "C" "0.0" "D" "1.0" "D" 0 "D" 1 "D" "4.44" "C" 0 5450 0 0 5010 0 0 4058 0 0 2334 0 1 32948 0.0000303509 0 450 0 0 11226 0 1 61476 0.0000162665
492098 "chr21:37833912:G>A" "CLDN14" "NM_144492:p.Pro28Ser" "NM_144492:c.82C>T" "EXON3" "Unknown significance" "rs758081638" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.0" "D" "1.0" "D" 0 "D" 0.999996 "D" "4.65" "C" 0 5320 0 0 4830 0 1 3930 0.000254453 0 2256 0 0 32180 0 0 442 0 0 11102 0 1 60060 0.00001665
492099 "chr21:37833920:G>A" "CLDN14" "NM_144492:p.Thr25Ile" "NM_144492:c.74C>T" "EXON3" "Unknown significance" "rs779937857" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.005" "D" "1.0" "D" 0 "D" 0.999998 "D" "4.65" "C" 0 4826 0 0 4138 0 0 3314 0 0 1884 0 1 28624 0.0000349357 0 398 0 0 10594 0 1 53778 0.000018595
492100 "chr21:37833921:T>G" "CLDN14" "NM_144492:p.Thr25Pro" "NM_144492:c.73A>C" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.005" "D" "1.0" "D" 0 "D" 0.999999 "D" "5.54" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
492101 "chr21:37833922:G>A" "CLDN14" "NM_144492:p.Thr24Thr" "NM_144492:c.72C>T" "EXON3" "Unknown significance" "rs549639383" "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 4594 0 0 3782 0 0 3030 0 0 1740 0 0 26964 0 0 384 0 4 10356 0.00038625 4 50850 0.0000786627
492102 "chr21:37833924:T>G" "CLDN14" "NM_144492:p.Thr24Pro" "NM_144492:c.70A>C" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.007" "D" "0.988" "D" 0.000038 "D" 0.885124 "D" "4.41" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
492103 "chr21:37833926:A>G" "CLDN14" "NM_144492:p.Ile23Thr" "NM_144492:c.68T>C" "EXON3" "Unknown significance" "rs768411939" "This variant is a VUS because it does not have enough information." 1.199 "C" "0.477" "T" "0.008" "B" 0.020346 "N" 0.951688 "D" "4.4" "C" 0 4376 0 0 3464 0 0 2776 0 0 1566 0 1 25416 0.0000393453 0 376 0 0 10116 0 1 48090 0.0000207943
492104 "chr21:37833927:T>G" "CLDN14" "NM_144492:p.Ile23Leu" "NM_144492:c.67A>C" "EXON3" "Unknown significance" "rs780834768" "This variant is a VUS because it does not have enough information." 1.061 "C" "0.071" "T" "0.001" "B" 0.020346 "N" 0.723679 "D" "3.1" "C" 0 4334 0 0 3430 0 1 2746 0.000364166 0 1540 0 0 25214 0 0 374 0 0 10076 0 1 47714 0.0000209582
492105 "chr21:37833928:CAA>-" "CLDN14" "NM_144492:c.66_70delTTG" "EXON3" "Unknown significance" "rs762948927" "This variant is a VUS because it does not have enough information." 0 4334 0 0 3430 0 0 2746 0 0 1540 0 1 25214 0.0000396605 0 374 0 0 10076 0 1 47714 0.0000209582
492106 "chr21:37833931:C>T" "CLDN14" "NM_144492:p.Thr21Thr" "NM_144492:c.63G>A" "EXON3" "Benign" "rs117560775" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 261 8600 0.0303488 23 4400 0.00522727 284 13000 0.0218462 0 400 0 44 320 0.1375 13 320 0.040625 0 400 0 0 360 0 1 200 0.005 58 2000 0.029 5 1322 0.0038 31 1006 0.0308 58 694 0.0836 1 1008 0.001 17 978 0.0174 112 5008 0.0223642 39 4108 0.00949367 398 2992 0.133021 0 2418 0 20 1378 0.0145138 1022 23160 0.0441278 10 358 0.027933 268 9792 0.0273693 1757 44206 0.0397457
492107 "chr21:37833932:G>A" "CLDN14" "NM_144492:p.Thr21Met" "NM_144492:c.62C>T" "EXON3" "Unknown significance" "rs532176130" "This variant is a VUS because it does not have enough information." 1.048 "C" "0.002" "D" "1.0" "D" 0 "D" 1 "D" "5.54" "C" 0 1322 0 1 1006 0.001 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
492108 "chr21:37833934:G>A" "CLDN14" "NM_144492:p.Gly20Gly" "NM_144492:c.60C>T" "EXON3" "Unknown significance" "rs387907415" "Pathogenicity is based on ClinVar submissions. All submitters agree with this pathogenicity."
492109 "chr21:37833935:C>T" "CLDN14" "NM_144492:p.Gly20Asp" "NM_144492:c.59G>A" "EXON3" "Unknown significance" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.0" "D" "1.0" "D" 0 "D" 1 "D" "5.54" "C" 0 400 0 0 320 0 0 320 0 0 400 0 0 360 0 0 200 0 0 2000 0
492110 "chr21:37833939:C>A" "CLDN14" "NM_144492:p.Val19Leu" "NM_144492:c.55G>T" "EXON3" "Likely benign" "rs769320772" "Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic." 0.935 "N" "0.771" "T" "0.059" "B" 0.003041 "N" 0.86535 "N" "2.63" "C"
492111 "chr21:37833942:T>C" "CLDN14" "NM_144492:p.Met18Val" "NM_144492:c.52A>G" "EXON3" "Likely benign" "rs369883669" "Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic." -0.315 "N" "0.253" "T" "0.013" "B" 0.031481 "N" 0.99717 "N" "-3.99" "N" 2 1322 0.0015 0 1006 0 0 694 0 0 1008 0 0 978 0 2 5008 0.000399361 1 3392 0.000294811 0 1682 0 0 1650 0 0 878 0 0 16648 0 0 262 0 0 8972 0 1 33484 0.000029865
492112 "chr21:37833943:G>A" "CLDN14" "NM_144492:p.Gly17Gly" "NM_144492:c.51C>T" "EXON3" "Unknown significance" "rs150040476" "This variant is a VUS because it does not have enough information." 1 8594 0.00011636 0 4396 0 1 12990 0.0000769823 0 3268 0 0 1540 0 0 1546 0 0 806 0 1 15946 0.0000627117 0 250 0 0 8904 0 1 32260 0.0000309981
492113 "chr21:37833966:C>G" "CLDN14" "NM_144492:p.Gly10Arg" "NM_144492:c.28G>C" "EXON3" "Unknown significance" "rs772295911" "This variant is a VUS because it does not have enough information." 0.069 "N" "0.001" "D" "1.0" "D" 0 "D" 1 "D" "5.54" "C"
492114 "chr21:37833976:C>T" "CLDN14" "NM_144492:p.Val6Val" "NM_144492:c.18G>A" "EXON3" "Unknown significance" "rs387907417" "Pathogenicity is based on ClinVar submissions. All submitters agree with this pathogenicity."
492115 "chr21:37833978:C>T" "CLDN14" "NM_144492:p.Val6Met" "NM_144492:c.16G>A" "EXON3" "Unknown significance" "rs202117396" "This variant is a VUS because it does not have enough information." 0.935 "N" "0.014" "D" "0.999" "D" 0.000158 "D" 0.993694 "D" "5.54" "C" 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
492116 "chr21:37833979:G>A" "CLDN14" "NM_144492:p.Ala5Ala" "NM_144492:c.15C>T" "EXON3" "Unknown significance" "rs387907416" "Pathogenicity is based on ClinVar submissions. All submitters agree with this pathogenicity."
492117 "chr21:37833982:C>T" "CLDN14" "NM_144492:p.Thr4Thr" "NM_144492:c.12G>A" "EXON3" "Unknown significance" "rs764358289" "This variant is a VUS because it does not have enough information." 1 1384 0.000722543 0 338 0 0 422 0 0 46 0 0 5572 0 0 154 0 0 7794 0 1 15710 0.0000636537
492118 "chr21:37833983:G>A" "CLDN14" "NM_144492:p.Thr4Met" "NM_144492:c.11C>T" "EXON3" "Benign" "rs113831133" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0.126 "N" "0.365" "T" "0.315" "B" 0.018627 "N" 1 "N" "3.63" "C" 149 8286 0.0179821 402 4252 0.0945437 551 12538 0.0439464 0 400 0 0 320 0 2 320 0.00625 0 400 0 0 360 0 9 200 0.045 11 2000 0.0055 170 1322 0.1286 17 1006 0.0169 19 694 0.0274 3 1008 0.003 27 978 0.0276 236 5008 0.0471246 179 1378 0.129898 10 340 0.0294118 8 408 0.0196078 0 40 0 142 5552 0.0255764 4 152 0.0263158 288 7790 0.0369705 631 15660 0.0402937
492119 "chr21:37833984:T>C" "CLDN14" "NM_144492:p.Thr4Ala" "NM_144492:c.10A>G" "EXON3" "Likely benign" "rs374578221" "Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic." 1.061 "C" "0.817" "T" "0.075" "B" 0.018627 "N" 1 "N" "0.152" "C" 1 8264 0.000121007 0 4242 0 1 12506 0.0000799616 0 1276 0 0 336 0 0 398 0 0 36 0 2 5386 0.000371333 0 150 0 0 7764 0 2 15346 0.000130327
492120 "chr21:37833998:C>T" "CLDN14" "NM_144492:c.-5G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs368231049" "This variant is a VUS because it does not have enough information." 0 980 0 0 274 0 1 322 0.00310559 0 16 0 0 4720 0 0 148 0 0 7656 0 1 14116 0.0000708416
492121 "chr21:37834018:C>G" "CLDN14" "NM_144492:c.-25G>C" "FIVE_PRIME_EXON" "Unknown significance" "rs750364874" "This variant is a VUS because it does not have enough information." 3 740 0.00405405 0 222 0 0 288 0 0 8 0 0 4106 0 0 138 0 0 7572 0 3 13074 0.000229463
492122 "chr21:37834019:C>T" "CLDN14" "NM_144492:c.-26G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs758426367" "This variant is a VUS because it does not have enough information."
492123 "chr21:37834026:C>A" "CLDN14" "NM_144492:c.-33G>T" "FIVE_PRIME_EXON" "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
492124 "chr21:37834030:C>T" "CLDN14" "NM_144492:c.-37G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs149049781" "This variant is a VUS because it does not have enough information."
492125 "chr21:37834039:C>T" "CLDN14" "NM_144492:c.-46G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs779699092" "This variant is a VUS because it does not have enough information." 0 642 0 0 214 0 0 268 0 0 6 0 5 3896 0.00128337 0 134 0 0 7526 0 5 12686 0.000394135
492126 "chr21:37834044:T>G" "CLDN14" "NM_144492:c.-51A>C" "FIVE_PRIME_EXON" "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
492127 "chr21:37834046:A>C" "CLDN14" "NM_144492:c.-53T>G" "FIVE_PRIME_EXON" "Unknown significance" "rs548165835" "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
492128 "chr21:37834050:C>T" "CLDN14" "NM_144492:c.-57G>A" "FIVE_PRIME_EXON" "Benign" "rs188479887" "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 2 400 0.005 0 360 0 0 200 0 2 2000 0.001 0 1322 0 0 1006 0 0 694 0 2 1008 0.002 0 978 0 2 5008 0.000399361
492129 "chr21:37834051:G>A" "CLDN14" "NM_144492:c.-58C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs759652223" "This variant is a VUS because it does not have enough information."
492130 "chr21:37834061:T>G" "CLDN14" "NM_144492:c.-68A>C" "FIVE_PRIME_EXON" "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
492131 "chr21:37834068:C>A" "CLDN14" "NM_144492:c.-75G>T" "FIVE_PRIME_EXON" "Unknown significance" "rs537529014" "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
492132 "chr21:37834068:C>T" "CLDN14" "NM_144492:c.-75G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs537529014" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 4 5008 0.000798722
492133 "chr21:37834069:G>A" "CLDN14" "NM_144492:c.-76C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs557122405" "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 0 1322 0 0 1006 0 0 694 0 0 1008 0 2 978 0.002 2 5008 0.000399361
492134 "chr21:37834103:G>A" "CLDN14" "NM_144492:c.-81-29C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs577282684" "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
492135 "chr21:37834154:C>T" "CLDN14" "NM_144492:c.-81-80G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs143768024" "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
492136 "chr21:37834155:G>A" "CLDN14" "NM_144492:c.-81-81C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs181629254" "This variant is a VUS because it does not have enough information."
492137 "chr21:37834155:G>T" "CLDN14" "NM_144492:c.-81-81C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs181629254" "This variant is a VUS because it does not have enough information."
492138 "chr21:37834161:A>C" "CLDN14" "NM_144492:c.-81-87T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs553607941" "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
492139 "chr21:37834258:T>C" "CLDN14" "NM_144492:c.-81-184A>G" "FIVE_PRIME_INTRON" "Benign" "rs128494" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 979 1322 0.7405 762 1006 0.7575 498 694 0.7176 441 1008 0.4375 460 978 0.4703 3140 5008 0.626997
492140 "chr21:37834271:G>T" "CLDN14" "NM_144492:c.-81-197C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs770494249" "This variant is a VUS because it does not have enough information."
492141 "chr21:37834281:G>A" "CLDN14" "NM_144492:c.-81-207C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs542574660" "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
492142 "chr21:37834284:C>T" "CLDN14" "NM_144492:c.-81-210G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs546952683" "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 2 978 0.002 4 5008 0.000798722
492143 "chr21:37834308:G>C" "CLDN14" "NM_144492:c.-81-234C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs577487299" "This variant is a VUS because it does not have enough information."
492144 "chr21:37834310:C>T" "CLDN14" "NM_144492:c.-81-236G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759249067" "This variant is a VUS because it does not have enough information."
492145 "chr21:37834318:G>A" "CLDN14" "NM_144492:c.-81-244C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs764414792" "This variant is a VUS because it does not have enough information."
492146 "chr21:37834336:C>T" "CLDN14" "NM_144492:c.-81-262G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs574324704" "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
492147 "chr21:37834359:T>C" "CLDN14" "NM_144492:c.-81-285A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs151077154" "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
492148 "chr21:37834405:G>T" "CLDN14" "NM_144492:c.-81-331C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs141042225" "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
492149 "chr21:37834432:G>A" "CLDN14" "NM_144492:c.-81-358C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs535211039" "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
492150 "chr21:37834437:G>C" "CLDN14" "NM_144492:c.-81-363C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs751919974" "This variant is a VUS because it does not have enough information."
492151 "chr21:37834484:C>G" "CLDN14" "NM_144492:c.-81-410G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs561135778" "This variant is a VUS because it does not have enough information."
492152 "chr21:37834499:G>A" "CLDN14" "NM_144492:c.-81-425C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs762042544" "This variant is a VUS because it does not have enough information."
492153 "chr21:37834526:C>T" "CLDN14" "NM_144492:c.-81-452G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs528381330" "This variant is a VUS because it does not have enough information."
492154 "chr21:37834545:G>A" "CLDN14" "NM_144492:c.-81-471C>T" "FIVE_PRIME_INTRON" "Benign" "rs150280873" "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
492155 "chr21:37834564:C>G" "CLDN14" "NM_144492:c.-81-490G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs768092897" "This variant is a VUS because it does not have enough information."
492156 "chr21:37834564:C>T" "CLDN14" "NM_144492:c.-81-490G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs768092897" "This variant is a VUS because it does not have enough information."
492157 "chr21:37834570:G>A" "CLDN14" "NM_144492:c.-81-496C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs139330688" "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
492158 "chr21:37834580:A>G" "CLDN14" "NM_144492:c.-81-506T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs750874131" "This variant is a VUS because it does not have enough information."
492159 "chr21:37834584:T>C" "CLDN14" "NM_144492:c.-81-510A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs756190771" "This variant is a VUS because it does not have enough information."
492160 "chr21:37834604:T>G" "CLDN14" "NM_144492:c.-81-530A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs766443351" "This variant is a VUS because it does not have enough information."
492161 "chr21:37834636:G>-" "CLDN14" "NM_144492:c.-81-562delC" "FIVE_PRIME_INTRON" "Benign" "rs141129591" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 191 1322 0.1445 1 1006 0.001 14 694 0.0202 0 1008 0 0 978 0 206 5008 0.0411342
492162 "chr21:37834636:G>A" "CLDN14" "NM_144492:c.-81-562C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs184320207" "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
492163 "chr21:37834639:GCA>CG" "CLDN14" "Unknown significance" "rs386818300" "This variant is a VUS because it does not have enough information."
492164 "chr21:37834641:A>G" "CLDN14" "NM_144492:c.-81-567T>C" "FIVE_PRIME_INTRON" "Benign" "rs219778" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 708 1322 0.5356 251 1006 0.2495 173 694 0.2493 6 1008 0.006 132 978 0.135 1270 5008 0.253594
492165 "chr21:37834675:C>T" "CLDN14" "NM_144492:c.-81-601G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568367754" "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 1 978 0.001 5 5008 0.000998403
492166 "chr21:37834704:C>T" "CLDN14" "NM_144492:c.-81-630G>A" "FIVE_PRIME_INTRON" "Benign" "rs2068750" "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 1 694 0.0014 0 1008 0 0 978 0 23 5008 0.00459265
492167 "chr21:37834712:C>T" "CLDN14" "NM_144492:c.-81-638G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs550962834" "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
492168 "chr21:37834713:G>T" "CLDN14" "NM_144492:c.-81-639C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs559334652" "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
492169 "chr21:37834720:C>T" "CLDN14" "NM_144492:c.-81-646G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs539985533" "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
492170 "chr21:37834721:G>A" "CLDN14" "NM_144492:c.-81-647C>T" "FIVE_PRIME_INTRON" "Benign" "rs219777" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 425 1322 0.3215 237 1006 0.2356 151 694 0.2176 3 1008 0.003 108 978 0.1104 924 5008 0.184505
492171 "chr21:37834722:C>T" "CLDN14" "NM_144492:c.-81-648G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs573504916" "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
492172 "chr21:37834731:C>T" "CLDN14" "NM_144492:c.-81-657G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs551338362" "This variant is a VUS because it does not have enough information."
492173 "chr21:37834752:G>T" "CLDN14" "NM_144492:c.-81-678C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs143026727" "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
492174 "chr21:37834775:C>T" "CLDN14" "NM_144492:c.-81-701G>A" "FIVE_PRIME_INTRON" "Benign" "rs78250838" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 17 1322 0.0129 43 1006 0.0427 66 694 0.0951 4 1008 0.004 41 978 0.0419 171 5008 0.0341454
492175 "chr21:37834835:T>C" "CLDN14" "NM_144492:c.-81-761A>G" "FIVE_PRIME_INTRON" "Benign" "rs219776" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 709 1322 0.5363 251 1006 0.2495 173 694 0.2493 6 1008 0.006 132 978 0.135 1271 5008 0.253794
492176 "chr21:37834879:T>C" "CLDN14" "NM_144492:c.-81-805A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs543002246" "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
492177 "chr21:37834892:T>C" "CLDN14" "NM_144492:c.-81-818A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs199572406" "This variant is a VUS because it does not have enough information."
492178 "chr21:37834914:A>T" "CLDN14" "NM_144492:c.-81-840T>A" "FIVE_PRIME_INTRON" "Benign" "rs2835363" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 705 1322 0.5333 251 1006 0.2495 173 694 0.2493 6 1008 0.006 132 978 0.135 1267 5008 0.252995
492179 "chr21:37834937:G>A" "CLDN14" "NM_144492:c.-81-863C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs567801476" "This variant is a VUS because it does not have enough information."
492180 "chr21:37834944:A>G" "CLDN14" "NM_144492:c.-81-870T>C" "FIVE_PRIME_INTRON" "Benign" "rs219775" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 705 1322 0.5333 251 1006 0.2495 173 694 0.2493 6 1008 0.006 132 978 0.135 1267 5008 0.252995
492181 "chr21:37834993:C>T" "CLDN14" "NM_144492:c.-81-919G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs545531226" "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
492182 "chr21:37835009:C>T" "CLDN14" "NM_144492:c.-81-935G>A" "FIVE_PRIME_INTRON" "Benign" "rs147028391" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 191 1322 0.1445 1 1006 0.001 14 694 0.0202 0 1008 0 1 978 0.001 207 5008 0.0413339
492183 "chr21:37835025:C>G" "CLDN14" "NM_144492:c.-81-951G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs528245620" "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
492184 "chr21:37835043:C>T" "CLDN14" "NM_144492:c.-81-969G>A" "FIVE_PRIME_INTRON" "Benign" "rs219774" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 346 1322 0.2617 236 1006 0.2346 140 694 0.2017 3 1008 0.003 108 978 0.1104 833 5008 0.166334
492185 "chr21:37835047:G>T" "CLDN14" "NM_144492:c.-81-973C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs561795274" "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
492186 "chr21:37835053:->C" "CLDN14" "NM_144492:c.-81-979_-81-978insG" "FIVE_PRIME_INTRON" "Unknown significance" "rs754044509" "This variant is a VUS because it does not have enough information."
492187 "chr21:37835078:T>C" "CLDN14" "NM_144492:c.-81-1004A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs571949070" "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
492188 "chr21:37835093:G>A" "CLDN14" "NM_144492:c.-81-1019C>T" "FIVE_PRIME_INTRON" "Benign" "rs112005761" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 8 1006 0.008 2 694 0.0029 0 1008 0 1 978 0.001 15 5008 0.00299521
492189 "chr21:37835093:G>T" "CLDN14" "NM_144492:c.-81-1019C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs112005761" "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
492190 "chr21:37835108:C>T" "CLDN14" "NM_144492:c.-81-1034G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs762254073" "This variant is a VUS because it does not have enough information."
492191 "chr21:37835109:G>A" "CLDN14" "NM_144492:c.-81-1035C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs767708369" "This variant is a VUS because it does not have enough information."
492192 "chr21:37835111:G>T" "CLDN14" "NM_144492:c.-81-1037C>A" "FIVE_PRIME_INTRON" "Benign" "rs144044511" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 5 1322 0.0038 30 1006 0.0298 58 694 0.0836 1 1008 0.001 17 978 0.0174 111 5008 0.0221645
492193 "chr21:37835131:G>A" "CLDN14" "NM_144492:c.-81-1057C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs182162891" "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
492194 "chr21:37835152:G>A" "CLDN14" "NM_144492:c.-81-1078C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566985176" "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
492195 "chr21:37835164:C>T" "CLDN14" "NM_144492:c.-81-1090G>A" "FIVE_PRIME_INTRON" "Benign" "rs60419768" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 52 1322 0.0393 11 1006 0.0109 10 694 0.0144 17 1008 0.0169 15 978 0.0153 105 5008 0.0209665
492196 "chr21:37835170:C>G" "CLDN14" "NM_144492:c.-81-1096G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs559328028" "This variant is a VUS because it does not have enough information."
492197 "chr21:37835173:G>T" "CLDN14" "NM_144492:c.-81-1099C>A" "FIVE_PRIME_INTRON" "Benign" "rs141254132" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 31 1006 0.0308 2 694 0.0029 0 1008 0 16 978 0.0164 49 5008 0.00978435
492198 "chr21:37835185:C>-" "CLDN14" "NM_144492:c.-81-1111delG" "FIVE_PRIME_INTRON" "Benign" "rs34627708" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 218 1322 0.1649 584 1006 0.5805 347 694 0.5 434 1008 0.4306 333 978 0.3405 1916 5008 0.382588
492199 "chr21:37835185:->C" "CLDN14" "NM_144492:c.-81-1111_-81-1110insG" "FIVE_PRIME_INTRON" "Unknown significance" "rs774539908" "This variant is a VUS because it does not have enough information."
492200 "chr21:37835185:C>T" "CLDN14" "NM_144492:c.-81-1111G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs113895166" "This variant is a VUS because it does not have enough information."
492201 "chr21:37835194:C>T" "CLDN14" "NM_144492:c.-81-1120G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs369746995" "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
492202 "chr21:37835207:C>T" "CLDN14" "NM_144492:c.-81-1133G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs753886527" "This variant is a VUS because it does not have enough information."
492203 "chr21:37835211:G>A" "CLDN14" "NM_144492:c.-81-1137C>T" "FIVE_PRIME_INTRON" "Benign" "rs139388371" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 74 1322 0.056 1 1006 0.001 3 694 0.0043 0 1008 0 1 978 0.001 79 5008 0.0157748
492204 "chr21:37835239:AC>-" "CLDN14" "NM_144492:c.-81-1165_-81-1162delGT" "FIVE_PRIME_INTRON" "Benign" "rs199565725" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 199 1322 0.1505 33 1006 0.0328 73 694 0.1052 3 1008 0.003 32 978 0.0327 340 5008 0.0678914
492205 "chr21:37835240:C>-" "CLDN14" "NM_144492:c.-81-1166delG" "FIVE_PRIME_INTRON" "Benign" "rs148792260" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 497 1322 0.3759 217 1006 0.2157 99 694 0.1427 1 1008 0.001 101 978 0.1033 915 5008 0.182708
492206 "chr21:37835240:C>A" "CLDN14" "NM_144492:c.-81-1166G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs113320652" "This variant is a VUS because it does not have enough information."
492207 "chr21:37835241:->A" "CLDN14" "NM_144492:c.-81-1167_-81-1166insT" "FIVE_PRIME_INTRON" "Unknown significance" "rs199909665" "This variant is a VUS because it does not have enough information."
492208 "chr21:37835247:A>G" "CLDN14" "NM_144492:c.-81-1173T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs187204092" "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
492209 "chr21:37835259:A>G" "CLDN14" "NM_144492:c.-81-1185T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs144001761" "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
492210 "chr21:37835291:A>G" "CLDN14" "NM_144492:c.-81-1217T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs752793779" "This variant is a VUS because it does not have enough information."
492211 "chr21:37835295:G>-" "CLDN14" "NM_144492:c.-81-1221delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs767525449" "This variant is a VUS because it does not have enough information."
492212 "chr21:37835296:G>A" "CLDN14" "NM_144492:c.-81-1222C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545419730" "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
492213 "chr21:37835323:G>A" "CLDN14" "NM_144492:c.-81-1249C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs369912737" "This variant is a VUS because it does not have enough information."
492214 "chr21:37835333:G>A" "CLDN14" "NM_144492:c.-81-1259C>T" "FIVE_PRIME_INTRON" "Benign" "rs219773" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 706 1322 0.534 251 1006 0.2495 173 694 0.2493 6 1008 0.006 132 978 0.135 1268 5008 0.253195
492215 "chr21:37835340:G>A" "CLDN14" "NM_144492:c.-81-1266C>T" "FIVE_PRIME_INTRON" "Benign" "rs377296138" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 190 1322 0.1437 1 1006 0.001 14 694 0.0202 0 1008 0 0 978 0 205 5008 0.0409345
492216 "chr21:37835344:G>A" "CLDN14" "NM_144492:c.-81-1270C>T" "FIVE_PRIME_INTRON" "Benign" "rs368713104" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 191 1322 0.1445 1 1006 0.001 14 694 0.0202 0 1008 0 0 978 0 206 5008 0.0411342
492217 "chr21:37835347:A>T" "CLDN14" "NM_144492:c.-81-1273T>A" "FIVE_PRIME_INTRON" "Benign" "rs219772" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 709 1322 0.5363 251 1006 0.2495 173 694 0.2493 6 1008 0.006 132 978 0.135 1271 5008 0.253794
492218 "chr21:37835405:G>T" "CLDN14" "NM_144492:c.-81-1331C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs190871138" "This variant is a VUS because it does not have enough information."
492219 "chr21:37835421:T>A" "CLDN14" "NM_144492:c.-81-1347A>T" "FIVE_PRIME_INTRON" "Benign" "rs146410264" "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 16 694 0.0231 3 1008 0.003 0 978 0 19 5008 0.00379393
492220 "chr21:37835423:G>A" "CLDN14" "NM_144492:c.-81-1349C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs746991947" "This variant is a VUS because it does not have enough information."
492221 "chr21:37835438:C>T" "CLDN14" "NM_144492:c.-81-1364G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs544523414" "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
492222 "chr21:37835445:G>A" "CLDN14" "NM_144492:c.-81-1371C>T" "FIVE_PRIME_INTRON" "Benign" "rs116699215" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 12 1322 0.0091 13 1006 0.0129 8 694 0.0115 3 1008 0.003 24 978 0.0245 60 5008 0.0119808
492223 "chr21:37835453:G>A" "CLDN14" "NM_144492:c.-81-1379C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs180745041" "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
492224 "chr21:37835457:C>T" "CLDN14" "NM_144492:c.-81-1383G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs745392970" "This variant is a VUS because it does not have enough information."
492225 "chr21:37835473:C>T" "CLDN14" "NM_144492:c.-81-1399G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs185843956" "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
492226 "chr21:37835486:C>T" "CLDN14" "NM_144492:c.-81-1412G>A" "FIVE_PRIME_INTRON" "Benign" "rs190169964" "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
492227 "chr21:37835487:G>A" "CLDN14" "NM_144492:c.-81-1413C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs769129712" "This variant is a VUS because it does not have enough information."
492228 "chr21:37835497:T>C" "CLDN14" "NM_144492:c.-81-1423A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs540177440" "This variant is a VUS because it does not have enough information."
492229 "chr21:37835501:C>T" "CLDN14" "NM_144492:c.-81-1427G>A" "FIVE_PRIME_INTRON" "Benign" "rs219771" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 626 1322 0.4735 251 1006 0.2495 174 694 0.2507 6 1008 0.006 132 978 0.135 1189 5008 0.23742
492230 "chr21:37835551:G>A" "CLDN14" "NM_144492:c.-81-1477C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs748890458" "This variant is a VUS because it does not have enough information."
492231 "chr21:37835553:C>T" "CLDN14" "NM_144492:c.-81-1479G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs571145959" "This variant is a VUS because it does not have enough information."
492232 "chr21:37835568:G>T" "CLDN14" "NM_144492:c.-81-1494C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs772547092" "This variant is a VUS because it does not have enough information."
492233 "chr21:37835578:C>T" "CLDN14" "NM_144492:c.-81-1504G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs549298563" "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
492234 "chr21:37835579:G>A" "CLDN14" "NM_144492:c.-81-1505C>T" "FIVE_PRIME_INTRON" "Benign" "rs375897772" "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 1 694 0.0014 5 1008 0.005 1 978 0.001 8 5008 0.00159744
492235 "chr21:37835599:C>A" "CLDN14" "NM_144492:c.-81-1525G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs773546697" "This variant is a VUS because it does not have enough information."
492236 "chr21:37835617:T>G" "CLDN14" "NM_144492:c.-81-1543A>C" "FIVE_PRIME_INTRON" "Benign" "rs538137714" "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 25 978 0.0256 25 5008 0.00499201
492237 "chr21:37835635:T>G" "CLDN14" "NM_144492:c.-81-1561A>C" "FIVE_PRIME_INTRON" "Benign" "rs139516886" "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
492238 "chr21:37835648:A>G" "CLDN14" "NM_144492:c.-81-1574T>C" "FIVE_PRIME_INTRON" "Benign" "rs219770" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 518 1322 0.3918 250 1006 0.2485 160 694 0.2305 6 1008 0.006 131 978 0.1339 1065 5008 0.21266
492239 "chr21:37835662:C>A" "CLDN14" "NM_144492:c.-81-1588G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs777061848" "This variant is a VUS because it does not have enough information."
492240 "chr21:37835675:C>A" "CLDN14" "NM_144492:c.-81-1601G>T" "FIVE_PRIME_INTRON" "Benign" "rs219769" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 519 1322 0.3926 250 1006 0.2485 160 694 0.2305 6 1008 0.006 131 978 0.1339 1066 5008 0.212859
492241 "chr21:37835699:A>G" "CLDN14" "NM_144492:c.-81-1625T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs149705100" "This variant is a VUS because it does not have enough information."
492242 "chr21:37835730:C>T" "CLDN14" "NM_144492:c.-81-1656G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs765225896" "This variant is a VUS because it does not have enough information."
492243 "chr21:37835737:C>T" "CLDN14" "NM_144492:c.-81-1663G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs552554268" "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
492244 "chr21:37835748:G>A" "CLDN14" "NM_144492:c.-81-1674C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs572601563" "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
492245 "chr21:37835749:C>T" "CLDN14" "NM_144492:c.-81-1675G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs535578002" "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
492246 "chr21:37835750:C>T" "CLDN14" "NM_144492:c.-81-1676G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs555249911" "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
492247 "chr21:37835764:C>G" "CLDN14" "NM_144492:c.-81-1690G>C" "FIVE_PRIME_INTRON" "Benign" "rs219768" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 518 1322 0.3918 250 1006 0.2485 160 694 0.2305 6 1008 0.006 131 978 0.1339 1065 5008 0.21266
492248 "chr21:37835778:G>A" "CLDN14" "NM_144492:c.-81-1704C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs544091109" "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
492249 "chr21:37835781:G>A" "CLDN14" "NM_144492:c.-81-1707C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs564331385" "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
492250 "chr21:37835816:C>T" "CLDN14" "NM_144492:c.-81-1742G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs763062893" "This variant is a VUS because it does not have enough information."
492251 "chr21:37835846:C>T" "CLDN14" "NM_144492:c.-81-1772G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs149200035" "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
492252 "chr21:37835870:C>T" "CLDN14" "NM_144492:c.-81-1796G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs540625407" "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
492253 "chr21:37835919:G>A" "CLDN14" "NM_144492:c.-81-1845C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs530912369" "This variant is a VUS because it does not have enough information."
492254 "chr21:37835925:C>T" "CLDN14" "NM_144492:c.-81-1851G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs560510026" "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
492255 "chr21:37835935:G>A" "CLDN14" "NM_144492:c.-81-1861C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs757639278" "This variant is a VUS because it does not have enough information."
492256 "chr21:37835982:C>G" "CLDN14" "NM_144492:c.-81-1908G>C" "FIVE_PRIME_INTRON" "Benign" "rs12626330" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 99 1322 0.0749 502 1006 0.499 320 694 0.4611 420 1008 0.4167 316 978 0.3231 1657 5008 0.330871
492257 "chr21:37836027:AAATG>-" "CLDN14" "NM_144492:c.-81-1953_-81-1947delCATTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs533056471" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 8 5008 0.00159744
492258 "chr21:37836070:T>G" "CLDN14" "NM_144492:c.-81-1996A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs549486982" "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
492259 "chr21:37836156:G>A" "CLDN14" "NM_144492:c.-81-2082C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs751431982" "This variant is a VUS because it does not have enough information."
492260 "chr21:37836207:T>G" "CLDN14" "NM_144492:c.-81-2133A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs562865546" "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
492261 "chr21:37836226:A>T" "CLDN14" "NM_144492:c.-81-2152T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs757069317" "This variant is a VUS because it does not have enough information."
492262 "chr21:37836230:A>G" "CLDN14" "NM_144492:c.-81-2156T>C" "FIVE_PRIME_INTRON" "Benign" "rs79725062" "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 0 694 0 0 1008 0 0 978 0 96 5008 0.0191693
492263 "chr21:37836239:C>A" "CLDN14" "NM_144492:c.-81-2165G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs183167070" "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
492264 "chr21:37836281:A>G" "CLDN14" "NM_144492:c.-81-2207T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs188404131" "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
492265 "chr21:37836290:G>A" "CLDN14" "NM_144492:c.-81-2216C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs534268933" "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
492266 "chr21:37836290:G>C" "CLDN14" "NM_144492:c.-81-2216C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs534268933" "This variant is a VUS because it does not have enough information."
492267 "chr21:37836291:G>T" "CLDN14" "NM_144492:c.-81-2217C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs545776319" "This variant is a VUS because it does not have enough information."
492268 "chr21:37836297:A>T" "CLDN14" "NM_144492:c.-81-2223T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs546180526" "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
492269 "chr21:37836310:C>T" "CLDN14" "NM_144492:c.-81-2236G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs755718509" "This variant is a VUS because it does not have enough information."
492270 "chr21:37836324:C>T" "CLDN14" "NM_144492:c.-81-2250G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs146713870" "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
492271 "chr21:37836342:G>A" "CLDN14" "NM_144492:c.-81-2268C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs191629872" "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
492272 "chr21:37836349:G>A" "CLDN14" "NM_144492:c.-81-2275C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs555405846" "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
492273 "chr21:37836378:C>T" "CLDN14" "NM_144492:c.-81-2304G>A" "FIVE_PRIME_INTRON" "Benign" "rs219767" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 328 1322 0.2481 235 1006 0.2336 134 694 0.1931 2 1008 0.002 97 978 0.0992 796 5008 0.158946
492274 "chr21:37836428:C>T" "CLDN14" "NM_144492:c.-81-2354G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs537997111" "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
492275 "chr21:37836436:G>A" "CLDN14" "NM_144492:c.-81-2362C>T" "FIVE_PRIME_INTRON" "Benign" "rs367618642" "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
492276 "chr21:37836471:CT>-" "CLDN14" "NM_144492:c.-81-2397_-81-2394delAG" "FIVE_PRIME_INTRON" "Unknown significance" "rs779846392" "This variant is a VUS because it does not have enough information."
492277 "chr21:37836473:C>T" "CLDN14" "NM_144492:c.-81-2399G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs371735848" "This variant is a VUS because it does not have enough information."
492278 "chr21:37836477:C>G" "CLDN14" "NM_144492:c.-81-2403G>C" "FIVE_PRIME_INTRON" "Benign" "rs219766" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 535 1322 0.4047 245 1006 0.2435 168 694 0.2421 32 1008 0.0317 125 978 0.1278 1105 5008 0.220647
492279 "chr21:37836483:C>T" "CLDN14" "NM_144492:c.-81-2409G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs183962685" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 1 1006 0.001 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
492280 "chr21:37836493:G>A" "CLDN14" "NM_144492:c.-81-2419C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs188912231" "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
492281 "chr21:37836496:C>T" "CLDN14" "NM_144492:c.-81-2422G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs117634720" "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
492282 "chr21:37836529:G>A" "CLDN14" "NM_144492:c.-81-2455C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs768164982" "This variant is a VUS because it does not have enough information."
492283 "chr21:37836562:C>T" "CLDN14" "NM_144492:c.-81-2488G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs749430704" "This variant is a VUS because it does not have enough information."
492284 "chr21:37836563:G>A" "CLDN14" "NM_144492:c.-81-2489C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs542673507" "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
492285 "chr21:37836580:T>G" "CLDN14" "NM_144492:c.-81-2506A>C" "FIVE_PRIME_INTRON" "Benign" "rs116380929" "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
492286 "chr21:37836588:A>G" "CLDN14" "NM_144492:c.-81-2514T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs778501458" "This variant is a VUS because it does not have enough information."
492287 "chr21:37836590:T>C" "CLDN14" "NM_144492:c.-81-2516A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs768972737" "This variant is a VUS because it does not have enough information."
492288 "chr21:37836619:G>A" "CLDN14" "NM_144492:c.-81-2545C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs747399595" "This variant is a VUS because it does not have enough information."
492289 "chr21:37836634:T>C" "CLDN14" "NM_144492:c.-81-2560A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs531717742" "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
492290 "chr21:37836647:C>T" "CLDN14" "NM_144492:c.-81-2573G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs369173435" "This variant is a VUS because it does not have enough information."
492291 "chr21:37836658:C>T" "CLDN14" "NM_144492:c.-81-2584G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs141819946" "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
492292 "chr21:37836659:G>A" "CLDN14" "NM_144492:c.-81-2585C>T" "FIVE_PRIME_INTRON" "Benign" "rs73902528" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 29 1322 0.0219 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 30 5008 0.00599042
492293 "chr21:37836671:C>T" "CLDN14" "NM_144492:c.-81-2597G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs527962836" "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
492294 "chr21:37836672:G>A" "CLDN14" "NM_144492:c.-81-2598C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566891307" "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 3 978 0.0031 4 5008 0.000798722
492295 "chr21:37836674:G>C" "CLDN14" "NM_144492:c.-81-2600C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs567879003" "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
492296 "chr21:37836677:TTTTTCTGCTGCTG>-" "CLDN14" "NM_144492:c.-81-2603_-81-2588delCAGCAGCAGAAAAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs754418945" "This variant is a VUS because it does not have enough information."
492297 "chr21:37836711:G>A" "CLDN14" "NM_144492:c.-81-2637C>T" "FIVE_PRIME_INTRON" "Benign" "rs219765" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1192 1322 0.9017 857 1006 0.8519 634 694 0.9135 663 1008 0.6577 794 978 0.8119 4140 5008 0.826677
492298 "chr21:37836718:T>C" "CLDN14" "NM_144492:c.-81-2644A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs191414470" "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
492299 "chr21:37836745:C>T" "CLDN14" "NM_144492:c.-81-2671G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs539340314" "This variant is a VUS because it does not have enough information."
492300 "chr21:37836794:C>A" "CLDN14" "NM_144492:c.-81-2720G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs183549856" "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
492301 "chr21:37836794:C>G" "CLDN14" "NM_144492:c.-81-2720G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs183549856" "This variant is a VUS because it does not have enough information."
492302 "chr21:37836801:C>T" "CLDN14" "NM_144492:c.-81-2727G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs147039278" "This variant is a VUS because it does not have enough information."
492303 "chr21:37836816:G>A" "CLDN14" "NM_144492:c.-81-2742C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs537978106" "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
492304 "chr21:37836819:G>T" "CLDN14" "NM_144492:c.-81-2745C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs775399280" "This variant is a VUS because it does not have enough information."
492305 "chr21:37836827:C>T" "CLDN14" "NM_144492:c.-81-2753G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs557965585" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 1 1006 0.001 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
492306 "chr21:37836834:A>G" "CLDN14" "NM_144492:c.-81-2760T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs763045927" "This variant is a VUS because it does not have enough information."
492307 "chr21:37836860:C>T" "CLDN14" "NM_144492:c.-81-2786G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs767437551" "This variant is a VUS because it does not have enough information."
492308 "chr21:37836866:C>T" "CLDN14" "NM_144492:c.-81-2792G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs764432273" "This variant is a VUS because it does not have enough information."
492309 "chr21:37836887:C>T" "CLDN14" "NM_144492:c.-81-2813G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs529401644" "This variant is a VUS because it does not have enough information."
492310 "chr21:37836966:T>C" "CLDN14" "NM_144492:c.-81-2892A>G" "FIVE_PRIME_INTRON" "Benign" "rs148075105" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 26 1322 0.0197 2 1006 0.002 5 694 0.0072 0 1008 0 0 978 0 33 5008 0.00658946
492311 "chr21:37836973:T>C" "CLDN14" "NM_144492:c.-81-2899A>G" "FIVE_PRIME_INTRON" "Benign" "rs7277076" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 542 1322 0.41 582 1006 0.5785 373 694 0.5375 480 1008 0.4762 391 978 0.3998 2368 5008 0.472843
492312 "chr21:37837010:A>G" "CLDN14" "NM_144492:c.-81-2936T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs554002654" "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
492313 "chr21:37837017:G>T" "CLDN14" "NM_144492:c.-81-2943C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs573864207" "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
492314 "chr21:37837060:G>A" "CLDN14" "NM_144492:c.-81-2986C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs542963141" "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
492315 "chr21:37837079:C>A" "CLDN14" "NM_144492:c.-81-3005G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs556329991" "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
492316 "chr21:37837100:C>T" "CLDN14" "NM_144492:c.-81-3026G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs187182708" "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
492317 "chr21:37837101:G>A" "CLDN14" "NM_144492:c.-81-3027C>T" "FIVE_PRIME_INTRON" "Benign" "rs76739387" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 105 1322 0.0794 12 1006 0.0119 16 694 0.0231 26 1008 0.0258 12 978 0.0123 171 5008 0.0341454
492318 "chr21:37837164:C>T" "CLDN14" "NM_144492:c.-81-3090G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs565115913" "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
492319 "chr21:37837282:C>G" "CLDN14" "NM_144492:c.-81-3208G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs191643462" "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
492320 "chr21:37837283:C>T" "CLDN14" "NM_144492:c.-81-3209G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs541235664" "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
492321 "chr21:37837298:G>T" "CLDN14" "NM_144492:c.-81-3224C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs373321128" "This variant is a VUS because it does not have enough information."
492322 "chr21:37837333:G>C" "CLDN14" "NM_144492:c.-81-3259C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs561579853" "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
492323 "chr21:37837370:C>A" "CLDN14" "NM_144492:c.-81-3296G>T" "FIVE_PRIME_INTRON" "Benign" "rs77562443" "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 0 694 0 0 1008 0 11 978 0.0112 48 5008 0.00958466
492324 "chr21:37837382:C>T" "CLDN14" "NM_144492:c.-81-3308G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs548952727" "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
492325 "chr21:37837384:G>A" "CLDN14" "NM_144492:c.-81-3310C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs141839603" "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
492326 "chr21:37837388:C>T" "CLDN14" "NM_144492:c.-81-3314G>A" "FIVE_PRIME_INTRON" "Benign" "rs549451818" "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 11 978 0.0112 11 5008 0.00219649
492327 "chr21:37837389:A>G" "CLDN14" "NM_144492:c.-81-3315T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs551471061" "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
492328 "chr21:37837408:G>T" "CLDN14" "NM_144492:c.-81-3334C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs571383246" "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
492329 "chr21:37837431:C>T" "CLDN14" "NM_144492:c.-81-3357G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs753321597" "This variant is a VUS because it does not have enough information."
492330 "chr21:37837435:T>G" "CLDN14" "NM_144492:c.-81-3361A>C" "FIVE_PRIME_INTRON" "Benign" "rs78262992" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 105 1322 0.0794 11 1006 0.0109 16 694 0.0231 26 1008 0.0258 13 978 0.0133 171 5008 0.0341454
492331 "chr21:37837485:C>T" "CLDN14" "NM_144492:c.-81-3411G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs778538126" "This variant is a VUS because it does not have enough information."
492332 "chr21:37837496:G>A" "CLDN14" "NM_144492:c.-81-3422C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs553689498" "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
492333 "chr21:37837497:G>A" "CLDN14" "NM_144492:c.-81-3423C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs567550774" "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
492334 "chr21:37837522:G>A" "CLDN14" "NM_144492:c.-81-3448C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs536194777" "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
492335 "chr21:37837604:G>T" "CLDN14" "NM_144492:c.-81-3530C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs183835612" "This variant is a VUS because it does not have enough information." 0 1322 0 4 1006 0.004 1 694 0.0014 0 1008 0 1 978 0.001 6 5008 0.00119808
492336 "chr21:37837614:T>A" "CLDN14" "NM_144492:c.-81-3540A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs576056929" "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
492337 "chr21:37837699:C>G" "CLDN14" "NM_144492:c.-81-3625G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs764821701" "This variant is a VUS because it does not have enough information."
492338 "chr21:37837725:A>G" "CLDN14" "NM_144492:c.-81-3651T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs545016678" "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
492339 "chr21:37837774:C>T" "CLDN14" "NM_144492:c.-81-3700G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs771340692" "This variant is a VUS because it does not have enough information."
492340 "chr21:37837835:C>T" "CLDN14" "NM_144492:c.-81-3761G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs558586309" "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
492341 "chr21:37837864:A>G" "CLDN14" "NM_144492:c.-81-3790T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs572209916" "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
492342 "chr21:37837888:C>T" "CLDN14" "NM_144492:c.-81-3814G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs373023892" "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 3 978 0.0031 4 5008 0.000798722
492343 "chr21:37837889:G>A" "CLDN14" "NM_144492:c.-81-3815C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs576773679" "This variant is a VUS because it does not have enough information."
492344 "chr21:37837930:C>T" "CLDN14" "NM_144492:c.-81-3856G>A" "FIVE_PRIME_INTRON" "Benign" "rs219764" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 663 1322 0.5015 260 1006 0.2584 194 694 0.2795 120 1008 0.119 384 978 0.3926 1621 5008 0.323682
492345 "chr21:37837932:G>T" "CLDN14" "NM_144492:c.-81-3858C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs776016007" "This variant is a VUS because it does not have enough information."
492346 "chr21:37837936:C>T" "CLDN14" "NM_144492:c.-81-3862G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs569082243" "This variant is a VUS because it does not have enough information."
492347 "chr21:37837951:G>A" "CLDN14" "NM_144492:c.-81-3877C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs370438825" "This variant is a VUS because it does not have enough information."
492348 "chr21:37838001:C>T" "CLDN14" "NM_144492:c.-81-3927G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs150229898" "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
492349 "chr21:37838003:G>T" "CLDN14" "NM_144492:c.-81-3929C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs543784415" "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
492350 "chr21:37838030:C>T" "CLDN14" "NM_144492:c.-81-3956G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs564028567" "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
492351 "chr21:37838039:T>C" "CLDN14" "NM_144492:c.-81-3965A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs538002176" "This variant is a VUS because it does not have enough information."
492352 "chr21:37838053:A>C" "CLDN14" "NM_144492:c.-81-3979T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs531302258" "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
492353 "chr21:37838094:G>A" "CLDN14" "NM_144492:c.-81-4020C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs190003115" "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
492354 "chr21:37838111:G>A" "CLDN14" "NM_144492:c.-81-4037C>T" "FIVE_PRIME_INTRON" "Benign" "rs2835364" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 69 1322 0.0522 95 1006 0.0944 37 694 0.0533 0 1008 0 36 978 0.0368 237 5008 0.0473243
492355 "chr21:37838123:C>T" "CLDN14" "NM_144492:c.-81-4049G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs527432181" "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
492356 "chr21:37838141:C>T" "CLDN14" "NM_144492:c.-81-4067G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs768790743" "This variant is a VUS because it does not have enough information."
492357 "chr21:37838142:G>C" "CLDN14" "NM_144492:c.-81-4068C>G" "FIVE_PRIME_INTRON" "Benign" "rs138790694" "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 2 694 0.0029 0 1008 0 2 978 0.002 12 5008 0.00239617
492358 "chr21:37838153:T>C" "CLDN14" "NM_144492:c.-81-4079A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs567384772" "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
492359 "chr21:37838252:G>T" "CLDN14" "NM_144492:c.-81-4178C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs193056047" "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
492360 "chr21:37838306:G>A" "CLDN14" "NM_144492:c.-81-4232C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs549780527" "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
492361 "chr21:37838332:C>A" "CLDN14" "NM_144492:c.-81-4258G>T" "FIVE_PRIME_INTRON" "Benign" "rs149305332" "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 0 978 0 17 5008 0.00339457
492362 "chr21:37838415:G>A" "CLDN14" "NM_144492:c.-81-4341C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs538601393" "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
492363 "chr21:37838421:A>G" "CLDN14" "NM_144492:c.-81-4347T>C" "FIVE_PRIME_INTRON" "Benign" "rs219763" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 722 1322 0.5461 293 1006 0.2913 261 694 0.3761 121 1008 0.12 408 978 0.4172 1805 5008 0.360423
492364 "chr21:37838430:G>A" "CLDN14" "NM_144492:c.-81-4356C>T" "FIVE_PRIME_INTRON" "Benign" "rs185622353" "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 1 694 0.0014 0 1008 0 0 978 0 8 5008 0.00159744
492365 "chr21:37838458:C>T" "CLDN14" "NM_144492:c.-81-4384G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs190582023" "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
492366 "chr21:37838465:C>T" "CLDN14" "NM_144492:c.-81-4391G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs772854849" "This variant is a VUS because it does not have enough information."
492367 "chr21:37838466:G>A" "CLDN14" "NM_144492:c.-81-4392C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs113829974" "This variant is a VUS because it does not have enough information."
492368 "chr21:37838498:C>A" "CLDN14" "NM_144492:c.-81-4424G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs555121598" "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
492369 "chr21:37838582:G>A" "CLDN14" "NM_144492:c.-81-4508C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs574904523" "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
492370 "chr21:37838623:G>A" "CLDN14" "NM_144492:c.-81-4549C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs180983477" "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
492371 "chr21:37838637:A>G" "CLDN14" "NM_144492:c.-81-4563T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs200809491" "This variant is a VUS because it does not have enough information."
492372 "chr21:37838647:G>A" "CLDN14" "NM_144492:c.-81-4573C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs563933564" "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
492373 "chr21:37838670:C>T" "CLDN14" "NM_012130:c.-87G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs376127472" "This variant is a VUS because it does not have enough information."
492374 "chr21:37838671:G>A" "CLDN14" "NM_012130:c.-88C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs371272476" "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
492375 "chr21:37838685:G>T" "CLDN14" "NM_144492:c.-81-4611C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs545020329" "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
492376 "chr21:37838705:C>G" "CLDN14" "NM_144492:c.-81-4631G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs564915811" "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
492377 "chr21:37838709:C>T" "CLDN14" "NM_144492:c.-81-4635G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs760480583" "This variant is a VUS because it does not have enough information."
492378 "chr21:37838718:A>G" "CLDN14" "NM_144492:c.-81-4644T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs768883066" "This variant is a VUS because it does not have enough information."
492379 "chr21:37838773:C>T" "CLDN14" "NM_144492:c.-81-4699G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs528569226" "This variant is a VUS because it does not have enough information."
492380 "chr21:37838775:A>G" "CLDN14" "NM_144492:c.-81-4701T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs146235327" "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
492381 "chr21:37838778:G>A" "CLDN14" "NM_144492:c.-81-4704C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs766253749" "This variant is a VUS because it does not have enough information."
492382 "chr21:37838826:T>G" "CLDN14" "NM_144492:c.-81-4752A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs547205304" "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
492383 "chr21:37838870:C>A" "CLDN14" "NM_144492:c.-81-4796G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs561061436" "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
492384 "chr21:37838884:C>T" "CLDN14" "NM_144492:c.-81-4810G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs528736332" "This variant is a VUS because it does not have enough information."
492385 "chr21:37838960:A>G" "CLDN14" "NM_144492:c.-81-4886T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs529809733" "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
492386 "chr21:37838970:G>T" "CLDN14" "NM_144492:c.-81-4896C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs753755056" "This variant is a VUS because it does not have enough information."
492387 "chr21:37839084:C>T" "CLDN14" "NM_144492:c.-81-5010G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs754546241" "This variant is a VUS because it does not have enough information."
492388 "chr21:37839085:G>A" "CLDN14" "NM_144492:c.-81-5011C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs764709203" "This variant is a VUS because it does not have enough information."
492389 "chr21:37839093:C>T" "CLDN14" "NM_144492:c.-81-5019G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs549951034" "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
492390 "chr21:37839096:G>A" "CLDN14" "NM_144492:c.-81-5022C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs185311480" "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
492391 "chr21:37839135:C>G" "CLDN14" "NM_144492:c.-81-5061G>C" "FIVE_PRIME_INTRON" "Benign" "rs219762" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 388 1322 0.2935 166 1006 0.165 156 694 0.2248 119 1008 0.1181 335 978 0.3425 1164 5008 0.232428
492392 "chr21:37839143:T>G" "CLDN14" "NM_144492:c.-81-5069A>C" "FIVE_PRIME_INTRON" "Benign" "rs139418350" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 25 1322 0.0189 2 1006 0.002 5 694 0.0072 0 1008 0 0 978 0 32 5008 0.00638978
492393 "chr21:37839164:G>A" "CLDN14" "NM_144492:c.-81-5090C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs777440671" "This variant is a VUS because it does not have enough information."
492394 "chr21:37839165:G>T" "CLDN14" "NM_144492:c.-81-5091C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs565762475" "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
492395 "chr21:37839210:A>G" "CLDN14" "NM_144492:c.-81-5136T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs535036739" "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
492396 "chr21:37839246:G>A" "CLDN14" "NM_144492:c.-81-5172C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs554728858" "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
492397 "chr21:37839287:G>C" "CLDN14" "NM_144492:c.-81-5213C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs142616983" "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
492398 "chr21:37839320:C>T" "CLDN14" "NM_144492:c.-81-5246G>A" "FIVE_PRIME_INTRON" "Benign" "rs73204259" "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 0 978 0 12 5008 0.00239617
492399 "chr21:37839323:C>G" "CLDN14" "NM_144492:c.-81-5249G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs756443101" "This variant is a VUS because it does not have enough information."
492400 "chr21:37839325:G>C" "CLDN14" "NM_144492:c.-81-5251C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs557636349" "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
492401 "chr21:37839328:C>T" "CLDN14" "NM_144492:c.-81-5254G>A" "FIVE_PRIME_INTRON" "Benign" "rs557786937" "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
492402 "chr21:37839330:G>A" "CLDN14" "NM_144492:c.-81-5256C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs749808910" "This variant is a VUS because it does not have enough information."
492403 "chr21:37839405:G>C" "CLDN14" "NM_144492:c.-81-5331C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs768915511" "This variant is a VUS because it does not have enough information."
492404 "chr21:37839410:A>G" "CLDN14" "NM_144492:c.-81-5336T>C" "FIVE_PRIME_INTRON" "Benign" "rs219761" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 990 1322 0.7489 827 1006 0.8221 588 694 0.8473 548 1008 0.5437 713 978 0.729 3666 5008 0.732029
492405 "chr21:37839412:G>C" "CLDN14" "NM_144492:c.-81-5338C>G" "FIVE_PRIME_INTRON" "Benign" "rs564852937" "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
492406 "chr21:37839437:T>C" "CLDN14" "NM_144492:c.-81-5363A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs188115205" "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
492407 "chr21:37839483:T>C" "CLDN14" "NM_144492:c.-81-5409A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs541037607" "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
492408 "chr21:37839488:C>T" "CLDN14" "NM_144492:c.-81-5414G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs59625180" "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
492409 "chr21:37839504:T>G" "CLDN14" "NM_144492:c.-81-5430A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs748422807" "This variant is a VUS because it does not have enough information."
492410 "chr21:37839522:TG>-" "CLDN14" "NM_144492:c.-81-5448_-81-5445delCA" "FIVE_PRIME_INTRON" "Unknown significance" "rs370023702" "This variant is a VUS because it does not have enough information."
492411 "chr21:37839588:A>C" "CLDN14" "NM_144492:c.-81-5514T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs772871342" "This variant is a VUS because it does not have enough information."
492412 "chr21:37839631:G>T" "CLDN14" "NM_144492:c.-81-5557C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs529843664" "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
492413 "chr21:37839637:C>T" "CLDN14" "NM_144492:c.-81-5563G>A" "FIVE_PRIME_INTRON" "Benign" "rs118133539" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 26 1006 0.0258 35 694 0.0504 106 1008 0.1052 30 978 0.0307 199 5008 0.0397364
492414 "chr21:37839638:G>A" "CLDN14" "NM_144492:c.-81-5564C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs563176594" "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
492415 "chr21:37839640:C>T" "CLDN14" "NM_144492:c.-81-5566G>A" "FIVE_PRIME_INTRON" "Benign" "rs146029576" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 31 1006 0.0308 58 694 0.0836 1 1008 0.001 24 978 0.0245 118 5008 0.0235623
492416 "chr21:37839645:C>T" "CLDN14" "NM_144492:c.-81-5571G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs552023163" "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
492417 "chr21:37839662:C>T" "CLDN14" "NM_144492:c.-81-5588G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs565649602" "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
492418 "chr21:37839663:G>A" "CLDN14" "NM_144492:c.-81-5589C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs181281971" "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
492419 "chr21:37839688:A>C" "CLDN14" "NM_144492:c.-81-5614T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs548569616" "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
492420 "chr21:37839689:C>T" "CLDN14" "NM_144492:c.-81-5615G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568461526" "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
492421 "chr21:37839692:C>A" "CLDN14" "NM_144492:c.-81-5618G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs537594020" "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
492422 "chr21:37839710:G>A" "CLDN14" "NM_144492:c.-81-5636C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs776651458" "This variant is a VUS because it does not have enough information."
492423 "chr21:37839710:G>C" "CLDN14" "NM_144492:c.-81-5636C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs776651458" "This variant is a VUS because it does not have enough information."
492424 "chr21:37839742:C>T" "CLDN14" "NM_144492:c.-81-5668G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs547863452" "This variant is a VUS because it does not have enough information."
492425 "chr21:37839798:A>T" "CLDN14" "NM_144492:c.-81-5724T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs557575283" "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
492426 "chr21:37839800:G>A" "CLDN14" "NM_144492:c.-81-5726C>T" "FIVE_PRIME_INTRON" "Benign" "rs148622363" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 31 1006 0.0308 58 694 0.0836 1 1008 0.001 24 978 0.0245 118 5008 0.0235623
492427 "chr21:37839815:G>A" "CLDN14" "NM_144492:c.-81-5741C>T" "FIVE_PRIME_INTRON" "Benign" "rs219760" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 496 1322 0.3752 196 1006 0.1948 228 694 0.3285 120 1008 0.119 361 978 0.3691 1401 5008 0.279752
492428 "chr21:37839816:C>T" "CLDN14" "NM_144492:c.-81-5742G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs553668649" "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
492429 "chr21:37839820:G>A" "CLDN14" "NM_144492:c.-81-5746C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs558334411" "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
492430 "chr21:37839827:C>T" "CLDN14" "NM_144492:c.-81-5753G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759443896" "This variant is a VUS because it does not have enough information."
492431 "chr21:37839829:A>G" "CLDN14" "NM_144492:c.-81-5755T>C" "FIVE_PRIME_INTRON" "Benign" "rs219759" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1205 1322 0.9115 873 1006 0.8678 640 694 0.9222 679 1008 0.6736 790 978 0.8078 4187 5008 0.836062
492432 "chr21:37839864:T>C" "CLDN14" "NM_144492:c.-81-5790A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs752233181" "This variant is a VUS because it does not have enough information."
492433 "chr21:37839905:G>A" "CLDN14" "NM_144492:c.-81-5831C>T" "FIVE_PRIME_INTRON" "Benign" "rs142051161" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 26 1322 0.0197 1 1006 0.001 0 694 0 0 1008 0 0 978 0 27 5008 0.00539137
492434 "chr21:37839914:G>A" "CLDN14" "NM_144492:c.-81-5840C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs574433250" "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
492435 "chr21:37839916:G>A" "CLDN14" "NM_144492:c.-81-5842C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs543139657" "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
492436 "chr21:37839924:A>C" "CLDN14" "NM_144492:c.-81-5850T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs757852126" "This variant is a VUS because it does not have enough information."
492437 "chr21:37839974:G>A" "CLDN14" "NM_144492:c.-81-5900C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs563063355" "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
492438 "chr21:37839977:G>A" "CLDN14" "NM_144492:c.-81-5903C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs368275602" "This variant is a VUS because it does not have enough information."
492439 "chr21:37840011:T>C" "CLDN14" "NM_144492:c.-81-5937A>G" "FIVE_PRIME_INTRON" "Benign" "rs532139908" "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
492440 "chr21:37840112:G>A" "CLDN14" "NM_144492:c.-81-6038C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545600818" "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
492441 "chr21:37840157:A>T" "CLDN14" "NM_144492:c.-81-6083T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs559340543" "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
492442 "chr21:37840164:G>A" "CLDN14" "NM_144492:c.-81-6090C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs528436050" "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
492443 "chr21:37840173:A>T" "CLDN14" "NM_144492:c.-81-6099T>A" "FIVE_PRIME_INTRON" "Benign" "rs219758" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 783 1322 0.5923 291 1006 0.2893 272 694 0.3919 120 1008 0.119 409 978 0.4182 1875 5008 0.374401
492444 "chr21:37840180:C>T" "CLDN14" "NM_144492:c.-81-6106G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568479382" "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
492445 "chr21:37840203:G>A" "CLDN14" "NM_144492:c.-81-6129C>T" "FIVE_PRIME_INTRON" "Benign" "rs368060184" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
492446 "chr21:37840204:T>C" "CLDN14" "NM_144492:c.-81-6130A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs751155392" "This variant is a VUS because it does not have enough information."
492447 "chr21:37840312:G>C" "CLDN14" "NM_144492:c.-81-6238C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs551066558" "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
492448 "chr21:37840318:G>A" "CLDN14" "NM_144492:c.-81-6244C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs756535229" "This variant is a VUS because it does not have enough information."
492449 "chr21:37840325:T>C" "CLDN14" "NM_144492:c.-81-6251A>G" "FIVE_PRIME_INTRON" "Benign" "rs151176096" "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 0 694 0 0 1008 0 0 978 0 23 5008 0.00459265
492450 "chr21:37840445:C>T" "CLDN14" "NM_144492:c.-81-6371G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs186390705" "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
492451 "chr21:37840446:C>T" "CLDN14" "NM_144492:c.-81-6372G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs191638166" "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
492452 "chr21:37840461:A>G" "CLDN14" "NM_144492:c.-81-6387T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs139076602" "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
492453 "chr21:37840468:T>A" "CLDN14" "NM_144492:c.-81-6394A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs536181295" "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
492454 "chr21:37840481:G>A" "CLDN14" "NM_144492:c.-81-6407C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs144837778" "This variant is a VUS because it does not have enough information."
492455 "chr21:37840486:T>C" "CLDN14" "NM_144492:c.-81-6412A>G" "FIVE_PRIME_INTRON" "Benign" "rs78874031" "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 10 694 0.0144 0 1008 0 11 978 0.0112 27 5008 0.00539137
492456 "chr21:37840494:C>T" "CLDN14" "NM_144492:c.-81-6420G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs749861770" "This variant is a VUS because it does not have enough information."
492457 "chr21:37840512:G>A" "CLDN14" "NM_144492:c.-81-6438C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs755511993" "This variant is a VUS because it does not have enough information."
492458 "chr21:37840548:C>G" "CLDN14" "NM_144492:c.-81-6474G>C" "FIVE_PRIME_INTRON" "Benign" "rs73902529" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 51 1322 0.0386 37 1006 0.0368 44 694 0.0634 109 1008 0.1081 53 978 0.0542 294 5008 0.0587061
492459 "chr21:37840568:G>A" "CLDN14" "NM_144492:c.-81-6494C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs147919717" "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
492460 "chr21:37840595:C>T" "CLDN14" "NM_144492:c.-81-6521G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs370059267" "This variant is a VUS because it does not have enough information."
492461 "chr21:37840597:G>A" "CLDN14" "NM_144492:c.-81-6523C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs372233426" "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
492462 "chr21:37840617:G>A" "CLDN14" "NM_144492:c.-81-6543C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs576531151" "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
492463 "chr21:37840623:C>T" "CLDN14" "NM_144492:c.-81-6549G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs545592573" "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
492464 "chr21:37840641:G>A" "CLDN14" "NM_144492:c.-81-6567C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs559541034" "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
492465 "chr21:37840661:G>-" "CLDN14" "NM_144492:c.-81-6587delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs755453968" "This variant is a VUS because it does not have enough information."
492466 "chr21:37840664:C>T" "CLDN14" "NM_144492:c.-81-6590G>A" "FIVE_PRIME_INTRON" "Benign" "rs528362603" "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 0 694 0 0 1008 0 0 978 0 10 5008 0.00199681
492467 "chr21:37840760:A>G" "CLDN14" "NM_144492:c.-81-6686T>C" "FIVE_PRIME_INTRON" "Benign" "rs542137777" "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
492468 "chr21:37840788:C>T" "CLDN14" "NM_144492:c.-81-6714G>A" "FIVE_PRIME_INTRON" "Benign" "rs114438555" "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 3 694 0.0043 0 1008 0 0 978 0 21 5008 0.00419329
492469 "chr21:37840789:G>A" "CLDN14" "NM_144492:c.-81-6715C>T" "FIVE_PRIME_INTRON" "Benign" "rs60482546" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 126 1322 0.0953 12 1006 0.0119 13 694 0.0187 21 1008 0.0208 14 978 0.0143 186 5008 0.0371406
492470 "chr21:37840869:G>T" "CLDN14" "NM_144492:c.-81-6795C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs141863530" "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
492471 "chr21:37840875:AAAC>-" "CLDN14" "NM_144492:c.-81-6801_-81-6796delGTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs775391152" "This variant is a VUS because it does not have enough information."
492472 "chr21:37840876:A>G" "CLDN14" "NM_144492:c.-81-6802T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs183594309" "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 3 978 0.0031 6 5008 0.00119808
492473 "chr21:37840915:A>G" "CLDN14" "NM_144492:c.-81-6841T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs533504086" "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
492474 "chr21:37840920:AG>-" "CLDN14" "NM_144492:c.-81-6846_-81-6843delCT" "FIVE_PRIME_INTRON" "Benign" "rs57979644" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 770 1322 0.5825 290 1006 0.2883 274 694 0.3948 119 1008 0.1181 406 978 0.4151 1859 5008 0.371206
492475 "chr21:37840920:->AG" "CLDN14" "NM_144492:c.-81-6846_-81-6845insCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs760141694" "This variant is a VUS because it does not have enough information."
492476 "chr21:37840938:T>A" "CLDN14" "NM_144492:c.-81-6864A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs546863405" "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
492477 "chr21:37840950:A>G" "CLDN14" "NM_144492:c.-81-6876T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs776376747" "This variant is a VUS because it does not have enough information."
492478 "chr21:37840950:A>T" "CLDN14" "NM_144492:c.-81-6876T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs776376747" "This variant is a VUS because it does not have enough information."
492479 "chr21:37840962:C>T" "CLDN14" "NM_144492:c.-81-6888G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs567082524" "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
492480 "chr21:37840973:AG>-" "CLDN14" "NM_144492:c.-81-6899_-81-6896delCT" "FIVE_PRIME_INTRON" "Benign" "rs200329979" "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 0 694 0 0 1008 0 0 978 0 26 5008 0.00519169
492481 "chr21:37840999:A>G" "CLDN14" "NM_144492:c.-81-6925T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs759284152" "This variant is a VUS because it does not have enough information."
492482 "chr21:37841046:->TTTC" "CLDN14" "NM_144492:c.-81-6972_-81-6971insGAAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs759737399" "This variant is a VUS because it does not have enough information."
492483 "chr21:37841046:TTTC>-" "CLDN14" "NM_144492:c.-81-6972_-81-6967delGAAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs749433177" "This variant is a VUS because it does not have enough information."
492484 "chr21:37841062:->T" "CLDN14" "NM_144492:c.-81-6988_-81-6987insA" "FIVE_PRIME_INTRON" "Unknown significance" "rs767054187" "This variant is a VUS because it does not have enough information."
492485 "chr21:37841062:TTTCT>-" "CLDN14" "NM_144492:c.-81-6988_-81-6982delAGAAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs771155620" "This variant is a VUS because it does not have enough information."
492486 "chr21:37841065:C>-" "CLDN14" "NM_144492:c.-81-6991delG" "FIVE_PRIME_INTRON" "Unknown significance" "rs200418281" "This variant is a VUS because it does not have enough information."
492487 "chr21:37841065:C>T" "CLDN14" "NM_144492:c.-81-6991G>A" "FIVE_PRIME_INTRON" "Benign" "rs2845763" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 759 1322 0.5741 259 1006 0.2575 225 694 0.3242 118 1008 0.1171 387 978 0.3957 1748 5008 0.349042
492488 "chr21:37841069:T>C" "CLDN14" "NM_144492:c.-81-6995A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs187320283" "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
492489 "chr21:37841076:G>T" "CLDN14" "NM_144492:c.-81-7002C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs77781953" "This variant is a VUS because it does not have enough information."
492490 "chr21:37841089:G>T" "CLDN14" "NM_144492:c.-81-7015C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs565491593" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 1 1006 0.001 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
492491 "chr21:37841093:T>C" "CLDN14" "NM_144492:c.-81-7019A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs111884106" "This variant is a VUS because it does not have enough information."
492492 "chr21:37841094:G>C" "CLDN14" "NM_144492:c.-81-7020C>G" "FIVE_PRIME_INTRON" "Benign" "rs372228267" "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 3 694 0.0043 0 1008 0 0 978 0 21 5008 0.00419329
492493 "chr21:37841120:C>T" "CLDN14" "NM_144492:c.-81-7046G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs762454895" "This variant is a VUS because it does not have enough information."
492494 "chr21:37841135:G>A" "CLDN14" "NM_144492:c.-81-7061C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs145714412" "This variant is a VUS because it does not have enough information."
492495 "chr21:37841164:T>A" "CLDN14" "NM_144492:c.-81-7090A>T" "FIVE_PRIME_INTRON" "Benign" "rs145403854" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 25 1322 0.0189 2 1006 0.002 5 694 0.0072 0 1008 0 0 978 0 32 5008 0.00638978
492496 "chr21:37841185:G>A" "CLDN14" "NM_144492:c.-81-7111C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs576522966" "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
492497 "chr21:37841202:C>A" "CLDN14" "NM_144492:c.-81-7128G>T" "FIVE_PRIME_INTRON" "Benign" "rs149147533" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 31 1006 0.0308 58 694 0.0836 1 1008 0.001 24 978 0.0245 118 5008 0.0235623
492498 "chr21:37841203:C>T" "CLDN14" "NM_144492:c.-81-7129G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs552872481" "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
492499 "chr21:37841267:A>T" "CLDN14" "NM_144492:c.-81-7193T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs190876269" "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
492500 "chr21:37841269:G>A" "CLDN14" "NM_144492:c.-81-7195C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs368968854" "This variant is a VUS because it does not have enough information."
492501 "chr21:37841286:G>A" "CLDN14" "NM_144492:c.-81-7212C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs761504751" "This variant is a VUS because it does not have enough information."
492502 "chr21:37841293:A>G" "CLDN14" "NM_144492:c.-81-7219T>C" "FIVE_PRIME_INTRON" "Benign" "rs182336451" "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
492503 "chr21:37841318:->A" "CLDN14" "NM_144492:c.-81-7244_-81-7243insT" "FIVE_PRIME_INTRON" "Unknown significance" "rs71326691" "This variant is a VUS because it does not have enough information."
492504 "chr21:37841327:G>A" "CLDN14" "NM_144492:c.-81-7253C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs561979161" "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
492505 "chr21:37841334:A>G" "CLDN14" "NM_144492:c.-81-7260T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs1537102" "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
492506 "chr21:37841335:G>A" "CLDN14" "NM_144492:c.-81-7261C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs544607817" "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
492507 "chr21:37841354:G>A" "CLDN14" "NM_144492:c.-81-7280C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs186689228" "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 1 978 0.001 5 5008 0.000998403
492508 "chr21:37841356:A>C" "CLDN14" "NM_144492:c.-81-7282T>G" "FIVE_PRIME_INTRON" "Benign" "rs178150" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 893 1322 0.6755 300 1006 0.2982 285 694 0.4107 140 1008 0.1389 420 978 0.4294 2038 5008 0.406949
492509 "chr21:37841387:A>G" "CLDN14" "NM_144492:c.-81-7313T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs755347579" "This variant is a VUS because it does not have enough information."
492510 "chr21:37841409:G>A" "CLDN14" "NM_144492:c.-81-7335C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs375908807" "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
492511 "chr21:37841410:C>T" "CLDN14" "NM_144492:c.-81-7336G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs370606370" "This variant is a VUS because it does not have enough information."
492512 "chr21:37841412:AAAC>-" "CLDN14" "NM_144492:c.-81-7338_-81-7333delGTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs767367475" "This variant is a VUS because it does not have enough information."
492513 "chr21:37841419:C>T" "CLDN14" "NM_144492:c.-81-7345G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs779579187" "This variant is a VUS because it does not have enough information."
492514 "chr21:37841422:A>G" "CLDN14" "NM_144492:c.-81-7348T>C" "FIVE_PRIME_INTRON" "Benign" "rs148331174" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 25 1322 0.0189 2 1006 0.002 5 694 0.0072 0 1008 0 0 978 0 32 5008 0.00638978
492515 "chr21:37841424:A>G" "CLDN14" "NM_144492:c.-81-7350T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs758478730" "This variant is a VUS because it does not have enough information."
492516 "chr21:37841471:C>T" "CLDN14" "NM_144492:c.-81-7397G>A" "FIVE_PRIME_INTRON" "Benign" "rs529445171" "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
492517 "chr21:37841488:A>G" "CLDN14" "NM_144492:c.-81-7414T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs140581369" "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
492518 "chr21:37841508:C>T" "CLDN14" "NM_144492:c.-81-7434G>A" "FIVE_PRIME_INTRON" "Benign" "rs117392071" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 31 1006 0.0308 58 694 0.0836 1 1008 0.001 24 978 0.0245 118 5008 0.0235623
492519 "chr21:37841515:G>A" "CLDN14" "NM_144492:c.-81-7441C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566298382" "This variant is a VUS because it does not have enough information."
492520 "chr21:37841545:A>G" "CLDN14" "NM_144492:c.-81-7471T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs538189835" "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
492521 "chr21:37841559:A>G" "CLDN14" "NM_144492:c.-81-7485T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs550147538" "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
492522 "chr21:37841587:A>G" "CLDN14" "NM_144492:c.-81-7513T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs570144718" "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
492523 "chr21:37841604:A>C" "CLDN14" "NM_144492:c.-81-7530T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs527395236" "This variant is a VUS because it does not have enough information."
492524 "chr21:37841613:TT>-" "CLDN14" "NM_144492:c.-81-7539_-81-7536delAA" "FIVE_PRIME_INTRON" "Benign" "rs10563479" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 745 1322 0.5635 288 1006 0.2863 269 694 0.3876 119 1008 0.1181 407 978 0.4162 1828 5008 0.365016
492525 "chr21:37841613:T>C" "CLDN14" "NM_144492:c.-81-7539A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs539070803" "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
492526 "chr21:37841614:T>C" "CLDN14" "NM_144492:c.-81-7540A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs199549611" "This variant is a VUS because it does not have enough information."
492527 "chr21:37841652:G>A" "CLDN14" "NM_144492:c.-81-7578C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs747232831" "This variant is a VUS because it does not have enough information."
492528 "chr21:37841692:C>T" "CLDN14" "NM_144492:c.-81-7618G>A" "FIVE_PRIME_INTRON" "Benign" "rs56183874" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 259 1322 0.1959 98 1006 0.0974 41 694 0.0591 0 1008 0 48 978 0.0491 446 5008 0.0890575
492529 "chr21:37841693:G>T" "CLDN14" "NM_144492:c.-81-7619C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs781341032" "This variant is a VUS because it does not have enough information."
492530 "chr21:37841696:T>A" "CLDN14" "NM_144492:c.-81-7622A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs145453413" "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
492531 "chr21:37841699:->AGTC" "CLDN14" "NM_144492:c.-81-7625_-81-7624insGACT" "FIVE_PRIME_INTRON" "Unknown significance" "rs763459914" "This variant is a VUS because it does not have enough information."
492532 "chr21:37841717:T>C" "CLDN14" "NM_144492:c.-81-7643A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs535592604" "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
492533 "chr21:37841720:A>-" "CLDN14" "NM_144492:c.-81-7646delT" "FIVE_PRIME_INTRON" "Unknown significance" "rs368530113" "This variant is a VUS because it does not have enough information."
492534 "chr21:37841734:C>T" "CLDN14" "NM_144492:c.-81-7660G>A" "FIVE_PRIME_INTRON" "Benign" "rs571494825" "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
492535 "chr21:37841751:T>C" "CLDN14" "NM_144492:c.-81-7677A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs769510974" "This variant is a VUS because it does not have enough information."
492536 "chr21:37841753:C>T" "CLDN14" "NM_144492:c.-81-7679G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs575593867" "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
492537 "chr21:37841765:A>G" "CLDN14" "NM_144492:c.-81-7691T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs544546396" "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
492538 "chr21:37841781:C>T" "CLDN14" "NM_144492:c.-81-7707G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs537682991" "This variant is a VUS because it does not have enough information."
492539 "chr21:37841876:T>C" "CLDN14" "NM_144492:c.-82+7796A>G" "FIVE_PRIME_INTRON" "Benign" "rs138073961" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 25 1322 0.0189 2 1006 0.002 5 694 0.0072 0 1008 0 0 978 0 32 5008 0.00638978
492540 "chr21:37841904:A>T" "CLDN14" "NM_144492:c.-82+7768T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs762935289" "This variant is a VUS because it does not have enough information."
492541 "chr21:37841906:AAG>-" "CLDN14" "NM_144492:c.-82+7766_-82+7770delCTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs796266371" "This variant is a VUS because it does not have enough information."
492542 "chr21:37841918:G>C" "CLDN14" "NM_144492:c.-82+7754C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs9984229" "This variant is a VUS because it does not have enough information."
492543 "chr21:37841931:T>C" "CLDN14" "NM_144492:c.-82+7741A>G" "FIVE_PRIME_INTRON" "Benign" "rs191101074" "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
492544 "chr21:37841936:A>C" "CLDN14" "NM_144492:c.-82+7736T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs545917722" "This variant is a VUS because it does not have enough information."
492545 "chr21:37841952:T>C" "CLDN14" "NM_144492:c.-82+7720A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs768101447" "This variant is a VUS because it does not have enough information."
492546 "chr21:37841987:A>G" "CLDN14" "NM_144492:c.-82+7685T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs79719027" "This variant is a VUS because it does not have enough information."
492547 "chr21:37842009:A>G" "CLDN14" "NM_144492:c.-82+7663T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs568387967" "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
492548 "chr21:37842020:G>A" "CLDN14" "NM_144492:c.-82+7652C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs560585768" "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
492549 "chr21:37842039:C>G" "CLDN14" "NM_144492:c.-82+7633G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs376848703" "This variant is a VUS because it does not have enough information."
492550 "chr21:37842040:A>G" "CLDN14" "NM_144492:c.-82+7632T>C" "FIVE_PRIME_INTRON" "Benign" "rs219757" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 767 1322 0.5802 266 1006 0.2644 205 694 0.2954 139 1008 0.1379 417 978 0.4264 1794 5008 0.358227
492551 "chr21:37842049:A>G" "CLDN14" "NM_144492:c.-82+7623T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs761190387" "This variant is a VUS because it does not have enough information."
492552 "chr21:37842062:C>T" "CLDN14" "NM_144492:c.-82+7610G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs183097826" "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
492553 "chr21:37842070:G>A" "CLDN14" "NM_144492:c.-82+7602C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs767302912" "This variant is a VUS because it does not have enough information."
492554 "chr21:37842074:G>A" "CLDN14" "NM_144492:c.-82+7598C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs750041759" "This variant is a VUS because it does not have enough information."
492555 "chr21:37842099:C>G" "CLDN14" "NM_144492:c.-82+7573G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs562777671" "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
492556 "chr21:37842144:A>T" "CLDN14" "NM_144492:c.-82+7528T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs531864718" "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
492557 "chr21:37842161:C>A" "CLDN14" "NM_144492:c.-82+7511G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs528095188" "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
492558 "chr21:37842165:T>C" "CLDN14" "NM_144492:c.-82+7507A>G" "FIVE_PRIME_INTRON" "Benign" "rs74276156" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 139 1322 0.1051 12 1006 0.0119 16 694 0.0231 21 1008 0.0208 14 978 0.0143 202 5008 0.0403355
492559 "chr21:37842205:G>T" "CLDN14" "NM_144492:c.-82+7467C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs532900760" "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
492560 "chr21:37842242:TTG>-" "CLDN14" "NM_144492:c.-82+7430_-82+7434delCAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs201904668" "This variant is a VUS because it does not have enough information."
492561 "chr21:37842243:T>C" "CLDN14" "NM_144492:c.-82+7429A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs546283105" "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
492562 "chr21:37842252:T>A" "CLDN14" "NM_144492:c.-82+7420A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs765696746" "This variant is a VUS because it does not have enough information."
492563 "chr21:37842295:C>T" "CLDN14" "NM_144492:c.-82+7377G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs142548069" "This variant is a VUS because it does not have enough information."
492564 "chr21:37842302:T>G" "CLDN14" "NM_144492:c.-82+7370A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs753302330" "This variant is a VUS because it does not have enough information."
492565 "chr21:37842341:A>C" "CLDN14" "NM_144492:c.-82+7331T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs758903629" "This variant is a VUS because it does not have enough information."
492566 "chr21:37842358:C>-" "CLDN14" "NM_144492:c.-82+7314delG" "FIVE_PRIME_INTRON" "Benign" "rs553798267" "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
492567 "chr21:37842377:G>A" "CLDN14" "NM_144492:c.-82+7295C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566560424" "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
492568 "chr21:37842424:C>T" "CLDN14" "NM_144492:c.-82+7248G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs535230531" "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
492569 "chr21:37842446:G>A" "CLDN14" "NM_144492:c.-82+7226C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs188132580" "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
492570 "chr21:37842468:A>G" "CLDN14" "NM_144492:c.-82+7204T>C" "FIVE_PRIME_INTRON" "Benign" "rs219756" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 891 1322 0.674 301 1006 0.2992 285 694 0.4107 141 1008 0.1399 458 978 0.4683 2076 5008 0.414537
492571 "chr21:37842525:C>A" "CLDN14" "NM_144492:c.-82+7147G>T" "FIVE_PRIME_INTRON" "Benign" "rs146039768" "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 0 694 0 0 1008 0 0 978 0 61 5008 0.0121805
492572 "chr21:37842538:C>A" "CLDN14" "NM_144492:c.-82+7134G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs540755054" "This variant is a VUS because it does not have enough information."
492573 "chr21:37842561:G>A" "CLDN14" "NM_144492:c.-82+7111C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs558041508" "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
492574 "chr21:37842591:C>T" "CLDN14" "NM_144492:c.-82+7081G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs577999519" "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
492575 "chr21:37842592:G>A" "CLDN14" "NM_144492:c.-82+7080C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs540617344" "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
492576 "chr21:37842608:C>G" "CLDN14" "NM_144492:c.-82+7064G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs553917213" "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
492577 "chr21:37842613:G>A" "CLDN14" "NM_144492:c.-82+7059C>T" "FIVE_PRIME_INTRON" "Benign" "rs74276157" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 144 1322 0.1089 12 1006 0.0119 16 694 0.0231 21 1008 0.0208 14 978 0.0143 207 5008 0.0413339
492578 "chr21:37842650:A>G" "CLDN14" "NM_144492:c.-82+7022T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs769634500" "This variant is a VUS because it does not have enough information."
492579 "chr21:37842652:G>T" "CLDN14" "NM_144492:c.-82+7020C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs542783867" "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
492580 "chr21:37842682:C>T" "CLDN14" "NM_144492:c.-82+6990G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs562668046" "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
492581 "chr21:37842689:AG>-" "CLDN14" "NM_144492:c.-82+6983_-82+6986delCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs777797826" "This variant is a VUS because it does not have enough information."
492582 "chr21:37842694:G>A" "CLDN14" "NM_144492:c.-82+6978C>T" "FIVE_PRIME_INTRON" "Benign" "rs74535100" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 15 1006 0.0149 6 694 0.0086 0 1008 0 1 978 0.001 24 5008 0.00479233
492583 "chr21:37842699:G>A" "CLDN14" "NM_144492:c.-82+6973C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs749223849" "This variant is a VUS because it does not have enough information."
492584 "chr21:37842729:G>C" "CLDN14" "NM_144492:c.-82+6943C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs768671341" "This variant is a VUS because it does not have enough information."
492585 "chr21:37842731:ATCGCCAGCAACCCGCGGAGA>-" "CLDN14" "NM_144492:c.-82+6941_-82+6963delTCTCCGCGGGTTGCTGGCGAT" "FIVE_PRIME_INTRON" "Unknown significance" "rs781700848" "This variant is a VUS because it does not have enough information."
492586 "chr21:37842733:C>T" "CLDN14" "NM_144492:c.-82+6939G>A" "FIVE_PRIME_INTRON" "Benign" "rs77704788" "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 5 694 0.0072 0 1008 0 2 978 0.002 22 5008 0.00439297
492587 "chr21:37842734:G>A" "CLDN14" "NM_144492:c.-82+6938C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs747709629" "This variant is a VUS because it does not have enough information."
492588 "chr21:37842744:C>T" "CLDN14" "NM_144492:c.-82+6928G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs771644717" "This variant is a VUS because it does not have enough information."
492589 "chr21:37842745:G>A" "CLDN14" "NM_144492:c.-82+6927C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs565191233" "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
492590 "chr21:37842746:C>T" "CLDN14" "NM_144492:c.-82+6926G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs550757230" "This variant is a VUS because it does not have enough information."
492591 "chr21:37842754:C>T" "CLDN14" "NM_144492:c.-82+6918G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773070293" "This variant is a VUS because it does not have enough information."
492592 "chr21:37842788:A>G" "CLDN14" "NM_144492:c.-82+6884T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs528023497" "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
492593 "chr21:37842800:C>T" "CLDN14" "NM_144492:c.-82+6872G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs760395078" "This variant is a VUS because it does not have enough information."
492594 "chr21:37842814:G>A" "CLDN14" "NM_144492:c.-82+6858C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs546567564" "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
492595 "chr21:37842840:G>A" "CLDN14" "NM_144492:c.-82+6832C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs765733384" "This variant is a VUS because it does not have enough information."
492596 "chr21:37842853:A>G" "CLDN14" "NM_144492:c.-82+6819T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs776960256" "This variant is a VUS because it does not have enough information."
492597 "chr21:37842865:C>T" "CLDN14" "NM_144492:c.-82+6807G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs566372380" "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
492598 "chr21:37842891:C>G" "CLDN14" "NM_144492:c.-82+6781G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs528903845" "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
492599 "chr21:37842906:G>A" "CLDN14" "NM_144492:c.-82+6766C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs138632716" "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
492600 "chr21:37842907:T>C" "CLDN14" "NM_144492:c.-82+6765A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs568979762" "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
492601 "chr21:37842925:G>C" "CLDN14" "NM_144492:c.-82+6747C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs370122491" "This variant is a VUS because it does not have enough information."
492602 "chr21:37842930:A>G" "CLDN14" "NM_144492:c.-82+6742T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs374943888" "This variant is a VUS because it does not have enough information."
492603 "chr21:37842935:A>G" "CLDN14" "NM_144492:c.-82+6737T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs537990424" "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
492604 "chr21:37842948:A>G" "CLDN14" "NM_144492:c.-82+6724T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs558029261" "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
492605 "chr21:37842961:T>C" "CLDN14" "NM_144492:c.-82+6711A>G" "FIVE_PRIME_INTRON" "Benign" "rs60267772" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492606 "chr21:37842976:C>A" "CLDN14" "NM_144492:c.-82+6696G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs533878849" "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
492607 "chr21:37842986:G>T" "CLDN14" "NM_144492:c.-82+6686C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs554117057" "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
492608 "chr21:37842990:G>A" "CLDN14" "NM_144492:c.-82+6682C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs573926465" "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
492609 "chr21:37843010:G>A" "CLDN14" "NM_144492:c.-82+6662C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs192974799" "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
492610 "chr21:37843023:A>G" "CLDN14" "NM_144492:c.-82+6649T>C" "FIVE_PRIME_INTRON" "Benign" "rs59358275" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492611 "chr21:37843055:T>C" "CLDN14" "NM_144492:c.-82+6617A>G" "FIVE_PRIME_INTRON" "Benign" "rs57321509" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 82 1322 0.062 2 1006 0.002 11 694 0.0159 0 1008 0 0 978 0 95 5008 0.0189696
492612 "chr21:37843055:T>G" "CLDN14" "NM_144492:c.-82+6617A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs57321509" "This variant is a VUS because it does not have enough information."
492613 "chr21:37843092:T>A" "CLDN14" "NM_144492:c.-82+6580A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs764672843" "This variant is a VUS because it does not have enough information."
492614 "chr21:37843116:->A" "CLDN14" "NM_144492:c.-82+6556_-82+6557insT" "FIVE_PRIME_INTRON" "Benign" "rs200002130" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 25 1322 0.0189 1 1006 0.001 2 694 0.0029 0 1008 0 1 978 0.001 29 5008 0.00579073
492615 "chr21:37843175:G>T" "CLDN14" "NM_144492:c.-82+6497C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs751943552" "This variant is a VUS because it does not have enough information."
492616 "chr21:37843191:T>C" "CLDN14" "NM_144492:c.-82+6481A>G" "FIVE_PRIME_INTRON" "Benign" "rs115064780" "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 3 694 0.0043 0 1008 0 0 978 0 23 5008 0.00459265
492617 "chr21:37843240:C>T" "CLDN14" "NM_144492:c.-82+6432G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs757423787" "This variant is a VUS because it does not have enough information."
492618 "chr21:37843242:C>G" "CLDN14" "NM_144492:c.-82+6430G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs565180670" "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
492619 "chr21:37843243:C>T" "CLDN14" "NM_144492:c.-82+6429G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs572676554" "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
492620 "chr21:37843251:G>A" "CLDN14" "NM_144492:c.-82+6421C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs533585098" "This variant is a VUS because it does not have enough information."
492621 "chr21:37843252:T>G" "CLDN14" "NM_144492:c.-82+6420A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs767571872" "This variant is a VUS because it does not have enough information."
492622 "chr21:37843264:A>G" "CLDN14" "NM_144492:c.-82+6408T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs367947720" "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
492623 "chr21:37843280:CAAA>-" "CLDN14" "NM_144492:c.-82+6392_-82+6397delTTTG" "FIVE_PRIME_INTRON" "Benign" "rs138615906" "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 3 694 0.0043 0 1008 0 0 978 0 23 5008 0.00459265
492624 "chr21:37843321:G>A" "CLDN14" "NM_144492:c.-82+6351C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs185206406" "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
492625 "chr21:37843374:T>C" "CLDN14" "NM_144492:c.-82+6298A>G" "FIVE_PRIME_INTRON" "Benign" "rs61406199" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492626 "chr21:37843376:A>G" "CLDN14" "NM_144492:c.-82+6296T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs548999130" "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
492627 "chr21:37843377:T>C" "CLDN14" "NM_144492:c.-82+6295A>G" "FIVE_PRIME_INTRON" "Benign" "rs77075163" "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 61 1008 0.0605 34 978 0.0348 98 5008 0.0195687
492628 "chr21:37843414:C>G" "CLDN14" "NM_144492:c.-82+6258G>C" "FIVE_PRIME_INTRON" "Benign" "rs145082996" "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
492629 "chr21:37843432:A>G" "CLDN14" "NM_144492:c.-82+6240T>C" "FIVE_PRIME_INTRON" "Benign" "rs78832953" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 86 1322 0.0651 11 1006 0.0109 7 694 0.0101 21 1008 0.0208 14 978 0.0143 139 5008 0.0277556
492630 "chr21:37843444:C>T" "CLDN14" "NM_144492:c.-82+6228G>A" "FIVE_PRIME_INTRON" "Benign" "rs57457629" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492631 "chr21:37843457:G>A" "CLDN14" "NM_144492:c.-82+6215C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs534016017" "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
492632 "chr21:37843502:A>G" "CLDN14" "NM_144492:c.-82+6170T>C" "FIVE_PRIME_INTRON" "Benign" "rs56751568" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492633 "chr21:37843515:AAA>-" "CLDN14" "NM_144492:c.-82+6157_-82+6161delTTT" "FIVE_PRIME_INTRON" "Benign" "rs528151196" "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
492634 "chr21:37843518:->C" "CLDN14" "NM_144492:c.-82+6154_-82+6155insG" "FIVE_PRIME_INTRON" "Benign" "rs539993699" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 880 1322 0.6657 300 1006 0.2982 282 694 0.4063 141 1008 0.1399 430 978 0.4397 2033 5008 0.40595
492635 "chr21:37843519:A>C" "CLDN14" "NM_144492:c.-82+6153T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs2633328" "This variant is a VUS because it does not have enough information."
492636 "chr21:37843520:T>-" "CLDN14" "NM_144492:c.-82+6152delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs202192020" "This variant is a VUS because it does not have enough information."
492637 "chr21:37843519:AT>CAA" "CLDN14" "Unknown significance" "rs386818301" "This variant is a VUS because it does not have enough information."
492638 "chr21:37843520:T>A" "CLDN14" "NM_144492:c.-82+6152A>T" "FIVE_PRIME_INTRON" "Benign" "rs35303583" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 891 1322 0.674 299 1006 0.2972 282 694 0.4063 141 1008 0.1399 429 978 0.4387 2042 5008 0.407748
492639 "chr21:37843537:G>A" "CLDN14" "NM_144492:c.-82+6135C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs536199693" "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
492640 "chr21:37843596:A>G" "CLDN14" "NM_144492:c.-82+6076T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs371188254" "This variant is a VUS because it does not have enough information."
492641 "chr21:37843629:C>A" "CLDN14" "NM_144492:c.-82+6043G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs112214744" "This variant is a VUS because it does not have enough information."
492642 "chr21:37843656:A>T" "CLDN14" "NM_144492:c.-82+6016T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs560110094" "This variant is a VUS because it does not have enough information."
492643 "chr21:37843679:A>G" "CLDN14" "NM_144492:c.-82+5993T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs556185364" "This variant is a VUS because it does not have enough information." 4 1322 0.003 0 1006 0 1 694 0.0014 1 1008 0.001 0 978 0 6 5008 0.00119808
492644 "chr21:37843746:T>C" "CLDN14" "NM_144492:c.-82+5926A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs754673654" "This variant is a VUS because it does not have enough information."
492645 "chr21:37843763:C>T" "CLDN14" "NM_144492:c.-82+5909G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs576120559" "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
492646 "chr21:37843775:C>G" "CLDN14" "NM_144492:c.-82+5897G>C" "FIVE_PRIME_INTRON" "Benign" "rs538783148" "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
492647 "chr21:37843777:A>G" "CLDN14" "NM_144492:c.-82+5895T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs147165861" "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
492648 "chr21:37843781:G>A" "CLDN14" "NM_144492:c.-82+5891C>T" "FIVE_PRIME_INTRON" "Benign" "rs117651866" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 24 1006 0.0239 14 694 0.0202 0 1008 0 2 978 0.002 42 5008 0.00838658
492649 "chr21:37843789:A>G" "CLDN14" "NM_144492:c.-82+5883T>C" "FIVE_PRIME_INTRON" "Benign" "rs57067750" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492650 "chr21:37843789:AT>GTACCCA" "CLDN14" "Unknown significance" "rs386818302" "This variant is a VUS because it does not have enough information."
492651 "chr21:37843791:->ACCCA" "CLDN14" "NM_144492:c.-82+5881_-82+5882insTGGGT" "FIVE_PRIME_INTRON" "Benign" "rs143716253" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 57 1322 0.0431 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 63 5008 0.0125799
492652 "chr21:37843804:C>T" "CLDN14" "NM_144492:c.-82+5868G>A" "FIVE_PRIME_INTRON" "Benign" "rs56866008" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492653 "chr21:37843805:C>G" "CLDN14" "NM_144492:c.-82+5867G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs368369805" "This variant is a VUS because it does not have enough information."
492654 "chr21:37843867:G>A" "CLDN14" "NM_144492:c.-82+5805C>T" "FIVE_PRIME_INTRON" "Benign" "rs117892750" "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 0 181 1008 0.1796 4 978 0.0041 185 5008 0.0369409
492655 "chr21:37843931:C>G" "CLDN14" "NM_144492:c.-82+5741G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs542633087" "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
492656 "chr21:37843955:A>G" "CLDN14" "NM_144492:c.-82+5717T>C" "FIVE_PRIME_INTRON" "Benign" "rs2850102" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1129 1322 0.854 878 1006 0.8728 638 694 0.9193 683 1008 0.6776 774 978 0.7914 4102 5008 0.819089
492657 "chr21:37843961:C>T" "CLDN14" "NM_144492:c.-82+5711G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs531414846" "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
492658 "chr21:37843972:A>G" "CLDN14" "NM_144492:c.-82+5700T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs192538842" "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
492659 "chr21:37844017:A>G" "CLDN14" "NM_144492:c.-82+5655T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs565009641" "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
492660 "chr21:37844018:A>G" "CLDN14" "NM_144492:c.-82+5654T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs771769568" "This variant is a VUS because it does not have enough information."
492661 "chr21:37844019:T>C" "CLDN14" "NM_144492:c.-82+5653A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs527457289" "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
492662 "chr21:37844057:T>A" "CLDN14" "NM_144492:c.-82+5615A>T" "FIVE_PRIME_INTRON" "Benign" "rs115381856" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492663 "chr21:37844079:C>T" "CLDN14" "NM_144492:c.-82+5593G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs567446078" "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
492664 "chr21:37844080:G>A" "CLDN14" "NM_144492:c.-82+5592C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs184724507" "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
492665 "chr21:37844094:A>G" "CLDN14" "NM_144492:c.-82+5578T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs549751032" "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
492666 "chr21:37844141:->TGG" "CLDN14" "NM_144492:c.-82+5531_-82+5532insCCA" "FIVE_PRIME_INTRON" "Unknown significance" "rs369042813" "This variant is a VUS because it does not have enough information."
492667 "chr21:37844142:->GTG" "CLDN14" "NM_144492:c.-82+5530_-82+5531insCAC" "FIVE_PRIME_INTRON" "Benign" "rs10624094" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1207 1322 0.913 873 1006 0.8678 637 694 0.9179 681 1008 0.6756 770 978 0.7873 4168 5008 0.832268
492668 "chr21:37844144:->G" "CLDN14" "NM_144492:c.-82+5528_-82+5529insC" "FIVE_PRIME_INTRON" "Unknown significance" "rs375298936" "This variant is a VUS because it does not have enough information."
492669 "chr21:37844144:->GTG" "CLDN14" "NM_144492:c.-82+5528_-82+5529insCAC" "FIVE_PRIME_INTRON" "Unknown significance" "rs375298936" "This variant is a VUS because it does not have enough information."
492670 "chr21:37844179:G>T" "CLDN14" "NM_144492:c.-82+5493C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs188363187" "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
492671 "chr21:37844228:->TT" "CLDN14" "NM_144492:c.-82+5444_-82+5445insAA" "FIVE_PRIME_INTRON" "Benign" "rs142787937" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492672 "chr21:37844231:A>C" "CLDN14" "NM_144492:c.-82+5441T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs538663024" "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
492673 "chr21:37844243:C>T" "CLDN14" "NM_144492:c.-82+5429G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs11701578" "This variant is a VUS because it does not have enough information."
492674 "chr21:37844254:A>G" "CLDN14" "NM_144492:c.-82+5418T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs772812616" "This variant is a VUS because it does not have enough information."
492675 "chr21:37844266:T>C" "CLDN14" "NM_144492:c.-82+5406A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs796598182" "This variant is a VUS because it does not have enough information."
492676 "chr21:37844275:T>C" "CLDN14" "NM_144492:c.-82+5397A>G" "FIVE_PRIME_INTRON" "Benign" "rs180723446" "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 7 694 0.0101 0 1008 0 0 978 0 7 5008 0.00139776
492677 "chr21:37844287:C>T" "CLDN14" "NM_144492:c.-82+5385G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs746473178" "This variant is a VUS because it does not have enough information."
492678 "chr21:37844291:C>T" "CLDN14" "NM_144492:c.-82+5381G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs770726966" "This variant is a VUS because it does not have enough information."
492679 "chr21:37844321:T>C" "CLDN14" "NM_144492:c.-82+5351A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs376256096" "This variant is a VUS because it does not have enough information."
492680 "chr21:37844367:AAAC>-" "CLDN14" "NM_144492:c.-82+5305_-82+5310delGTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs774297488" "This variant is a VUS because it does not have enough information."
492681 "chr21:37844382:C>T" "CLDN14" "NM_144492:c.-82+5290G>A" "FIVE_PRIME_INTRON" "Benign" "rs145540755" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 24 1322 0.0182 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 27 5008 0.00539137
492682 "chr21:37844383:G>A" "CLDN14" "NM_144492:c.-82+5289C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs553721305" "This variant is a VUS because it does not have enough information."
492683 "chr21:37844424:T>C" "CLDN14" "NM_144492:c.-82+5248A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs763378091" "This variant is a VUS because it does not have enough information."
492684 "chr21:37844437:T>C" "CLDN14" "NM_144492:c.-82+5235A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs369931133" "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
492685 "chr21:37844455:G>T" "CLDN14" "NM_144492:c.-82+5217C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs764361344" "This variant is a VUS because it does not have enough information."
492686 "chr21:37844503:A>G" "CLDN14" "NM_144492:c.-82+5169T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs555183099" "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 0 978 0 3 5008 0.000599042
492687 "chr21:37844525:G>A" "CLDN14" "NM_144492:c.-82+5147C>T" "FIVE_PRIME_INTRON" "Benign" "rs74883685" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 31 1006 0.0308 58 694 0.0836 2 1008 0.002 38 978 0.0389 133 5008 0.0265575
492688 "chr21:37844572:T>C" "CLDN14" "NM_144492:c.-82+5100A>G" "FIVE_PRIME_INTRON" "Benign" "rs186491798" "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 7 694 0.0101 0 1008 0 0 978 0 7 5008 0.00139776
492689 "chr21:37844575:A>G" "CLDN14" "NM_144492:c.-82+5097T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs762285429" "This variant is a VUS because it does not have enough information."
492690 "chr21:37844583:G>C" "CLDN14" "NM_144492:c.-82+5089C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs767625169" "This variant is a VUS because it does not have enough information."
492691 "chr21:37844593:C>A" "CLDN14" "NM_144492:c.-82+5079G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs573449987" "This variant is a VUS because it does not have enough information."
492692 "chr21:37844599:G>A" "CLDN14" "NM_144492:c.-82+5073C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs767134177" "This variant is a VUS because it does not have enough information."
492693 "chr21:37844614:C>T" "CLDN14" "NM_144492:c.-82+5058G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs557710141" "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
492694 "chr21:37844618:G>A" "CLDN14" "NM_144492:c.-82+5054C>T" "FIVE_PRIME_INTRON" "Benign" "rs79008732" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 10 1006 0.0099 5 694 0.0072 21 1008 0.0208 14 978 0.0143 111 5008 0.0221645
492695 "chr21:37844662:G>-" "CLDN14" "NM_144492:c.-82+5010delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs750291910" "This variant is a VUS because it does not have enough information."
492696 "chr21:37844684:T>C" "CLDN14" "NM_144492:c.-82+4988A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs756139569" "This variant is a VUS because it does not have enough information."
492697 "chr21:37844722:G>T" "CLDN14" "NM_144492:c.-82+4950C>A" "FIVE_PRIME_INTRON" "Benign" "rs77147525" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 61 1322 0.0461 10 1006 0.0099 5 694 0.0072 21 1008 0.0208 14 978 0.0143 111 5008 0.0221645
492698 "chr21:37844768:G>T" "CLDN14" "NM_144492:c.-82+4904C>A" "FIVE_PRIME_INTRON" "Benign" "rs115456476" "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 3 694 0.0043 0 1008 0 0 978 0 21 5008 0.00419329
492699 "chr21:37844776:A>G" "CLDN14" "NM_144492:c.-82+4896T>C" "FIVE_PRIME_INTRON" "Benign" "rs76720201" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 78 1322 0.059 0 1006 0 0 694 0 0 1008 0 0 978 0 78 5008 0.0155751
492700 "chr21:37844791:A>G" "CLDN14" "NM_144492:c.-82+4881T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs540860140" "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
492701 "chr21:37844828:G>A" "CLDN14" "NM_144492:c.-82+4844C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs189754873" "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
492702 "chr21:37844842:C>T" "CLDN14" "NM_144492:c.-82+4830G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs529917730" "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
492703 "chr21:37844851:C>T" "CLDN14" "NM_144492:c.-82+4821G>A" "FIVE_PRIME_INTRON" "Benign" "rs75804435" "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 4 694 0.0058 0 1008 0 0 978 0 49 5008 0.00978435
492704 "chr21:37844856:T>C" "CLDN14" "NM_144492:c.-82+4816A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs141084471" "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
492705 "chr21:37844874:C>A" "CLDN14" "NM_144492:c.-82+4798G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs547344603" "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
492706 "chr21:37844874:C>T" "CLDN14" "NM_144492:c.-82+4798G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs547344603" "This variant is a VUS because it does not have enough information."
492707 "chr21:37844875:C>T" "CLDN14" "NM_144492:c.-82+4797G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs765801008" "This variant is a VUS because it does not have enough information."
492708 "chr21:37844892:A>G" "CLDN14" "NM_144492:c.-82+4780T>C" "FIVE_PRIME_INTRON" "Benign" "rs114763855" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 48 1322 0.0363 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 54 5008 0.0107827
492709 "chr21:37844899:A>C" "CLDN14" "NM_144492:c.-82+4773T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs566028698" "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
492710 "chr21:37844973:C>T" "CLDN14" "NM_144492:c.-82+4699G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs748170078" "This variant is a VUS because it does not have enough information."
492711 "chr21:37844997:C>T" "CLDN14" "NM_144492:c.-82+4675G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs149776602" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 2 1008 0.002 0 978 0 3 5008 0.000599042
492712 "chr21:37845005:G>A" "CLDN14" "NM_144492:c.-82+4667C>T" "FIVE_PRIME_INTRON" "Benign" "rs77793033" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 61 5008 0.0121805
492713 "chr21:37845047:G>A" "CLDN14" "NM_144492:c.-82+4625C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs746528147" "This variant is a VUS because it does not have enough information."
492714 "chr21:37845062:G>A" "CLDN14" "NM_144492:c.-82+4610C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs117745663" "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
492715 "chr21:37845065:T>G" "CLDN14" "NM_144492:c.-82+4607A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs181898636" "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
492716 "chr21:37845093:TC>-" "CLDN14" "NM_144492:c.-82+4579_-82+4582delGA" "FIVE_PRIME_INTRON" "Unknown significance" "rs780876347" "This variant is a VUS because it does not have enough information."
492717 "chr21:37845140:C>T" "CLDN14" "NM_144492:c.-82+4532G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs534222415" "This variant is a VUS because it does not have enough information."
492718 "chr21:37845141:C>T" "CLDN14" "NM_144492:c.-82+4531G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs758341521" "This variant is a VUS because it does not have enough information."
492719 "chr21:37845146:T>C" "CLDN14" "NM_144492:c.-82+4526A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs201803732" "This variant is a VUS because it does not have enough information."
492720 "chr21:37845167:A>G" "CLDN14" "NM_144492:c.-82+4505T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs372882820" "This variant is a VUS because it does not have enough information."
492721 "chr21:37845186:G>A" "CLDN14" "NM_144492:c.-82+4486C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs557650434" "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
492722 "chr21:37845194:A>G" "CLDN14" "NM_144492:c.-82+4478T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs577617738" "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
492723 "chr21:37845199:A>G" "CLDN14" "NM_144492:c.-82+4473T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs374652824" "This variant is a VUS because it does not have enough information."
492724 "chr21:37845201:C>T" "CLDN14" "NM_144492:c.-82+4471G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs770496265" "This variant is a VUS because it does not have enough information."
492725 "chr21:37845207:G>A" "CLDN14" "NM_144492:c.-82+4465C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs544676150" "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
492726 "chr21:37845226:T>C" "CLDN14" "NM_144492:c.-82+4446A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs534345122" "This variant is a VUS because it does not have enough information."
492727 "chr21:37845306:G>A" "CLDN14" "NM_144492:c.-82+4366C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs377275458" "This variant is a VUS because it does not have enough information."
492728 "chr21:37845333:C>T" "CLDN14" "NM_144492:c.-82+4339G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs558984592" "This variant is a VUS because it does not have enough information."
492729 "chr21:37845342:TCTATAGCAGGCTG>-" "CLDN14" "NM_144492:c.-82+4330_-82+4345delCAGCCTGCTATAGA" "FIVE_PRIME_INTRON" "Benign" "rs573593243" "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
492730 "chr21:37845343:C>T" "CLDN14" "NM_144492:c.-82+4329G>A" "FIVE_PRIME_INTRON" "Benign" "rs116091175" "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
492731 "chr21:37845346:T>C" "CLDN14" "NM_144492:c.-82+4326A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs572032154" "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
492732 "chr21:37845380:C>T" "CLDN14" "NM_144492:c.-82+4292G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs541150073" "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
492733 "chr21:37845381:G>A" "CLDN14" "NM_144492:c.-82+4291C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs780963027" "This variant is a VUS because it does not have enough information."
492734 "chr21:37845391:G>A" "CLDN14" "NM_144492:c.-82+4281C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs745493712" "This variant is a VUS because it does not have enough information."
492735 "chr21:37845495:C>T" "CLDN14" "NM_144492:c.-82+4177G>A" "FIVE_PRIME_INTRON" "Benign" "rs145678531" "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
492736 "chr21:37845496:C>G" "CLDN14" "NM_144492:c.-82+4176G>C" "FIVE_PRIME_INTRON" "Benign" "rs529797944" "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
492737 "chr21:37845524:G>T" "CLDN14" "NM_144492:c.-82+4148C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs543215915" "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
492738 "chr21:37845541:T>A" "CLDN14" "NM_144492:c.-82+4131A>T" "FIVE_PRIME_INTRON" "Benign" "rs116353730" "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 3 694 0.0043 0 1008 0 0 978 0 23 5008 0.00459265
492739 "chr21:37845567:A>C" "CLDN14" "NM_144492:c.-82+4105T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs764230123" "This variant is a VUS because it does not have enough information."
492740 "chr21:37845595:G>A" "CLDN14" "NM_144492:c.-82+4077C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs751644798" "This variant is a VUS because it does not have enough information."
492741 "chr21:37845634:C>G" "CLDN14" "NM_144492:c.-82+4038G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs535948893" "This variant is a VUS because it does not have enough information."
492742 "chr21:37845644:C>T" "CLDN14" "NM_144492:c.-82+4028G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs769112892" "This variant is a VUS because it does not have enough information."
492743 "chr21:37845648:G>C" "CLDN14" "NM_144492:c.-82+4024C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs555801498" "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
492744 "chr21:37845666:G>T" "CLDN14" "NM_144492:c.-82+4006C>A" "FIVE_PRIME_INTRON" "Benign" "rs140504886" "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 5 1008 0.005 0 978 0 6 5008 0.00119808
492745 "chr21:37845670:G>A" "CLDN14" "NM_144492:c.-82+4002C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs370856904" "This variant is a VUS because it does not have enough information."
492746 "chr21:37845707:G>-" "CLDN14" "NM_144492:c.-82+3965delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs769824523" "This variant is a VUS because it does not have enough information."
492747 "chr21:37845710:A>G" "CLDN14" "NM_144492:c.-82+3962T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs145731829" "This variant is a VUS because it does not have enough information."
492748 "chr21:37845771:A>G" "CLDN14" "NM_144492:c.-82+3901T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs566090969" "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
492749 "chr21:37845931:G>A" "CLDN14" "NM_144492:c.-82+3741C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs528497952" "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
492750 "chr21:37845939:T>C" "CLDN14" "NM_144492:c.-82+3733A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs186929104" "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
492751 "chr21:37845949:TGTT>-" "CLDN14" "NM_144492:c.-82+3723_-82+3728delAACA" "FIVE_PRIME_INTRON" "Benign" "rs374383937" "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 3 694 0.0043 0 1008 0 0 978 0 23 5008 0.00459265
492752 "chr21:37845964:C>T" "CLDN14" "NM_144492:c.-82+3708G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568579493" "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
492753 "chr21:37845965:G>A" "CLDN14" "NM_144492:c.-82+3707C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs537598804" "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
492754 "chr21:37845965:G>T" "CLDN14" "NM_144492:c.-82+3707C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs537598804" "This variant is a VUS because it does not have enough information."
492755 "chr21:37845980:T>C" "CLDN14" "NM_144492:c.-82+3692A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs138300518" "This variant is a VUS because it does not have enough information."
492756 "chr21:37846013:G>A" "CLDN14" "NM_144492:c.-82+3659C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs772590797" "This variant is a VUS because it does not have enough information."
492757 "chr21:37846048:T>A" "CLDN14" "NM_144492:c.-82+3624A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs773653080" "This variant is a VUS because it does not have enough information."
492758 "chr21:37846064:C>T" "CLDN14" "NM_144492:c.-82+3608G>A" "FIVE_PRIME_INTRON" "Benign" "rs115068221" "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 3 694 0.0043 0 1008 0 0 978 0 23 5008 0.00459265
492759 "chr21:37846109:C>T" "CLDN14" "NM_144492:c.-82+3563G>A" "FIVE_PRIME_INTRON" "Benign" "rs114009917" "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 3 694 0.0043 0 1008 0 0 978 0 23 5008 0.00459265
492760 "chr21:37846110:G>A" "CLDN14" "NM_144492:c.-82+3562C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs190340048" "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
492761 "chr21:37846115:G>A" "CLDN14" "NM_144492:c.-82+3557C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs754151555" "This variant is a VUS because it does not have enough information."
492762 "chr21:37846118:G>A" "CLDN14" "NM_144492:c.-82+3554C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs375195442" "This variant is a VUS because it does not have enough information."
492763 "chr21:37846119:G>A" "CLDN14" "NM_144492:c.-82+3553C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs781430821" "This variant is a VUS because it does not have enough information."
492764 "chr21:37846126:C>T" "CLDN14" "NM_144492:c.-82+3546G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759659713" "This variant is a VUS because it does not have enough information."
492765 "chr21:37846144:C>A" "CLDN14" "NM_144492:c.-82+3528G>T" "FIVE_PRIME_INTRON" "Benign" "rs114572696" "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
492766 "chr21:37846166:G>A" "CLDN14" "NM_144492:c.-82+3506C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs765455126" "This variant is a VUS because it does not have enough information."
492767 "chr21:37846197:C>T" "CLDN14" "NM_144492:c.-82+3475G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs752558554" "This variant is a VUS because it does not have enough information."
492768 "chr21:37846221:AAATC>-" "CLDN14" "NM_144492:c.-82+3451_-82+3457delGATTT" "FIVE_PRIME_INTRON" "Benign" "rs371127384" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 15 1322 0.0113 2 1006 0.002 2 694 0.0029 0 1008 0 0 978 0 19 5008 0.00379393
492769 "chr21:37846273:G>A" "CLDN14" "NM_144492:c.-82+3399C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs577462675" "This variant is a VUS because it does not have enough information."
492770 "chr21:37846282:G>A" "CLDN14" "NM_144492:c.-82+3390C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs571980786" "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
492771 "chr21:37846289:A>G" "CLDN14" "NM_144492:c.-82+3383T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs758206172" "This variant is a VUS because it does not have enough information."
492772 "chr21:37846303:G>A" "CLDN14" "NM_144492:c.-82+3369C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs534330261" "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
492773 "chr21:37846306:G>A" "CLDN14" "NM_144492:c.-82+3366C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs183247614" "This variant is a VUS because it does not have enough information."
492774 "chr21:37846381:G>A" "CLDN14" "NM_144492:c.-82+3291C>T" "FIVE_PRIME_INTRON" "Benign" "rs80177565" "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 3 694 0.0043 0 1008 0 0 978 0 23 5008 0.00459265
492775 "chr21:37846435:T>G" "CLDN14" "NM_144492:c.-82+3237A>C" "FIVE_PRIME_INTRON" "Benign" "rs141039530" "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 3 694 0.0043 0 1008 0 0 978 0 23 5008 0.00459265
492776 "chr21:37846460:A>T" "CLDN14" "NM_144492:c.-82+3212T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs543201436" "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
492777 "chr21:37846506:T>C" "CLDN14" "NM_144492:c.-82+3166A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs563176737" "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
492778 "chr21:37846511:C>G" "CLDN14" "NM_144492:c.-82+3161G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs755928882" "This variant is a VUS because it does not have enough information."
492779 "chr21:37846568:A>G" "CLDN14" "NM_144492:c.-82+3104T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs779912016" "This variant is a VUS because it does not have enough information."
492780 "chr21:37846608:A>G" "CLDN14" "NM_144492:c.-82+3064T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs749232295" "This variant is a VUS because it does not have enough information."
492781 "chr21:37846619:C>T" "CLDN14" "NM_144492:c.-82+3053G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs756848693" "This variant is a VUS because it does not have enough information."
492782 "chr21:37846620:G>A" "CLDN14" "NM_144492:c.-82+3052C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs186148936" "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
492783 "chr21:37846623:T>C" "CLDN14" "NM_144492:c.-82+3049A>G" "FIVE_PRIME_INTRON" "Benign" "rs116168116" "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
492784 "chr21:37846627:A>T" "CLDN14" "NM_144492:c.-82+3045T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs189779829" "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
492785 "chr21:37846630:C>A" "CLDN14" "NM_144492:c.-82+3042G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs780545261" "This variant is a VUS because it does not have enough information."
492786 "chr21:37846631:G>A" "CLDN14" "NM_144492:c.-82+3041C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs182736886" "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
492787 "chr21:37846641:C>G" "CLDN14" "NM_144492:c.-82+3031G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs188108342" "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
492788 "chr21:37846649:G>A" "CLDN14" "NM_144492:c.-82+3023C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs562160834" "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
492789 "chr21:37846668:A>G" "CLDN14" "NM_144492:c.-82+3004T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs531070891" "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
492790 "chr21:37846691:T>C" "CLDN14" "NM_144492:c.-82+2981A>G" "FIVE_PRIME_INTRON" "Benign" "rs148276782" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 19 1322 0.0144 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 22 5008 0.00439297
492791 "chr21:37846723:T>C" "CLDN14" "NM_144492:c.-82+2949A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs773899818" "This variant is a VUS because it does not have enough information."
492792 "chr21:37846730:G>A" "CLDN14" "NM_144492:c.-82+2942C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs141303066" "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 0 978 0 6 5008 0.00119808
492793 "chr21:37846733:C>T" "CLDN14" "NM_144492:c.-82+2939G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs539669481" "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
492794 "chr21:37846777:TA>-" "CLDN14" "NM_144492:c.-82+2895_-82+2898delTA" "FIVE_PRIME_INTRON" "Unknown significance" "rs773985646" "This variant is a VUS because it does not have enough information."
492795 "chr21:37846795:A>T" "CLDN14" "NM_144492:c.-82+2877T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs779716820" "This variant is a VUS because it does not have enough information."
492796 "chr21:37846816:G>A" "CLDN14" "NM_144492:c.-82+2856C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs374374851" "This variant is a VUS because it does not have enough information."
492797 "chr21:37846873:G>A" "CLDN14" "NM_144492:c.-82+2799C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs542531445" "This variant is a VUS because it does not have enough information."
492798 "chr21:37846911:G>A" "CLDN14" "NM_144492:c.-82+2761C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs150720100" "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
492799 "chr21:37846921:A>G" "CLDN14" "NM_144492:c.-82+2751T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs567053111" "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
492800 "chr21:37846929:G>A" "CLDN14" "NM_144492:c.-82+2743C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs560447411" "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
492801 "chr21:37846931:T>C" "CLDN14" "NM_144492:c.-82+2741A>G" "FIVE_PRIME_INTRON" "Benign" "rs192889453" "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 1 978 0.001 8 5008 0.00159744
492802 "chr21:37846932:AAC>-" "CLDN14" "NM_144492:c.-82+2740_-82+2744delGTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs773031661" "This variant is a VUS because it does not have enough information."
492803 "chr21:37846945:A>T" "CLDN14" "NM_144492:c.-82+2727T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs574179125" "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
492804 "chr21:37846995:C>G" "CLDN14" "NM_144492:c.-82+2677G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs772362811" "This variant is a VUS because it does not have enough information."
492805 "chr21:37846998:T>C" "CLDN14" "NM_144492:c.-82+2674A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs572396078" "This variant is a VUS because it does not have enough information."
492806 "chr21:37847064:A>G" "CLDN14" "NM_144492:c.-82+2608T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs536778216" "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
492807 "chr21:37847067:G>A" "CLDN14" "NM_144492:c.-82+2605C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545438409" "This variant is a VUS because it does not have enough information."
492808 "chr21:37847086:->G" "CLDN14" "NM_144492:c.-82+2586_-82+2587insC" "FIVE_PRIME_INTRON" "Unknown significance" "rs36118053" "This variant is a VUS because it does not have enough information."
492809 "chr21:37847107:G>A" "CLDN14" "NM_144492:c.-82+2565C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs771079890" "This variant is a VUS because it does not have enough information."
492810 "chr21:37847120:C>-" "CLDN14" "NM_144492:c.-82+2552delG" "FIVE_PRIME_INTRON" "Unknown significance" "rs759123701" "This variant is a VUS because it does not have enough information."
492811 "chr21:37847139:A>G" "CLDN14" "NM_144492:c.-82+2533T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs575449263" "This variant is a VUS because it does not have enough information."
492812 "chr21:37847158:G>A" "CLDN14" "NM_144492:c.-82+2514C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs556658032" "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
492813 "chr21:37847167:G>C" "CLDN14" "NM_144492:c.-82+2505C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs576933251" "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
492814 "chr21:37847170:G>A" "CLDN14" "NM_144492:c.-82+2502C>T" "FIVE_PRIME_INTRON" "Benign" "rs219755" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 692 1322 0.5234 254 1006 0.2525 209 694 0.3012 115 1008 0.1141 382 978 0.3906 1652 5008 0.329872
492815 "chr21:37847227:C>T" "CLDN14" "NM_144492:c.-82+2445G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs559553228" "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
492816 "chr21:37847247:A>T" "CLDN14" "NM_144492:c.-82+2425T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs531314036" "This variant is a VUS because it does not have enough information."
492817 "chr21:37847257:T>C" "CLDN14" "NM_144492:c.-82+2415A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs183618709" "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
492818 "chr21:37847291:C>T" "CLDN14" "NM_144492:c.-82+2381G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs542235689" "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
492819 "chr21:37847302:A>C" "CLDN14" "NM_144492:c.-82+2370T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs765385616" "This variant is a VUS because it does not have enough information."
492820 "chr21:37847328:->C" "CLDN14" "NM_144492:c.-82+2344_-82+2345insG" "FIVE_PRIME_INTRON" "Unknown significance" "rs376626468" "This variant is a VUS because it does not have enough information."
492821 "chr21:37847329:C>T" "CLDN14" "NM_144492:c.-82+2343G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs752912198" "This variant is a VUS because it does not have enough information."
492822 "chr21:37847341:C>A" "CLDN14" "NM_144492:c.-82+2331G>T" "FIVE_PRIME_INTRON" "Benign" "rs219754" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1049 1322 0.7935 303 1006 0.3012 267 694 0.3847 247 1008 0.245 465 978 0.4755 2331 5008 0.465455
492823 "chr21:37847342:G>A" "CLDN14" "NM_144492:c.-82+2330C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs137956834" "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
492824 "chr21:37847361:A>G" "CLDN14" "NM_144492:c.-82+2311T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs551068586" "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
492825 "chr21:37847375:A>G" "CLDN14" "NM_144492:c.-82+2297T>C" "FIVE_PRIME_INTRON" "Benign" "rs219753" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1061 1322 0.8026 304 1006 0.3022 270 694 0.389 251 1008 0.249 464 978 0.4744 2350 5008 0.469249
492826 "chr21:37847383:->C" "CLDN14" "NM_144492:c.-82+2289_-82+2290insG" "FIVE_PRIME_INTRON" "Unknown significance" "rs776886704" "This variant is a VUS because it does not have enough information."
492827 "chr21:37847384:C>T" "CLDN14" "NM_144492:c.-82+2288G>A" "FIVE_PRIME_INTRON" "Benign" "rs117977562" "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 1 978 0.001 12 5008 0.00239617
492828 "chr21:37847385:G>A" "CLDN14" "NM_144492:c.-82+2287C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs187551675" "This variant is a VUS because it does not have enough information."
492829 "chr21:37847390:C>T" "CLDN14" "NM_144492:c.-82+2282G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs192028523" "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
492830 "chr21:37847392:G>C" "CLDN14" "NM_144492:c.-82+2280C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs529106979" "This variant is a VUS because it does not have enough information."
492831 "chr21:37847426:A>G" "CLDN14" "NM_144492:c.-82+2246T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs781134738" "This variant is a VUS because it does not have enough information."
492832 "chr21:37847431:G>A" "CLDN14" "NM_144492:c.-82+2241C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs749932731" "This variant is a VUS because it does not have enough information."
492833 "chr21:37847446:C>T" "CLDN14" "NM_144492:c.-82+2226G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs185007116" "This variant is a VUS because it does not have enough information."
492834 "chr21:37847458:A>C" "CLDN14" "NM_144492:c.-82+2214T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs547556928" "This variant is a VUS because it does not have enough information."
492835 "chr21:37847466:G>A" "CLDN14" "NM_144492:c.-82+2206C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs370579309" "This variant is a VUS because it does not have enough information."
492836 "chr21:37847468:G>A" "CLDN14" "NM_144492:c.-82+2204C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566021896" "This variant is a VUS because it does not have enough information."
492837 "chr21:37847470:G>C" "CLDN14" "NM_144492:c.-82+2202C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs567141627" "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
492838 "chr21:37847489:G>A" "CLDN14" "NM_144492:c.-82+2183C>T" "FIVE_PRIME_INTRON" "Benign" "rs219752" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1035 1322 0.7829 335 1006 0.333 277 694 0.3991 248 1008 0.246 463 978 0.4734 2358 5008 0.470847
492839 "chr21:37847557:G>A" "CLDN14" "NM_144492:c.-82+2115C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs371882344" "This variant is a VUS because it does not have enough information."
492840 "chr21:37847571:G>C" "CLDN14" "NM_144492:c.-82+2101C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs143409582" "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
492841 "chr21:37847607:G>A" "CLDN14" "NM_144492:c.-82+2065C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs567688986" "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
492842 "chr21:37847618:C>T" "CLDN14" "NM_144492:c.-82+2054G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs376449896" "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
492843 "chr21:37847644:T>C" "CLDN14" "NM_144492:c.-82+2028A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs556599604" "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
492844 "chr21:37847649:G>C" "CLDN14" "NM_144492:c.-82+2023C>G" "FIVE_PRIME_INTRON" "Benign" "rs219751" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 891 1322 0.674 287 1006 0.2853 226 694 0.3256 117 1008 0.1161 376 978 0.3845 1897 5008 0.378794
492845 "chr21:37847651:G>A" "CLDN14" "NM_144492:c.-82+2021C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs187815538" "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 1 978 0.001 3 5008 0.000599042
492846 "chr21:37847659:C>T" "CLDN14" "NM_144492:c.-82+2013G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs538352401" "This variant is a VUS because it does not have enough information."
492847 "chr21:37847697:G>A" "CLDN14" "NM_144492:c.-82+1975C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs552933497" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 5 5008 0.000998403
492848 "chr21:37847700:G>A" "CLDN14" "NM_144492:c.-82+1972C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs219750" "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
492849 "chr21:37847725:C>T" "CLDN14" "NM_144492:c.-82+1947G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs192463128" "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
492850 "chr21:37847758:C>T" "CLDN14" "NM_144492:c.-82+1914G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs555724038" "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
492851 "chr21:37847762:G>C" "CLDN14" "NM_144492:c.-82+1910C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs575677586" "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
492852 "chr21:37847771:G>A" "CLDN14" "NM_144492:c.-82+1901C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs184437793" "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
492853 "chr21:37847804:C>T" "CLDN14" "NM_144492:c.-82+1868G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs564599367" "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
492854 "chr21:37847808:C>G" "CLDN14" "NM_144492:c.-82+1864G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs533302268" "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
492855 "chr21:37847812:C>T" "CLDN14" "NM_144492:c.-82+1860G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs189782844" "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
492856 "chr21:37847842:A>-" "CLDN14" "NM_144492:c.-82+1830delT" "FIVE_PRIME_INTRON" "Unknown significance" "rs762201633" "This variant is a VUS because it does not have enough information."
492857 "chr21:37847917:C>T" "CLDN14" "NM_144492:c.-82+1755G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs560551126" "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
492858 "chr21:37847926:G>A" "CLDN14" "NM_144492:c.-82+1746C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs529466201" "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
492859 "chr21:37847973:C>T" "CLDN14" "NM_144492:c.-82+1699G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs76382731" "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
492860 "chr21:37848016:G>A" "CLDN14" "NM_144492:c.-82+1656C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs779824412" "This variant is a VUS because it does not have enough information."
492861 "chr21:37848026:T>C" "CLDN14" "NM_144492:c.-82+1646A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs769906863" "This variant is a VUS because it does not have enough information."
492862 "chr21:37848033:A>T" "CLDN14" "NM_144492:c.-82+1639T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs374384776" "This variant is a VUS because it does not have enough information."
492863 "chr21:37848034:A>C" "CLDN14" "NM_144492:c.-82+1638T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs556354345" "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
492864 "chr21:37848035:C>T" "CLDN14" "NM_144492:c.-82+1637G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs530379849" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 4 5008 0.000798722
492865 "chr21:37848036:->TTTT" "CLDN14" "NM_144492:c.-82+1636_-82+1637insAAAA" "FIVE_PRIME_INTRON" "Benign" "rs557800353" "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 3 694 0.0043 0 1008 0 0 978 0 26 5008 0.00519169
492866 "chr21:37848038:T>A" "CLDN14" "NM_144492:c.-82+1634A>T" "FIVE_PRIME_INTRON" "Benign" "rs145581775" "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 1 1008 0.001 0 978 0 12 5008 0.00239617
492867 "chr21:37848080:C>T" "CLDN14" "NM_144492:c.-82+1592G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs570518980" "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
492868 "chr21:37848088:C>G" "CLDN14" "NM_144492:c.-82+1584G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs539193340" "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
492869 "chr21:37848101:A>G" "CLDN14" "NM_144492:c.-82+1571T>C" "FIVE_PRIME_INTRON" "Benign" "rs2850108" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1100 1322 0.8321 816 1006 0.8111 563 694 0.8112 673 1008 0.6677 736 978 0.7526 3888 5008 0.776358
492870 "chr21:37848101:A>T" "CLDN14" "NM_144492:c.-82+1571T>A" "FIVE_PRIME_INTRON" "Benign" "rs2850108" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 1322 0.0068 2 1006 0.002 4 694 0.0058 0 1008 0 0 978 0 15 5008 0.00299521
492871 "chr21:37848121:C>T" "CLDN14" "NM_144492:c.-82+1551G>A" "FIVE_PRIME_INTRON" "Benign" "rs144321230" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 24 1322 0.0182 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 25 5008 0.00499201
492872 "chr21:37848121:C>G" "CLDN14" "NM_144492:c.-82+1551G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs144321230" "This variant is a VUS because it does not have enough information."
492873 "chr21:37848147:A>C" "CLDN14" "NM_144492:c.-82+1525T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs750316056" "This variant is a VUS because it does not have enough information."
492874 "chr21:37848162:G>A" "CLDN14" "NM_144492:c.-82+1510C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs555661442" "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
492875 "chr21:37848174:C>T" "CLDN14" "NM_144492:c.-82+1498G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs575655219" "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
492876 "chr21:37848175:G>A" "CLDN14" "NM_144492:c.-82+1497C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs181380475" "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
492877 "chr21:37848182:C>T" "CLDN14" "NM_144492:c.-82+1490G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs184583821" "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
492878 "chr21:37848197:C>T" "CLDN14" "NM_144492:c.-82+1475G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs578027754" "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
492879 "chr21:37848280:A>G" "CLDN14" "NM_144492:c.-82+1392T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs540339745" "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
492880 "chr21:37848319:A>G" "CLDN14" "NM_144492:c.-82+1353T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs188996501" "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
492881 "chr21:37848320:C>T" "CLDN14" "NM_144492:c.-82+1352G>A" "FIVE_PRIME_INTRON" "Benign" "rs115900808" "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
492882 "chr21:37848321:G>A" "CLDN14" "NM_144492:c.-82+1351C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs753525443" "This variant is a VUS because it does not have enough information."
492883 "chr21:37848329:AG>-" "CLDN14" "NM_144492:c.-82+1343_-82+1346delCT" "FIVE_PRIME_INTRON" "Benign" "rs373475187" "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
492884 "chr21:37848334:G>A" "CLDN14" "NM_144492:c.-82+1338C>T" "FIVE_PRIME_INTRON" "Benign" "rs170183" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 58 1322 0.0439 543 1006 0.5398 311 694 0.4481 402 1008 0.3988 341 978 0.3487 1655 5008 0.330471
492885 "chr21:37848346:A>C" "CLDN14" "NM_144492:c.-82+1326T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs778484807" "This variant is a VUS because it does not have enough information."
492886 "chr21:37848359:T>C" "CLDN14" "NM_144492:c.-82+1313A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs546045460" "This variant is a VUS because it does not have enough information."
492887 "chr21:37848381:G>A" "CLDN14" "NM_144492:c.-82+1291C>T" "FIVE_PRIME_INTRON" "Benign" "rs79514755" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 65 1322 0.0492 11 1006 0.0109 5 694 0.0072 21 1008 0.0208 13 978 0.0133 115 5008 0.0229633
492888 "chr21:37848396:T>C" "CLDN14" "NM_144492:c.-82+1276A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs531922459" "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
492889 "chr21:37848397:C>G" "CLDN14" "NM_144492:c.-82+1275G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs775974160" "This variant is a VUS because it does not have enough information."
492890 "chr21:37848438:T>C" "CLDN14" "NM_144492:c.-82+1234A>G" "FIVE_PRIME_INTRON" "Benign" "rs219749" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1007 1322 0.7617 272 1006 0.2704 250 694 0.3602 276 1008 0.2738 395 978 0.4039 2200 5008 0.439297
492891 "chr21:37848440:G>A" "CLDN14" "NM_144492:c.-82+1232C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs781611104" "This variant is a VUS because it does not have enough information."
492892 "chr21:37848479:C>T" "CLDN14" "NM_144492:c.-82+1193G>A" "FIVE_PRIME_INTRON" "Benign" "rs219748" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1007 1322 0.7617 272 1006 0.2704 250 694 0.3602 276 1008 0.2738 395 978 0.4039 2200 5008 0.439297
492893 "chr21:37848562:G>A" "CLDN14" "NM_144492:c.-82+1110C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs375334824" "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
492894 "chr21:37848564:T>C" "CLDN14" "NM_144492:c.-82+1108A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs372989969" "This variant is a VUS because it does not have enough information."
492895 "chr21:37848567:G>C" "CLDN14" "NM_144492:c.-82+1105C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs561669971" "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
492896 "chr21:37848567:G>T" "CLDN14" "NM_144492:c.-82+1105C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs561669971" "This variant is a VUS because it does not have enough information."
492897 "chr21:37848603:C>T" "CLDN14" "NM_144492:c.-82+1069G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs57665331" "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
492898 "chr21:37848625:C>T" "CLDN14" "NM_144492:c.-82+1047G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs181437441" "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
492899 "chr21:37848626:G>A" "CLDN14" "NM_144492:c.-82+1046C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs549237945" "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
492900 "chr21:37848646:T>C" "CLDN14" "NM_144492:c.-82+1026A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs569155631" "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
492901 "chr21:37848692:C>A" "CLDN14" "NM_144492:c.-82+980G>T" "FIVE_PRIME_INTRON" "Benign" "rs148800228" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 29 1322 0.0219 0 1006 0 0 694 0 0 1008 0 0 978 0 29 5008 0.00579073
492902 "chr21:37848697:T>C" "CLDN14" "NM_144492:c.-82+975A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs770035370" "This variant is a VUS because it does not have enough information."
492903 "chr21:37848754:->T" "CLDN14" "NM_144492:c.-82+918_-82+919insA" "FIVE_PRIME_INTRON" "Benign" "rs11457181" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 365 1322 0.2761 414 1006 0.4115 267 694 0.3847 348 1008 0.3452 311 978 0.318 1705 5008 0.340455
492904 "chr21:37848767:T>G" "CLDN14" "NM_144492:c.-82+905A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs76473362" "This variant is a VUS because it does not have enough information."
492905 "chr21:37848789:C>T" "CLDN14" "NM_144492:c.-82+883G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs796770157" "This variant is a VUS because it does not have enough information."
492906 "chr21:37848796:G>A" "CLDN14" "NM_144492:c.-82+876C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs558055167" "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
492907 "chr21:37848799:G>A" "CLDN14" "NM_144492:c.-82+873C>T" "FIVE_PRIME_INTRON" "Benign" "rs142481270" "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
492908 "chr21:37848811:T>C" "CLDN14" "NM_144492:c.-82+861A>G" "FIVE_PRIME_INTRON" "Benign" "rs2845764" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1210 1322 0.9153 862 1006 0.8569 622 694 0.8963 674 1008 0.6687 753 978 0.7699 4121 5008 0.822883
492909 "chr21:37848812:G>A" "CLDN14" "NM_144492:c.-82+860C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs569164438" "This variant is a VUS because it does not have enough information."
492910 "chr21:37848843:C>A" "CLDN14" "NM_144492:c.-82+829G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs796303281" "This variant is a VUS because it does not have enough information."
492911 "chr21:37848855:A>T" "CLDN14" "NM_144492:c.-82+817T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs553928599" "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
492912 "chr21:37848891:C>T" "CLDN14" "NM_144492:c.-82+781G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs749332865" "This variant is a VUS because it does not have enough information."
492913 "chr21:37848895:C>T" "CLDN14" "NM_144492:c.-82+777G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs139548328" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 4 5008 0.000798722
492914 "chr21:37848896:G>A" "CLDN14" "NM_144492:c.-82+776C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs542804979" "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
492915 "chr21:37849023:G>A" "CLDN14" "NM_144492:c.-82+649C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs562777366" "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
492916 "chr21:37849028:C>T" "CLDN14" "NM_144492:c.-82+644G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs541276302" "This variant is a VUS because it does not have enough information."
492917 "chr21:37849029:G>A" "CLDN14" "NM_144492:c.-82+643C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs374095824" "This variant is a VUS because it does not have enough information."
492918 "chr21:37849075:C>T" "CLDN14" "NM_144492:c.-82+597G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs146583842" "This variant is a VUS because it does not have enough information." 0 1322 0 4 1006 0.004 1 694 0.0014 0 1008 0 1 978 0.001 6 5008 0.00119808
492919 "chr21:37849078:C>A" "CLDN14" "NM_144492:c.-82+594G>T" "FIVE_PRIME_INTRON" "Benign" "rs141279841" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 22 1006 0.0219 6 694 0.0086 0 1008 0 3 978 0.0031 31 5008 0.0061901
492920 "chr21:37849083:C>A" "CLDN14" "NM_144492:c.-82+589G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs201867910" "This variant is a VUS because it does not have enough information."
492921 "chr21:37849107:C>T" "CLDN14" "NM_144492:c.-82+565G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs565590175" "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
492922 "chr21:37849124:G>C" "CLDN14" "NM_144492:c.-82+548C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs186376799" "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
492923 "chr21:37849128:G>A" "CLDN14" "NM_144492:c.-82+544C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs546580007" "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
492924 "chr21:37849144:C>G" "CLDN14" "NM_144492:c.-82+528G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs560278268" "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
492925 "chr21:37849147:G>A" "CLDN14" "NM_144492:c.-82+525C>T" "FIVE_PRIME_INTRON" "Benign" "rs150142713" "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
492926 "chr21:37849169:T>G" "CLDN14" "NM_144492:c.-82+503A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs544763463" "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
492927 "chr21:37849181:T>G" "CLDN14" "NM_144492:c.-82+491A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs551668742" "This variant is a VUS because it does not have enough information."
492928 "chr21:37849239:C>A" "CLDN14" "NM_144492:c.-82+433G>T" "FIVE_PRIME_INTRON" "Benign" "rs2249115" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1211 1322 0.916 873 1006 0.8678 628 694 0.9049 676 1008 0.6706 779 978 0.7965 4167 5008 0.832069
492929 "chr21:37849280:A>C" "CLDN14" "NM_144492:c.-82+392T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs113083723" "This variant is a VUS because it does not have enough information."
492930 "chr21:37849323:G>A" "CLDN14" "NM_144492:c.-82+349C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs538059096" "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
492931 "chr21:37849330:A>G" "CLDN14" "NM_144492:c.-82+342T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs765919483" "This variant is a VUS because it does not have enough information."
492932 "chr21:37849343:C>T" "CLDN14" "NM_144492:c.-82+329G>A" "FIVE_PRIME_INTRON" "Benign" "rs145540140" "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 2 694 0.0029 1 1008 0.001 27 978 0.0276 38 5008 0.00758786
492933 "chr21:37849353:G>A" "CLDN14" "NM_144492:c.-82+319C>T" "FIVE_PRIME_INTRON" "Benign" "rs190823390" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 20 1006 0.0199 3 694 0.0043 0 1008 0 1 978 0.001 24 5008 0.00479233
492934 "chr21:37849381:T>A" "CLDN14" "NM_144492:c.-82+291A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566666378" "This variant is a VUS because it does not have enough information."
492935 "chr21:37849425:A>C" "CLDN14" "NM_144492:c.-82+247T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs533937060" "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
492936 "chr21:37849448:C>T" "CLDN14" "NM_144492:c.-82+224G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs764887097" "This variant is a VUS because it does not have enough information."
492937 "chr21:37849471:C>G" "CLDN14" "NM_144492:c.-82+201G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs369898854" "This variant is a VUS because it does not have enough information."
492938 "chr21:37849478:C>T" "CLDN14" "NM_144492:c.-82+194G>A" "FIVE_PRIME_INTRON" "Benign" "rs75840464" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 52 1322 0.0393 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 53 5008 0.0105831
492939 "chr21:37849501:A>G" "CLDN14" "NM_144492:c.-82+171T>C" "FIVE_PRIME_INTRON" "Benign" "rs2850110" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1212 1322 0.9168 873 1006 0.8678 628 694 0.9049 676 1008 0.6706 779 978 0.7965 4168 5008 0.832268
492940 "chr21:37849517:G>A" "CLDN14" "NM_144492:c.-82+155C>T" "FIVE_PRIME_INTRON" "Benign" "rs55828480" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 191 1322 0.1445 48 1006 0.0477 55 694 0.0793 158 1008 0.1567 77 978 0.0787 529 5008 0.105631
492941 "chr21:37849518:C>A" "CLDN14" "NM_144492:c.-82+154G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs556262995" "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
492942 "chr21:37849521:T>A" "CLDN14" "NM_144492:c.-82+151A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs754761552" "This variant is a VUS because it does not have enough information."
492943 "chr21:37849545:G>A" "CLDN14" "NM_144492:c.-82+127C>T" "FIVE_PRIME_INTRON" "Benign" "rs138192235" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 23 1006 0.0229 10 694 0.0144 0 1008 0 2 978 0.002 36 5008 0.0071885
492944 "chr21:37849552:G>C" "CLDN14" "NM_144492:c.-82+120C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs76552750" "This variant is a VUS because it does not have enough information."
492945 "chr21:37849553:A>T" "CLDN14" "NM_144492:c.-82+119T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs77007044" "This variant is a VUS because it does not have enough information."
492946 "chr21:37849556:T>C" "CLDN14" "NM_144492:c.-82+116A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs545595529" "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
492947 "chr21:37849559:G>C" "CLDN14" "NM_144492:c.-82+113C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs564655623" "This variant is a VUS because it does not have enough information."
492948 "chr21:37849566:C>T" "CLDN14" "NM_144492:c.-82+106G>A" "FIVE_PRIME_INTRON" "Benign" "rs143450623" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 24 1006 0.0239 14 694 0.0202 0 1008 0 2 978 0.002 42 5008 0.00838658
492949 "chr21:37849568:C>T" "CLDN14" "NM_144492:c.-82+104G>A" "FIVE_PRIME_INTRON" "Benign" "rs114289814" "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 1 694 0.0014 0 1008 0 0 978 0 19 5008 0.00379393
492950 "chr21:37849596:A>T" "CLDN14" "NM_144492:c.-82+76T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs539830032" "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
492951 "chr21:37849604:GAAAG>-" "CLDN14" "NM_144492:c.-82+68_-82+74delCTTTC" "FIVE_PRIME_INTRON" "Unknown significance" "rs755622286" "This variant is a VUS because it does not have enough information."
492952 "chr21:37849618:C>T" "CLDN14" "NM_144492:c.-82+54G>A" "FIVE_PRIME_INTRON" "Benign" "rs55801805" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 54 1006 0.0537 55 694 0.0793 1 1008 0.001 42 978 0.0429 155 5008 0.0309505
492953 "chr21:37849624:T>G" "CLDN14" "NM_144492:c.-82+48A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs528916528" "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
492954 "chr21:37849628:G>A" "CLDN14" "NM_144492:c.-82+44C>T" "FIVE_PRIME_INTRON" "Benign" "rs56260012" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 168 1322 0.1271 53 1006 0.0527 55 694 0.0793 158 1008 0.1567 78 978 0.0798 512 5008 0.102236
492955 "chr21:37849634:T>C" "CLDN14" "NM_144492:c.-82+38A>G" "FIVE_PRIME_INTRON" "Benign" "rs8132785" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 29 1322 0.0219 0 1006 0 0 694 0 0 1008 0 0 978 0 29 5008 0.00579073
492956 "chr21:37849642:C>T" "CLDN14" "NM_144492:c.-82+30G>A" "FIVE_PRIME_INTRON" "Benign" "rs145740910" "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
492957 "chr21:37849643:G>A" "CLDN14" "NM_144492:c.-82+29C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs779061727" "This variant is a VUS because it does not have enough information."
492958 "chr21:37849703:G>A" "CLDN14" "NM_144492:c.-113C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs28653283" "This variant is a VUS because it does not have enough information."
492959 "chr21:37849738:G>T" "CLDN14" "NM_144492:c.-148C>A" "FIVE_PRIME_EXON" "Unknown significance" "rs748396698" "This variant is a VUS because it does not have enough information."
492960 "chr21:37849748:G>T" "CLDN14" "NM_144492:c.-158C>A" "FIVE_PRIME_EXON" "Unknown significance" "rs771801058" "This variant is a VUS because it does not have enough information."
492961 "chr21:37849750:C>T" "CLDN14" "NM_144492:c.-160G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs181028658" "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
492962 "chr21:37849769:C>T" "CLDN14" "NM_144492:c.-179G>A" "FIVE_PRIME_EXON" "Benign" "rs73902533" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 18 400 0.045 22 320 0.06875 10 320 0.03125 120 400 0.3 13 360 0.0361111 13 200 0.065 196 2000 0.098 167 1322 0.1263 30 1006 0.0298 45 694 0.0648 158 1008 0.1567 75 978 0.0767 475 5008 0.0948482
492963 "chr21:37849782:C>G" "CLDN14" "NM_144492:c.-192G>C" "FIVE_PRIME_EXON" "Unknown significance" "rs543094379" "This variant is a VUS because it does not have enough information."
492964 "chr21:37849791:T>G" "CLDN14" "NM_144492:c.-201A>C" "FIVE_PRIME_EXON" "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
492965 "chr21:37849848:G>A" "CLDN14" "NM_144492:c.-258C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs760334550" "This variant is a VUS because it does not have enough information."
492966 "chr21:37849855:T>G" "CLDN14" "NM_144492:c.-265A>C" "FIVE_PRIME_EXON" "Unknown significance" "rs527619994" "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
492967 "chr21:37849885:G>A" "CLDN14" "NM_144492:c.-271-24C>T" "FIVE_PRIME_INTRON" "Benign" "rs219747" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 193 400 0.4825 120 320 0.375 119 320 0.371875 246 400 0.615 134 360 0.372222 117 200 0.585 929 2000 0.4645 1006 1322 0.761 251 1006 0.2495 240 694 0.3458 276 1008 0.2738 394 978 0.4029 2167 5008 0.432708
492968 "chr21:37849886:G>C" "CLDN14" "NM_144492:c.-271-25C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs746566908" "This variant is a VUS because it does not have enough information."
492969 "chr21:37849914:A>G" "CLDN14" "NM_144492:c.-271-53T>C" "FIVE_PRIME_INTRON" "Benign" "rs141183125" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 1322 0.0068 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 12 5008 0.00239617
492970 "chr21:37849932:A>C" "CLDN14" "NM_144492:c.-271-71T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs770671958" "This variant is a VUS because it does not have enough information."
492971 "chr21:37849944:C>-" "CLDN14" "NM_144492:c.-271-83delG" "FIVE_PRIME_INTRON" "Benign" "rs11365554" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1006 1322 0.761 251 1006 0.2495 240 694 0.3458 276 1008 0.2738 394 978 0.4029 2167 5008 0.432708
492972 "chr21:37849944:->C" "CLDN14" "NM_144492:c.-271-83_-271-82insG" "FIVE_PRIME_INTRON" "Unknown significance" "rs796885170" "This variant is a VUS because it does not have enough information."
492973 "chr21:37849947:C>T" "CLDN14" "NM_144492:c.-271-86G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs536264879" "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
492974 "chr21:37849951:A>G" "CLDN14" "NM_144492:c.-271-90T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs541088164" "This variant is a VUS because it does not have enough information."
492975 "chr21:37849964:G>T" "CLDN14" "NM_144492:c.-271-103C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs186061681" "This variant is a VUS because it does not have enough information."
492976 "chr21:37849978:A>G" "CLDN14" "NM_144492:c.-271-117T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs73204262" "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
492977 "chr21:37850026:C>A" "CLDN14" "NM_144492:c.-271-165G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs776498592" "This variant is a VUS because it does not have enough information."
492978 "chr21:37850027:G>A" "CLDN14" "NM_144492:c.-271-166C>T" "FIVE_PRIME_INTRON" "Benign" "rs219746" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1006 1322 0.761 251 1006 0.2495 240 694 0.3458 276 1008 0.2738 394 978 0.4029 2167 5008 0.432708
492979 "chr21:37850130:C>T" "CLDN14" "NM_144492:c.-271-269G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs538856983" "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
492980 "chr21:37850143:C>T" "CLDN14" "NM_144492:c.-271-282G>A" "FIVE_PRIME_INTRON" "Benign" "rs219745" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1006 1322 0.761 251 1006 0.2495 240 694 0.3458 276 1008 0.2738 394 978 0.4029 2167 5008 0.432708
492981 "chr21:37850154:A>G" "CLDN14" "NM_144492:c.-271-293T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs752335915" "This variant is a VUS because it does not have enough information."
492982 "chr21:37850192:C>T" "CLDN14" "NM_144492:c.-271-331G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs572628401" "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
492983 "chr21:37850258:C>G" "CLDN14" "NM_144492:c.-271-397G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs541715070" "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
492984 "chr21:37850270:G>A" "CLDN14" "NM_144492:c.-271-409C>T" "FIVE_PRIME_INTRON" "Benign" "rs219744" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1007 1322 0.7617 251 1006 0.2495 240 694 0.3458 276 1008 0.2738 394 978 0.4029 2168 5008 0.432907
492985 "chr21:37850327:C>T" "CLDN14" "NM_144492:c.-271-466G>A" "FIVE_PRIME_INTRON" "Benign" "rs76729843" "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 0 694 0 0 1008 0 0 978 0 21 5008 0.00419329
492986 "chr21:37850328:G>A" "CLDN14" "NM_144492:c.-271-467C>T" "FIVE_PRIME_INTRON" "Benign" "rs73902534" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 190 1322 0.1437 30 1006 0.0298 46 694 0.0663 158 1008 0.1567 75 978 0.0767 499 5008 0.0996406
492987 "chr21:37850390:C>G" "CLDN14" "NM_144492:c.-271-529G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs750831593" "This variant is a VUS because it does not have enough information."
492988 "chr21:37850445:A>T" "CLDN14" "NM_144492:c.-271-584T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs756479478" "This variant is a VUS because it does not have enough information."
492989 "chr21:37850468:A>G" "CLDN14" "NM_144492:c.-271-607T>C" "FIVE_PRIME_INTRON" "Benign" "rs2249234" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 788 1322 0.5961 223 1006 0.2217 196 694 0.2824 118 1008 0.1171 318 978 0.3252 1643 5008 0.328075
492990 "chr21:37850491:G>A" "CLDN14" "NM_144492:c.-271-630C>T" "FIVE_PRIME_INTRON" "Benign" "rs190585954" "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 6 978 0.0061 7 5008 0.00139776
492991 "chr21:37850522:T>C" "CLDN14" "NM_144492:c.-271-661A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs544861391" "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
492992 "chr21:37850543:C>G" "CLDN14" "NM_144492:c.-271-682G>C" "FIVE_PRIME_INTRON" "Benign" "rs115850652" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 100 1322 0.0756 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 104 5008 0.0207668
492993 "chr21:37850606:A>G" "CLDN14" "NM_144492:c.-271-745T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs183342456" "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
492994 "chr21:37850618:G>T" "CLDN14" "NM_144492:c.-271-757C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs547257436" "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
492995 "chr21:37850710:G>A" "CLDN14" "NM_144492:c.-271-849C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs549909451" "This variant is a VUS because it does not have enough information."
492996 "chr21:37850714:C>T" "CLDN14" "NM_144492:c.-271-853G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs187070979" "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
492997 "chr21:37850785:A>G" "CLDN14" "NM_144492:c.-271-924T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs748365040" "This variant is a VUS because it does not have enough information."
492998 "chr21:37850837:C>T" "CLDN14" "NM_144492:c.-272+956G>A" "FIVE_PRIME_INTRON" "Benign" "rs116230478" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 29 1322 0.0219 0 1006 0 0 694 0 0 1008 0 0 978 0 29 5008 0.00579073
492999 "chr21:37850838:G>A" "CLDN14" "NM_144492:c.-272+955C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs371326236" "This variant is a VUS because it does not have enough information."
493000 "chr21:37850844:A>T" "CLDN14" "NM_144492:c.-272+949T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs190754608" "This variant is a VUS because it does not have enough information."
493001 "chr21:37850869:C>T" "CLDN14" "NM_144492:c.-272+924G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568400309" "This variant is a VUS because it does not have enough information."
493002 "chr21:37850899:A>G" "CLDN14" "NM_144492:c.-272+894T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs375947545" "This variant is a VUS because it does not have enough information."
493003 "chr21:37850909:A>G" "CLDN14" "NM_144492:c.-272+884T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs376020833" "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
493004 "chr21:37850927:C>T" "CLDN14" "NM_144492:c.-272+866G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs760784435" "This variant is a VUS because it does not have enough information."
493005 "chr21:37850940:C>T" "CLDN14" "NM_144492:c.-272+853G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs182983686" "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
493006 "chr21:37850941:G>A" "CLDN14" "NM_144492:c.-272+852C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs746823619" "This variant is a VUS because it does not have enough information."
493007 "chr21:37850976:A>G" "CLDN14" "NM_144492:c.-272+817T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs188056875" "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
493008 "chr21:37851020:C>T" "CLDN14" "NM_144492:c.-272+773G>A" "FIVE_PRIME_INTRON" "Benign" "rs150743822" "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 12 978 0.0123 13 5008 0.00259585
493009 "chr21:37851077:G>A" "CLDN14" "NM_144492:c.-272+716C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs139922158" "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
493010 "chr21:37851080:C>T" "CLDN14" "NM_144492:c.-272+713G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs770703035" "This variant is a VUS because it does not have enough information."
493011 "chr21:37851095:A>C" "CLDN14" "NM_144492:c.-272+698T>G" "FIVE_PRIME_INTRON" "Benign" "rs219743" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 858 1322 0.649 221 1006 0.2197 194 694 0.2795 120 1008 0.119 323 978 0.3303 1716 5008 0.342652
493012 "chr21:37851123:G>A" "CLDN14" "NM_144492:c.-272+670C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs193251006" "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
493013 "chr21:37851130:C>T" "CLDN14" "NM_144492:c.-272+663G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs149398998" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 3 1008 0.003 0 978 0 5 5008 0.000998403
493014 "chr21:37851149:C>T" "CLDN14" "NM_144492:c.-272+644G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs542634864" "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
493015 "chr21:37851159:G>A" "CLDN14" "NM_144492:c.-272+634C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs556159121" "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
493016 "chr21:37851167:T>C" "CLDN14" "NM_144492:c.-272+626A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs576035147" "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
493017 "chr21:37851200:C>G" "CLDN14" "NM_144492:c.-272+593G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs113316664" "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 3 978 0.0031 4 5008 0.000798722
493018 "chr21:37851201:G>A" "CLDN14" "NM_144492:c.-272+592C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs187902110" "This variant is a VUS because it does not have enough information."
493019 "chr21:37851229:T>G" "CLDN14" "NM_144492:c.-272+564A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs13046416" "This variant is a VUS because it does not have enough information."
493020 "chr21:37851247:C>T" "CLDN14" "NM_144492:c.-272+546G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs564845894" "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
493021 "chr21:37851251:T>C" "CLDN14" "NM_144492:c.-272+542A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs769238193" "This variant is a VUS because it does not have enough information."
493022 "chr21:37851253:GA>-" "CLDN14" "NM_144492:c.-272+540_-272+543delTC" "FIVE_PRIME_INTRON" "Unknown significance" "rs796650447" "This variant is a VUS because it does not have enough information."
493023 "chr21:37851271:->C" "CLDN14" "NM_144492:c.-272+522_-272+523insG" "FIVE_PRIME_INTRON" "Unknown significance" "rs565811359" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 3 1006 0.003 0 694 0 1 1008 0.001 0 978 0 5 5008 0.000998403
493024 "chr21:37851271:C>-" "CLDN14" "NM_144492:c.-272+522delG" "FIVE_PRIME_INTRON" "Benign" "rs529578323" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 29 1322 0.0219 0 1006 0 0 694 0 0 1008 0 0 978 0 29 5008 0.00579073
493025 "chr21:37851274:C>G" "CLDN14" "NM_144492:c.-272+519G>C" "FIVE_PRIME_INTRON" "Benign" "rs146400661" "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 1 694 0.0014 0 1008 0 0 978 0 24 5008 0.00479233
493026 "chr21:37851276:C>G" "CLDN14" "NM_144492:c.-272+517G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs540833958" "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
493027 "chr21:37851277:C>G" "CLDN14" "NM_144492:c.-272+516G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs139743683" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 4 1008 0.004 0 978 0 5 5008 0.000998403
493028 "chr21:37851293:A>G" "CLDN14" "NM_144492:c.-272+500T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs529979530" "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
493029 "chr21:37851352:C>G" "CLDN14" "NM_144492:c.-272+441G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs549740880" "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
493030 "chr21:37851353:T>C" "CLDN14" "NM_144492:c.-272+440A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs192191224" "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 1 978 0.001 4 5008 0.000798722
493031 "chr21:37851361:C>T" "CLDN14" "NM_144492:c.-272+432G>A" "FIVE_PRIME_INTRON" "Benign" "rs78249536" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 18 1006 0.0179 9 694 0.013 0 1008 0 2 978 0.002 29 5008 0.00579073
493032 "chr21:37851362:G>A" "CLDN14" "NM_144492:c.-272+431C>T" "FIVE_PRIME_INTRON" "Benign" "rs552598214" "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
493033 "chr21:37851370:C>T" "CLDN14" "NM_144492:c.-272+423G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs144210481" "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
493034 "chr21:37851388:A>C" "CLDN14" "NM_144492:c.-272+405T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs184065708" "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
493035 "chr21:37851395:C>T" "CLDN14" "NM_144492:c.-272+398G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs763812305" "This variant is a VUS because it does not have enough information."
493036 "chr21:37851429:C>T" "CLDN14" "NM_144492:c.-272+364G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs548839901" "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
493037 "chr21:37851547:A>G" "CLDN14" "NM_144492:c.-272+246T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs568754137" "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
493038 "chr21:37851552:C>T" "CLDN14" "NM_144492:c.-272+241G>A" "FIVE_PRIME_INTRON" "Benign" "rs146534747" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 1322 0.0068 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 12 5008 0.00239617
493039 "chr21:37851553:G>A" "CLDN14" "NM_144492:c.-272+240C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs140078412" "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
493040 "chr21:37851569:G>C" "CLDN14" "NM_144492:c.-272+224C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs759768364" "This variant is a VUS because it does not have enough information."
493041 "chr21:37851650:G>C" "CLDN14" "NM_144492:c.-272+143C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs575958804" "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
493042 "chr21:37851659:G>A" "CLDN14" "NM_144492:c.-272+134C>T" "FIVE_PRIME_INTRON" "Benign" "rs111674447" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 8 1006 0.008 0 694 0 0 1008 0 0 978 0 11 5008 0.00219649
493043 "chr21:37851709:C>T" "CLDN14" "NM_144492:c.-272+84G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs558578944" "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
493044 "chr21:37851737:A>T" "CLDN14" "NM_144492:c.-272+56T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs571857174" "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
493045 "chr21:37851749:C>T" "CLDN14" "NM_144492:c.-272+44G>A" "FIVE_PRIME_INTRON" "Benign" "rs142376144" "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 1 694 0.0014 0 1008 0 7 978 0.0072 13 5008 0.00259585
493046 "chr21:37851756:C>T" "CLDN14" "NM_144492:c.-272+37G>A" "FIVE_PRIME_INTRON" "Benign" "rs115560288" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 78 1322 0.059 0 1006 0 0 694 0 0 1008 0 0 978 0 78 5008 0.0155751
493047 "chr21:37851760:C>T" "CLDN14" "NM_144492:c.-272+33G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs574311920" "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
493048 "chr21:37851762:C>A" "CLDN14" "NM_144492:c.-272+31G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs777896976" "This variant is a VUS because it does not have enough information."
493049 "chr21:37851781:C>T" "CLDN14" "NM_144492:c.-272+12G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs188456322" "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
493050 "chr21:37851806:C>T" "CLDN14" "NM_144492:c.-285G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs563441963" "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
493051 "chr21:37851841:C>T" "CLDN14" "NM_144492:c.-320G>A" "FIVE_PRIME_EXON" "Benign" "rs537704763" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 400 0 2 320 0.00625 0 320 0 0 400 0 0 360 0 0 200 0 2 2000 0.001
493052 "chr21:37851842:G>A" "CLDN14" "NM_144492:c.-321C>T" "FIVE_PRIME_EXON" "Benign" "rs114492024" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 400 0 2 320 0.00625 0 320 0 0 400 0 0 360 0 0 200 0 2 2000 0.001 77 1322 0.0582 0 1006 0 0 694 0 0 1008 0 0 978 0 77 5008 0.0153754
493053 "chr21:37851848:G>A" "CLDN14" "NM_144492:c.-327C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs372217521" "This variant is a VUS because it does not have enough information."
493054 "chr21:37851855:A>G" "CLDN14" "NM_144492:c.-334T>C" "FIVE_PRIME_EXON" "Unknown significance" "rs754434925" "This variant is a VUS because it does not have enough information."
493055 "chr21:37851866:A>C" "CLDN14" "NM_144492:c.-345T>G" "FIVE_PRIME_EXON" "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
493056 "chr21:37851881:T>C" "CLDN14" "NM_144492:c.-360A>G" "FIVE_PRIME_EXON" "Unknown significance" "rs552336543" "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
493057 "chr21:37851890:A>C" "CLDN14" "NM_144492:c.-369T>G" "FIVE_PRIME_EXON" "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
493058 "chr21:37851894:A>G" "CLDN14" "NM_144492:c.-373T>C" "FIVE_PRIME_EXON" "Unknown significance" "rs376974087" "This variant is a VUS because it does not have enough information."
493059 "chr21:37851897:C>T" "CLDN14" "NM_144492:c.-376G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs181645276" "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
493060 "chr21:37851902:C>T" "CLDN14" "NM_144492:c.-381G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs528630078" "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
493061 "chr21:37851906:G>A" "CLDN14" "NM_144492:c.-385C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs548778387" "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
493062 "chr21:37851909:A>C" "CLDN14" "NM_144492:c.-388T>G" "FIVE_PRIME_EXON" "Benign" "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 0 360 0 1 200 0.005 1 2000 0.0005
493063 "chr21:37851941:C>T" "CLDN14" "NM_144492:c.-420G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs151272065" "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
493064 "chr21:37851950:G>A" "CLDN14" "NM_144492:c.-429C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs369614226" "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
493065 "chr21:37851952:C>T" "CLDN14" "NM_144492:c.-431G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs551215354" "This variant is a VUS because it does not have enough information." 0 400 0 1 320 0.003125 0 320 0 0 400 0 0 360 0 0 200 0 1 2000 0.0005 1 1322 0.0008 0 1006 0 0 694 0 1 1008 0.001 0 978 0 2 5008 0.000399361
493066 "chr21:37851953:G>A" "CLDN14" "NM_144492:c.-432C>T" "FIVE_PRIME_EXON" "Benign" "rs78291168" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 29 1322 0.0219 0 1006 0 0 694 0 0 1008 0 0 978 0 29 5008 0.00579073
493067 "chr21:37851975:C>G" "CLDN14" "NM_144492:c.-454G>C" "FIVE_PRIME_EXON" "Benign" "rs188733" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 140 400 0.35 81 320 0.253125 91 320 0.284375 70 400 0.175 106 360 0.294444 61 200 0.305 549 2000 0.2745 889 1322 0.6725 223 1006 0.2217 199 694 0.2867 118 1008 0.1171 315 978 0.3221 1744 5008 0.348243
493068 "chr21:37852001:T>C" "CLDN14" "NM_144492:c.-480A>G" "FIVE_PRIME_EXON" "Benign" "rs219742" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 136 400 0.34 79 320 0.246875 92 320 0.2875 70 400 0.175 110 360 0.305556 62 200 0.31 549 2000 0.2745 839 1322 0.6346 223 1006 0.2217 198 694 0.2853 119 1008 0.1181 315 978 0.3221 1694 5008 0.338259
493069 "chr21:37852008:C>T" "CLDN14" "NM_144492:c.-487G>A" "FIVE_PRIME_EXON" "Benign" "rs140333712" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 400 0.0225 4 320 0.0125 2 320 0.00625 0 400 0 1 360 0.00277778 3 200 0.015 19 2000 0.0095 1 1322 0.0008 11 1006 0.0109 8 694 0.0115 0 1008 0 4 978 0.0041 24 5008 0.00479233
493070 "chr21:37852019:G>A" "CLDN14" "NM_144492:c.-498C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs778118245" "This variant is a VUS because it does not have enough information."
493071 "chr21:37852042:A>-" "CLDN14" "NM_144492:c.-521delT" "FIVE_PRIME_EXON" "Unknown significance" "rs758408442" "This variant is a VUS because it does not have enough information."
493072 "chr21:37852048:G>C" "CLDN14" "NM_144492:c.-527C>G" "FIVE_PRIME_EXON" "Benign" "rs117804848" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 400 0 1 320 0.003125 2 320 0.00625 0 400 0 5 360 0.0138889 1 200 0.005 9 2000 0.0045 0 1322 0 3 1006 0.003 3 694 0.0043 0 1008 0 0 978 0 6 5008 0.00119808
493073 "chr21:37852050:T>G" "CLDN14" "NM_144492:c.-529A>C" "FIVE_PRIME_EXON" "Benign" "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 0 400 0 0 360 0 1 200 0.005 2 2000 0.001
493074 "chr21:37852101:C>T" "CLDN14" "NM_144492:c.-580G>A" "FIVE_PRIME_EXON" "Benign" "rs150344346" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 400 0.0075 0 320 0 0 320 0 0 400 0 0 360 0 1 200 0.005 4 2000 0.002 0 1322 0 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 4 5008 0.000798722
493075 "chr21:37852107:A>G" "CLDN14" "NM_144492:c.-586T>C" "FIVE_PRIME_EXON" "Unknown significance" "rs574250923" "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
493076 "chr21:37852115:T>A" "CLDN14" "NM_144492:c.-594A>T" "FIVE_PRIME_EXON" "Unknown significance" "rs370189669" "This variant is a VUS because it does not have enough information."
493077 "chr21:37852125:A>C" "CLDN14" "NM_144492:c.-604T>G" "FIVE_PRIME_EXON" "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
493078 "chr21:37852147:C>T" "CLDN14" "NM_144492:c.-626G>A" "FIVE_PRIME_EXON" "Benign" "rs543253636" "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
493079 "chr21:37852156:C>T" "CLDN14" "NM_144492:c.-635G>A" "FIVE_PRIME_EXON" "Benign" "rs557217395" "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 0 360 0 1 200 0.005 1 2000 0.0005 1 1322 0.0008 0 1006 0 0 694 0 0 1008 0 0 978 0 1 5008 0.000199681
493080 "chr21:37852190:A>G" "CLDN14" "NM_144492:c.-669T>C" "FIVE_PRIME_EXON" "Unknown significance" "rs376942377" "This variant is a VUS because it does not have enough information."
493081 "chr21:37852236:C>G" "CLDN14" "NM_144492:c.-715G>C" "FIVE_PRIME_EXON" "Benign" "rs116629563" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 77 1322 0.0582 0 1006 0 0 694 0 0 1008 0 0 978 0 77 5008 0.0153754
493082 "chr21:37852242:C>T" "CLDN14" "NM_144492:c.-721G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs372584176" "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
493083 "chr21:37852243:G>A" "CLDN14" "NM_144492:c.-722C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs559813058" "This variant is a VUS because it does not have enough information." 0 400 0 0 320 0 0 320 0 1 400 0.0025 0 360 0 0 200 0 1 2000 0.0005 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
493084 "chr21:37852249:A>G" "CLDN14" "NM_144492:c.-728T>C" "FIVE_PRIME_EXON" "Unknown significance" "This variant is a VUS because it does not have enough information." 0 400 0 1 320 0.003125 0 320 0 0 400 0 0 360 0 0 200 0 1 2000 0.0005
493085 "chr21:37852334:C>T" "CLDN14" "NM_144492:c.-813G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs528517263" "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
493086 "chr21:37852341:A>C" "CLDN14" "NM_144492:c.-820T>G" "FIVE_PRIME_EXON" "Unknown significance" "rs375811545" "This variant is a VUS because it does not have enough information."
493087 "chr21:37852344:A>C" "CLDN14" "NM_144492:c.-823T>G" "FIVE_PRIME_EXON" "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
493088 "chr21:37852364:TCC>-" "CLDN14" "NM_144492:c.-843_-839delGGA" "FIVE_PRIME_EXON" "Unknown significance" "rs139003220" "This variant is a VUS because it does not have enough information."
493089 "chr21:37852388:G>A" "CLDN14" "NM_144492:c.-867C>T" "FIVE_PRIME_EXON" "Unknown significance" "rs553132355" "This variant is a VUS because it does not have enough information."
493090 "chr21:37852444:C>G" "CLDN14" "NM_001146078:c.-81-18370G>C" "FIVE_PRIME_INTRON" "Benign" "rs75853875" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 65 1322 0.0492 10 1006 0.0099 5 694 0.0072 21 1008 0.0208 12 978 0.0123 113 5008 0.0225639
493091 "chr21:37852459:G>A" "CLDN14" "NM_001146078:c.-81-18385C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs769802817" "This variant is a VUS because it does not have enough information."
493092 "chr21:37852477:G>A" "CLDN14" "NM_001146078:c.-81-18403C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs562174866" "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
493093 "chr21:37852489:C>G" "CLDN14" "NM_001146078:c.-81-18415G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs531088988" "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
493094 "chr21:37852579:C>T" "CLDN14" "NM_001146078:c.-81-18505G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs775224760" "This variant is a VUS because it does not have enough information."
493095 "chr21:37852584:C>T" "CLDN14" "NM_001146078:c.-81-18510G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs550942577" "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
493096 "chr21:37852595:G>A" "CLDN14" "NM_001146078:c.-81-18521C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs571117714" "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
493097 "chr21:37852607:G>A" "CLDN14" "NM_001146078:c.-81-18533C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs748842696" "This variant is a VUS because it does not have enough information."
493098 "chr21:37852639:A>G" "CLDN14" "NM_001146078:c.-81-18565T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs768038120" "This variant is a VUS because it does not have enough information."
493099 "chr21:37852639:A>T" "CLDN14" "NM_001146078:c.-81-18565T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs768038120" "This variant is a VUS because it does not have enough information."
493100 "chr21:37852658:G>A" "CLDN14" "NM_001146078:c.-81-18584C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545269704" "This variant is a VUS because it does not have enough information."
493101 "chr21:37852662:T>G" "CLDN14" "NM_001146078:c.-81-18588A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs761525805" "This variant is a VUS because it does not have enough information."
493102 "chr21:37852665:C>T" "CLDN14" "NM_001146078:c.-81-18591G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs370248396" "This variant is a VUS because it does not have enough information."
493103 "chr21:37852669:A>G" "CLDN14" "NM_001146078:c.-81-18595T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs533493029" "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
493104 "chr21:37852674:G>C" "CLDN14" "NM_001146078:c.-81-18600C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs547292074" "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
493105 "chr21:37852697:C>T" "CLDN14" "NM_001146078:c.-81-18623G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs147647931" "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
493106 "chr21:37852711:C>G" "CLDN14" "NM_001146078:c.-81-18637G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs142239719" "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
493107 "chr21:37852712:G>A" "CLDN14" "NM_001146078:c.-81-18638C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs184294427" "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
493108 "chr21:37852723:G>A" "CLDN14" "NM_001146078:c.-81-18649C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs567860583" "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
493109 "chr21:37852782:G>A" "CLDN14" "NM_001146078:c.-81-18708C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs777155075" "This variant is a VUS because it does not have enough information."
493110 "chr21:37852787:G>C" "CLDN14" "NM_001146078:c.-81-18713C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs537239494" "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
493111 "chr21:37852796:C>T" "CLDN14" "NM_001146078:c.-81-18722G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759775647" "This variant is a VUS because it does not have enough information."
493112 "chr21:37852797:G>T" "CLDN14" "NM_001146078:c.-81-18723C>A" "FIVE_PRIME_INTRON" "Benign" "rs73902535" "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 1 694 0.0014 0 1008 0 0 978 0 27 5008 0.00539137
493113 "chr21:37852820:T>C" "CLDN14" "NM_001146078:c.-81-18746A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs773740856" "This variant is a VUS because it does not have enough information."
493114 "chr21:37852884:T>A" "CLDN14" "NM_001146078:c.-81-18810A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs577045128" "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
493115 "chr21:37852885:A>G" "CLDN14" "NM_001146078:c.-81-18811T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs563449761" "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
493116 "chr21:37852902:C>G" "CLDN14" "NM_001146078:c.-81-18828G>C" "FIVE_PRIME_INTRON" "Benign" "rs7278260" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 77 1322 0.0582 0 1006 0 0 694 0 0 1008 0 0 978 0 77 5008 0.0153754
493117 "chr21:37852907:T>C" "CLDN14" "NM_001146078:c.-81-18833A>G" "FIVE_PRIME_INTRON" "Benign" "rs114212535" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 54 1322 0.0408 0 1006 0 5 694 0.0072 0 1008 0 1 978 0.001 60 5008 0.0119808
493118 "chr21:37852971:G>A" "CLDN14" "NM_001146078:c.-81-18897C>T" "FIVE_PRIME_INTRON" "Benign" "rs145779858" "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
493119 "chr21:37852979:C>T" "CLDN14" "NM_001146078:c.-81-18905G>A" "FIVE_PRIME_INTRON" "Benign" "rs16994155" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 24 1322 0.0182 0 1006 0 1 694 0.0014 0 1008 0 12 978 0.0123 37 5008 0.00738818
493120 "chr21:37853008:G>A" "CLDN14" "NM_001146078:c.-81-18934C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs530950679" "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
493121 "chr21:37853020:A>G" "CLDN14" "NM_001146078:c.-81-18946T>C" "FIVE_PRIME_INTRON" "Benign" "rs75639826" "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 18 694 0.0259 0 1008 0 2 978 0.002 87 5008 0.0173722
493122 "chr21:37853036:C>T" "CLDN14" "NM_001146078:c.-81-18962G>A" "FIVE_PRIME_INTRON" "Benign" "rs219741" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 842 1322 0.6369 223 1006 0.2217 195 694 0.281 119 1008 0.1181 315 978 0.3221 1694 5008 0.338259
493123 "chr21:37853045:G>C" "CLDN14" "NM_001146078:c.-81-18971C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs189498388" "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
493124 "chr21:37853045:G>T" "CLDN14" "NM_001146078:c.-81-18971C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs189498388" "This variant is a VUS because it does not have enough information."
493125 "chr21:37853059:C>T" "CLDN14" "NM_001146078:c.-81-18985G>A" "FIVE_PRIME_INTRON" "Benign" "rs143515056" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 0 1006 0 63 694 0.0908 32 1008 0.0317 2 978 0.002 101 5008 0.0201677
493126 "chr21:37853060:G>A" "CLDN14" "NM_001146078:c.-81-18986C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566825533" "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
493127 "chr21:37853079:G>C" "CLDN14" "NM_001146078:c.-81-19005C>G" "FIVE_PRIME_INTRON" "Benign" "rs2845765" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 842 1322 0.6369 223 1006 0.2217 195 694 0.281 119 1008 0.1181 315 978 0.3221 1694 5008 0.338259
493128 "chr21:37853089:G>A" "CLDN14" "NM_001146078:c.-81-19015C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs148001192" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 6 5008 0.00119808
493129 "chr21:37853092:C>A" "CLDN14" "NM_001146078:c.-81-19018G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs182398814" "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
493130 "chr21:37853099:G>A" "CLDN14" "NM_001146078:c.-81-19025C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs536774325" "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
493131 "chr21:37853106:C>T" "CLDN14" "NM_001146078:c.-81-19032G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs557040976" "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
493132 "chr21:37853124:C>T" "CLDN14" "NM_001146078:c.-81-19050G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs559457829" "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
493133 "chr21:37853126:C>T" "CLDN14" "NM_001146078:c.-81-19052G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs539628952" "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
493134 "chr21:37853135:G>A" "CLDN14" "NM_001146078:c.-81-19061C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs553259004" "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
493135 "chr21:37853153:A>G" "CLDN14" "NM_001146078:c.-81-19079T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs533251015" "This variant is a VUS because it does not have enough information."
493136 "chr21:37853154:A>G" "CLDN14" "NM_001146078:c.-81-19080T>C" "FIVE_PRIME_INTRON" "Benign" "rs187061735" "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 2 694 0.0029 0 1008 0 0 978 0 12 5008 0.00239617
493137 "chr21:37853162:C>T" "CLDN14" "NM_001146078:c.-81-19088G>A" "FIVE_PRIME_INTRON" "Benign" "rs219740" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 841 1322 0.6362 223 1006 0.2217 195 694 0.281 119 1008 0.1181 315 978 0.3221 1693 5008 0.338059
493138 "chr21:37853186:G>A" "CLDN14" "NM_001146078:c.-81-19112C>T" "FIVE_PRIME_INTRON" "Benign" "rs77229245" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 55 1322 0.0416 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 56 5008 0.0111821
493139 "chr21:37853235:C>T" "CLDN14" "NM_001146078:c.-81-19161G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs537360140" "This variant is a VUS because it does not have enough information."
493140 "chr21:37853292:C>T" "CLDN14" "NM_001146078:c.-81-19218G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs768250334" "This variant is a VUS because it does not have enough information."
493141 "chr21:37853293:G>A" "CLDN14" "NM_001146078:c.-81-19219C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs773974559" "This variant is a VUS because it does not have enough information."
493142 "chr21:37853296:A>G" "CLDN14" "NM_001146078:c.-81-19222T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs747609430" "This variant is a VUS because it does not have enough information."
493143 "chr21:37853322:G>C" "CLDN14" "NM_001146078:c.-81-19248C>G" "FIVE_PRIME_INTRON" "Benign" "rs115270476" "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 3 694 0.0043 0 1008 0 0 978 0 41 5008 0.0081869
493144 "chr21:37853342:T>C" "CLDN14" "NM_001146078:c.-81-19268A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs369032126" "This variant is a VUS because it does not have enough information."
493145 "chr21:37853360:T>C" "CLDN14" "NM_001146078:c.-81-19286A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs544343171" "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
493146 "chr21:37853362:T>-" "CLDN14" "NM_001146078:c.-81-19288delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs780811884" "This variant is a VUS because it does not have enough information."
493147 "chr21:37853387:A>G" "CLDN14" "NM_001146078:c.-81-19313T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs771879796" "This variant is a VUS because it does not have enough information."
493148 "chr21:37853421:A>G" "CLDN14" "NM_001146078:c.-81-19347T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs564611462" "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
493149 "chr21:37853471:A>G" "CLDN14" "NM_001146078:c.-81-19397T>C" "FIVE_PRIME_INTRON" "Benign" "rs578074583" "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
493150 "chr21:37853486:C>T" "CLDN14" "NM_001146078:c.-81-19412G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs146352231" "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
493151 "chr21:37853487:G>A" "CLDN14" "NM_001146078:c.-81-19413C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs759955096" "This variant is a VUS because it does not have enough information."
493152 "chr21:37853500:G>T" "CLDN14" "NM_001146078:c.-81-19426C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs770053420" "This variant is a VUS because it does not have enough information."
493153 "chr21:37853516:C>T" "CLDN14" "NM_001146078:c.-81-19442G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs191126404" "This variant is a VUS because it does not have enough information."
493154 "chr21:37853517:G>A" "CLDN14" "NM_001146078:c.-81-19443C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs776109706" "This variant is a VUS because it does not have enough information."
493155 "chr21:37853525:->C" "CLDN14" "NM_001146078:c.-81-19451_-81-19450insG" "FIVE_PRIME_INTRON" "Unknown significance" "rs148023392" "This variant is a VUS because it does not have enough information."
493156 "chr21:37853526:C>A" "CLDN14" "NM_001146078:c.-81-19452G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs180792898" "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
493157 "chr21:37853576:G>T" "CLDN14" "NM_001146078:c.-81-19502C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs764539650" "This variant is a VUS because it does not have enough information."
493158 "chr21:37853598:A>G" "CLDN14" "NM_001146078:c.-81-19524T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs185840722" "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
493159 "chr21:37853609:A>G" "CLDN14" "NM_001146078:c.-81-19535T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs547760989" "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
493160 "chr21:37853614:->C" "CLDN14" "NM_001146078:c.-81-19540_-81-19539insG" "FIVE_PRIME_INTRON" "Benign" "rs138188005" "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 1 978 0.001 13 5008 0.00259585
493161 "chr21:37853617:C>T" "CLDN14" "NM_001146078:c.-81-19543G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs190213282" "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
493162 "chr21:37853618:G>A" "CLDN14" "NM_001146078:c.-81-19544C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs139762897" "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
493163 "chr21:37853630:C>T" "CLDN14" "NM_001146078:c.-81-19556G>A" "FIVE_PRIME_INTRON" "Benign" "rs55723668" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 167 1322 0.1263 25 1006 0.0249 44 694 0.0634 158 1008 0.1567 74 978 0.0757 468 5008 0.0934505
493164 "chr21:37853659:G>A" "CLDN14" "NM_001146078:c.-81-19585C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs570531455" "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
493165 "chr21:37853665:C>T" "CLDN14" "NM_001146078:c.-81-19591G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs539641662" "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
493166 "chr21:37853676:T>C" "CLDN14" "NM_001146078:c.-81-19602A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs546858597" "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
493167 "chr21:37853688:A>G" "CLDN14" "NM_001146078:c.-81-19614T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs578185894" "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
493168 "chr21:37853736:T>C" "CLDN14" "NM_001146078:c.-81-19662A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs767739906" "This variant is a VUS because it does not have enough information."
493169 "chr21:37853739:CTTTGT>-" "CLDN14" "NM_001146078:c.-81-19665_-81-19658delACAAAG" "FIVE_PRIME_INTRON" "Unknown significance" "rs534639759" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 1 694 0.0014 1 1008 0.001 1 978 0.001 5 5008 0.000998403
493170 "chr21:37853771:A>G" "CLDN14" "NM_001146078:c.-81-19697T>C" "FIVE_PRIME_INTRON" "Benign" "rs17283840" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 205 1322 0.1551 25 1006 0.0249 47 694 0.0677 159 1008 0.1577 74 978 0.0757 510 5008 0.101837
493171 "chr21:37853811:C>T" "CLDN14" "NM_001146078:c.-81-19737G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs577816579" "This variant is a VUS because it does not have enough information."
493172 "chr21:37853812:G>A" "CLDN14" "NM_001146078:c.-81-19738C>T" "FIVE_PRIME_INTRON" "Benign" "rs2850111" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 748 1322 0.5658 223 1006 0.2217 191 694 0.2752 118 1008 0.1171 303 978 0.3098 1583 5008 0.316094
493173 "chr21:37853835:G>A" "CLDN14" "NM_001146078:c.-81-19761C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs201012704" "This variant is a VUS because it does not have enough information."
493174 "chr21:37853912:T>C" "CLDN14" "NM_001146078:c.-81-19838A>G" "FIVE_PRIME_INTRON" "Benign" "rs2845766" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1211 1322 0.916 874 1006 0.8688 628 694 0.9049 677 1008 0.6716 774 978 0.7914 4164 5008 0.83147
493175 "chr21:37853913:G>A" "CLDN14" "NM_001146078:c.-81-19839C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs768193094" "This variant is a VUS because it does not have enough information."
493176 "chr21:37853922:G>A" "CLDN14" "NM_001146078:c.-81-19848C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs575366812" "This variant is a VUS because it does not have enough information."
493177 "chr21:37853926:C>T" "CLDN14" "NM_001146078:c.-81-19852G>A" "FIVE_PRIME_INTRON" "Benign" "rs183198930" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
493178 "chr21:37853944:->T" "CLDN14" "NM_001146078:c.-81-19870_-81-19869insA" "FIVE_PRIME_INTRON" "Unknown significance" "rs35037216" "This variant is a VUS because it does not have enough information."
493179 "chr21:37853959:A>G" "CLDN14" "NM_001146078:c.-81-19885T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs369260212" "This variant is a VUS because it does not have enough information."
493180 "chr21:37853968:->G" "CLDN14" "NM_001146078:c.-81-19894_-81-19893insC" "FIVE_PRIME_INTRON" "Benign" "rs575392034" "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 3 694 0.0043 0 1008 0 0 978 0 24 5008 0.00479233
493181 "chr21:37854011:G>A" "CLDN14" "NM_001146078:c.-81-19937C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs537507278" "This variant is a VUS because it does not have enough information."
493182 "chr21:37854013:A>C" "CLDN14" "NM_001146078:c.-81-19939T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs542433746" "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
493183 "chr21:37854016:T>C" "CLDN14" "NM_001146078:c.-81-19942A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs578076852" "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
493184 "chr21:37854048:T>C" "CLDN14" "NM_001146078:c.-81-19974A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs143011618" "This variant is a VUS because it does not have enough information."
493185 "chr21:37854056:A>-" "CLDN14" "NM_001146078:c.-81-19982delT" "FIVE_PRIME_INTRON" "Unknown significance" "rs756032898" "This variant is a VUS because it does not have enough information."
493186 "chr21:37854061:A>T" "CLDN14" "NM_001146078:c.-81-19987T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs561267852" "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
493187 "chr21:37854107:G>A" "CLDN14" "NM_001146078:c.-81-20033C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs560341096" "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
493188 "chr21:37854126:A>G" "CLDN14" "NM_001146078:c.-81-20052T>C" "FIVE_PRIME_INTRON" "Benign" "rs540314843" "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 8 978 0.0082 9 5008 0.00179712
493189 "chr21:37854131:T>G" "CLDN14" "NM_001146078:c.-81-20057A>C" "FIVE_PRIME_INTRON" "Benign" "rs114354346" "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 1 694 0.0014 0 1008 0 0 978 0 24 5008 0.00479233
493190 "chr21:37854140:C>T" "CLDN14" "NM_001146078:c.-81-20066G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs563206409" "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
493191 "chr21:37854167:G>A" "CLDN14" "NM_001146078:c.-81-20093C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs560540439" "This variant is a VUS because it does not have enough information."
493192 "chr21:37854171:G>A" "CLDN14" "NM_001146078:c.-81-20097C>T" "FIVE_PRIME_INTRON" "Benign" "rs56083599" "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 25 694 0.036 0 1008 0 6 978 0.0061 95 5008 0.0189696
493193 "chr21:37854198:A>C" "CLDN14" "NM_001146078:c.-81-20124T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs570884018" "This variant is a VUS because it does not have enough information."
493194 "chr21:37854201:A>G" "CLDN14" "NM_001146078:c.-81-20127T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs541075543" "This variant is a VUS because it does not have enough information."
493195 "chr21:37854202:C>T" "CLDN14" "NM_001146078:c.-81-20128G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs550599357" "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
493196 "chr21:37854265:G>C" "CLDN14" "NM_001146078:c.-81-20191C>G" "FIVE_PRIME_INTRON" "Benign" "rs187526759" "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 3 694 0.0043 0 1008 0 0 978 0 24 5008 0.00479233
493197 "chr21:37854286:A>C" "CLDN14" "NM_001146078:c.-81-20212T>G" "FIVE_PRIME_INTRON" "Benign" "rs117271359" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 13 1006 0.0129 3 694 0.0043 0 1008 0 5 978 0.0051 24 5008 0.00479233
493198 "chr21:37854296:C>T" "CLDN14" "NM_001146078:c.-81-20222G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs546798849" "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
493199 "chr21:37854297:C>G" "CLDN14" "NM_001146078:c.-81-20223G>C" "FIVE_PRIME_INTRON" "Benign" "rs529264445" "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 0 1008 0 12 978 0.0123 14 5008 0.00279553
493200 "chr21:37854307:A>G" "CLDN14" "NM_001146078:c.-81-20233T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs775742580" "This variant is a VUS because it does not have enough information."
493201 "chr21:37854344:G>T" "CLDN14" "NM_001146078:c.-81-20270C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs535653100" "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
493202 "chr21:37854353:A>G" "CLDN14" "NM_001146078:c.-81-20279T>C" "FIVE_PRIME_INTRON" "Benign" "rs116544039" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 77 1322 0.0582 0 1006 0 0 694 0 0 1008 0 0 978 0 77 5008 0.0153754
493203 "chr21:37854363:A>G" "CLDN14" "NM_001146078:c.-81-20289T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs763338782" "This variant is a VUS because it does not have enough information."
493204 "chr21:37854364:C>T" "CLDN14" "NM_001146078:c.-81-20290G>A" "FIVE_PRIME_INTRON" "Benign" "rs2845768" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 747 1322 0.5651 225 1006 0.2237 191 694 0.2752 119 1008 0.1181 303 978 0.3098 1585 5008 0.316494
493205 "chr21:37854365:G>A" "CLDN14" "NM_001146078:c.-81-20291C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs774782331" "This variant is a VUS because it does not have enough information."
493206 "chr21:37854414:T>C" "CLDN14" "NM_001146078:c.-81-20340A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs146151919" "This variant is a VUS because it does not have enough information."
493207 "chr21:37854419:C>T" "CLDN14" "NM_001146078:c.-81-20345G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs761939419" "This variant is a VUS because it does not have enough information."
493208 "chr21:37854430:C>T" "CLDN14" "NM_001146078:c.-81-20356G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs537840533" "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
493209 "chr21:37854432:C>T" "CLDN14" "NM_001146078:c.-81-20358G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs368224931" "This variant is a VUS because it does not have enough information."
493210 "chr21:37854463:A>G" "CLDN14" "NM_001146078:c.-81-20389T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs558165768" "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
493211 "chr21:37854485:G>A" "CLDN14" "NM_001146078:c.-81-20411C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs571384264" "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
493212 "chr21:37854492:A>G" "CLDN14" "NM_001146078:c.-81-20418T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs534001943" "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
493213 "chr21:37854493:A>G" "CLDN14" "NM_001146078:c.-81-20419T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs553863693" "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
493214 "chr21:37854507:A>G" "CLDN14" "NM_001146078:c.-81-20433T>C" "FIVE_PRIME_INTRON" "Benign" "rs2850112" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 747 1322 0.5651 223 1006 0.2217 191 694 0.2752 119 1008 0.1181 303 978 0.3098 1583 5008 0.316094
493215 "chr21:37854586:T>C" "CLDN14" "NM_001146078:c.-81-20512A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs542815547" "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
493216 "chr21:37854616:A>G" "CLDN14" "NM_001146078:c.-81-20542T>C" "FIVE_PRIME_INTRON" "Benign" "rs139716587" "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 0 694 0 0 1008 0 12 978 0.0123 22 5008 0.00439297
493217 "chr21:37854627:GATGGATG>-" "CLDN14" "NM_001146078:c.-81-20553_-81-20544delCATCCATC" "FIVE_PRIME_INTRON" "Benign" "rs111623787" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 163 1322 0.1233 572 1006 0.5686 337 694 0.4856 399 1008 0.3958 354 978 0.362 1825 5008 0.364417
493218 "chr21:37854627:GATGGATGGATG>-" "CLDN14" "NM_001146078:c.-81-20553_-81-20540delCATCCATCCATC" "FIVE_PRIME_INTRON" "Benign" "rs140502654" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1038 1322 0.7852 301 1006 0.2992 291 694 0.4193 277 1008 0.2748 418 978 0.4274 2325 5008 0.464257
493219 "chr21:37854650:G>A" "CLDN14" "NM_001146078:c.-81-20576C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111832554" "This variant is a VUS because it does not have enough information."
493220 "chr21:37854654:G>A" "CLDN14" "NM_001146078:c.-81-20580C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs117251883" "This variant is a VUS because it does not have enough information."
493221 "chr21:37854657:T>C" "CLDN14" "NM_001146078:c.-81-20583A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs151159532" "This variant is a VUS because it does not have enough information."
493222 "chr21:37854662:AGAC>-" "CLDN14" "NM_001146078:c.-81-20588_-81-20583delGTCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs748485058" "This variant is a VUS because it does not have enough information."
493223 "chr21:37854662:AGACTGAC>-" "CLDN14" "NM_001146078:c.-81-20588_-81-20579delGTCAGTCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs770506492" "This variant is a VUS because it does not have enough information."
493224 "chr21:37854666:TGACGGATGGATGGATGGATGGATGGATGGATGGATGGATAGACGGAT>-" "CLDN14" "NM_001146078:c.-81-20592_-81-20543delATCCGTCTATCCATCCATCCATCCATCCATCCATCCATCCATCCGTCA" "FIVE_PRIME_INTRON" "Unknown significance" "rs148668977" "This variant is a VUS because it does not have enough information."
493225 "chr21:37854667:GACG>-" "CLDN14" "NM_001146078:c.-81-20593_-81-20588delCGTC" "FIVE_PRIME_INTRON" "Unknown significance" "rs777926744" "This variant is a VUS because it does not have enough information."
493226 "chr21:37854667:GACGGATGGATGGATGGATGGATGGATGGATGGATGGATA>-" "CLDN14" "NM_001146078:c.-81-20593_-81-20552delTATCCATCCATCCATCCATCCATCCATCCATCCATCCGTC" "FIVE_PRIME_INTRON" "Unknown significance" "rs147342622" "This variant is a VUS because it does not have enough information."
493227 "chr21:37854669:C>T" "CLDN14" "NM_001146078:c.-81-20595G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs55822624" "This variant is a VUS because it does not have enough information."
493228 "chr21:37854670:->GGAT" "CLDN14" "NM_001146078:c.-81-20596_-81-20595insATCC" "FIVE_PRIME_INTRON" "Unknown significance" "rs767207806" "This variant is a VUS because it does not have enough information."
493229 "chr21:37854670:GGAT>-" "CLDN14" "NM_001146078:c.-81-20596_-81-20591delATCC" "FIVE_PRIME_INTRON" "Unknown significance" "rs770151069" "This variant is a VUS because it does not have enough information."
493230 "chr21:37854673:T>C" "CLDN14" "NM_001146078:c.-81-20599A>G" "FIVE_PRIME_INTRON" "Benign" "rs549513247" "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 0 694 0 2 1008 0.002 12 978 0.0123 24 5008 0.00479233
493231 "chr21:37854677:T>C" "CLDN14" "NM_001146078:c.-81-20603A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs543849815" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 0 694 0 1 1008 0.001 0 978 0 6 5008 0.00119808
493232 "chr21:37854698:G>A" "CLDN14" "NM_001146078:c.-81-20624C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs56142246" "This variant is a VUS because it does not have enough information."
493233 "chr21:37854701:T>C" "CLDN14" "NM_001146078:c.-81-20627A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs766573569" "This variant is a VUS because it does not have enough information."
493234 "chr21:37854703:->GATC" "CLDN14" "NM_001146078:c.-81-20629_-81-20628insGATC" "FIVE_PRIME_INTRON" "Unknown significance" "rs745994383" "This variant is a VUS because it does not have enough information."
493235 "chr21:37854703:GATA>-" "CLDN14" "NM_001146078:c.-81-20629_-81-20624delTATC" "FIVE_PRIME_INTRON" "Unknown significance" "rs773654913" "This variant is a VUS because it does not have enough information."
493236 "chr21:37854706:AGAC>-" "CLDN14" "NM_001146078:c.-81-20632_-81-20627delGTCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs751562517" "This variant is a VUS because it does not have enough information."
493237 "chr21:37854706:A>G" "CLDN14" "NM_001146078:c.-81-20632T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs376111783" "This variant is a VUS because it does not have enough information."
493238 "chr21:37854709:C>T" "CLDN14" "NM_001146078:c.-81-20635G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs56208514" "This variant is a VUS because it does not have enough information."
493239 "chr21:37854710:->GGAT" "CLDN14" "NM_001146078:c.-81-20636_-81-20635insATCC" "FIVE_PRIME_INTRON" "Unknown significance" "rs201509970" "This variant is a VUS because it does not have enough information."
493240 "chr21:37854710:GGAT>-" "CLDN14" "NM_001146078:c.-81-20636_-81-20631delATCC" "FIVE_PRIME_INTRON" "Unknown significance" "rs75061949" "This variant is a VUS because it does not have enough information."
493241 "chr21:37854712:A>G" "CLDN14" "NM_001146078:c.-81-20638T>C" "FIVE_PRIME_INTRON" "Benign" "rs564138438" "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 11 978 0.0112 11 5008 0.00219649
493242 "chr21:37854721:T>C" "CLDN14" "NM_001146078:c.-81-20647A>G" "FIVE_PRIME_INTRON" "Benign" "rs532982461" "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 1 694 0.0014 1 1008 0.001 5 978 0.0051 9 5008 0.00179712
493243 "chr21:37854725:T>C" "CLDN14" "NM_001146078:c.-81-20651A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs540299262" "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
493244 "chr21:37854726:G>A" "CLDN14" "NM_001146078:c.-81-20652C>T" "FIVE_PRIME_INTRON" "Benign" "rs560290289" "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 0 1008 0 12 978 0.0123 15 5008 0.00299521
493245 "chr21:37854734:G>A" "CLDN14" "NM_001146078:c.-81-20660C>T" "FIVE_PRIME_INTRON" "Benign" "rs149768072" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 77 1322 0.0582 0 1006 0 0 694 0 0 1008 0 0 978 0 77 5008 0.0153754
493246 "chr21:37854737:T>C" "CLDN14" "NM_001146078:c.-81-20663A>G" "FIVE_PRIME_INTRON" "Benign" "rs144748429" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 77 1322 0.0582 0 1006 0 0 694 0 0 1008 0 0 978 0 77 5008 0.0153754
493247 "chr21:37854746:G>A" "CLDN14" "NM_001146078:c.-81-20672C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs370854306" "This variant is a VUS because it does not have enough information."
493248 "chr21:37854750:A>G" "CLDN14" "NM_001146078:c.-81-20676T>C" "FIVE_PRIME_INTRON" "Benign" "rs373974648" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 271 1322 0.205 77 1006 0.0765 60 694 0.0865 39 1008 0.0387 134 978 0.137 581 5008 0.116014
493249 "chr21:37854793:G>T" "CLDN14" "NM_001146078:c.-81-20719C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs779003681" "This variant is a VUS because it does not have enough information."
493250 "chr21:37854804:T>C" "CLDN14" "NM_001146078:c.-81-20730A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs531659885" "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
493251 "chr21:37854823:C>T" "CLDN14" "NM_001146078:c.-81-20749G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs191418396" "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
493252 "chr21:37854827:C>T" "CLDN14" "NM_001146078:c.-81-20753G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs549296225" "This variant is a VUS because it does not have enough information."
493253 "chr21:37854844:C>T" "CLDN14" "NM_001146078:c.-81-20770G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs142626006" "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
493254 "chr21:37854860:C>G" "CLDN14" "NM_001146078:c.-81-20786G>C" "FIVE_PRIME_INTRON" "Benign" "rs115582368" "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 3 694 0.0043 0 1008 0 0 978 0 41 5008 0.0081869
493255 "chr21:37854906:G>A" "CLDN14" "NM_001146078:c.-81-20832C>T" "FIVE_PRIME_INTRON" "Benign" "rs2633324" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 769 1322 0.5817 223 1006 0.2217 191 694 0.2752 119 1008 0.1181 298 978 0.3047 1600 5008 0.319489
493256 "chr21:37854936:C>T" "CLDN14" "NM_001146078:c.-81-20862G>A" "FIVE_PRIME_INTRON" "Benign" "rs13047046" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 5 1322 0.0038 30 1006 0.0298 9 694 0.013 1 1008 0.001 4 978 0.0041 49 5008 0.00978435
493257 "chr21:37854939:T>G" "CLDN14" "NM_001146078:c.-81-20865A>C" "FIVE_PRIME_INTRON" "Benign" "rs147604729" "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
493258 "chr21:37854961:C>T" "CLDN14" "NM_001146078:c.-81-20887G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs142278962" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 3 5008 0.000599042
493259 "chr21:37855021:T>A" "CLDN14" "NM_001146078:c.-81-20947A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs576641564" "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
493260 "chr21:37855029:GTG>-" "CLDN14" "NM_001146078:c.-81-20955_-81-20951delCAC" "FIVE_PRIME_INTRON" "Unknown significance" "rs759712284" "This variant is a VUS because it does not have enough information."
493261 "chr21:37855082:C>T" "CLDN14" "NM_001146078:c.-81-21008G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs184109768" "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
493262 "chr21:37855082:C>A" "CLDN14" "NM_001146078:c.-81-21008G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs184109768" "This variant is a VUS because it does not have enough information."
493263 "chr21:37855105:T>C" "CLDN14" "NM_001146078:c.-81-21031A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs373917702" "This variant is a VUS because it does not have enough information."
493264 "chr21:37855121:T>G" "CLDN14" "NM_001146078:c.-81-21047A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs749629982" "This variant is a VUS because it does not have enough information."
493265 "chr21:37855143:G>C" "CLDN14" "NM_001146078:c.-81-21069C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs768995766" "This variant is a VUS because it does not have enough information."
493266 "chr21:37855154:G>A" "CLDN14" "NM_001146078:c.-81-21080C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs762776179" "This variant is a VUS because it does not have enough information."
493267 "chr21:37855170:C>A" "CLDN14" "NM_001146078:c.-81-21096G>T" "FIVE_PRIME_INTRON" "Benign" "rs78405027" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 26 1322 0.0197 53 1006 0.0527 56 694 0.0807 1 1008 0.001 42 978 0.0429 178 5008 0.0355431
493268 "chr21:37855197:C>T" "CLDN14" "NM_001146078:c.-81-21123G>A" "FIVE_PRIME_INTRON" "Benign" "rs144556564" "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 0 1008 0 0 978 0 12 5008 0.00239617
493269 "chr21:37855211:T>A" "CLDN14" "NM_001146078:c.-81-21137A>T" "FIVE_PRIME_INTRON" "Benign" "rs147845559" "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 1 694 0.0014 0 1008 0 18 978 0.0184 21 5008 0.00419329
493270 "chr21:37855216:G>T" "CLDN14" "NM_001146078:c.-81-21142C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs772186841" "This variant is a VUS because it does not have enough information."
493271 "chr21:37855237:C>T" "CLDN14" "NM_001146078:c.-81-21163G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs560278162" "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
493272 "chr21:37855238:G>A" "CLDN14" "NM_001146078:c.-81-21164C>T" "FIVE_PRIME_INTRON" "Benign" "rs140119285" "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 33 1008 0.0327 0 978 0 33 5008 0.00658946
493273 "chr21:37855280:T>C" "CLDN14" "NM_001146078:c.-81-21206A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs773185592" "This variant is a VUS because it does not have enough information."
493274 "chr21:37855285:C>T" "CLDN14" "NM_001146078:c.-81-21211G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs760765456" "This variant is a VUS because it does not have enough information."
493275 "chr21:37855298:T>C" "CLDN14" "NM_001146078:c.-81-21224A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs188661869" "This variant is a VUS because it does not have enough information."
493276 "chr21:37855332:G>A" "CLDN14" "NM_001146078:c.-81-21258C>T" "FIVE_PRIME_INTRON" "Benign" "rs73902536" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 170 1322 0.1286 25 1006 0.0249 44 694 0.0634 158 1008 0.1567 86 978 0.0879 483 5008 0.0964457
493277 "chr21:37855383:C>T" "CLDN14" "NM_001146078:c.-81-21309G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs562673916" "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
493278 "chr21:37855396:C>A" "CLDN14" "NM_001146078:c.-81-21322G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs372747752" "This variant is a VUS because it does not have enough information."
493279 "chr21:37855421:C>T" "CLDN14" "NM_001146078:c.-81-21347G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs562939191" "This variant is a VUS because it does not have enough information."
493280 "chr21:37855436:C>T" "CLDN14" "NM_001146078:c.-81-21362G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs765096506" "This variant is a VUS because it does not have enough information."
493281 "chr21:37855474:A>G" "CLDN14" "NM_001146078:c.-81-21400T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs375896466" "This variant is a VUS because it does not have enough information."
493282 "chr21:37855485:A>G" "CLDN14" "NM_001146078:c.-81-21411T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs752734441" "This variant is a VUS because it does not have enough information."
493283 "chr21:37855529:C>T" "CLDN14" "NM_001146078:c.-81-21455G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs531421891" "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
493284 "chr21:37855531:G>A" "CLDN14" "NM_001146078:c.-81-21457C>T" "FIVE_PRIME_INTRON" "Benign" "rs75430464" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 18 1006 0.0179 8 694 0.0115 0 1008 0 2 978 0.002 28 5008 0.00559105
493285 "chr21:37855540:TGT>-" "CLDN14" "NM_001146078:c.-81-21466_-81-21462delACA" "FIVE_PRIME_INTRON" "Benign" "rs139362637" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
493286 "chr21:37855542:T>G" "CLDN14" "NM_001146078:c.-81-21468A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs571212459" "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
493287 "chr21:37855570:C>G" "CLDN14" "NM_001146078:c.-81-21496G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs192769438" "This variant is a VUS because it does not have enough information."
493288 "chr21:37855575:C>T" "CLDN14" "NM_001146078:c.-81-21501G>A" "FIVE_PRIME_INTRON" "Benign" "rs77868469" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 169 1322 0.1278 25 1006 0.0249 60 694 0.0865 162 1008 0.1607 74 978 0.0757 490 5008 0.0978435
493289 "chr21:37855578:C>T" "CLDN14" "NM_001146078:c.-81-21504G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs547428327" "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
493290 "chr21:37855579:G>A" "CLDN14" "NM_001146078:c.-81-21505C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs567408488" "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
493291 "chr21:37855589:G>-" "CLDN14" "NM_001146078:c.-81-21515delC" "FIVE_PRIME_INTRON" "Benign" "rs66518968" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1210 1322 0.9153 873 1006 0.8678 628 694 0.9049 676 1008 0.6706 769 978 0.7863 4156 5008 0.829872
493292 "chr21:37855589:G>A" "CLDN14" "NM_001146078:c.-81-21515C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs200745243" "This variant is a VUS because it does not have enough information."
493293 "chr21:37855595:C>T" "CLDN14" "NM_001146078:c.-81-21521G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs536783312" "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
493294 "chr21:37855603:G>T" "CLDN14" "NM_001146078:c.-81-21529C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs778096459" "This variant is a VUS because it does not have enough information."
493295 "chr21:37855604:C>T" "CLDN14" "NM_001146078:c.-81-21530G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs150288921" "This variant is a VUS because it does not have enough information."
493296 "chr21:37855605:G>C" "CLDN14" "NM_001146078:c.-81-21531C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs550030384" "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
493297 "chr21:37855605:G>A" "CLDN14" "NM_001146078:c.-81-21531C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs550030384" "This variant is a VUS because it does not have enough information."
493298 "chr21:37855611:G>A" "CLDN14" "NM_001146078:c.-81-21537C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs570199479" "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
493299 "chr21:37855640:C>G" "CLDN14" "NM_001146078:c.-81-21566G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs756734277" "This variant is a VUS because it does not have enough information."
493300 "chr21:37855644:G>T" "CLDN14" "NM_001146078:c.-81-21570C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs538871519" "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
493301 "chr21:37855664:G>A" "CLDN14" "NM_001146078:c.-81-21590C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs577298761" "This variant is a VUS because it does not have enough information."
493302 "chr21:37855700:C>T" "CLDN14" "NM_001146078:c.-81-21626G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs559288211" "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
493303 "chr21:37855701:G>A" "CLDN14" "NM_001146078:c.-81-21627C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs540099348" "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
493304 "chr21:37855731:C>A" "CLDN14" "NM_001146078:c.-81-21657G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs533751825" "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
493305 "chr21:37855740:G>C" "CLDN14" "NM_001146078:c.-81-21666C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs553829834" "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
493306 "chr21:37855760:G>A" "CLDN14" "NM_001146078:c.-81-21686C>T" "FIVE_PRIME_INTRON" "Benign" "rs9636632" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 387 1322 0.2927 597 1006 0.5934 379 694 0.5461 556 1008 0.5516 416 978 0.4254 2335 5008 0.466254
493307 "chr21:37855792:G>A" "CLDN14" "NM_001146078:c.-81-21718C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs137990636" "This variant is a VUS because it does not have enough information."
493308 "chr21:37855854:G>A" "CLDN14" "NM_001146078:c.-81-21780C>T" "FIVE_PRIME_INTRON" "Benign" "rs13051241" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 228 1322 0.1725 622 1006 0.6183 385 694 0.5548 399 1008 0.3958 396 978 0.4049 2030 5008 0.405351
493309 "chr21:37855873:C>G" "CLDN14" "NM_001146078:c.-81-21799G>C" "FIVE_PRIME_INTRON" "Benign" "rs73902538" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 169 1322 0.1278 25 1006 0.0249 44 694 0.0634 158 1008 0.1567 74 978 0.0757 470 5008 0.0938498
493310 "chr21:37855884:A>T" "CLDN14" "NM_001146078:c.-81-21810T>A" "FIVE_PRIME_INTRON" "Benign" "rs116414345" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 44 1322 0.0333 1 1006 0.001 7 694 0.0101 0 1008 0 0 978 0 52 5008 0.0103834
493311 "chr21:37855897:G>T" "CLDN14" "NM_001146078:c.-81-21823C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs149048360" "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
493312 "chr21:37855899:G>T" "CLDN14" "NM_001146078:c.-81-21825C>A" "FIVE_PRIME_INTRON" "Benign" "rs145798950" "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 0 694 0 0 1008 0 0 978 0 23 5008 0.00459265
493313 "chr21:37855911:C>T" "CLDN14" "NM_001146078:c.-81-21837G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs527616407" "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
493314 "chr21:37855912:G>A" "CLDN14" "NM_001146078:c.-81-21838C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs547366710" "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
493315 "chr21:37855923:C>A" "CLDN14" "NM_001146078:c.-81-21849G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs540274524" "This variant is a VUS because it does not have enough information."
493316 "chr21:37855923:C>G" "CLDN14" "NM_001146078:c.-81-21849G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs540274524" "This variant is a VUS because it does not have enough information."
493317 "chr21:37855945:G>T" "CLDN14" "NM_001146078:c.-81-21871C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs745882318" "This variant is a VUS because it does not have enough information."
493318 "chr21:37855969:G>A" "CLDN14" "NM_001146078:c.-81-21895C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs376161967" "This variant is a VUS because it does not have enough information."
493319 "chr21:37855974:T>C" "CLDN14" "NM_001146078:c.-81-21900A>G" "FIVE_PRIME_INTRON" "Benign" "rs13051987" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 111 1322 0.084 572 1006 0.5686 334 694 0.4813 398 1008 0.3948 342 978 0.3497 1757 5008 0.350839
493320 "chr21:37855998:G>A" "CLDN14" "NM_001146078:c.-81-21924C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs138450323" "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
493321 "chr21:37856001:C>T" "CLDN14" "NM_001146078:c.-81-21927G>A" "FIVE_PRIME_INTRON" "Benign" "rs35734452" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 57 1322 0.0431 570 1006 0.5666 324 694 0.4669 397 1008 0.3938 341 978 0.3487 1689 5008 0.33726
493322 "chr21:37856009:T>A" "CLDN14" "NM_001146078:c.-81-21935A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs747069112" "This variant is a VUS because it does not have enough information."
493323 "chr21:37856025:G>C" "CLDN14" "NM_001146078:c.-81-21951C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs771027108" "This variant is a VUS because it does not have enough information."
493324 "chr21:37856026:G>A" "CLDN14" "NM_001146078:c.-81-21952C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs776781902" "This variant is a VUS because it does not have enough information."
493325 "chr21:37856048:G>T" "CLDN14" "NM_001146078:c.-81-21974C>A" "FIVE_PRIME_INTRON" "Benign" "rs142947869" "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 2 694 0.0029 0 1008 0 0 978 0 22 5008 0.00439297
493326 "chr21:37856054:C>G" "CLDN14" "NM_001146078:c.-81-21980G>C" "FIVE_PRIME_INTRON" "Benign" "rs146163570" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
493327 "chr21:37856093:C>A" "CLDN14" "NM_001146078:c.-81-22019G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs115602239" "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
493328 "chr21:37856116:A>G" "CLDN14" "NM_001146078:c.-81-22042T>C" "FIVE_PRIME_INTRON" "Benign" "rs148371221" "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 5 694 0.0072 0 1008 0 0 978 0 43 5008 0.00858626
493329 "chr21:37856118:G>A" "CLDN14" "NM_001146078:c.-81-22044C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs749515266" "This variant is a VUS because it does not have enough information."
493330 "chr21:37856177:A>T" "CLDN14" "NM_001146078:c.-81-22103T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs535307011" "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
493331 "chr21:37856180:T>C" "CLDN14" "NM_001146078:c.-81-22106A>G" "FIVE_PRIME_INTRON" "Benign" "rs59125211" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 156 1322 0.118 92 1006 0.0915 39 694 0.0562 0 1008 0 23 978 0.0235 310 5008 0.061901
493332 "chr21:37856207:G>A" "CLDN14" "NM_001146078:c.-81-22133C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs561427307" "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
493333 "chr21:37856208:C>G" "CLDN14" "NM_001146078:c.-81-22134G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs535874161" "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
493334 "chr21:37856271:G>A" "CLDN14" "NM_001146078:c.-81-22197C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs556220493" "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
493335 "chr21:37856288:C>T" "CLDN14" "NM_001146078:c.-81-22214G>A" "FIVE_PRIME_INTRON" "Benign" "rs141426588" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 8 1322 0.0061 7 1006 0.007 4 694 0.0058 0 1008 0 0 978 0 19 5008 0.00379393
493336 "chr21:37856296:C>G" "CLDN14" "NM_001146078:c.-81-22222G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs150816312" "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
493337 "chr21:37856333:G>T" "CLDN14" "NM_001146078:c.-81-22259C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs547285545" "This variant is a VUS because it does not have enough information."
493338 "chr21:37856346:T>C" "CLDN14" "NM_001146078:c.-81-22272A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs182144974" "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
493339 "chr21:37856351:C>T" "CLDN14" "NM_001146078:c.-81-22277G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs762774115" "This variant is a VUS because it does not have enough information."
493340 "chr21:37856360:G>A" "CLDN14" "NM_001146078:c.-81-22286C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs113251334" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 1 1006 0.001 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
493341 "chr21:37856400:G>A" "CLDN14" "NM_001146078:c.-81-22326C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs761711199" "This variant is a VUS because it does not have enough information."
493342 "chr21:37856401:G>A" "CLDN14" "NM_001146078:c.-81-22327C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs540895316" "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
493343 "chr21:37856415:C>T" "CLDN14" "NM_001146078:c.-81-22341G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs145402139" "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
493344 "chr21:37856416:C>T" "CLDN14" "NM_001146078:c.-81-22342G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs147272285" "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
493345 "chr21:37856421:G>A" "CLDN14" "NM_001146078:c.-81-22347C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs549944492" "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
493346 "chr21:37856422:C>T" "CLDN14" "NM_001146078:c.-81-22348G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs532165276" "This variant is a VUS because it does not have enough information."
493347 "chr21:37856432:G>A" "CLDN14" "NM_001146078:c.-81-22358C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs751500902" "This variant is a VUS because it does not have enough information."
493348 "chr21:37856449:C>T" "CLDN14" "NM_001146078:c.-81-22375G>A" "FIVE_PRIME_INTRON" "Benign" "rs140539944" "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 3 694 0.0043 0 1008 0 0 978 0 12 5008 0.00239617
493349 "chr21:37856480:C>T" "CLDN14" "NM_001146078:c.-81-22406G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs570994613" "This variant is a VUS because it does not have enough information."
493350 "chr21:37856487:C>T" "CLDN14" "NM_001146078:c.-81-22413G>A" "FIVE_PRIME_INTRON" "Benign" "rs79227324" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 77 1322 0.0582 0 1006 0 0 694 0 0 1008 0 0 978 0 77 5008 0.0153754
493351 "chr21:37856514:C>T" "CLDN14" "NM_001146078:c.-81-22440G>A" "FIVE_PRIME_INTRON" "Benign" "rs75921250" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 30 1006 0.0298 8 694 0.0115 1 1008 0.001 4 978 0.0041 47 5008 0.00938498
493352 "chr21:37856528:G>A" "CLDN14" "NM_001146078:c.-81-22454C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566241962" "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
493353 "chr21:37856536:G>A" "CLDN14" "NM_001146078:c.-81-22462C>T" "FIVE_PRIME_INTRON" "Benign" "rs219739" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 768 1322 0.5809 223 1006 0.2217 190 694 0.2738 119 1008 0.1181 299 978 0.3057 1599 5008 0.319289
493354 "chr21:37856596:C>T" "CLDN14" "NM_001146078:c.-81-22522G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs565548800" "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
493355 "chr21:37856621:A>G" "CLDN14" "NM_001146078:c.-81-22547T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs755783454" "This variant is a VUS because it does not have enough information."
493356 "chr21:37856660:C>T" "CLDN14" "NM_001146078:c.-81-22586G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568706996" "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
493357 "chr21:37856668:G>C" "CLDN14" "NM_001146078:c.-81-22594C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs368678586" "This variant is a VUS because it does not have enough information."
493358 "chr21:37856682:T>C" "CLDN14" "NM_001146078:c.-81-22608A>G" "FIVE_PRIME_INTRON" "Benign" "rs219738" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 804 1322 0.6082 223 1006 0.2217 190 694 0.2738 119 1008 0.1181 311 978 0.318 1647 5008 0.328874
493359 "chr21:37856700:AC>-" "CLDN14" "NM_001146078:c.-81-22626_-81-22623delGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs753415019" "This variant is a VUS because it does not have enough information."
493360 "chr21:37856703:C>T" "CLDN14" "NM_001146078:c.-81-22629G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs748513733" "This variant is a VUS because it does not have enough information."
493361 "chr21:37856721:G>T" "CLDN14" "NM_001146078:c.-81-22647C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs115290795" "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
493362 "chr21:37856736:A>G" "CLDN14" "NM_001146078:c.-81-22662T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs375415084" "This variant is a VUS because it does not have enough information."
493363 "chr21:37856773:G>C" "CLDN14" "NM_001146078:c.-81-22699C>G" "FIVE_PRIME_INTRON" "Benign" "rs76269285" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 54 1006 0.0537 55 694 0.0793 1 1008 0.001 42 978 0.0429 155 5008 0.0309505
493364 "chr21:37856776:C>A" "CLDN14" "NM_001146078:c.-81-22702G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs76121568" "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
493365 "chr21:37856776:C>T" "CLDN14" "NM_001146078:c.-81-22702G>A" "FIVE_PRIME_INTRON" "Benign" "rs76121568" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 65 1322 0.0492 11 1006 0.0109 5 694 0.0072 21 1008 0.0208 12 978 0.0123 114 5008 0.0227636
493366 "chr21:37856787:C>A" "CLDN14" "NM_001146078:c.-81-22713G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs144386008" "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
493367 "chr21:37856787:C>T" "CLDN14" "NM_001146078:c.-81-22713G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs144386008" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 6 5008 0.00119808
493368 "chr21:37856821:G>T" "CLDN14" "NM_001146078:c.-81-22747C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs111732028" "This variant is a VUS because it does not have enough information."
493369 "chr21:37856842:A>G" "CLDN14" "NM_001146078:c.-81-22768T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs187161892" "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
493370 "chr21:37856854:T>C" "CLDN14" "NM_001146078:c.-81-22780A>G" "FIVE_PRIME_INTRON" "Benign" "rs114539090" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 80 1322 0.0605 1 1006 0.001 7 694 0.0101 0 1008 0 12 978 0.0123 100 5008 0.0199681
493371 "chr21:37856881:C>T" "CLDN14" "NM_001146078:c.-81-22807G>A" "FIVE_PRIME_INTRON" "Benign" "rs2633334" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1127 1322 0.8525 819 1006 0.8141 566 694 0.8156 674 1008 0.6687 715 978 0.7311 3901 5008 0.778954
493372 "chr21:37856901:A>G" "CLDN14" "NM_001146078:c.-81-22827T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs563504954" "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
493373 "chr21:37856916:A>G" "CLDN14" "NM_001146078:c.-81-22842T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs577267066" "This variant is a VUS because it does not have enough information."
493374 "chr21:37856924:G>A" "CLDN14" "NM_001146078:c.-81-22850C>T" "FIVE_PRIME_INTRON" "Benign" "rs115976669" "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 5 694 0.0072 0 1008 0 0 978 0 43 5008 0.00858626
493375 "chr21:37856929:C>T" "CLDN14" "NM_001146078:c.-81-22855G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs745907621" "This variant is a VUS because it does not have enough information."
493376 "chr21:37856947:T>C" "CLDN14" "NM_001146078:c.-81-22873A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs546278348" "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
493377 "chr21:37856952:C>T" "CLDN14" "NM_001146078:c.-81-22878G>A" "FIVE_PRIME_INTRON" "Benign" "rs2845769" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1164 1322 0.8805 819 1006 0.8141 571 694 0.8228 674 1008 0.6687 715 978 0.7311 3943 5008 0.78734
493378 "chr21:37856956:G>A" "CLDN14" "NM_001146078:c.-81-22882C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs191658728" "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
493379 "chr21:37856988:G>C" "CLDN14" "NM_001146078:c.-81-22914C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs145644416" "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
493380 "chr21:37857007:A>G" "CLDN14" "NM_001146078:c.-81-22933T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs148893351" "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
493381 "chr21:37857011:T>-" "CLDN14" "NM_001146078:c.-81-22937delA" "FIVE_PRIME_INTRON" "Benign" "rs373280104" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 53 1006 0.0527 55 694 0.0793 1 1008 0.001 42 978 0.0429 158 5008 0.0315495
493382 "chr21:37857013:T>C" "CLDN14" "NM_001146078:c.-81-22939A>G" "FIVE_PRIME_INTRON" "Benign" "rs531139304" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 53 1006 0.0527 55 694 0.0793 1 1008 0.001 42 978 0.0429 158 5008 0.0315495
493383 "chr21:37857024:T>G" "CLDN14" "NM_001146078:c.-81-22950A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs775798203" "This variant is a VUS because it does not have enough information."
493384 "chr21:37857046:T>G" "CLDN14" "NM_001146078:c.-81-22972A>C" "FIVE_PRIME_INTRON" "Benign" "rs115462541" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 41 1322 0.031 53 1006 0.0527 60 694 0.0865 1 1008 0.001 42 978 0.0429 197 5008 0.0393371
493385 "chr21:37857077:T>G" "CLDN14" "NM_001146078:c.-81-23003A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs569517700" "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
493386 "chr21:37857097:C>T" "CLDN14" "NM_001146078:c.-81-23023G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs538248881" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 1 1006 0.001 0 694 0 1 1008 0.001 0 978 0 3 5008 0.000599042
493387 "chr21:37857104:C>T" "CLDN14" "NM_001146078:c.-81-23030G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs558187202" "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
493388 "chr21:37857136:C>T" "CLDN14" "NM_001146078:c.-81-23062G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs565475592" "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
493389 "chr21:37857150:A>C" "CLDN14" "NM_001146078:c.-81-23076T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs559661494" "This variant is a VUS because it does not have enough information."
493390 "chr21:37857159:C>A" "CLDN14" "NM_001146078:c.-81-23085G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs534490345" "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
493391 "chr21:37857163:G>A" "CLDN14" "NM_001146078:c.-81-23089C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs142515371" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 1 1006 0.001 2 694 0.0029 0 1008 0 0 978 0 8 5008 0.00159744
493392 "chr21:37857252:C>T" "CLDN14" "NM_001146078:c.-81-23178G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs369681776" "This variant is a VUS because it does not have enough information."
493393 "chr21:37857253:G>A" "CLDN14" "NM_001146078:c.-81-23179C>T" "FIVE_PRIME_INTRON" "Benign" "rs141184876" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 169 1322 0.1278 25 1006 0.0249 44 694 0.0634 157 1008 0.1558 75 978 0.0767 470 5008 0.0938498
493394 "chr21:37857257:G>A" "CLDN14" "NM_001146078:c.-81-23183C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs543325402" "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
493395 "chr21:37857261:C>T" "CLDN14" "NM_001146078:c.-81-23187G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs561487641" "This variant is a VUS because it does not have enough information."
493396 "chr21:37857262:G>A" "CLDN14" "NM_001146078:c.-81-23188C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs373148144" "This variant is a VUS because it does not have enough information."
493397 "chr21:37857273:G>T" "CLDN14" "NM_001146078:c.-81-23199C>A" "FIVE_PRIME_INTRON" "Benign" "rs557225714" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 11 1006 0.0109 8 694 0.0115 0 1008 0 13 978 0.0133 33 5008 0.00658946
493398 "chr21:37857274:T>A" "CLDN14" "NM_001146078:c.-81-23200A>T" "FIVE_PRIME_INTRON" "Benign" "rs577269707" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 11 1006 0.0109 8 694 0.0115 0 1008 0 13 978 0.0133 32 5008 0.00638978
493399 "chr21:37857280:G>C" "CLDN14" "NM_001146078:c.-81-23206C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs546260188" "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
493400 "chr21:37857293:A>C" "CLDN14" "NM_001146078:c.-81-23219T>G" "FIVE_PRIME_INTRON" "Benign" "rs559883279" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 33 1006 0.0328 30 694 0.0432 0 1008 0 8 978 0.0082 71 5008 0.0141773
493401 "chr21:37857325:T>C" "CLDN14" "NM_001146078:c.-81-23251A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs573403087" "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
493402 "chr21:37857334:C>A" "CLDN14" "NM_001146078:c.-81-23260G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs542392419" "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
493403 "chr21:37857390:A>G" "CLDN14" "NM_001146078:c.-81-23316T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs140702212" "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
493404 "chr21:37857402:G>T" "CLDN14" "NM_001146078:c.-81-23328C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs542485754" "This variant is a VUS because it does not have enough information."
493405 "chr21:37857416:T>G" "CLDN14" "NM_001146078:c.-81-23342A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs531155650" "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
493406 "chr21:37857421:T>G" "CLDN14" "NM_001146078:c.-81-23347A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs550944714" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 4 5008 0.000798722
493407 "chr21:37857428:G>A" "CLDN14" "NM_001146078:c.-81-23354C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs564447761" "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
493408 "chr21:37857447:C>G" "CLDN14" "NM_001146078:c.-81-23373G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs531969300" "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
493409 "chr21:37857460:T>C" "CLDN14" "NM_001146078:c.-81-23386A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs560829027" "This variant is a VUS because it does not have enough information."
493410 "chr21:37857462:T>C" "CLDN14" "NM_001146078:c.-81-23388A>G" "FIVE_PRIME_INTRON" "Benign" "rs76633772" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 42 1322 0.0318 1 1006 0.001 2 694 0.0029 0 1008 0 12 978 0.0123 57 5008 0.0113818
493411 "chr21:37857483:A>G" "CLDN14" "NM_001146078:c.-81-23409T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs565615947" "This variant is a VUS because it does not have enough information."
493412 "chr21:37857525:T>A" "CLDN14" "NM_001146078:c.-81-23451A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs565424136" "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
493413 "chr21:37857527:A>C" "CLDN14" "NM_001146078:c.-81-23453T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs73204268" "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
493414 "chr21:37857567:G>A" "CLDN14" "NM_001146078:c.-81-23493C>T" "FIVE_PRIME_INTRON" "Benign" "rs114669931" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 42 1322 0.0318 1 1006 0.001 2 694 0.0029 0 1008 0 12 978 0.0123 57 5008 0.0113818
493415 "chr21:37857585:C>A" "CLDN14" "NM_001146078:c.-81-23511G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs568117809" "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
493416 "chr21:37857600:A>T" "CLDN14" "NM_001146078:c.-81-23526T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs753471891" "This variant is a VUS because it does not have enough information."
493417 "chr21:37857624:A>G" "CLDN14" "NM_001146078:c.-81-23550T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs531562402" "This variant is a VUS because it does not have enough information."
493418 "chr21:37857636:A>C" "CLDN14" "NM_001146078:c.-81-23562T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs537261627" "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
493419 "chr21:37857637:G>T" "CLDN14" "NM_001146078:c.-81-23563C>A" "FIVE_PRIME_INTRON" "Benign" "rs144714609" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 42 1322 0.0318 1 1006 0.001 2 694 0.0029 0 1008 0 12 978 0.0123 57 5008 0.0113818
493420 "chr21:37857663:T>G" "CLDN14" "NM_001146078:c.-81-23589A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs183805589" "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
493421 "chr21:37857691:G>A" "CLDN14" "NM_001146078:c.-81-23617C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs190264460" "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
493422 "chr21:37857751:C>-" "CLDN14" "NM_001146078:c.-81-23677delG" "FIVE_PRIME_INTRON" "Unknown significance" "rs537966196" "This variant is a VUS because it does not have enough information." 0 1322 0 3 1006 0.003 1 694 0.0014 1 1008 0.001 3 978 0.0031 8 5008 0.00159744
493423 "chr21:37857754:G>A" "CLDN14" "NM_001146078:c.-81-23680C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs529813109" "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
493424 "chr21:37857781:A>G" "CLDN14" "NM_001146078:c.-81-23707T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs573289650" "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
493425 "chr21:37857822:G>A" "CLDN14" "NM_001146078:c.-81-23748C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs541930056" "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
493426 "chr21:37857834:C>T" "CLDN14" "NM_001146078:c.-81-23760G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs562213012" "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
493427 "chr21:37857835:G>A" "CLDN14" "NM_001146078:c.-81-23761C>T" "FIVE_PRIME_INTRON" "Benign" "rs76572519" "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 0 978 0 15 5008 0.00299521
493428 "chr21:37857843:TC>-" "CLDN14" "NM_001146078:c.-81-23769_-81-23766delGA" "FIVE_PRIME_INTRON" "Benign" "rs146102381" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 5 1322 0.0038 111 1006 0.1103 47 694 0.0677 0 1008 0 35 978 0.0358 198 5008 0.0395367
493429 "chr21:37857843:->TC" "CLDN14" "NM_001146078:c.-81-23769_-81-23768insGA" "FIVE_PRIME_INTRON" "Unknown significance" "rs778794815" "This variant is a VUS because it does not have enough information."
493430 "chr21:37857854:C>T" "CLDN14" "NM_001146078:c.-81-23780G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs544829461" "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
493431 "chr21:37857860:C>G" "CLDN14" "NM_001146078:c.-81-23786G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs564433853" "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
493432 "chr21:37857904:C>T" "CLDN14" "NM_001146078:c.-81-23830G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs533483709" "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 1 978 0.001 3 5008 0.000599042
493433 "chr21:37857937:G>A" "CLDN14" "NM_001146078:c.-81-23863C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs546907080" "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
493434 "chr21:37857962:C>T" "CLDN14" "NM_001146078:c.-81-23888G>A" "FIVE_PRIME_INTRON" "Benign" "rs138576900" "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 2 694 0.0029 0 1008 0 0 978 0 22 5008 0.00439297
493435 "chr21:37857981:G>C" "CLDN14" "NM_001146078:c.-81-23907C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs781738819" "This variant is a VUS because it does not have enough information."
493436 "chr21:37857989:A>G" "CLDN14" "NM_001146078:c.-81-23915T>C" "FIVE_PRIME_INTRON" "Benign" "rs551536116" "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
493437 "chr21:37858004:CAGA>-" "CLDN14" "NM_001146078:c.-81-23930_-81-23925delTCTG" "FIVE_PRIME_INTRON" "Unknown significance" "rs371227535" "This variant is a VUS because it does not have enough information."
493438 "chr21:37858023:A>T" "CLDN14" "NM_001146078:c.-81-23949T>A" "FIVE_PRIME_INTRON" "Benign" "rs170182" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1211 1322 0.916 873 1006 0.8678 629 694 0.9063 673 1008 0.6677 760 978 0.7771 4146 5008 0.827875
493439 "chr21:37858061:C>A" "CLDN14" "NM_001146078:c.-81-23987G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs769982028" "This variant is a VUS because it does not have enough information."
493440 "chr21:37858124:C>T" "CLDN14" "NM_001146078:c.-81-24050G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs771918213" "This variant is a VUS because it does not have enough information."
493441 "chr21:37858136:G>C" "CLDN14" "NM_001146078:c.-81-24062C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs568189823" "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
493442 "chr21:37858152:->T" "CLDN14" "NM_001146078:c.-81-24078_-81-24077insA" "FIVE_PRIME_INTRON" "Benign" "rs763779986" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 16 458 0.0349345 9 106 0.0849057 5 198 0.0252525 8 298 0.0268456 64 1588 0.0403023 1 26 0.0384615 2 58 0.0344828 105 2732 0.0384334
493443 "chr21:37858152:->TT" "CLDN14" "NM_001146078:c.-81-24078_-81-24077insAA" "FIVE_PRIME_INTRON" "Benign" "rs763779986" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 458 0 0 106 0 1 198 0.00505051 0 298 0 2 1588 0.00125945 0 26 0 0 58 0 3 2732 0.0010981
493444 "chr21:37858152:T>-" "CLDN14" "NM_001146078:c.-81-24078delA" "FIVE_PRIME_INTRON" "Benign" "rs751417030" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 106 458 0.231441 23 106 0.216981 59 198 0.29798 37 298 0.124161 457 1588 0.287783 5 26 0.192308 12 58 0.206897 699 2732 0.255857
493445 "chr21:37858152:TT>-" "CLDN14" "NM_001146078:c.-81-24078_-81-24075delAA" "FIVE_PRIME_INTRON" "Benign" "rs756825394" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 17 458 0.0371179 1 106 0.00943396 0 198 0 1 298 0.0033557 29 1588 0.018262 2 26 0.0769231 1 58 0.0172414 51 2732 0.0186676
493446 "chr21:37858152:TTT>-" "CLDN14" "NM_001146078:c.-81-24078_-81-24074delAAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs749851406" "This variant is a VUS because it does not have enough information." 2 458 0.00436681 0 106 0 0 198 0 0 298 0 0 1588 0 0 26 0 0 58 0 2 2732 0.000732064
493447 "chr21:37858156:T>C" "CLDN14" "NM_001146078:c.-81-24082A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs536850979" "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 1 938 0.0010661 0 248 0 0 434 0 0 1112 0 0 3438 0 0 82 0 0 190 0 1 6442 0.000155231
493448 "chr21:37858166:A>T" "CLDN14" "NM_001146078:c.-81-24092T>A" "FIVE_PRIME_INTRON" "Benign" "rs754732989" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 472 0.00423729 1 120 0.00833333 1 220 0.00454545 3 268 0.011194 18 1450 0.0124138 1 36 0.0277778 2 98 0.0204082 28 2664 0.0105105
493449 "chr21:37858168:G>T" "CLDN14" "NM_001146078:c.-81-24094C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs780779531" "This variant is a VUS because it does not have enough information." 0 958 0 0 258 0 0 434 0 0 914 0 1 3276 0.00030525 0 78 0 0 190 0 1 6108 0.00016372
493450 "chr21:37858171:G>A" "CLDN14" "NM_001146078:c.-81-24097C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs747816571" "This variant is a VUS because it does not have enough information." 1 1070 0.000934579 0 288 0 0 476 0 0 1238 0 0 3742 0 0 92 0 0 224 0 1 7130 0.000140252
493451 "chr21:37858187:G>T" "CLDN14" "NM_001146078:c.-81-24113C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs533771901" "This variant is a VUS because it does not have enough information." 0 1424 0 0 390 0 0 584 0 5 1674 0.00298686 10 5052 0.00197941 0 118 0 0 372 0 15 9614 0.00156022
493452 "chr21:37858190:G>A" "CLDN14" "NM_001146078:c.-81-24116C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs753784003" "This variant is a VUS because it does not have enough information."
493453 "chr21:37858198:T>C" "CLDN14" "NM_001146078:c.-81-24124A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs551945437" "This variant is a VUS because it does not have enough information."
493454 "chr21:37858219:C>T" "CLDN14" "NM_001146078:c.-81-24145G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs777302905" "This variant is a VUS because it does not have enough information." 0 2610 0 0 760 0 0 1114 0 0 2140 0 1 11396 0.0000877501 0 202 0 0 998 0 1 19220 0.0000520291
493455 "chr21:37858220:C>T" "CLDN14" "NM_001146078:c.-81-24146G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs746360065" "This variant is a VUS because it does not have enough information." 0 2678 0 0 798 0 0 1198 0 0 2182 0 1 11900 0.0000840336 0 214 0 0 1022 0 1 19992 0.00005002
493456 "chr21:37858222:A>G" "CLDN14" "NM_001146078:c.-81-24148T>C" "FIVE_PRIME_INTRON" "Benign" "rs192853373" "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 1 694 0.0014 0 1008 0 0 978 0 4 5008 0.000798722 2 2832 0.000706215 5 880 0.00568182 0 1326 0 4 2274 0.00175901 84 12890 0.00651668 0 228 0 0 1124 0 95 21554 0.00440753
493457 "chr21:37858230:T>-" "CLDN14" "NM_001146078:c.-81-24156delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs755698983" "This variant is a VUS because it does not have enough information." 1 3272 0.000305623 0 1174 0 0 1644 0 0 2576 0 0 16488 0 0 268 0 0 1494 0 1 26916 0.0000371526
493458 "chr21:37858232:C>T" "CLDN14" "NM_001146078:c.-81-24158G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs775877620" "This variant is a VUS because it does not have enough information." 0 3494 0 0 1322 0 0 1864 0 0 2706 0 5 18126 0.000275847 0 284 0 1 1706 0.000586166 6 29502 0.000203376
493459 "chr21:37858233:G>A" "CLDN14" "NM_001146078:c.-81-24159C>T" "FIVE_PRIME_INTRON" "Benign" "rs141364962" "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 33 3642 0.00906096 1 1510 0.000662252 0 2012 0 13 2828 0.00459689 6 19410 0.000309119 0 300 0 0 1908 0 53 31610 0.00167668
493460 "chr21:37858245:C>T" "CLDN14" "NM_001146078:c.-81-24171G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs769174939" "This variant is a VUS because it does not have enough information." 2 4754 0.000420698 0 2744 0 0 3172 0 0 3616 0 0 28042 0 0 380 0 0 3194 0 2 45902 0.0000435711
493461 "chr21:37858260:A>G" "CLDN14" "NM_001146078:c.-81-24186T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs776946363" "This variant is a VUS because it does not have enough information." 1 6190 0.000161551 0 4842 0 0 4912 0 0 4532 0 4 39654 0.000100873 0 550 0 0 5400 0 5 66080 0.0000756659
493462 "chr21:37858266:C>T" "CLDN14" "NM_001146078:c.-81-24192G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs762176141" "This variant is a VUS because it does not have enough information." 1 6860 0.000145773 1 5862 0.00017059 0 5632 0 0 4916 0 0 44046 0 0 594 0 0 6444 0 2 74354 0.0000268984
493463 "chr21:37858267:C>G" "CLDN14" "NM_001146078:c.-81-24193G>C" "FIVE_PRIME_INTRON" "Benign" "rs7277324" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 706 1322 0.534 220 1006 0.2187 187 694 0.2695 119 1008 0.1181 300 978 0.3067 1532 5008 0.305911 4548 9068 0.501544 3123 8460 0.369149 949 6320 0.150158 1275 5488 0.232325 14764 52702 0.280141 188 698 0.269341 3476 9690 0.35872 28323 92426 0.30644
493464 "chr21:37858267:C>A" "CLDN14" "NM_001146078:c.-81-24193G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs7277324" "This variant is a VUS because it does not have enough information." 1 9068 0.000110278 0 8460 0 0 6320 0 0 5488 0 1 52702 0.0000189746 0 698 0 0 9690 0 2 92426 0.0000216389
493465 "chr21:37858271:C>T" "CLDN14" "NM_001146078:c.-81-24197G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs185807374" "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 0 9234 0 1 8976 0.000111408 0 6680 0 0 5724 0 2 54648 0.0000365979 0 708 0 3 10146 0.000295683 6 96116 0.0000624246
493466 "chr21:37858274:T>C" "CLDN14" "NM_001146078:c.-81-24200A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs766273046" "This variant is a VUS because it does not have enough information." 0 9322 0 0 9204 0 0 6930 0 0 5824 0 1 55734 0.0000179424 0 720 0 0 10546 0 1 98280 0.000010175
493467 "chr21:37858280:C>A" "CLDN14" "NM_001146078:c.-81-24206G>T" "FIVE_PRIME_INTRON" "Benign" "rs138952890" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 6 1322 0.0045 52 1006 0.0517 55 694 0.0793 1 1008 0.001 53 978 0.0542 167 5008 0.0333466 116 9516 0.01219 978 10046 0.0973522 0 7336 0 103 6022 0.017104 2256 58412 0.0386222 25 766 0.0326371 756 11752 0.0643295 4234 103850 0.0407703
493468 "chr21:37858283:A>C" "CLDN14" "NM_001146078:c.-81-24209T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs754750024" "This variant is a VUS because it does not have enough information." 0 9572 0 0 10236 0 0 7480 0 0 6082 0 1 59224 0.000016885 0 772 0 0 12094 0 1 105460 0.00000948227
493469 "chr21:37858284:C>G" "CLDN14" "NM_001146078:c.-81-24210G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs767345481" "This variant is a VUS because it does not have enough information."
493470 "chr21:37858301:T>C" "CLDN14" "NM_001146078:c.-81-24227A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs752312738" "This variant is a VUS because it does not have enough information." 0 9750 0 0 10644 0 0 7924 0 0 6288 0 0 61484 0 0 820 0 1 13482 0.000074173 1 110392 0.00000905863
493471 "chr21:37858312:T>C" "CLDN14" "NM_001146078:c.-81-24238A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs755834323" "This variant is a VUS because it does not have enough information." 0 9846 0 0 10816 0 0 8138 0 0 6408 0 1 62718 0.0000159444 0 838 0 0 14534 0 1 113298 0.00000882628
493472 "chr21:37858313:T>G" "CLDN14" "NM_001146078:c.-81-24239A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs190330667" "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 9864 0 0 10836 0 1 8148 0.00012273 0 6404 0 0 62830 0 0 840 0 0 14618 0 1 113540 0.00000880747
493473 "chr21:37858321:T>G" "CLDN14" "NM_001146078:c.-81-24247A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs748777229" "This variant is a VUS because it does not have enough information." 0 9924 0 0 10928 0 0 8226 0 0 6466 0 1 63668 0.0000157065 0 858 0 0 15250 0 1 115320 0.00000867152
493474 "chr21:37858346:C>A" "CLDN14" "NM_001146078:c.-81-24272G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs149420767" "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 45 10108 0.00445192 2 11212 0.00017838 0 8434 0 0 6550 0 1 65256 0.0000153243 0 886 0 1 16154 0.0000619042 49 118600 0.000413153
493475 "chr21:37858347:C>T" "CLDN14" "NM_001146078:c.-81-24273G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs780570486" "This variant is a VUS because it does not have enough information." 0 10114 0 0 11222 0 0 8440 0 0 6554 0 1 65280 0.0000153186 0 882 0 0 16158 0 1 118650 0.00000842815
493476 "chr21:37858348:A>G" "CLDN14" "NM_001146078:c.-81-24274T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs747494196" "This variant is a VUS because it does not have enough information." 0 10124 0 0 11224 0 0 8448 0 0 6556 0 1 65358 0.0000153003 0 884 0 0 16172 0 1 118766 0.00000841992
493477 "chr21:37858350:A>G" "CLDN14" "NM_001146078:c.-81-24276T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs769121919" "This variant is a VUS because it does not have enough information." 0 10144 0 0 11236 0 0 8458 0 0 6558 0 1 65448 0.0000152793 0 884 0 0 16194 0 1 118922 0.00000840887
493478 "chr21:37858351:G>A" "CLDN14" "NM_001146078:c.-81-24277C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs575737922" "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 10146 0 0 11238 0 0 8456 0 0 6558 0 0 65490 0 0 886 0 40 16212 0.00246731 40 118986 0.000336174
493479 "chr21:37858352:C>T" "CLDN14" "NM_001146078:c.-81-24278G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs748365714" "This variant is a VUS because it does not have enough information." 0 10156 0 1 11248 0.0000889047 0 8458 0 0 6560 0 2 65492 0.0000305381 0 884 0 0 16220 0 3 119018 0.0000252063
493480 "chr21:37858353:G>A" "CLDN14" "NM_001146078:c.-81-24279C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs770082934" "This variant is a VUS because it does not have enough information." 1 10168 0.0000983478 0 11260 0 3 8474 0.000354024 0 6564 0 2 65576 0.000030499 0 884 0 0 16226 0 6 119152 0.0000503558
493481 "chr21:37858360:A>G" "CLDN14" "NM_001146078:c.-81-24286T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs773310485" "This variant is a VUS because it does not have enough information." 0 10218 0 0 11304 0 0 8522 0 0 6570 0 2 65832 0.0000303804 0 890 0 0 16270 0 2 119606 0.0000167216
493482 "chr21:37858362:G>A" "CLDN14" "NM_001146078:c.-81-24288C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs763047859" "This variant is a VUS because it does not have enough information." 0 10226 0 0 11316 0 1 8520 0.000117371 0 6572 0 0 65878 0 0 890 0 0 16272 0 1 119674 0.00000835603
493483 "chr21:37858363:G>C" "CLDN14" "NM_001146078:c.-81-24289C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs766386831" "This variant is a VUS because it does not have enough information." 0 10228 0 2 11316 0.000176741 0 8524 0 0 6576 0 0 65898 0 0 890 0 0 16282 0 2 119714 0.0000167065
493484 "chr21:37858363:G>T" "CLDN14" "NM_001146078:c.-81-24289C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs766386831" "This variant is a VUS because it does not have enough information." 0 10228 0 0 11316 0 0 8524 0 0 6576 0 2 65898 0.0000303499 0 890 0 0 16282 0 2 119714 0.0000167065
493485 "chr21:37858380:C>T" "CLDN14" "NM_001146078:c.-82+24281G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759506950" "This variant is a VUS because it does not have enough information." 0 10278 0 0 11376 0 0 8568 0 0 6596 0 1 66164 0.000015114 0 894 0 0 16324 0 1 120200 0.00000831947
493486 "chr21:37858382:C>T" "CLDN14" "NM_001146078:c.-82+24279G>A" "FIVE_PRIME_INTRON" "Benign" "rs116823059" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 24 1322 0.0182 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 25 5008 0.00499201 227 10286 0.0220688 8 11376 0.000703235 0 8570 0 0 6598 0 19 66176 0.000287113 0 894 0 0 16334 0 254 120234 0.00211255
493487 "chr21:37858388:G>A" "CLDN14" "NM_001146078:c.-82+24273C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs752549518" "This variant is a VUS because it does not have enough information." 0 10304 0 0 11382 0 8 8580 0.000932401 0 6602 0 0 66242 0 0 894 0 0 16350 0 8 120354 0.0000664706
493488 "chr21:37858407:C>T" "CLDN14" "NM_001146078:c.-82+24254G>A" "FIVE_PRIME_INTRON" "Benign" "rs113240027" "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 3 694 0.0043 0 1008 0 0 978 0 30 5008 0.00599042 151 10300 0.0146602 23 11378 0.00202144 0 8608 0 0 6604 0 19 66282 0.000286654 1 896 0.00111607 1 16360 0.0000611247 195 120428 0.00161922
493489 "chr21:37858410:A>G" "CLDN14" "NM_001146078:c.-82+24251T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs763739743" "This variant is a VUS because it does not have enough information." 0 10306 0 0 11380 0 0 8604 0 0 6606 0 1 66298 0.0000150834 0 898 0 0 16360 0 1 120452 0.00000830206
493490 "chr21:37858412:G>A" "CLDN14" "NM_001146078:c.-82+24249C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs753464535" "This variant is a VUS because it does not have enough information." 0 10300 0 0 11382 0 0 8600 0 5 6604 0.000757117 0 66262 0 0 898 0 0 16362 0 5 120408 0.0000415255
493491 "chr21:37858416:C>G" "CLDN14" "NM_001146078:c.-82+24245G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs756742704" "This variant is a VUS because it does not have enough information." 0 10286 0 0 11378 0 0 8596 0 0 6604 0 0 66240 0 0 898 0 1 16348 0.0000611696 1 120350 0.0000083091
493492 "chr21:37858420:G>A" "CLDN14" "NM_001146078:c.-82+24241C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs577840391" "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 10282 0 0 11372 0 0 8596 0 0 6600 0 9 66220 0.000135911 0 896 0 0 16340 0 9 120306 0.0000748092
493493 "chr21:37858425:C>T" "CLDN14" "NM_001146078:c.-82+24236G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs540479289" "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 10254 0.000292569 0 11354 0 0 8584 0 0 6596 0 0 66182 0 1 898 0.00111359 0 16322 0 4 120190 0.0000332806
493494 "chr21:37858427:G>A" "CLDN14" "NM_001146078:c.-82+24234C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs755598407" "This variant is a VUS because it does not have enough information." 0 10236 0 0 11346 0 0 8582 0 0 6590 0 0 66142 0 0 896 0 1 16310 0.0000613121 1 120102 0.00000832626
493495 "chr21:37858429:A>T" "CLDN14" "NM_001146078:c.-82+24232T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs781767663" "This variant is a VUS because it does not have enough information." 0 10230 0 0 11354 0 0 8580 0 0 6586 0 1 66132 0.0000151213 0 896 0 0 16304 0 1 120082 0.00000832764
493496 "chr21:37858433:C>T" "CLDN14" "NM_001146078:c.-82+24228G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs148100059" "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 9 10210 0.000881489 3 11338 0.000264597 1 8574 0.000116632 0 6588 0 0 66102 0 0 896 0 0 16304 0 13 120012 0.000108323
493497 "chr21:37858434:G>A" "CLDN14" "NM_001146078:c.-82+24227C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs770314029" "This variant is a VUS because it does not have enough information." 1 10218 0.0000978665 0 11338 0 0 8572 0 0 6584 0 2 66074 0.0000302691 0 896 0 0 16296 0 3 119978 0.0000250046
493498 "chr21:37858435:T>C" "CLDN14" "NM_001146078:c.-82+24226A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs56061241" "This variant is a VUS because it does not have enough information."
493499 "chr21:37858436:C>T" "CLDN14" "NM_001146078:c.-82+24225G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773431634" "This variant is a VUS because it does not have enough information." 0 10200 0 1 11326 0.0000882924 0 8564 0 0 6582 0 0 66030 0 0 896 0 1 16276 0.0000614402 2 119874 0.0000166842
493500 "chr21:37858437:G>A" "CLDN14" "NM_001146078:c.-82+24224C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs181048296" "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 1 978 0.001 4 5008 0.000798722 29 10198 0.00284369 23 11324 0.00203108 0 8564 0 0 6582 0 52 66030 0.000787521 1 896 0.00111607 1 16272 0.0000614553 106 119866 0.000884321
493501 "chr21:37858440:A>C" "CLDN14" "NM_001146078:c.-82+24221T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs761474128" "This variant is a VUS because it does not have enough information." 0 10180 0 0 11306 0 0 8558 0 0 6574 0 1 65960 0.0000151607 0 894 0 0 16258 0 1 119730 0.00000835213
493502 "chr21:37858441:T>C" "CLDN14" "NM_001146078:c.-82+24220A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs774359231" "This variant is a VUS because it does not have enough information." 0 10154 0 0 11286 0 0 8544 0 0 6568 0 1 65906 0.0000151731 0 894 0 0 16238 0 1 119590 0.0000083619
493503 "chr21:37858444:TCC>-" "CLDN14" "NM_001146078:c.-82+24217_-82+24221delGGA" "FIVE_PRIME_INTRON" "Unknown significance" "rs780640783" "This variant is a VUS because it does not have enough information." 0 10142 0 0 11282 0 0 8540 0 0 6560 0 2 65880 0.0000303582 0 894 0 0 16238 0 2 119536 0.0000167314
493504 "chr21:37858447:T>C" "CLDN14" "NM_001146078:c.-82+24214A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs759459801" "This variant is a VUS because it does not have enough information." 0 10108 0 2 11234 0.000178031 0 8516 0 0 6550 0 0 65654 0 0 888 0 0 16190 0 2 119140 0.000016787
493505 "chr21:37858453:T>C" "CLDN14" "NM_001146078:c.-82+24208A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs143817787" "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 2 10044 0.000199124 0 11136 0 0 8484 0 20 6528 0.00306373 130 65282 0.00199136 0 888 0 0 16108 0 152 118470 0.00128303
493506 "chr21:37858455:G>A" "CLDN14" "NM_001146078:c.-82+24206C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs775414546" "This variant is a VUS because it does not have enough information." 0 10014 0 1 11078 0.000090269 0 8472 0 0 6520 0 0 65100 0 0 880 0 0 16068 0 1 118132 0.00000846511
493507 "chr21:37858460:GCTGGCAAGTGTCCATGGCTGA>-" "CLDN14" "NM_001146078:c.-82+24201_-82+24224delTCAGCCATGGACACTTGCCAGC" "FIVE_PRIME_INTRON" "Unknown significance" "rs749800591" "This variant is a VUS because it does not have enough information."
493508 "chr21:37858467:A>G" "CLDN14" "NM_001146078:c.-82+24194T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs760426729" "This variant is a VUS because it does not have enough information." 0 9906 0 0 10824 0 0 8374 0 0 6464 0 1 64162 0.0000155855 0 866 0 0 15880 0 1 116476 0.00000858546
493509 "chr21:37858468:G>A" "CLDN14" "NM_001146078:c.-82+24193C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs763817417" "This variant is a VUS because it does not have enough information." 0 9884 0 0 10790 0 0 8366 0 4 6460 0.000619195 6 64078 0.0000936359 1 864 0.00115741 0 15854 0 11 116296 0.0000945862
493510 "chr21:37858474:A>G" "CLDN14" "NM_001146078:c.-82+24187T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs561606383" "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 2 9774 0.000204625 0 10584 0 0 8260 0 0 6378 0 0 63388 0 0 858 0 0 15722 0 2 114964 0.0000173968
493511 "chr21:37858484:T>A" "CLDN14" "NM_001146078:c.-82+24177A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs761413190" "This variant is a VUS because it does not have enough information." 0 9576 0 0 10202 0 0 8038 0 0 6270 0 0 61952 0 0 842 0 1 15484 0.0000645828 1 112364 0.00000889965
493512 "chr21:37858484:T>C" "CLDN14" "NM_001146078:c.-82+24177A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs761413190" "This variant is a VUS because it does not have enough information." 0 9576 0 0 10202 0 0 8038 0 0 6270 0 1 61952 0.0000161415 0 842 0 0 15484 0 1 112364 0.00000889965
493513 "chr21:37858492:A>G" "CLDN14" "NM_001146078:c.-82+24169T>C" "FIVE_PRIME_INTRON" "Benign" "rs147279578" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 27 1006 0.0268 12 694 0.0173 0 1008 0 2 978 0.002 42 5008 0.00838658 20 9380 0.0021322 78 9822 0.00794136 0 7850 0 354 6140 0.0576547 1240 60480 0.0205026 18 830 0.0216867 76 15252 0.00498295 1786 109754 0.0162728
493514 "chr21:37858494:G>A" "CLDN14" "NM_001146078:c.-82+24167C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs757985305" "This variant is a VUS because it does not have enough information." 0 9364 0 0 9772 0 0 7836 0 0 6050 0 1 60186 0.0000166152 0 822 0 0 15234 0 1 109264 0.00000915215
493515 "chr21:37858500:T>G" "CLDN14" "NM_001146078:c.-82+24161A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs781750002" "This variant is a VUS because it does not have enough information." 27 9168 0.00294503 2 9336 0.000214225 0 7544 0 0 5924 0 0 58256 0 0 792 0 0 14936 0 29 105956 0.000273699
493516 "chr21:37858506:C>T" "CLDN14" "NM_001146078:c.-82+24155G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs753278127" "This variant is a VUS because it does not have enough information." 0 9054 0 0 9152 0 0 7404 0 0 5852 0 7 57242 0.000122288 0 784 0 2 14804 0.000135099 9 104292 0.0000862962
493517 "chr21:37858507:G>A" "CLDN14" "NM_001146078:c.-82+24154C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs756475594" "This variant is a VUS because it does not have enough information." 0 9016 0 0 9050 0 0 7380 0 0 5806 0 1 56966 0.0000175543 0 780 0 0 14722 0 1 103720 0.00000964134
493518 "chr21:37858512:G>T" "CLDN14" "NM_001146078:c.-82+24149C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs778035846" "This variant is a VUS because it does not have enough information." 0 8754 0 0 8614 0 0 7152 0 0 5646 0 0 55250 0 0 752 0 1 14456 0.0000691754 1 100624 0.00000993799
493519 "chr21:37858522:G>T" "CLDN14" "NM_001146078:c.-82+24139C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs749518559" "This variant is a VUS because it does not have enough information." 0 8402 0 0 8060 0 0 6764 0 0 5416 0 0 52222 0 0 714 0 1 14052 0.0000711642 1 95630 0.000010457
493520 "chr21:37858526:C>A" "CLDN14" "NM_001146078:c.-82+24135G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs771114301" "This variant is a VUS because it does not have enough information." 0 8292 0 0 7806 0 21 6618 0.00317316 0 5344 0 0 51174 0 0 702 0 0 13860 0 21 93796 0.00022389
493521 "chr21:37858533:G>A" "CLDN14" "NM_001146078:c.-82+24128C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs779212502" "This variant is a VUS because it does not have enough information." 0 8004 0 0 7266 0 0 6282 0 0 5180 0 1 48824 0.0000204817 0 676 0 0 13500 0 1 89732 0.0000111443
493522 "chr21:37858540:T>G" "CLDN14" "NM_001146078:c.-82+24121A>C" "FIVE_PRIME_INTRON" "Benign" "rs114872540" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 120 1322 0.0908 52 1006 0.0517 55 694 0.0793 1 1008 0.001 53 978 0.0542 281 5008 0.0561102 785 7694 0.102028 940 6860 0.137026 0 6028 0 100 5024 0.0199045 2177 47052 0.046268 24 654 0.0366972 776 13210 0.0587434 4802 86522 0.0555003
493523 "chr21:37858541:C>T" "CLDN14" "NM_001146078:c.-82+24120G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs765866531" "This variant is a VUS because it does not have enough information."
493524 "chr21:37858543:T>C" "CLDN14" "NM_001146078:c.-82+24118A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs772174613" "This variant is a VUS because it does not have enough information." 1 7118 0.000140489 0 6294 0 0 5904 0 0 4906 0 0 45282 0 0 632 0 0 12754 0 1 82890 0.0000120642
493525 "chr21:37858548:T>A" "CLDN14" "NM_001146078:c.-82+24113A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs775357406" "This variant is a VUS because it does not have enough information." 0 6486 0 2 5538 0.000361141 0 5720 0 0 4730 0 0 42918 0 0 604 0 0 12174 0 2 78170 0.0000255853
493526 "chr21:37858551:G>A" "CLDN14" "NM_001146078:c.-82+24110C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs760655716" "This variant is a VUS because it does not have enough information." 0 6140 0 0 5180 0 4 5584 0.000716332 0 4636 0 0 41620 0 0 604 0 1 11832 0.0000845166 5 75596 0.0000661411
493527 "chr21:37858556:C>T" "CLDN14" "NM_001146078:c.-82+24105G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs768468709" "This variant is a VUS because it does not have enough information."
493528 "chr21:37858560:T>A" "CLDN14" "NM_001146078:c.-82+24101A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs776359125" "This variant is a VUS because it does not have enough information."
493529 "chr21:37858565:->CTCAGTCACACTG" "CLDN14" "NM_001146078:c.-82+24096_-82+24097insCAGTGTGACTGAG" "FIVE_PRIME_INTRON" "Benign" "rs147383938" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 162 1322 0.1225 53 1006 0.0527 68 694 0.098 1 1008 0.001 53 978 0.0542 337 5008 0.0672923
493530 "chr21:37858567:->CAGTCACAC" "CLDN14" "NM_001146078:c.-82+24094_-82+24095insGTGTGACTG" "FIVE_PRIME_INTRON" "Unknown significance" "rs60694231" "This variant is a VUS because it does not have enough information." 0 5202 0 0 4088 0 0 5110 0 0 4328 0 0 37020 0 0 556 0 1 10212 0.000097924 1 66516 0.000015034
493531 "chr21:37858567:->CAGTCACACTGC" "CLDN14" "NM_001146078:c.-82+24094_-82+24095insGCAGTGTGACTG" "FIVE_PRIME_INTRON" "Unknown significance" "rs60694231" "This variant is a VUS because it does not have enough information." 0 5202 0 0 4088 0 0 5110 0 0 4328 0 0 37020 0 0 556 0 0 10212 0 0 66516 0
493532 "chr21:37858567:T>C" "CLDN14" "NM_001146078:c.-82+24094A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs761680195" "This variant is a VUS because it does not have enough information."
493533 "chr21:37858569:G>-" "CLDN14" "NM_001146078:c.-82+24092delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs772140284" "This variant is a VUS because it does not have enough information."
493534 "chr21:37858570:->TCACACT" "CLDN14" "NM_001146078:c.-82+24091_-82+24092insAGTGTGA" "FIVE_PRIME_INTRON" "Unknown significance" "rs773499360" "This variant is a VUS because it does not have enough information."
493535 "chr21:37858580:C>T" "CLDN14" "NM_001146078:c.-82+24081G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs764728818" "This variant is a VUS because it does not have enough information." 0 5696 0 0 4316 0 0 4784 0 0 4126 0 1 36128 0.0000276794 0 538 0 0 10068 0 1 65656 0.0000152309
493536 "chr21:37858581:C>T" "CLDN14" "NM_001146078:c.-82+24080G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs185304873" "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 5146 0 0 3792 0 0 4734 0 0 4030 0 8 34546 0.000231575 0 510 0 5 9446 0.000529325 13 62204 0.00020899
493537 "chr21:37858582:G>A" "CLDN14" "NM_001146078:c.-82+24079C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs762503090" "This variant is a VUS because it does not have enough information." 0 5780 0 1 4300 0.000232558 1 4718 0.000211954 0 4080 0 0 35916 0 0 526 0 0 9844 0 2 65164 0.0000306918
493538 "chr21:37858587:G>T" "CLDN14" "NM_001146078:c.-82+24074C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs766032227" "This variant is a VUS because it does not have enough information." 0 5586 0 1 4066 0.000245942 0 4754 0 0 4042 0 0 35296 0 0 514 0 0 9416 0 1 63674 0.000015705
493539 "chr21:37858594:C>G" "CLDN14" "NM_001146078:c.-82+24067G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs753220670" "This variant is a VUS because it does not have enough information." 0 5560 0 0 4002 0 0 4694 0 1 4000 0.00025 0 34868 0 0 518 0 0 8946 0 1 62588 0.0000159775
493540 "chr21:37858599:G>C" "CLDN14" "NM_001146078:c.-82+24062C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs756643295" "This variant is a VUS because it does not have enough information." 0 5492 0 0 3980 0 0 4666 0 0 3972 0 0 34520 0 0 520 0 1 8678 0.000115234 1 61828 0.0000161739
493541 "chr21:37858600:T>A" "CLDN14" "NM_001146078:c.-82+24061A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs778183602" "This variant is a VUS because it does not have enough information." 0 5524 0 1 4014 0.000249128 0 4680 0 0 3982 0 0 34642 0 0 520 0 0 8714 0 1 62076 0.0000161093
493542 "chr21:37858604:C>T" "CLDN14" "NM_001146078:c.-82+24057G>A" "FIVE_PRIME_INTRON" "Benign" "rs140783451" "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 0 5470 0 173 4074 0.0424644 0 4688 0 0 3956 0 2 34452 0.0000580518 0 508 0 0 8432 0 175 61580 0.00284183
493543 "chr21:37858605:T>A" "CLDN14" "NM_001146078:c.-82+24056A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs757648899" "This variant is a VUS because it does not have enough information."
493544 "chr21:37858613:A>G" "CLDN14" "NM_001146078:c.-82+24048T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs546872916" "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 5458 0 0 4196 0 10 4766 0.0020982 0 3988 0 0 34858 0 0 510 0 0 7962 0 10 61738 0.000161975
493545 "chr21:37858615:C>A" "CLDN14" "NM_001146078:c.-82+24046G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs746116036" "This variant is a VUS because it does not have enough information." 0 5444 0 0 4202 0 4 4730 0.000845666 0 4006 0 0 34786 0 0 506 0 0 7852 0 4 61526 0.0000650132
493546 "chr21:37858629:C>T" "CLDN14" "NM_001146078:c.-82+24032G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs772117469" "This variant is a VUS because it does not have enough information." 0 5494 0 0 4492 0 0 4868 0 0 4098 0 1 35536 0.0000281405 0 520 0 0 7204 0 1 62212 0.0000160741
493547 "chr21:37858630:G>A" "CLDN14" "NM_001146078:c.-82+24031C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs780148893" "This variant is a VUS because it does not have enough information." 0 5520 0 2 4542 0.000440335 0 4916 0 0 4126 0 0 35724 0 0 520 0 0 7126 0 2 62474 0.0000320133
493548 "chr21:37858631:T>C" "CLDN14" "NM_001146078:c.-82+24030A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs746946178" "This variant is a VUS because it does not have enough information." 0 5534 0 0 4598 0 0 4960 0 0 4170 0 1 36054 0.0000277362 0 520 0 0 7140 0 1 62976 0.0000158791
493549 "chr21:37858642:A>G" "CLDN14" "NM_001146078:c.-82+24019T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs768536640" "This variant is a VUS because it does not have enough information." 0 5720 0 0 4970 0 0 5214 0 0 4356 0 2 37644 0.0000531293 0 538 0 0 7246 0 2 65688 0.000030447
493550 "chr21:37858648:A>G" "CLDN14" "NM_001146078:c.-82+24013T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs776633230" "This variant is a VUS because it does not have enough information." 0 5782 0 0 5144 0 2 5360 0.000373134 0 4424 0 0 38482 0 0 538 0 0 7330 0 2 67060 0.000029824
493551 "chr21:37858661:C>T" "CLDN14" "NM_001146078:c.-82+24000G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs761474277" "This variant is a VUS because it does not have enough information." 0 5982 0 0 5610 0 0 5658 0 0 4648 0 0 40360 0 0 558 0 8 7562 0.00105792 8 70378 0.000113672
493552 "chr21:37858664:G>T" "CLDN14" "NM_001146078:c.-82+23997C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs769652424" "This variant is a VUS because it does not have enough information." 0 6036 0 0 5768 0 0 5704 0 0 4674 0 6 40852 0.000146872 0 576 0 0 7590 0 6 71200 0.0000842697
493553 "chr21:37858666:C>T" "CLDN14" "NM_001146078:c.-82+23995G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs772976585" "This variant is a VUS because it does not have enough information." 0 6098 0 0 5908 0 0 5794 0 0 4762 0 0 41546 0 0 574 0 1 7688 0.000130073 1 72370 0.0000138179
493554 "chr21:37858677:AGGCTGCAGCT>-" "CLDN14" "NM_001146078:c.-82+23984_-82+23996delAGCTGCAGCCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs200931210" "This variant is a VUS because it does not have enough information."
493555 "chr21:37858691:C>T" "CLDN14" "NM_001146078:c.-82+23970G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs762731282" "This variant is a VUS because it does not have enough information." 0 6388 0 1 7392 0.000135281 0 6382 0 0 5014 0 0 46344 0 0 614 0 0 8812 0 1 80946 0.0000123539
493556 "chr21:37858692:G>A" "CLDN14" "NM_001146078:c.-82+23969C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566796158" "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 6544 0.000152812 0 7622 0 1 6476 0.000154416 0 5110 0 0 47310 0 0 624 0 1 8906 0.000112284 3 82592 0.0000363231
493557 "chr21:37858692:G>C" "CLDN14" "NM_001146078:c.-82+23969C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs566796158" "This variant is a VUS because it does not have enough information." 0 6544 0 0 7622 0 0 6476 0 0 5110 0 1 47310 0.0000211372 0 624 0 0 8906 0 1 82592 0.0000121077
493558 "chr21:37858701:C>T" "CLDN14" "NM_001146078:c.-82+23960G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759096807" "This variant is a VUS because it does not have enough information." 0 6938 0 0 8442 0 1 6814 0.000146757 0 5400 0 0 50308 0 0 670 0 0 9606 0 1 88178 0.0000113407
493559 "chr21:37858704:C>T" "CLDN14" "NM_001146078:c.-82+23957G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs535475394" "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 7034 0 0 8600 0 0 6896 0 0 5458 0 4 51060 0.0000783392 0 678 0 0 9766 0 4 89492 0.0000446967
493560 "chr21:37858706:T>A" "CLDN14" "NM_001146078:c.-82+23955A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs555757364" "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 7096 0 0 8694 0 0 6968 0 0 5450 0 0 51536 0 0 676 0 17 9918 0.00171406 17 90338 0.000188182
493561 "chr21:37858707:C>A" "CLDN14" "NM_001146078:c.-82+23954G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs757518632" "This variant is a VUS because it does not have enough information."
493562 "chr21:37858709:T>C" "CLDN14" "NM_001146078:c.-82+23952A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs569177141" "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 0 7430 0 1 8938 0.000111882 0 7090 0 0 5676 0 0 53060 0 0 706 0 0 10142 0 1 93042 0.0000107478
493563 "chr21:37858712:C>T" "CLDN14" "NM_001146078:c.-82+23949G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs538311435" "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 3 7622 0.000393597 2 9220 0.00021692 2 7222 0.000276932 0 5810 0 1 54238 0.0000184373 0 720 0 2 10364 0.000192976 10 95196 0.000105046
493564 "chr21:37858713:G>A" "CLDN14" "NM_001146078:c.-82+23948C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs758687428" "This variant is a VUS because it does not have enough information." 0 7732 0 0 9408 0 0 7314 0 0 5888 0 3 54808 0.0000547365 0 722 0 0 10442 0 3 96314 0.0000311481
493565 "chr21:37858714:C>T" "CLDN14" "NM_001146078:c.-82+23947G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759258589" "This variant is a VUS because it does not have enough information." 0 7822 0 0 9550 0 0 7390 0 0 5938 0 4 55440 0.0000721501 0 740 0 0 10618 0 4 97498 0.0000410265
493566 "chr21:37858715:T>C" "CLDN14" "NM_001146078:c.-82+23946A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs746991757" "This variant is a VUS because it does not have enough information." 0 7912 0 0 9698 0 0 7490 0 0 6004 0 0 56094 0 0 746 0 1 10780 0.0000927644 1 98724 0.0000101292
493567 "chr21:37858718:T>C" "CLDN14" "NM_001146078:c.-82+23943A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs755113092" "This variant is a VUS because it does not have enough information." 0 8134 0 0 10066 0 0 7668 0 0 6142 0 1 57650 0.0000173461 0 764 0 0 11234 0 1 101658 0.0000098369
493568 "chr21:37858722:G>T" "CLDN14" "NM_001146078:c.-82+23939C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs780939692" "This variant is a VUS because it does not have enough information." 0 8346 0 0 10416 0 1 7874 0.000127 0 6270 0 0 59130 0 0 784 0 0 11650 0 1 104470 0.00000957213
493569 "chr21:37858725:C>G" "CLDN14" "NM_001146078:c.-82+23936G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs748161875" "This variant is a VUS because it does not have enough information." 0 8518 0 0 10618 0 0 7966 0 0 6340 0 1 60106 0.0000166373 0 804 0 0 11990 0 1 106342 0.00000940362
493570 "chr21:37858728:C>T" "CLDN14" "NM_001146078:c.-82+23933G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs769680621" "This variant is a VUS because it does not have enough information." 0 8644 0 0 10762 0 0 8076 0 0 6384 0 1 60758 0.0000164587 0 810 0 0 12294 0 1 107728 0.00000928264
493571 "chr21:37858731:T>C" "CLDN14" "NM_001146078:c.-82+23930A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs773207433" "This variant is a VUS because it does not have enough information." 0 8752 0 0 10882 0 0 8184 0 0 6420 0 10 61370 0.000162946 0 812 0 0 12510 0 10 108930 0.0000918021
493572 "chr21:37858731:T>G" "CLDN14" "NM_001146078:c.-82+23930A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs773207433" "This variant is a VUS because it does not have enough information." 0 8752 0 0 10882 0 0 8184 0 0 6420 0 5 61370 0.000081473 0 812 0 0 12510 0 5 108930 0.000045901
493573 "chr21:37858740:G>A" "CLDN14" "NM_001146078:c.-82+23921C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs770647525" "This variant is a VUS because it does not have enough information." 0 9134 0 0 11254 0 0 8456 0 0 6532 0 1 63014 0.0000158695 0 844 0 0 13478 0 1 112712 0.00000887217
493574 "chr21:37858747:A>C" "CLDN14" "NM_001146078:c.-82+23914T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs142812656" "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 10 9396 0.00106428 1 11420 0.0000875657 0 8570 0 0 6580 0 0 63880 0 0 858 0 0 14290 0 11 114994 0.0000956572
493575 "chr21:37858779:T>C" "CLDN14" "NM_001146078:c.-82+23882A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs758929779" "This variant is a VUS because it does not have enough information." 0 9874 0 0 11550 0 10 8630 0.00115875 0 6614 0 0 65452 0 0 892 0 0 16212 0 10 119224 0.0000838757
493576 "chr21:37858783:A>C" "CLDN14" "NM_001146078:c.-82+23878T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs752408094" "This variant is a VUS because it does not have enough information."
493577 "chr21:37858789:A>G" "CLDN14" "NM_001146078:c.-82+23872T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs767078263" "This variant is a VUS because it does not have enough information." 0 9922 0 0 11554 0 0 8630 0 0 6614 0 0 65634 0 0 892 0 1 16376 0.000061065 1 119622 0.00000835967
493578 "chr21:37858794:A>C" "CLDN14" "NM_001146078:c.-82+23867T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs776982557" "This variant is a VUS because it does not have enough information." 0 9948 0 0 11556 0 2 8630 0.00023175 0 6614 0 0 65740 0 0 892 0 0 16424 0 2 119804 0.0000166939
493579 "chr21:37858798:G>T" "CLDN14" "NM_001146078:c.-82+23863C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs577776582" "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 9982 0 0 11558 0 0 8632 0 0 6614 0 1 65828 0.0000151911 0 896 0 0 16456 0 1 119966 0.0000083357
493580 "chr21:37858802:C>T" "CLDN14" "NM_001146078:c.-82+23859G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs573361999" "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 5 10000 0.0005 4 11560 0.000346021 0 8632 0 0 6614 0 12 65894 0.000182111 0 894 0 0 16472 0 21 120066 0.000174904
493581 "chr21:37858802:C>A" "CLDN14" "NM_001146078:c.-82+23859G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs573361999" "This variant is a VUS because it does not have enough information." 1 10000 0.0001 0 11560 0 0 8632 0 0 6614 0 0 65894 0 0 894 0 0 16472 0 1 120066 0.00000832875
493582 "chr21:37858803:G>A" "CLDN14" "NM_001146078:c.-82+23858C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs554041213" "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 10010 0 0 11562 0 0 8634 0 0 6614 0 2 65908 0.0000303453 0 896 0 1 16482 0.0000606722 3 120106 0.0000249779
493583 "chr21:37858805:G>A" "CLDN14" "NM_001146078:c.-82+23856C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs766545921" "This variant is a VUS because it does not have enough information." 0 10042 0 0 11562 0 0 8636 0 0 6614 0 0 65980 0 0 896 0 1 16486 0.0000606575 1 120216 0.00000831836
493584 "chr21:37858810:A>G" "CLDN14" "NM_001146078:c.-82+23851T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs574304620" "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 10074 0 0 11564 0 0 8636 0 0 6614 0 0 66032 0 0 896 0 2 16492 0.000121271 2 120308 0.000016624
493585 "chr21:37858816:G>A" "CLDN14" "NM_001146078:c.-82+23845C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs541446134" "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 10108 0 0 11564 0 0 8638 0 0 6614 0 2 66130 0.0000302435 0 896 0 0 16496 0 2 120446 0.000016605
493586 "chr21:37858818:A>T" "CLDN14" "NM_001146078:c.-82+23843T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs781369059" "This variant is a VUS because it does not have enough information." 0 10136 0 0 11566 0 0 8638 0 0 6614 0 0 66160 0 0 898 0 6 16500 0.000363636 6 120512 0.0000497876
493587 "chr21:37858820:C>G" "CLDN14" "NM_001146078:c.-82+23841G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs748030203" "This variant is a VUS because it does not have enough information." 1 10146 0.000098561 0 11564 0 0 8638 0 0 6614 0 0 66186 0 0 900 0 0 16502 0 1 120550 0.00000829531
493588 "chr21:37858822:C>G" "CLDN14" "NM_001146078:c.-82+23839G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs756176979" "This variant is a VUS because it does not have enough information." 0 10154 0 0 11566 0 0 8638 0 0 6614 0 1 66206 0.0000151044 0 900 0 0 16504 0 1 120582 0.00000829311
493589 "chr21:37858822:C>T" "CLDN14" "NM_001146078:c.-82+23839G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs756176979" "This variant is a VUS because it does not have enough information." 0 10154 0 0 11566 0 0 8638 0 0 6614 0 1 66206 0.0000151044 0 900 0 0 16504 0 1 120582 0.00000829311
493590 "chr21:37858827:C>T" "CLDN14" "NM_001146078:c.-82+23834G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs561691498" "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 2 10184 0.000196386 0 11564 0 0 8642 0 0 6614 0 0 66258 0 0 900 0 0 16504 0 2 120666 0.0000165747
493591 "chr21:37858829:C>G" "CLDN14" "NM_001146078:c.-82+23832G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs770882487" "This variant is a VUS because it does not have enough information." 0 10188 0 0 11566 0 0 8642 0 0 6614 0 1 66282 0.0000150871 0 900 0 0 16506 0 1 120698 0.00000828514
493592 "chr21:37858837:A>T" "CLDN14" "NM_001146078:c.-82+23824T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773827778" "This variant is a VUS because it does not have enough information." 0 10256 0 0 11570 0 0 8644 0 0 6614 0 0 66384 0 0 902 0 2 16510 0.000121139 2 120880 0.0000165453
493593 "chr21:37858839:C>T" "CLDN14" "NM_001146078:c.-82+23822G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs751962904" "This variant is a VUS because it does not have enough information." 0 10258 0 0 11570 0 0 8644 0 0 6614 0 5 66386 0.0000753171 0 902 0 0 16512 0 5 120886 0.0000413613
493594 "chr21:37858840:G>A" "CLDN14" "NM_001146078:c.-82+23821C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs771451778" "This variant is a VUS because it does not have enough information." 0 10286 0 1 11570 0.0000864304 0 8646 0 0 6614 0 2 66446 0.0000300996 0 902 0 3 16512 0.000181686 6 120976 0.0000495966
493595 "chr21:37858844:A>T" "CLDN14" "NM_001146078:c.-82+23817T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs775136520" "This variant is a VUS because it does not have enough information." 2 10300 0.000194175 0 11570 0 0 8650 0 0 6614 0 0 66496 0 0 902 0 0 16512 0 2 121044 0.0000165229
493596 "chr21:37858848:G>A" "CLDN14" "NM_001146078:c.-82+23813C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs762216401" "This variant is a VUS because it does not have enough information." 0 10338 0 0 11570 0 0 8652 0 0 6614 0 1 66576 0.0000150204 0 902 0 0 16512 0 1 121164 0.00000825328
493597 "chr21:37858855:G>A" "CLDN14" "NM_001146078:c.-82+23806C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs770230869" "This variant is a VUS because it does not have enough information." 0 10360 0 0 11570 0 0 8652 0 0 6614 0 0 66620 0 0 904 0 17 16512 0.00102955 17 121232 0.000140227
493598 "chr21:37858862:C>T" "CLDN14" "NM_001146078:c.-82+23799G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773736927" "This variant is a VUS because it does not have enough information." 0 10368 0 1 11570 0.0000864304 0 8652 0 0 6614 0 0 66640 0 0 906 0 0 16510 0 1 121260 0.00000824674
493599 "chr21:37858865:A>G" "CLDN14" "NM_001146078:c.-82+23796T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs763251227" "This variant is a VUS because it does not have enough information." 0 10374 0 0 11568 0 0 8652 0 0 6614 0 2 66642 0.0000300111 0 906 0 0 16510 0 2 121266 0.0000164927
493600 "chr21:37858867:C>T" "CLDN14" "NM_001146078:c.-82+23794G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs766775089" "This variant is a VUS because it does not have enough information." 0 10374 0 0 11570 0 0 8652 0 4 6614 0.000604778 24 66646 0.000360112 0 906 0 0 16510 0 28 121272 0.000230886
493601 "chr21:37858869:G>A" "CLDN14" "NM_001146078:c.-82+23792C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs751696060" "This variant is a VUS because it does not have enough information." 0 10374 0 0 11570 0 0 8652 0 0 6614 0 0 66646 0 0 906 0 1 16510 0.0000605694 1 121272 0.00000824593
493602 "chr21:37858871:G>A" "CLDN14" "NM_001146078:c.-82+23790C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs759869283" "This variant is a VUS because it does not have enough information." 0 10378 0 2 11570 0.000172861 0 8652 0 0 6614 0 0 66644 0 0 906 0 0 16510 0 2 121274 0.0000164916
493603 "chr21:37858875:AGG>-" "CLDN14" "NM_001146078:c.-82+23786_-82+23790delCCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs762016112" "This variant is a VUS because it does not have enough information."
493604 "chr21:37858877:G>T" "CLDN14" "NM_001146078:c.-82+23784C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs767481526" "This variant is a VUS because it does not have enough information." 0 10388 0 0 11570 0 0 8652 0 0 6614 0 0 66666 0 0 906 0 1 16510 0.0000605694 1 121306 0.00000824362
493605 "chr21:37858879:G>A" "CLDN14" "NM_001146078:c.-82+23782C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs752763743" "This variant is a VUS because it does not have enough information." 0 10388 0 0 11570 0 0 8652 0 0 6614 0 0 66672 0 0 906 0 1 16508 0.0000605767 1 121310 0.00000824334
493606 "chr21:37858880:G>C" "CLDN14" "NM_001146078:c.-82+23781C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs757509246" "This variant is a VUS because it does not have enough information."
493607 "chr21:37858883:C>T" "CLDN14" "NM_001146078:c.-82+23778G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs756264913" "This variant is a VUS because it does not have enough information." 0 10388 0 1 11570 0.0000864304 0 8652 0 0 6614 0 0 66676 0 0 906 0 0 16508 0 1 121314 0.00000824307
493608 "chr21:37858885:G>C" "CLDN14" "NM_001146078:c.-82+23776C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs777815205" "This variant is a VUS because it does not have enough information." 0 10392 0 10 11570 0.000864304 0 8652 0 0 6614 0 0 66676 0 0 906 0 0 16506 0 10 121316 0.0000824294
493609 "chr21:37858902:G>A" "CLDN14" "NM_001146078:c.-82+23759C>T" "FIVE_PRIME_INTRON" "Benign" "rs150760850" "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 14 978 0.0143 22 5008 0.00439297
493610 "chr21:37858916:C>T" "CLDN14" "NM_001146078:c.-82+23745G>A" "FIVE_PRIME_INTRON" "Benign" "rs139201577" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 54 1322 0.0408 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 58 5008 0.0115815
493611 "chr21:37858922:A>G" "CLDN14" "NM_001146078:c.-82+23739T>C" "FIVE_PRIME_INTRON" "Benign" "rs73204269" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 387 1322 0.2927 175 1006 0.174 91 694 0.1311 0 1008 0 45 978 0.046 698 5008 0.139377
493612 "chr21:37858924:G>A" "CLDN14" "NM_001146078:c.-82+23737C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs750809701" "This variant is a VUS because it does not have enough information."
493613 "chr21:37858926:G>T" "CLDN14" "NM_001146078:c.-82+23735C>A" "FIVE_PRIME_INTRON" "Benign" "rs117833343" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 13 1006 0.0129 1 694 0.0014 0 1008 0 0 978 0 16 5008 0.00319489
493614 "chr21:37858947:T>C" "CLDN14" "NM_001146078:c.-82+23714A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs188103469" "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
493615 "chr21:37858951:C>G" "CLDN14" "NM_001146078:c.-82+23710G>C" "FIVE_PRIME_INTRON" "Benign" "rs8132946" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 468 1322 0.354 75 1006 0.0746 86 694 0.1239 22 1008 0.0218 75 978 0.0767 726 5008 0.144968
493616 "chr21:37858957:A>C" "CLDN14" "NM_001146078:c.-82+23704T>G" "FIVE_PRIME_INTRON" "Benign" "rs60605101" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 441 1322 0.3336 54 1006 0.0537 55 694 0.0793 31 1008 0.0308 48 978 0.0491 629 5008 0.125599
493617 "chr21:37858958:C>T" "CLDN14" "NM_001146078:c.-82+23703G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs549033005" "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
493618 "chr21:37858972:A>G" "CLDN14" "NM_001146078:c.-82+23689T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs569188063" "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
493619 "chr21:37858978:A>G" "CLDN14" "NM_001146078:c.-82+23683T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs537860719" "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
493620 "chr21:37858982:T>C" "CLDN14" "NM_001146078:c.-82+23679A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs557822684" "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
493621 "chr21:37858990:T>-" "CLDN14" "NM_001146078:c.-82+23671delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs562529008" "This variant is a VUS because it does not have enough information."
493622 "chr21:37858999:T>C" "CLDN14" "NM_001146078:c.-82+23662A>G" "FIVE_PRIME_INTRON" "Benign" "rs149969264" "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 2 694 0.0029 0 1008 0 0 978 0 10 5008 0.00199681
493623 "chr21:37859008:A>G" "CLDN14" "NM_001146078:c.-82+23653T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs755257925" "This variant is a VUS because it does not have enough information."
493624 "chr21:37859022:T>C" "CLDN14" "NM_001146078:c.-82+23639A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs534105390" "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
493625 "chr21:37859027:C>T" "CLDN14" "NM_001146078:c.-82+23634G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs181307519" "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
493626 "chr21:37859027:C>G" "CLDN14" "NM_001146078:c.-82+23634G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs181307519" "This variant is a VUS because it does not have enough information."
493627 "chr21:37859042:T>G" "CLDN14" "NM_001146078:c.-82+23619A>C" "FIVE_PRIME_INTRON" "Benign" "rs145081590" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 24 1006 0.0239 14 694 0.0202 0 1008 0 3 978 0.0031 43 5008 0.00858626
493628 "chr21:37859059:C>T" "CLDN14" "NM_001146078:c.-82+23602G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs536923329" "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
493629 "chr21:37859067:A>G" "CLDN14" "NM_001146078:c.-82+23594T>C" "FIVE_PRIME_INTRON" "Benign" "rs139831645" "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
493630 "chr21:37859100:C>T" "CLDN14" "NM_001146078:c.-82+23561G>A" "FIVE_PRIME_INTRON" "Benign" "rs143143791" "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
493631 "chr21:37859101:G>A" "CLDN14" "NM_001146078:c.-82+23560C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs544263865" "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
493632 "chr21:37859130:C>T" "CLDN14" "NM_001146078:c.-82+23531G>A" "FIVE_PRIME_INTRON" "Benign" "rs146701669" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
493633 "chr21:37859154:T>C" "CLDN14" "NM_001146078:c.-82+23507A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs577837415" "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
493634 "chr21:37859164:C>T" "CLDN14" "NM_001146078:c.-82+23497G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs140270401" "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
493635 "chr21:37859165:G>A" "CLDN14" "NM_001146078:c.-82+23496C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs560269432" "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
493636 "chr21:37859171:T>C" "CLDN14" "NM_001146078:c.-82+23490A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs771837514" "This variant is a VUS because it does not have enough information."
493637 "chr21:37859187:C>T" "CLDN14" "NM_001146078:c.-82+23474G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs758617465" "This variant is a VUS because it does not have enough information."
493638 "chr21:37859191:C>T" "CLDN14" "NM_001146078:c.-82+23470G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs374366549" "This variant is a VUS because it does not have enough information."
493639 "chr21:37859210:G>A" "CLDN14" "NM_001146078:c.-82+23451C>T" "FIVE_PRIME_INTRON" "Benign" "rs73204270" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 88 1322 0.0666 147 1006 0.1461 65 694 0.0937 48 1008 0.0476 54 978 0.0552 402 5008 0.0802716
493640 "chr21:37859225:G>A" "CLDN14" "NM_001146078:c.-82+23436C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs56205342" "This variant is a VUS because it does not have enough information."
493641 "chr21:37859251:T>C" "CLDN14" "NM_001146078:c.-82+23410A>G" "FIVE_PRIME_INTRON" "Benign" "rs549221238" "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
493642 "chr21:37859283:A>T" "CLDN14" "NM_001146078:c.-82+23378T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs62229459" "This variant is a VUS because it does not have enough information."
493643 "chr21:37859285:->T" "CLDN14" "NM_001146078:c.-82+23376_-82+23377insA" "FIVE_PRIME_INTRON" "Unknown significance" "rs796230026" "This variant is a VUS because it does not have enough information."
493644 "chr21:37859285:T>-" "CLDN14" "NM_001146078:c.-82+23376delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs57062881" "This variant is a VUS because it does not have enough information."
493645 "chr21:37859301:TG>-" "CLDN14" "NM_001146078:c.-82+23360_-82+23363delCA" "FIVE_PRIME_INTRON" "Unknown significance" "rs796365186" "This variant is a VUS because it does not have enough information."
493646 "chr21:37859301:G>-" "CLDN14" "NM_001146078:c.-82+23360delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs200617255" "This variant is a VUS because it does not have enough information."
493647 "chr21:37859301:G>C" "CLDN14" "NM_001146078:c.-82+23360C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs185568758" "This variant is a VUS because it does not have enough information."
493648 "chr21:37859336:G>T" "CLDN14" "NM_001146078:c.-82+23325C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs371380662" "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
493649 "chr21:37859344:G>A" "CLDN14" "NM_001146078:c.-82+23317C>T" "FIVE_PRIME_INTRON" "Benign" "rs56900455" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 21 1322 0.0159 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 25 5008 0.00499201
493650 "chr21:37859364:C>A" "CLDN14" "NM_001146078:c.-82+23297G>T" "FIVE_PRIME_INTRON" "Benign" "rs61540527" "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 2 694 0.0029 0 1008 0 0 978 0 22 5008 0.00439297
493651 "chr21:37859375:C>T" "CLDN14" "NM_001146078:c.-82+23286G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs571489196" "This variant is a VUS because it does not have enough information."
493652 "chr21:37859411:T>G" "CLDN14" "NM_001146078:c.-82+23250A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs571391925" "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
493653 "chr21:37859418:A>G" "CLDN14" "NM_001146078:c.-82+23243T>C" "FIVE_PRIME_INTRON" "Benign" "rs140549895" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 170 1322 0.1286 13 1006 0.0129 19 694 0.0274 0 1008 0 5 978 0.0051 207 5008 0.0413339
493654 "chr21:37859427:C>T" "CLDN14" "NM_001146078:c.-82+23234G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs570519515" "This variant is a VUS because it does not have enough information."
493655 "chr21:37859439:C>T" "CLDN14" "NM_001146078:c.-82+23222G>A" "FIVE_PRIME_INTRON" "Benign" "rs547595944" "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 24 978 0.0245 25 5008 0.00499201
493656 "chr21:37859444:G>A" "CLDN14" "NM_001146078:c.-82+23217C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs567801452" "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
493657 "chr21:37859449:A>C" "CLDN14" "NM_001146078:c.-82+23212T>G" "FIVE_PRIME_INTRON" "Benign" "rs150494374" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 65 1006 0.0646 18 694 0.0259 0 1008 0 2 978 0.002 88 5008 0.0175719
493658 "chr21:37859464:G>A" "CLDN14" "NM_001146078:c.-82+23197C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs534093433" "This variant is a VUS because it does not have enough information."
493659 "chr21:37859495:C>T" "CLDN14" "NM_001146078:c.-82+23166G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs764960429" "This variant is a VUS because it does not have enough information."
493660 "chr21:37859519:G>A" "CLDN14" "NM_001146078:c.-82+23142C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs556805607" "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
493661 "chr21:37859520:G>A" "CLDN14" "NM_001146078:c.-82+23141C>T" "FIVE_PRIME_INTRON" "Benign" "rs138314596" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 19 1006 0.0189 9 694 0.013 1 1008 0.001 2 978 0.002 32 5008 0.00638978
493662 "chr21:37859532:C>T" "CLDN14" "NM_001146078:c.-82+23129G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs537817675" "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
493663 "chr21:37859546:G>A" "CLDN14" "NM_001146078:c.-82+23115C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs557818225" "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
493664 "chr21:37859560:C>T" "CLDN14" "NM_001146078:c.-82+23101G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs577726179" "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
493665 "chr21:37859561:G>A" "CLDN14" "NM_001146078:c.-82+23100C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs767963499" "This variant is a VUS because it does not have enough information."
493666 "chr21:37859564:A>C" "CLDN14" "NM_001146078:c.-82+23097T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs751018005" "This variant is a VUS because it does not have enough information."
493667 "chr21:37859572:C>T" "CLDN14" "NM_001146078:c.-82+23089G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568327710" "This variant is a VUS because it does not have enough information."
493668 "chr21:37859576:C>T" "CLDN14" "NM_001146078:c.-82+23085G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs191963174" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 2 694 0.0029 0 1008 0 0 978 0 4 5008 0.000798722
493669 "chr21:37859578:G>T" "CLDN14" "NM_001146078:c.-82+23083C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs776182642" "This variant is a VUS because it does not have enough information."
493670 "chr21:37859617:G>A" "CLDN14" "NM_001146078:c.-82+23044C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs766951367" "This variant is a VUS because it does not have enough information."
493671 "chr21:37859637:G>A" "CLDN14" "NM_001146078:c.-82+23024C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs372232065" "This variant is a VUS because it does not have enough information."
493672 "chr21:37859660:T>C" "CLDN14" "NM_001146078:c.-82+23001A>G" "FIVE_PRIME_INTRON" "Benign" "rs219737" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 341 1322 0.2579 803 1006 0.7982 423 694 0.6095 706 1008 0.7004 605 978 0.6186 2878 5008 0.574681
493673 "chr21:37859667:ACTC>-" "CLDN14" "NM_001146078:c.-82+22994_-82+22999delGAGT" "FIVE_PRIME_INTRON" "Benign" "rs3216089" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 187 1322 0.1415 780 1006 0.7753 400 694 0.5764 384 1008 0.381 435 978 0.4448 2186 5008 0.436502
493674 "chr21:37859667:->ACTC" "CLDN14" "NM_001146078:c.-82+22994_-82+22995insGAGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs745715953" "This variant is a VUS because it does not have enough information."
493675 "chr21:37859670:C>T" "CLDN14" "NM_001146078:c.-82+22991G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs573772148" "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
493676 "chr21:37859694:C>T" "CLDN14" "NM_001146078:c.-82+22967G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs111933146" "This variant is a VUS because it does not have enough information."
493677 "chr21:37859695:G>A" "CLDN14" "NM_001146078:c.-82+22966C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs542505366" "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
493678 "chr21:37859711:C>G" "CLDN14" "NM_001146078:c.-82+22950G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs111588195" "This variant is a VUS because it does not have enough information."
493679 "chr21:37859711:C>T" "CLDN14" "NM_001146078:c.-82+22950G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs111588195" "This variant is a VUS because it does not have enough information."
493680 "chr21:37859757:A>G" "CLDN14" "NM_001146078:c.-82+22904T>C" "FIVE_PRIME_INTRON" "Benign" "rs143854384" "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
493681 "chr21:37859763:G>A" "CLDN14" "NM_001146078:c.-82+22898C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs12627729" "This variant is a VUS because it does not have enough information."
493682 "chr21:37859769:T>C" "CLDN14" "NM_001146078:c.-82+22892A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs753955086" "This variant is a VUS because it does not have enough information."
493683 "chr21:37859821:G>A" "CLDN14" "NM_001146078:c.-82+22840C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs574905488" "This variant is a VUS because it does not have enough information."
493684 "chr21:37859847:G>A" "CLDN14" "NM_001146078:c.-82+22814C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs531535030" "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
493685 "chr21:37859875:G>A" "CLDN14" "NM_001146078:c.-82+22786C>T" "FIVE_PRIME_INTRON" "Benign" "rs74933634" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 7 1322 0.0053 57 1006 0.0567 35 694 0.0504 50 1008 0.0496 59 978 0.0603 208 5008 0.0415335
493686 "chr21:37859877:G>A" "CLDN14" "NM_001146078:c.-82+22784C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs564906980" "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
493687 "chr21:37859898:AA>-" "CLDN14" "NM_001146078:c.-82+22763_-82+22766delTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs573376105" "This variant is a VUS because it does not have enough information."
493688 "chr21:37859958:G>T" "CLDN14" "NM_001146078:c.-82+22703C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs779253331" "This variant is a VUS because it does not have enough information."
493689 "chr21:37860013:C>T" "CLDN14" "NM_001146078:c.-82+22648G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs748309918" "This variant is a VUS because it does not have enough information."
493690 "chr21:37860016:A>G" "CLDN14" "NM_001146078:c.-82+22645T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs527682854" "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
493691 "chr21:37860055:C>T" "CLDN14" "NM_001146078:c.-82+22606G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs183333999" "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
493692 "chr21:37860096:A>G" "CLDN14" "NM_001146078:c.-82+22565T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs758227731" "This variant is a VUS because it does not have enough information."
493693 "chr21:37860099:T>C" "CLDN14" "NM_001146078:c.-82+22562A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs567693493" "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
493694 "chr21:37860102:A>G" "CLDN14" "NM_001146078:c.-82+22559T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs187609107" "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
493695 "chr21:37860114:G>A" "CLDN14" "NM_001146078:c.-82+22547C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs146302929" "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
493696 "chr21:37860123:T>C" "CLDN14" "NM_001146078:c.-82+22538A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs761153873" "This variant is a VUS because it does not have enough information."
493697 "chr21:37860146:C>T" "CLDN14" "NM_001146078:c.-82+22515G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs570345809" "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
493698 "chr21:37860147:G>A" "CLDN14" "NM_001146078:c.-82+22514C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs191928724" "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
493699 "chr21:37860158:C>A" "CLDN14" "NM_001146078:c.-82+22503G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs777519102" "This variant is a VUS because it does not have enough information."
493700 "chr21:37860160:T>-" "CLDN14" "NM_001146078:c.-82+22501delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs34584005" "This variant is a VUS because it does not have enough information."
493701 "chr21:37860163:T>G" "CLDN14" "NM_001146078:c.-82+22498A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs559298362" "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
493702 "chr21:37860165:G>C" "CLDN14" "NM_001146078:c.-82+22496C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs571225405" "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
493703 "chr21:37860166:A>G" "CLDN14" "NM_001146078:c.-82+22495T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs746770097" "This variant is a VUS because it does not have enough information."
493704 "chr21:37860178:C>T" "CLDN14" "NM_001146078:c.-82+22483G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs575885088" "This variant is a VUS because it does not have enough information."
493705 "chr21:37860283:C>T" "CLDN14" "NM_001146078:c.-82+22378G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs770862307" "This variant is a VUS because it does not have enough information."
493706 "chr21:37860298:A>C" "CLDN14" "NM_001146078:c.-82+22363T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs533594791" "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
493707 "chr21:37860325:G>T" "CLDN14" "NM_001146078:c.-82+22336C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs376988818" "This variant is a VUS because it does not have enough information."
493708 "chr21:37860328:A>G" "CLDN14" "NM_001146078:c.-82+22333T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs553831263" "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
493709 "chr21:37860355:C>T" "CLDN14" "NM_001146078:c.-82+22306G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs573683429" "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
493710 "chr21:37860366:A>C" "CLDN14" "NM_001146078:c.-82+22295T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs182344362" "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
493711 "chr21:37860369:C>T" "CLDN14" "NM_001146078:c.-82+22292G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs776379466" "This variant is a VUS because it does not have enough information."
493712 "chr21:37860370:G>A" "CLDN14" "NM_001146078:c.-82+22291C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs745445871" "This variant is a VUS because it does not have enough information."
493713 "chr21:37860396:C>T" "CLDN14" "NM_001146078:c.-82+22265G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs555905695" "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
493714 "chr21:37860413:C>T" "CLDN14" "NM_001146078:c.-82+22248G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs139148097" "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
493715 "chr21:37860447:A>G" "CLDN14" "NM_001146078:c.-82+22214T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs544855812" "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
493716 "chr21:37860450:C>T" "CLDN14" "NM_001146078:c.-82+22211G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs377266757" "This variant is a VUS because it does not have enough information."
493717 "chr21:37860495:C>T" "CLDN14" "NM_001146078:c.-82+22166G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs559124715" "This variant is a VUS because it does not have enough information."
493718 "chr21:37860503:C>T" "CLDN14" "NM_001146078:c.-82+22158G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs564845363" "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
493719 "chr21:37860518:C>T" "CLDN14" "NM_001146078:c.-82+22143G>A" "FIVE_PRIME_INTRON" "Benign" "rs116421037" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 58 1322 0.0439 2 1006 0.002 1 694 0.0014 3 1008 0.003 0 978 0 64 5008 0.0127796
493720 "chr21:37860519:->CCTT" "CLDN14" "NM_001146078:c.-82+22142_-82+22143insAAGG" "FIVE_PRIME_INTRON" "Unknown significance" "rs747508864" "This variant is a VUS because it does not have enough information."
493721 "chr21:37860519:->CCTTCCTT" "CLDN14" "NM_001146078:c.-82+22142_-82+22143insAAGGAAGG" "FIVE_PRIME_INTRON" "Unknown significance" "rs60820945" "This variant is a VUS because it does not have enough information."
493722 "chr21:37860519:->CCTTCCTTCCTT" "CLDN14" "NM_001146078:c.-82+22142_-82+22143insAAGGAAGGAAGG" "FIVE_PRIME_INTRON" "Unknown significance" "rs747508864" "This variant is a VUS because it does not have enough information."
493723 "chr21:37860519:->CCTTCCTTCCTTCCTT" "CLDN14" "NM_001146078:c.-82+22142_-82+22143insAAGGAAGGAAGGAAGG" "FIVE_PRIME_INTRON" "Unknown significance" "rs60820945" "This variant is a VUS because it does not have enough information."
493724 "chr21:37860519:->CCTTCCTTCCTTCCTTCCTTCCTTCCTT" "CLDN14" "NM_001146078:c.-82+22142_-82+22143insAAGGAAGGAAGGAAGGAAGGAAGGAAGG" "FIVE_PRIME_INTRON" "Unknown significance" "rs60820945" "This variant is a VUS because it does not have enough information."
493725 "chr21:37860520:C>T" "CLDN14" "NM_001146078:c.-82+22141G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs541113484" "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
493726 "chr21:37860561:T>A" "CLDN14" "NM_001146078:c.-82+22100A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs13047474" "This variant is a VUS because it does not have enough information."
493727 "chr21:37860566:T>C" "CLDN14" "NM_001146078:c.-82+22095A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs544773385" "This variant is a VUS because it does not have enough information."
493728 "chr21:37860569:T>C" "CLDN14" "NM_001146078:c.-82+22092A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs186657668" "This variant is a VUS because it does not have enough information."
493729 "chr21:37860573:C>T" "CLDN14" "NM_001146078:c.-82+22088G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs376306696" "This variant is a VUS because it does not have enough information."
493730 "chr21:37860578:TCTT>-" "CLDN14" "NM_001146078:c.-82+22083_-82+22088delAAGA" "FIVE_PRIME_INTRON" "Unknown significance" "rs145010742" "This variant is a VUS because it does not have enough information."
493731 "chr21:37860613:A>G" "CLDN14" "NM_001146078:c.-82+22048T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs561410034" "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
493732 "chr21:37860615:G>A" "CLDN14" "NM_001146078:c.-82+22046C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs530168653" "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
493733 "chr21:37860623:G>A" "CLDN14" "NM_001146078:c.-82+22038C>T" "FIVE_PRIME_INTRON" "Benign" "rs59059205" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 13 1322 0.0098 19 1006 0.0189 15 694 0.0216 315 1008 0.3125 163 978 0.1667 525 5008 0.104832
493734 "chr21:37860630:C>T" "CLDN14" "NM_001146078:c.-82+22031G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs532228451" "This variant is a VUS because it does not have enough information."
493735 "chr21:37860669:A>C" "CLDN14" "NM_001146078:c.-82+21992T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs374816633" "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
493736 "chr21:37860695:G>A" "CLDN14" "NM_001146078:c.-82+21966C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs532765116" "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
493737 "chr21:37860701:C>T" "CLDN14" "NM_001146078:c.-82+21960G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs552897539" "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
493738 "chr21:37860710:C>T" "CLDN14" "NM_001146078:c.-82+21951G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs566424143" "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
493739 "chr21:37860713:G>T" "CLDN14" "NM_001146078:c.-82+21948C>A" "FIVE_PRIME_INTRON" "Benign" "rs533762455" "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 0 1008 0 0 978 0 12 5008 0.00239617
493740 "chr21:37860717:G>A" "CLDN14" "NM_001146078:c.-82+21944C>T" "FIVE_PRIME_INTRON" "Benign" "rs112599647" "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 3 694 0.0043 0 1008 0 0 978 0 30 5008 0.00599042
493741 "chr21:37860717:G>T" "CLDN14" "NM_001146078:c.-82+21944C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs112599647" "This variant is a VUS because it does not have enough information."
493742 "chr21:37860782:A>G" "CLDN14" "NM_001146078:c.-82+21879T>C" "FIVE_PRIME_INTRON" "Benign" "rs59285877" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 13 1322 0.0098 19 1006 0.0189 15 694 0.0216 315 1008 0.3125 163 978 0.1667 525 5008 0.104832
493743 "chr21:37860785:A>G" "CLDN14" "NM_001146078:c.-82+21876T>C" "FIVE_PRIME_INTRON" "Benign" "rs219736" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 293 1322 0.2216 804 1006 0.7992 428 694 0.6167 703 1008 0.6974 637 978 0.6513 2865 5008 0.572085
493744 "chr21:37860857:C>T" "CLDN14" "NM_001146078:c.-82+21804G>A" "FIVE_PRIME_INTRON" "Benign" "rs141726850" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 57 1322 0.0431 174 1006 0.173 71 694 0.1023 0 1008 0 46 978 0.047 348 5008 0.0694888
493745 "chr21:37860862:C>T" "CLDN14" "NM_001146078:c.-82+21799G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs777885796" "This variant is a VUS because it does not have enough information."
493746 "chr21:37860863:C>T" "CLDN14" "NM_001146078:c.-82+21798G>A" "FIVE_PRIME_INTRON" "Benign" "rs59724458" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 13 1322 0.0098 19 1006 0.0189 15 694 0.0216 314 1008 0.3115 163 978 0.1667 524 5008 0.104633
493747 "chr21:37860931:C>T" "CLDN14" "NM_001146078:c.-82+21730G>A" "FIVE_PRIME_INTRON" "Benign" "rs117857503" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 45 1006 0.0447 49 694 0.0706 1 1008 0.001 32 978 0.0327 128 5008 0.0255591
493748 "chr21:37860995:C>T" "CLDN14" "NM_001146078:c.-82+21666G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs558425268" "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
493749 "chr21:37861013:T>C" "CLDN14" "NM_001146078:c.-82+21648A>G" "FIVE_PRIME_INTRON" "Benign" "rs572276871" "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 0 1008 0 0 978 0 12 5008 0.00239617
493750 "chr21:37861015:C>T" "CLDN14" "NM_001146078:c.-82+21646G>A" "FIVE_PRIME_INTRON" "Benign" "rs35599107" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 109 1322 0.0825 20 1006 0.0199 24 694 0.0346 318 1008 0.3155 201 978 0.2055 672 5008 0.134185
493751 "chr21:37861022:G>C" "CLDN14" "NM_001146078:c.-82+21639C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs561089482" "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
493752 "chr21:37861025:T>C" "CLDN14" "NM_001146078:c.-82+21636A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs531439864" "This variant is a VUS because it does not have enough information."
493753 "chr21:37861042:A>G" "CLDN14" "NM_001146078:c.-82+21619T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs182620097" "This variant is a VUS because it does not have enough information."
493754 "chr21:37861050:C>T" "CLDN14" "NM_001146078:c.-82+21611G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs530126254" "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
493755 "chr21:37861068:->G" "CLDN14" "NM_001146078:c.-82+21593_-82+21594insC" "FIVE_PRIME_INTRON" "Unknown significance" "rs35409319" "This variant is a VUS because it does not have enough information."
493756 "chr21:37861074:T>G" "CLDN14" "NM_001146078:c.-82+21587A>C" "FIVE_PRIME_INTRON" "Benign" "rs35857368" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 13 1322 0.0098 19 1006 0.0189 15 694 0.0216 315 1008 0.3125 163 978 0.1667 525 5008 0.104832
493757 "chr21:37861148:C>T" "CLDN14" "NM_001146078:c.-82+21513G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs775040526" "This variant is a VUS because it does not have enough information."
493758 "chr21:37861179:->T" "CLDN14" "NM_001146078:c.-82+21482_-82+21483insA" "FIVE_PRIME_INTRON" "Unknown significance" "rs35406478" "This variant is a VUS because it does not have enough information."
493759 "chr21:37861213:G>C" "CLDN14" "NM_001146078:c.-82+21448C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs748790501" "This variant is a VUS because it does not have enough information."
493760 "chr21:37861218:G>C" "CLDN14" "NM_001146078:c.-82+21443C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs112720656" "This variant is a VUS because it does not have enough information."
493761 "chr21:37861261:A>C" "CLDN14" "NM_001146078:c.-82+21400T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs370841653" "This variant is a VUS because it does not have enough information."
493762 "chr21:37861277:A>G" "CLDN14" "NM_001146078:c.-82+21384T>C" "FIVE_PRIME_INTRON" "Benign" "rs139957562" "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
493763 "chr21:37861287:G>A" "CLDN14" "NM_001146078:c.-82+21374C>T" "FIVE_PRIME_INTRON" "Benign" "rs219735" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 102 1322 0.0772 610 1006 0.6064 333 694 0.4798 375 1008 0.372 384 978 0.3926 1804 5008 0.360224
493764 "chr21:37861361:T>C" "CLDN14" "NM_001146078:c.-82+21300A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs529152783" "This variant is a VUS because it does not have enough information."
493765 "chr21:37861415:G>A" "CLDN14" "NM_001146078:c.-82+21246C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs370770690" "This variant is a VUS because it does not have enough information."
493766 "chr21:37861416:->AAAA" "CLDN14" "NM_001146078:c.-82+21245_-82+21246insTTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs59933730" "This variant is a VUS because it does not have enough information."
493767 "chr21:37861418:A>T" "CLDN14" "NM_001146078:c.-82+21243T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs13050446" "This variant is a VUS because it does not have enough information."
493768 "chr21:37861420:->AAAAT" "CLDN14" "NM_001146078:c.-82+21241_-82+21242insATTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs754506324" "This variant is a VUS because it does not have enough information."
493769 "chr21:37861427:->AT" "CLDN14" "NM_001146078:c.-82+21234_-82+21235insAT" "FIVE_PRIME_INTRON" "Unknown significance" "rs759681267" "This variant is a VUS because it does not have enough information."
493770 "chr21:37861429:A>T" "CLDN14" "NM_001146078:c.-82+21232T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs796590012" "This variant is a VUS because it does not have enough information."
493771 "chr21:37861430:->AATAT" "CLDN14" "NM_001146078:c.-82+21231_-82+21232insATATT" "FIVE_PRIME_INTRON" "Unknown significance" "rs369986633" "This variant is a VUS because it does not have enough information."
493772 "chr21:37861430:->ATAT" "CLDN14" "NM_001146078:c.-82+21231_-82+21232insATAT" "FIVE_PRIME_INTRON" "Unknown significance" "rs59933730" "This variant is a VUS because it does not have enough information."
493773 "chr21:37861430:->ATATATAT" "CLDN14" "NM_001146078:c.-82+21231_-82+21232insATATATAT" "FIVE_PRIME_INTRON" "Unknown significance" "rs71198816" "This variant is a VUS because it does not have enough information."
493774 "chr21:37861431:TATATAT>-" "CLDN14" "NM_001146078:c.-82+21230_-82+21238delATATATA" "FIVE_PRIME_INTRON" "Unknown significance" "rs371008340" "This variant is a VUS because it does not have enough information."
493775 "chr21:37861431:T>A" "CLDN14" "NM_001146078:c.-82+21230A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs11701326" "This variant is a VUS because it does not have enough information."
493776 "chr21:37861457:GA>-" "CLDN14" "NM_001146078:c.-82+21204_-82+21207delTC" "FIVE_PRIME_INTRON" "Unknown significance" "rs369533067" "This variant is a VUS because it does not have enough information."
493777 "chr21:37861488:G>A" "CLDN14" "NM_001146078:c.-82+21173C>T" "FIVE_PRIME_INTRON" "Benign" "rs219734" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 186 1322 0.1407 783 1006 0.7783 403 694 0.5807 384 1008 0.381 436 978 0.4458 2192 5008 0.4377
493778 "chr21:37861492:GAGAGAGAGAGAGAAAGAGA>-" "CLDN14" "NM_001146078:c.-82+21169_-82+21190delTCTCTTTCTCTCTCTCTCTC" "FIVE_PRIME_INTRON" "Unknown significance" "rs67920223" "This variant is a VUS because it does not have enough information."
493779 "chr21:37861495:AGAGAGAGAGAA>-" "CLDN14" "NM_001146078:c.-82+21166_-82+21179delTTCTCTCTCTCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs746126035" "This variant is a VUS because it does not have enough information."
493780 "chr21:37861507:->AG" "CLDN14" "NM_001146078:c.-82+21154_-82+21155insCT" "FIVE_PRIME_INTRON" "Benign" "rs551064855" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 43 1006 0.0427 51 694 0.0735 2 1008 0.002 32 978 0.0327 132 5008 0.0263578
493781 "chr21:37861590:T>C" "CLDN14" "NM_001146078:c.-82+21071A>G" "FIVE_PRIME_INTRON" "Benign" "rs115175616" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 66 1322 0.0499 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 67 5008 0.0133786
493782 "chr21:37861621:T>C" "CLDN14" "NM_001146078:c.-82+21040A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs369187783" "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
493783 "chr21:37861633:T>C" "CLDN14" "NM_001146078:c.-82+21028A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs371609428" "This variant is a VUS because it does not have enough information."
493784 "chr21:37861653:A>G" "CLDN14" "NM_001146078:c.-82+21008T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs548885498" "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
493785 "chr21:37861672:A>G" "CLDN14" "NM_001146078:c.-82+20989T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs193191070" "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 0 978 0 6 5008 0.00119808
493786 "chr21:37861721:C>T" "CLDN14" "NM_001146078:c.-82+20940G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs536253138" "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
493787 "chr21:37861803:G>A" "CLDN14" "NM_001146078:c.-82+20858C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs376208300" "This variant is a VUS because it does not have enough information."
493788 "chr21:37861849:C>T" "CLDN14" "NM_001146078:c.-82+20812G>A" "FIVE_PRIME_INTRON" "Benign" "rs219733" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 855 1322 0.6467 931 1006 0.9254 562 694 0.8098 785 1008 0.7788 750 978 0.7669 3883 5008 0.775359
493789 "chr21:37861853:G>A" "CLDN14" "NM_001146078:c.-82+20808C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs569457071" "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
493790 "chr21:37861859:G>C" "CLDN14" "NM_001146078:c.-82+20802C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs538424598" "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
493791 "chr21:37861869:T>C" "CLDN14" "NM_001146078:c.-82+20792A>G" "FIVE_PRIME_INTRON" "Benign" "rs55666618" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 239 1322 0.1808 34 1006 0.0338 36 694 0.0519 320 1008 0.3175 212 978 0.2168 841 5008 0.167931
493792 "chr21:37861886:G>A" "CLDN14" "NM_001146078:c.-82+20775C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs572219337" "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
493793 "chr21:37861890:C>T" "CLDN14" "NM_001146078:c.-82+20771G>A" "FIVE_PRIME_INTRON" "Benign" "rs7279128" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 441 1322 0.3336 69 1006 0.0686 74 694 0.1066 79 1008 0.0784 72 978 0.0736 735 5008 0.146765
493794 "chr21:37861896:C>G" "CLDN14" "NM_001146078:c.-82+20765G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs554848954" "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
493795 "chr21:37861899:C>T" "CLDN14" "NM_001146078:c.-82+20762G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs760110874" "This variant is a VUS because it does not have enough information."
493796 "chr21:37861900:G>A" "CLDN14" "NM_001146078:c.-82+20761C>T" "FIVE_PRIME_INTRON" "Benign" "rs73902541" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 48 1322 0.0363 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 50 5008 0.00998403
493797 "chr21:37861942:T>C" "CLDN14" "NM_001146078:c.-82+20719A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs745761739" "This variant is a VUS because it does not have enough information."
493798 "chr21:37861952:C>A" "CLDN14" "NM_001146078:c.-82+20709G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs769395116" "This variant is a VUS because it does not have enough information."
493799 "chr21:37861975:C>T" "CLDN14" "NM_001146078:c.-82+20686G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs369758898" "This variant is a VUS because it does not have enough information."
493800 "chr21:37862002:A>G" "CLDN14" "NM_001146078:c.-82+20659T>C" "FIVE_PRIME_INTRON" "Benign" "rs114309609" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 92 1322 0.0696 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 94 5008 0.01877
493801 "chr21:37862023:C>T" "CLDN14" "NM_001146078:c.-82+20638G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs185138572" "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
493802 "chr21:37862053:C>T" "CLDN14" "NM_001146078:c.-82+20608G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs577450543" "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
493803 "chr21:37862054:G>A" "CLDN14" "NM_001146078:c.-82+20607C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs748768536" "This variant is a VUS because it does not have enough information."
493804 "chr21:37862055:C>T" "CLDN14" "NM_001146078:c.-82+20606G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs768425561" "This variant is a VUS because it does not have enough information."
493805 "chr21:37862065:G>A" "CLDN14" "NM_001146078:c.-82+20596C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs149917568" "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
493806 "chr21:37862098:C>T" "CLDN14" "NM_001146078:c.-82+20563G>A" "FIVE_PRIME_INTRON" "Benign" "rs58621477" "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
493807 "chr21:37862118:C>T" "CLDN14" "NM_001146078:c.-82+20543G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs374503255" "This variant is a VUS because it does not have enough information."
493808 "chr21:37862141:C>A" "CLDN14" "NM_001146078:c.-82+20520G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs528689051" "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 2 978 0.002 3 5008 0.000599042
493809 "chr21:37862229:C>A" "CLDN14" "NM_001146078:c.-82+20432G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs28394132" "This variant is a VUS because it does not have enough information."
493810 "chr21:37862230:T>C" "CLDN14" "NM_001146078:c.-82+20431A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs774088231" "This variant is a VUS because it does not have enough information."
493811 "chr21:37862241:C>T" "CLDN14" "NM_001146078:c.-82+20420G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs548558024" "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
493812 "chr21:37862250:G>A" "CLDN14" "NM_001146078:c.-82+20411C>T" "FIVE_PRIME_INTRON" "Benign" "rs562444591" "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
493813 "chr21:37862328:C>T" "CLDN14" "NM_001146078:c.-82+20333G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs761178509" "This variant is a VUS because it does not have enough information."
493814 "chr21:37862329:G>A" "CLDN14" "NM_001146078:c.-82+20332C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs538096806" "This variant is a VUS because it does not have enough information."
493815 "chr21:37862336:G>C" "CLDN14" "NM_001146078:c.-82+20325C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs556713746" "This variant is a VUS because it does not have enough information."
493816 "chr21:37862356:C>T" "CLDN14" "NM_001146078:c.-82+20305G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs529654499" "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
493817 "chr21:37862357:G>A" "CLDN14" "NM_001146078:c.-82+20304C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs771195893" "This variant is a VUS because it does not have enough information."
493818 "chr21:37862380:A>G" "CLDN14" "NM_001146078:c.-82+20281T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs777230959" "This variant is a VUS because it does not have enough information."
493819 "chr21:37862381:G>T" "CLDN14" "NM_001146078:c.-82+20280C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs549393436" "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
493820 "chr21:37862473:T>C" "CLDN14" "NM_001146078:c.-82+20188A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs569394763" "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
493821 "chr21:37862560:G>A" "CLDN14" "NM_001146078:c.-82+20101C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs538310201" "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
493822 "chr21:37862564:C>T" "CLDN14" "NM_001146078:c.-82+20097G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs551874229" "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
493823 "chr21:37862565:G>A" "CLDN14" "NM_001146078:c.-82+20096C>T" "FIVE_PRIME_INTRON" "Benign" "rs13047783" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 20 1006 0.0199 14 694 0.0202 319 1008 0.3165 167 978 0.1708 523 5008 0.104433
493824 "chr21:37862568:C>T" "CLDN14" "NM_001146078:c.-82+20093G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs534861516" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 2 694 0.0029 1 1008 0.001 0 978 0 3 5008 0.000599042
493825 "chr21:37862569:G>A" "CLDN14" "NM_001146078:c.-82+20092C>T" "FIVE_PRIME_INTRON" "Benign" "rs7280480" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 80 1322 0.0605 4 1006 0.004 6 694 0.0086 0 1008 0 0 978 0 90 5008 0.0179712
493826 "chr21:37862583:C>G" "CLDN14" "NM_001146078:c.-82+20078G>C" "FIVE_PRIME_INTRON" "Benign" "rs117487724" "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 76 1008 0.0754 1 978 0.001 82 5008 0.0163738
493827 "chr21:37862588:A>C" "CLDN14" "NM_001146078:c.-82+20073T>G" "FIVE_PRIME_INTRON" "Benign" "rs144943328" "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 4 694 0.0058 0 1008 0 0 978 0 43 5008 0.00858626
493828 "chr21:37862648:C>T" "CLDN14" "NM_001146078:c.-82+20013G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs370468962" "This variant is a VUS because it does not have enough information."
493829 "chr21:37862657:A>G" "CLDN14" "NM_001146078:c.-82+20004T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs557359209" "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
493830 "chr21:37862681:T>A" "CLDN14" "NM_001146078:c.-82+19980A>T" "FIVE_PRIME_INTRON" "Benign" "rs547330394" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 6 1322 0.0045 0 1006 0 0 694 0 6 1008 0.006 2 978 0.002 14 5008 0.00279553
493831 "chr21:37862684:->TTTT" "CLDN14" "NM_001146078:c.-82+19977_-82+19978insAAAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs71326694" "This variant is a VUS because it does not have enough information."
493832 "chr21:37862684:->TTTTT" "CLDN14" "NM_001146078:c.-82+19977_-82+19978insAAAAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs748320712" "This variant is a VUS because it does not have enough information."
493833 "chr21:37862747:C>T" "CLDN14" "NM_001146078:c.-82+19914G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs190828205" "This variant is a VUS because it does not have enough information."
493834 "chr21:37862748:G>A" "CLDN14" "NM_001146078:c.-82+19913C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111796324" "This variant is a VUS because it does not have enough information."
493835 "chr21:37862753:C>T" "CLDN14" "NM_001146078:c.-82+19908G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs546274319" "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
493836 "chr21:37862775:C>T" "CLDN14" "NM_001146078:c.-82+19886G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs192531623" "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
493837 "chr21:37862787:A>G" "CLDN14" "NM_001146078:c.-82+19874T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs184756976" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 4 5008 0.000798722
493838 "chr21:37862826:A>G" "CLDN14" "NM_001146078:c.-82+19835T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs762965581" "This variant is a VUS because it does not have enough information."
493839 "chr21:37862840:C>T" "CLDN14" "NM_001146078:c.-82+19821G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs758427581" "This variant is a VUS because it does not have enough information."
493840 "chr21:37862848:G>A" "CLDN14" "NM_001146078:c.-82+19813C>T" "FIVE_PRIME_INTRON" "Benign" "rs542455379" "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
493841 "chr21:37862874:A>G" "CLDN14" "NM_001146078:c.-82+19787T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs562222581" "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
493842 "chr21:37862939:G>A" "CLDN14" "NM_001146078:c.-82+19722C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs372474563" "This variant is a VUS because it does not have enough information."
493843 "chr21:37862942:C>A" "CLDN14" "NM_001146078:c.-82+19719G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs377168898" "This variant is a VUS because it does not have enough information."
493844 "chr21:37862949:A>C" "CLDN14" "NM_001146078:c.-82+19712T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs751780785" "This variant is a VUS because it does not have enough information."
493845 "chr21:37862977:A>G" "CLDN14" "NM_001146078:c.-82+19684T>C" "FIVE_PRIME_INTRON" "Benign" "rs112047307" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 28 1322 0.0212 0 1006 0 3 694 0.0043 0 1008 0 0 978 0 31 5008 0.0061901
493846 "chr21:37863002:T>G" "CLDN14" "NM_001146078:c.-82+19659A>C" "FIVE_PRIME_INTRON" "Benign" "rs78013211" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 45 1006 0.0447 49 694 0.0706 1 1008 0.001 32 978 0.0327 128 5008 0.0255591
493847 "chr21:37863005:T>C" "CLDN14" "NM_001146078:c.-82+19656A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs751780582" "This variant is a VUS because it does not have enough information."
493848 "chr21:37863026:TC>-" "CLDN14" "NM_001146078:c.-82+19635_-82+19638delGA" "FIVE_PRIME_INTRON" "Unknown significance" "rs773601906" "This variant is a VUS because it does not have enough information."
493849 "chr21:37863031:C>G" "CLDN14" "NM_001146078:c.-82+19630G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs188347702" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 4 5008 0.000798722
493850 "chr21:37863034:T>C" "CLDN14" "NM_001146078:c.-82+19627A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs531981832" "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
493851 "chr21:37863039:C>T" "CLDN14" "NM_001146078:c.-82+19622G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs180759982" "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
493852 "chr21:37863040:G>A" "CLDN14" "NM_001146078:c.-82+19621C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs780951192" "This variant is a VUS because it does not have enough information."
493853 "chr21:37863049:T>A" "CLDN14" "NM_001146078:c.-82+19612A>T" "FIVE_PRIME_INTRON" "Benign" "rs186675546" "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 4 694 0.0058 0 1008 0 0 978 0 5 5008 0.000998403
493854 "chr21:37863115:C>T" "CLDN14" "NM_001146078:c.-82+19546G>A" "FIVE_PRIME_INTRON" "Benign" "rs112823433" "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 3 694 0.0043 0 1008 0 0 978 0 30 5008 0.00599042
493855 "chr21:37863118:G>A" "CLDN14" "NM_001146078:c.-82+19543C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs548402145" "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
493856 "chr21:37863123:C>T" "CLDN14" "NM_001146078:c.-82+19538G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs189504186" "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
493857 "chr21:37863129:T>G" "CLDN14" "NM_001146078:c.-82+19532A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs182140391" "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
493858 "chr21:37863147:C>T" "CLDN14" "NM_001146078:c.-82+19514G>A" "FIVE_PRIME_INTRON" "Benign" "rs117421817" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 17 1006 0.0169 4 694 0.0058 0 1008 0 4 978 0.0041 27 5008 0.00539137
493859 "chr21:37863159:->C" "CLDN14" "NM_001146078:c.-82+19502_-82+19503insG" "FIVE_PRIME_INTRON" "Unknown significance" "rs373023833" "This variant is a VUS because it does not have enough information."
493860 "chr21:37863164:C>T" "CLDN14" "NM_001146078:c.-82+19497G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs374208392" "This variant is a VUS because it does not have enough information."
493861 "chr21:37863167:->A" "CLDN14" "NM_001146078:c.-82+19494_-82+19495insT" "FIVE_PRIME_INTRON" "Unknown significance" "rs376057087" "This variant is a VUS because it does not have enough information."
493862 "chr21:37863170:->T" "CLDN14" "NM_001146078:c.-82+19491_-82+19492insA" "FIVE_PRIME_INTRON" "Unknown significance" "rs370205829" "This variant is a VUS because it does not have enough information."
493863 "chr21:37863170:A>G" "CLDN14" "NM_001146078:c.-82+19491T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs368691047" "This variant is a VUS because it does not have enough information."
493864 "chr21:37863177:T>G" "CLDN14" "NM_001146078:c.-82+19484A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs372183769" "This variant is a VUS because it does not have enough information."
493865 "chr21:37863181:C>G" "CLDN14" "NM_001146078:c.-82+19480G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs570820609" "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
493866 "chr21:37863198:C>A" "CLDN14" "NM_001146078:c.-82+19463G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs539881240" "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
493867 "chr21:37863219:C>T" "CLDN14" "NM_001146078:c.-82+19442G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs186738300" "This variant is a VUS because it does not have enough information." 0 1322 0 0 1006 0 1 694 0.0014 2 1008 0.002 0 978 0 3 5008 0.000599042
493868 "chr21:37863220:G>A" "CLDN14" "NM_001146078:c.-82+19441C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs573315708" "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
493869 "chr21:37863240:G>A" "CLDN14" "NM_001146078:c.-82+19421C>T" "FIVE_PRIME_INTRON" "Benign" "rs1318500" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 60 1322 0.0454 19 1006 0.0189 16 694 0.0231 321 1008 0.3185 166 978 0.1697 582 5008 0.116214
493870 "chr21:37863244:->ACAG" "CLDN14" "NM_001146078:c.-82+19417_-82+19418insCTGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs775319552" "This variant is a VUS because it does not have enough information."
493871 "chr21:37863244:ACAG>-" "CLDN14" "NM_001146078:c.-82+19417_-82+19422delCTGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs763348613" "This variant is a VUS because it does not have enough information."
493872 "chr21:37863248:ACAC>-" "CLDN14" "NM_001146078:c.-82+19413_-82+19418delGTGT" "FIVE_PRIME_INTRON" "Benign" "rs71827103" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 378 1322 0.2859 865 1006 0.8598 480 694 0.6916 704 1008 0.6984 673 978 0.6881 3100 5008 0.61901
493873 "chr21:37863248:->AC" "CLDN14" "NM_001146078:c.-82+19413_-82+19414insGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs3030068" "This variant is a VUS because it does not have enough information."
493874 "chr21:37863248:AC>-" "CLDN14" "NM_001146078:c.-82+19413_-82+19416delGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs367695478" "This variant is a VUS because it does not have enough information."
493875 "chr21:37863248:ACACAC>-" "CLDN14" "NM_001146078:c.-82+19413_-82+19420delGTGTGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs774981291" "This variant is a VUS because it does not have enough information."
493876 "chr21:37863248:ACACACACACACAC>-" "CLDN14" "NM_001146078:c.-82+19413_-82+19428delGTGTGTGTGTGTGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs200169110" "This variant is a VUS because it does not have enough information."
493877 "chr21:37863251:C>G" "CLDN14" "NM_001146078:c.-82+19410G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs73902542" "This variant is a VUS because it does not have enough information."
493878 "chr21:37863286:A>C" "CLDN14" "NM_001146078:c.-82+19375T>G" "FIVE_PRIME_INTRON" "Benign" "rs555892713" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 12 1322 0.0091 10 1006 0.0099 9 694 0.013 2 1008 0.002 4 978 0.0041 37 5008 0.00738818
493879 "chr21:37863359:G>A" "CLDN14" "NM_001146078:c.-82+19302C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs575451534" "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
493880 "chr21:37863361:A>C" "CLDN14" "NM_001146078:c.-82+19300T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs544455079" "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
493881 "chr21:37863384:G>A" "CLDN14" "NM_001146078:c.-82+19277C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs374928965" "This variant is a VUS because it does not have enough information."
493882 "chr21:37863440:G>A" "CLDN14" "NM_001146078:c.-82+19221C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs190308304" "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
493883 "chr21:37863448:C>T" "CLDN14" "NM_001146078:c.-82+19213G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs183268400" "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
493884 "chr21:37863453:C>-" "CLDN14" "NM_001146078:c.-82+19208delG" "FIVE_PRIME_INTRON" "Unknown significance" "rs759532820" "This variant is a VUS because it does not have enough information."
493885 "chr21:37863469:A>G" "CLDN14" "NM_001146078:c.-82+19192T>C" "FIVE_PRIME_INTRON" "Benign" "rs147748620" "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
493886 "chr21:37863473:T>C" "CLDN14" "NM_001146078:c.-82+19188A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs186111586" "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
493887 "chr21:37863525:T>C" "CLDN14" "NM_001146078:c.-82+19136A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs779972760" "This variant is a VUS because it does not have enough information."
493888 "chr21:37863529:G>A" "CLDN14" "NM_001146078:c.-82+19132C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs528158122" "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
493889 "chr21:37863580:C>T" "CLDN14" "NM_001146078:c.-82+19081G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs548002601" "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
493890 "chr21:37863659:C>G" "CLDN14" "NM_001146078:c.-82+19002G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs568214657" "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
493891 "chr21:37863668:AAG>-" "CLDN14" "NM_001146078:c.-82+18993_-82+18997delCTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs773971039" "This variant is a VUS because it does not have enough information."
493892 "chr21:37863670:G>A" "CLDN14" "NM_001146078:c.-82+18991C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs530736267" "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
493893 "chr21:37863673:G>A" "CLDN14" "NM_001146078:c.-82+18988C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs748819439" "This variant is a VUS because it does not have enough information."
493894 "chr21:37863679:C>T" "CLDN14" "NM_001146078:c.-82+18982G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs768268008" "This variant is a VUS because it does not have enough information."
493895 "chr21:37863697:G>A" "CLDN14" "NM_001146078:c.-82+18964C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs7280279" "This variant is a VUS because it does not have enough information." 5 1322 0.0038 0 1006 0 1 694 0.0014 1 1008 0.001 0 978 0 7 5008 0.00139776
493896 "chr21:37863702:G>A" "CLDN14" "NM_001146078:c.-82+18959C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs570806195" "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
493897 "chr21:37863715:G>C" "CLDN14" "NM_001146078:c.-82+18946C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs756045964" "This variant is a VUS because it does not have enough information."
493898 "chr21:37863718:C>T" "CLDN14" "NM_001146078:c.-82+18943G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs778774831" "This variant is a VUS because it does not have enough information."
493899 "chr21:37863721:G>A" "CLDN14" "NM_001146078:c.-82+18940C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545767623" "This variant is a VUS because it does not have enough information."
493900 "chr21:37863727:G>A" "CLDN14" "NM_001146078:c.-82+18934C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs539820277" "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
493901 "chr21:37863735:G>A" "CLDN14" "NM_001146078:c.-82+18926C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs553366109" "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
493902 "chr21:37863771:G>A" "CLDN14" "NM_001146078:c.-82+18890C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs142594367" "This variant is a VUS because it does not have enough information."
493903 "chr21:37863789:G>A" "CLDN14" "NM_001146078:c.-82+18872C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566767442" "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
493904 "chr21:37863846:T>C" "CLDN14" "NM_001146078:c.-82+18815A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs146362686" "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
493905 "chr21:37863897:A>G" "CLDN14" "NM_001146078:c.-82+18764T>C" "FIVE_PRIME_INTRON" "Benign" "rs139085673" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 1322 0 23 1006 0.0229 3 694 0.0043 0 1008 0 3 978 0.0031 29 5008 0.00579073
493906 "chr21:37863912:T>-" "CLDN14" "NM_001146078:c.-82+18749delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs34594670" "This variant is a VUS because it does not have enough information."
493907 "chr21:37863975:G>A" "CLDN14" "NM_001146078:c.-82+18686C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs531429763" "This variant is a VUS because it does not have enough information."
493908 "chr21:37863993:T>C" "CLDN14" "NM_001146078:c.-82+18668A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs142988599" "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
493909 "chr21:37864001:C>T" "CLDN14" "NM_001146078:c.-82+18660G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs543251914" "This variant is a VUS because it does not have enough information."
493910 "chr21:37864016:C>T" "CLDN14" "NM_001146078:c.-82+18645G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs776878501" "This variant is a VUS because it does not have enough information."
493911 "chr21:37864028:C>T" "CLDN14" "NM_001146078:c.-82+18633G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs369241822" "This variant is a VUS because it does not have enough information."
493912 "chr21:37864040:G>A" "CLDN14" "NM_001146078:c.-82+18621C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs558547585" "This variant is a VUS because it does not have enough information."
493913 "chr21:37864045:C>T" "CLDN14" "NM_001146078:c.-82+18616G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759902114" "This variant is a VUS because it does not have enough information."
493914 "chr21:37864059:G>C" "CLDN14" "NM_001146078:c.-82+18602C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs561878828" "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
493915 "chr21:37864072:C>T" "CLDN14" "NM_001146078:c.-82+18589G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs775966241" "This variant is a VUS because it does not have enough information."
493916 "chr21:37864078:T>A" "CLDN14" "NM_001146078:c.-82+18583A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs558009502" "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
493917 "chr21:37864099:T>C" "CLDN14" "NM_001146078:c.-82+18562A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs189836334" "This variant is a VUS because it does not have enough information." 0 1322 0 2 1006 0.002 2 694 0.0029 0 1008 0 2 978 0.002 6 5008 0.00119808
493918 "chr21:37864105:G>A" "CLDN14" "NM_001146078:c.-82+18556C>T" "FIVE_PRIME_INTRON" "Benign" "rs540588126" "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
493919 "chr21:37864127:C>T" "CLDN14" "NM_001146078:c.-82+18534G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs182157060" "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
493920 "chr21:37864137:C>G" "CLDN14" "NM_001146078:c.-82+18524G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs764132891" "This variant is a VUS because it does not have enough information."
493921 "chr21:37864147:C>T" "CLDN14" "NM_001146078:c.-82+18514G>A" "FIVE_PRIME_INTRON" "Benign" "rs219732" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 100 1322 0.0756 609 1006 0.6054 334 694 0.4813 375 1008 0.372 375 978 0.3834 1793 5008 0.358027
493922 "chr21:37864170:C>A" "CLDN14" "NM_001146078:c.-82+18491G>T" "FIVE_PRIME_INTRON" "Benign" "rs114926124" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 48 1322 0.0363 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 49 5008 0.00978435
493923 "chr21:37864260:C>T" "CLDN14" "NM_001146078:c.-82+18401G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs565960068" "This variant is a VUS because it does not have enough information."
493924 "chr21:37864308:A>C" "CLDN14" "NM_001146078:c.-82+18353T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs561808508" "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
493925 "chr21:37864340:G>A" "CLDN14" "NM_001146078:c.-82+18321C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs200855722" "This variant is a VUS because it does not have enough information."
493926 "chr21:37864341:C>T" "CLDN14" "NM_001146078:c.-82+18320G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs188433065" "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
493927 "chr21:37864405:C>A" "CLDN14" "NM_001146078:c.-82+18256G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs372827470" "This variant is a VUS because it does not have enough information."
493928 "chr21:37864409:C>G" "CLDN14" "NM_001146078:c.-82+18252G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs771910732" "This variant is a VUS because it does not have enough information."
493929 "chr21:37864449:->AAAATT" "CLDN14" "NM_001146078:c.-82+18212_-82+18213insAATTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs552473909" "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
493930 "chr21:37864455:G>A" "CLDN14" "NM_001146078:c.-82+18206C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs527723661" "This variant is a VUS because it does not have enough information."
493931 "chr21:37864459:G>A" "CLDN14" "NM_001146078:c.-82+18202C>T" "FIVE_PRIME_INTRON" "Benign" "rs550821172" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 268 1322 0.2027 27 1006 0.0268 31 694 0.0447 318 1008 0.3155 205 978 0.2096 849 5008 0.169529
493932 "chr21:37864460:C>T" "CLDN14" "NM_001146078:c.-82+18201G>A" "FIVE_PRIME_INTRON" "Benign" "rs564357866" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 278 1322 0.2103 27 1006 0.0268 31 694 0.0447 318 1008 0.3155 205 978 0.2096 859 5008 0.171526
493933 "chr21:37864467:T>G" "CLDN14" "NM_001146078:c.-82+18194A>C" "FIVE_PRIME_INTRON" "Benign" "rs533220067" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 253 1322 0.1914 29 1006 0.0288 35 694 0.0504 316 1008 0.3135 207 978 0.2117 840 5008 0.167732
493934 "chr21:37864468:C>A" "CLDN14" "NM_001146078:c.-82+18193G>T" "FIVE_PRIME_INTRON" "Benign" "rs546597675" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 253 1322 0.1914 29 1006 0.0288 35 694 0.0504 316 1008 0.3135 207 978 0.2117 840 5008 0.167732
493935 "chr21:37864469:A>G" "CLDN14" "NM_001146078:c.-82+18192T>C" "FIVE_PRIME_INTRON" "Benign" "rs566808313" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 253 1322 0.1914 29 1006 0.0288 35 694 0.0504 316 1008 0.3135 207 978 0.2117 840 5008 0.167732
493936 "chr21:37864471:G>A" "CLDN14" "NM_001146078:c.-82+18190C>T" "FIVE_PRIME_INTRON" "Benign" "rs184320" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 344 1322 0.2602 813 1006 0.8082 430 694 0.6196 701 1008 0.6954 631 978 0.6452 2919 5008 0.582867
493937 "chr21:37864486:A>T" "CLDN14" "NM_001146078:c.-82+18175T>A" "FIVE_PRIME_INTRON" "Benign" "rs549054564" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 160 1322 0.121 6 1006 0.006 17 694 0.0245 207 1008 0.2054 107 978 0.1094 497 5008 0.0992412
493938 "chr21:37864487:C>A" "CLDN14" "NM_001146078:c.-82+18174G>T" "FIVE_PRIME_INTRON" "Benign" "rs569039507" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 160 1322 0.121 6 1006 0.006 17 694 0.0245 207 1008 0.2054 107 978 0.1094 497 5008 0.0992412
493939 "chr21:37864498:C>T" "CLDN14" "NM_001146078:c.-82+18163G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs570904787" "This variant is a VUS because it does not have enough information."
493940 "chr21:37864517:G>T" "CLDN14" "NM_001146078:c.-82+18144C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs13048689" "This variant is a VUS because it does not have enough information."
493941 "chr21:37864528:C>T" "CLDN14" "NM_001146078:c.-82+18133G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs538035446" "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
493942 "chr21:37864532:A>G" "CLDN14" "NM_001146078:c.-82+18129T>C" "FIVE_PRIME_INTRON" "Benign" "rs377209469" "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 1 694 0.0014 0 1008 0 0 978 0 23 5008 0.00459265
493943 "chr21:37864538:C>T" "CLDN14" "NM_001146078:c.-82+18123G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs538292762" "This variant is a VUS because it does not have enough information."
493944 "chr21:37864559:C>T" "CLDN14" "NM_001146078:c.-82+18102G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs577840382" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 2 1006 0.002 0 694 0 0 1008 0 0 978 0 4 5008 0.000798722
493945 "chr21:37864560:G>A" "CLDN14" "NM_001146078:c.-82+18101C>T" "FIVE_PRIME_INTRON" "Benign" "rs534458948" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
493946 "chr21:37864567:C>A" "CLDN14" "NM_001146078:c.-82+18094G>T" "FIVE_PRIME_INTRON" "Benign" "rs554179271" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 63 1322 0.0477 3 1006 0.003 0 694 0 18 1008 0.0179 8 978 0.0082 92 5008 0.0183706
493947 "chr21:37864568:T>A" "CLDN14" "NM_001146078:c.-82+18093A>T" "FIVE_PRIME_INTRON" "Benign" "rs572788659" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 63 1322 0.0477 3 1006 0.003 0 694 0 18 1008 0.0179 8 978 0.0082 92 5008 0.0183706
493948 "chr21:37864586:G>C" "CLDN14" "NM_001146078:c.-82+18075C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs9798632" "This variant is a VUS because it does not have enough information."
493949 "chr21:37864589:G>A" "CLDN14" "NM_001146078:c.-82+18072C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs556490263" "This variant is a VUS because it does not have enough information."
493950 "chr21:37864594:C>T" "CLDN14" "NM_001146078:c.-82+18067G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs541509473" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 1 1006 0.001 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
493951 "chr21:37864595:G>A" "CLDN14" "NM_001146078:c.-82+18066C>T" "FIVE_PRIME_INTRON" "Benign" "rs568284831" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 149 1322 0.1127 1 1006 0.001 4 694 0.0058 0 1008 0 0 978 0 154 5008 0.0307508
493952 "chr21:37864600:C>T" "CLDN14" "NM_001146078:c.-82+18061G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs535630077" "This variant is a VUS because it does not have enough information."
493953 "chr21:37864604:C>T" "CLDN14" "NM_001146078:c.-82+18057G>A" "FIVE_PRIME_INTRON" "Benign" "rs554077863" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 4 1006 0.004 4 694 0.0058 0 1008 0 0 978 0 10 5008 0.00199681
493954 "chr21:37864647:G>T" "CLDN14" "NM_001146078:c.-82+18014C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs544339683" "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
493955 "chr21:37864697:A>G" "CLDN14" "NM_001146078:c.-82+17964T>C" "FIVE_PRIME_INTRON" "Benign" "rs564245502" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 1322 0.0068 1 1006 0.001 1 694 0.0014 1 1008 0.001 0 978 0 12 5008 0.00239617
493956 "chr21:37864707:C>T" "CLDN14" "NM_001146078:c.-82+17954G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs112693501" "This variant is a VUS because it does not have enough information."
493957 "chr21:37864733:C>T" "CLDN14" "NM_001146078:c.-82+17928G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs572396027" "This variant is a VUS because it does not have enough information."
493958 "chr21:37864737:C>T" "CLDN14" "NM_001146078:c.-82+17924G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs219731" "This variant is a VUS because it does not have enough information."
493959 "chr21:37864737:CCAAAAAAAAAAAAAAAAA>TC" "CLDN14" "Unknown significance" "rs747288451" "This variant is a VUS because it does not have enough information."
493960 "chr21:37864739:->AAA" "CLDN14" "NM_001146078:c.-82+17922_-82+17923insTTT" "FIVE_PRIME_INTRON" "Benign" "rs536878400" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 463 1322 0.3502 229 1006 0.2276 190 694 0.2738 157 1008 0.1558 226 978 0.2311 1265 5008 0.252596
493961 "chr21:37864739:A>-" "CLDN14" "NM_001146078:c.-82+17922delT" "FIVE_PRIME_INTRON" "Unknown significance" "rs58666814" "This variant is a VUS because it does not have enough information."
493962 "chr21:37864767:->TGC" "CLDN14" "NM_001146078:c.-82+17894_-82+17895insGCA" "FIVE_PRIME_INTRON" "Unknown significance" "rs71198818" "This variant is a VUS because it does not have enough information."
493963 "chr21:37864788:A>G" "CLDN14" "NM_001146078:c.-82+17873T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs532983153" "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
493964 "chr21:37864830:G>A" "CLDN14" "NM_001146078:c.-82+17831C>T" "FIVE_PRIME_INTRON" "Benign" "rs113118738" "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 2 694 0.0029 0 1008 0 0 978 0 38 5008 0.00758786
493965 "chr21:37864831:G>A" "CLDN14" "NM_001146078:c.-82+17830C>T" "FIVE_PRIME_INTRON" "Benign" "rs560227457" "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
493966 "chr21:37864852:G>A" "CLDN14" "NM_001146078:c.-82+17809C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566935504" "This variant is a VUS because it does not have enough information."
493967 "chr21:37864870:T>G" "CLDN14" "NM_001146078:c.-82+17791A>C" "FIVE_PRIME_INTRON" "Benign" "rs7277448" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 284 1322 0.2148 88 1006 0.0875 75 694 0.1081 76 1008 0.0754 128 978 0.1309 651 5008 0.129992
493968 "chr21:37864870:T>C" "CLDN14" "NM_001146078:c.-82+17791A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs7277448" "This variant is a VUS because it does not have enough information."
493969 "chr21:37864884:G>A" "CLDN14" "NM_001146078:c.-82+17777C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs549003320" "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
493970 "chr21:37864923:T>A" "CLDN14" "NM_001146078:c.-82+17738A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs191174381" "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
493971 "chr21:37864931:A>C" "CLDN14" "NM_001146078:c.-82+17730T>G" "FIVE_PRIME_INTRON" "Benign" "rs115498438" "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 1 694 0.0014 0 1008 0 0 978 0 54 5008 0.0107827
493972 "chr21:37864940:C>T" "CLDN14" "NM_001146078:c.-82+17721G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs183078136" "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
493973 "chr21:37864941:G>A" "CLDN14" "NM_001146078:c.-82+17720C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs571772676" "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
493974 "chr21:37864942:A>-" "CLDN14" "NM_001146078:c.-82+17719delT" "FIVE_PRIME_INTRON" "Unknown significance" "rs545299912" "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
493975 "chr21:37864999:A>G" "CLDN14" "NM_001146078:c.-82+17662T>C" "FIVE_PRIME_INTRON" "Benign" "rs534169483" "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
493976 "chr21:37865007:G>A" "CLDN14" "NM_001146078:c.-82+17654C>T" "FIVE_PRIME_INTRON" "Benign" "rs112972217" "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 3 694 0.0043 0 1008 0 0 978 0 30 5008 0.00599042
493977 "chr21:37865031:G>A" "CLDN14" "NM_001146078:c.-82+17630C>T" "FIVE_PRIME_INTRON" "Benign" "rs138764681" "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
493978 "chr21:37865063:A>G" "CLDN14" "NM_001146078:c.-82+17598T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs760008567" "This variant is a VUS because it does not have enough information."
493979 "chr21:37865069:A>C" "CLDN14" "NM_001146078:c.-82+17592T>G" "FIVE_PRIME_INTRON" "Benign" "rs113404454" "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 3 694 0.0043 0 1008 0 0 978 0 30 5008 0.00599042
493980 "chr21:37865097:C>A" "CLDN14" "NM_001146078:c.-82+17564G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs770283140" "This variant is a VUS because it does not have enough information."
493981 "chr21:37865111:G>A" "CLDN14" "NM_001146078:c.-82+17550C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs188414758" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 2 1006 0.002 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
493982 "chr21:37865167:A>G" "CLDN14" "NM_001146078:c.-82+17494T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs543468081" "This variant is a VUS because it does not have enough information."
493983 "chr21:37865171:T>C" "CLDN14" "NM_001146078:c.-82+17490A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs561888003" "This variant is a VUS because it does not have enough information."
493984 "chr21:37865196:G>A" "CLDN14" "NM_001146078:c.-82+17465C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs766284259" "This variant is a VUS because it does not have enough information."
493985 "chr21:37865207:ATG>-" "CLDN14" "NM_001146078:c.-82+17454_-82+17458delCAT" "FIVE_PRIME_INTRON" "Unknown significance" "rs750212151" "This variant is a VUS because it does not have enough information."
493986 "chr21:37865236:G>C" "CLDN14" "NM_001146078:c.-82+17425C>G" "FIVE_PRIME_INTRON" "Benign" "rs192019075" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 22 1322 0.0166 1 1006 0.001 9 694 0.013 0 1008 0 0 978 0 32 5008 0.00638978
493987 "chr21:37865281:G>T" "CLDN14" "NM_001146078:c.-82+17380C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs146272844" "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
493988 "chr21:37865281:G>C" "CLDN14" "NM_001146078:c.-82+17380C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs146272844" "This variant is a VUS because it does not have enough information."
493989 "chr21:37865291:G>A" "CLDN14" "NM_001146078:c.-82+17370C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs564177313" "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
493990 "chr21:37865297:G>A" "CLDN14" "NM_001146078:c.-82+17364C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs541214845" "This variant is a VUS because it does not have enough information."
493991 "chr21:37865297:G>C" "CLDN14" "NM_001146078:c.-82+17364C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs541214845" "This variant is a VUS because it does not have enough information."
493992 "chr21:37865329:G>A" "CLDN14" "NM_001146078:c.-82+17332C>T" "FIVE_PRIME_INTRON" "Benign" "rs139138612" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
493993 "chr21:37865339:G>T" "CLDN14" "NM_001146078:c.-82+17322C>A" "FIVE_PRIME_INTRON" "Benign" "rs2835365" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 784 1322 0.593 339 1006 0.337 238 694 0.3429 402 1008 0.3988 442 978 0.4519 2205 5008 0.440296
493994 "chr21:37865356:T>C" "CLDN14" "NM_001146078:c.-82+17305A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs777427969" "This variant is a VUS because it does not have enough information."
493995 "chr21:37865358:A>G" "CLDN14" "NM_001146078:c.-82+17303T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs560381609" "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
493996 "chr21:37865397:C>T" "CLDN14" "NM_001146078:c.-82+17264G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs533253887" "This variant is a VUS because it does not have enough information."
493997 "chr21:37865404:T>A" "CLDN14" "NM_001146078:c.-82+17257A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs770193282" "This variant is a VUS because it does not have enough information."
493998 "chr21:37865410:C>T" "CLDN14" "NM_001146078:c.-82+17251G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs529143229" "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
493999 "chr21:37865411:C>T" "CLDN14" "NM_001146078:c.-82+17250G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs184998016" "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
494000 "chr21:37865412:G>-" "CLDN14" "NM_001146078:c.-82+17249delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs752908002" "This variant is a VUS because it does not have enough information."
494001 "chr21:37865415:TTG>-" "CLDN14" "NM_001146078:c.-82+17246_-82+17250delCAA" "FIVE_PRIME_INTRON" "Benign" "rs544277434" "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
494002 "chr21:37865417:G>A" "CLDN14" "NM_001146078:c.-82+17244C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs77773244" "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
494003 "chr21:37865417:G>T" "CLDN14" "NM_001146078:c.-82+17244C>A" "FIVE_PRIME_INTRON" "Benign" "rs77773244" "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 0 694 0 1 1008 0.001 0 978 0 40 5008 0.00798722
494004 "chr21:37865427:C>T" "CLDN14" "NM_001146078:c.-82+17234G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs552291943" "This variant is a VUS because it does not have enough information."
494005 "chr21:37865438:G>A" "CLDN14" "NM_001146078:c.-82+17223C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs551452702" "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
494006 "chr21:37865447:G>A" "CLDN14" "NM_001146078:c.-82+17214C>T" "FIVE_PRIME_INTRON" "Benign" "rs35030913" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 262 1322 0.1982 15 1006 0.0149 32 694 0.0461 308 1008 0.3056 172 978 0.1759 789 5008 0.157548
494007 "chr21:37865477:C>T" "CLDN14" "NM_001146078:c.-82+17184G>A" "FIVE_PRIME_INTRON" "Benign" "rs142503474" "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 4 694 0.0058 0 1008 0 0 978 0 40 5008 0.00798722
494008 "chr21:37865491:G>A" "CLDN14" "NM_001146078:c.-82+17170C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs769103935" "This variant is a VUS because it does not have enough information."
494009 "chr21:37865502:G>A" "CLDN14" "NM_001146078:c.-82+17159C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs547708517" "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
494010 "chr21:37865522:G>A" "CLDN14" "NM_001146078:c.-82+17139C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs567863056" "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
494011 "chr21:37865537:C>G" "CLDN14" "NM_001146078:c.-82+17124G>C" "FIVE_PRIME_INTRON" "Benign" "rs113738085" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 2 1322 0.0015 11 1006 0.0109 1 694 0.0014 0 1008 0 0 978 0 14 5008 0.00279553
494012 "chr21:37865584:G>A" "CLDN14" "NM_001146078:c.-82+17077C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs761886970" "This variant is a VUS because it does not have enough information."
494013 "chr21:37865623:T>C" "CLDN14" "NM_001146078:c.-82+17038A>G" "FIVE_PRIME_INTRON" "Benign" "rs2850113" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 742 1322 0.5613 861 1006 0.8559 511 694 0.7363 734 1008 0.7282 625 978 0.6391 3473 5008 0.69349
494014 "chr21:37865637:C>T" "CLDN14" "NM_001146078:c.-82+17024G>A" "FIVE_PRIME_INTRON" "Benign" "rs201242355" "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 8 978 0.0082 8 5008 0.00159744
494015 "chr21:37865638:G>A" "CLDN14" "NM_001146078:c.-82+17023C>T" "FIVE_PRIME_INTRON" "Benign" "rs57149462" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 65 1322 0.0492 1 1006 0.001 7 694 0.0101 4 1008 0.004 23 978 0.0235 100 5008 0.0199681
494016 "chr21:37865660:T>C" "CLDN14" "NM_001146078:c.-82+17001A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs760452955" "This variant is a VUS because it does not have enough information."
494017 "chr21:37865671:T>A" "CLDN14" "NM_001146078:c.-82+16990A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs766245915" "This variant is a VUS because it does not have enough information."
494018 "chr21:37865736:A>T" "CLDN14" "NM_001146078:c.-82+16925T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs11910952" "This variant is a VUS because it does not have enough information."
494019 "chr21:37865802:G>A" "CLDN14" "NM_001146078:c.-82+16859C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs755884728" "This variant is a VUS because it does not have enough information."
494020 "chr21:37865832:A>G" "CLDN14" "NM_001146078:c.-82+16829T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs753871623" "This variant is a VUS because it does not have enough information."
494021 "chr21:37865837:C>A" "CLDN14" "NM_001146078:c.-82+16824G>T" "FIVE_PRIME_INTRON" "Benign" "rs187805904" "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 0 978 0 6 5008 0.00119808
494022 "chr21:37865843:A>G" "CLDN14" "NM_001146078:c.-82+16818T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs577691477" "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
494023 "chr21:37865902:C>A" "CLDN14" "NM_001146078:c.-82+16759G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs540340479" "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
494024 "chr21:37865904:C>T" "CLDN14" "NM_001146078:c.-82+16757G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs553658942" "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
494025 "chr21:37865905:G>A" "CLDN14" "NM_001146078:c.-82+16756C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs150541309" "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
494026 "chr21:37865920:A>G" "CLDN14" "NM_001146078:c.-82+16741T>C" "FIVE_PRIME_INTRON" "Benign" "rs2776289" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 686 1322 0.5189 857 1006 0.8519 502 694 0.7233 731 1008 0.7252 613 978 0.6268 3389 5008 0.676717
494027 "chr21:37865945:C>T" "CLDN14" "NM_001146078:c.-82+16716G>A" "FIVE_PRIME_INTRON" "Benign" "rs562482881" "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 24 978 0.0245 24 5008 0.00479233
494028 "chr21:37865946:G>A" "CLDN14" "NM_001146078:c.-82+16715C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs139496621" "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
494029 "chr21:37865947:C>T" "CLDN14" "NM_001146078:c.-82+16714G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs545030323" "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
494030 "chr21:37865954:G>A" "CLDN14" "NM_001146078:c.-82+16707C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs565364923" "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
494031 "chr21:37865960:G>A" "CLDN14" "NM_001146078:c.-82+16701C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs150037580" "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
494032 "chr21:37865978:A>G" "CLDN14" "NM_001146078:c.-82+16683T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs191557247" "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
494033 "chr21:37865979:T>C" "CLDN14" "NM_001146078:c.-82+16682A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs567707575" "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
494034 "chr21:37865987:C>T" "CLDN14" "NM_001146078:c.-82+16674G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs530324812" "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
494035 "chr21:37865988:G>A" "CLDN14" "NM_001146078:c.-82+16673C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs778557936" "This variant is a VUS because it does not have enough information."
494036 "chr21:37866022:C>T" "CLDN14" "NM_001146078:c.-82+16639G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs547581849" "This variant is a VUS because it does not have enough information."
494037 "chr21:37866036:T>C" "CLDN14" "NM_001146078:c.-82+16625A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs550484245" "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
494038 "chr21:37866042:G>A" "CLDN14" "NM_001146078:c.-82+16619C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs747712892" "This variant is a VUS because it does not have enough information."
494039 "chr21:37866064:G>C" "CLDN14" "NM_001146078:c.-82+16597C>G" "FIVE_PRIME_INTRON" "Benign" "rs147706788" "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 1 978 0.001 15 5008 0.00299521
494040 "chr21:37866067:T>C" "CLDN14" "NM_001146078:c.-82+16594A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs746645368" "This variant is a VUS because it does not have enough information."
494041 "chr21:37866090:T>C" "CLDN14" "NM_001146078:c.-82+16571A>G" "FIVE_PRIME_INTRON" "Benign" "rs2850114" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 464 1322 0.351 812 1006 0.8072 449 694 0.647 742 1008 0.7361 580 978 0.593 3047 5008 0.608427
494042 "chr21:37866123:C>T" "CLDN14" "NM_001146078:c.-82+16538G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs777588097" "This variant is a VUS because it does not have enough information."
494043 "chr21:37866124:G>A" "CLDN14" "NM_001146078:c.-82+16537C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs142533097" "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
494044 "chr21:37866210:C>T" "CLDN14" "NM_001146078:c.-82+16451G>A" "FIVE_PRIME_INTRON" "Benign" "rs2850115" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 207 1322 0.1566 61 1006 0.0606 48 694 0.0692 305 1008 0.3026 213 978 0.2178 834 5008 0.166534
494045 "chr21:37866231:G>A" "CLDN14" "NM_001146078:c.-82+16430C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs557482460" "This variant is a VUS because it does not have enough information."
494046 "chr21:37866245:C>G" "CLDN14" "NM_001146078:c.-82+16416G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs533607339" "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
494047 "chr21:37866266:G>C" "CLDN14" "NM_001146078:c.-82+16395C>G" "FIVE_PRIME_INTRON" "Benign" "rs144966133" "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
494048 "chr21:37866276:G>C" "CLDN14" "NM_001146078:c.-82+16385C>G" "FIVE_PRIME_INTRON" "Benign" "rs9982279" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 255 1322 0.1929 750 1006 0.7455 401 694 0.5778 434 1008 0.4306 366 978 0.3742 2206 5008 0.440495
494049 "chr21:37866293:->G" "CLDN14" "NM_001146078:c.-82+16368_-82+16369insC" "FIVE_PRIME_INTRON" "Unknown significance" "rs368848338" "This variant is a VUS because it does not have enough information."
494050 "chr21:37866324:A>G" "CLDN14" "NM_001146078:c.-82+16337T>C" "FIVE_PRIME_INTRON" "Benign" "rs2776290" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 127 1322 0.0961 63 1006 0.0626 44 694 0.0634 305 1008 0.3026 215 978 0.2198 754 5008 0.150559
494051 "chr21:37866361:C>T" "CLDN14" "NM_001146078:c.-82+16300G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs147952376" "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
494052 "chr21:37866362:G>A" "CLDN14" "NM_001146078:c.-82+16299C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs748232387" "This variant is a VUS because it does not have enough information."
494053 "chr21:37866380:C>G" "CLDN14" "NM_001146078:c.-82+16281G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs148936127" "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
494054 "chr21:37866381:G>A" "CLDN14" "NM_001146078:c.-82+16280C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs772187758" "This variant is a VUS because it does not have enough information."
494055 "chr21:37866395:C>T" "CLDN14" "NM_001146078:c.-82+16266G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs545303156" "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
494056 "chr21:37866456:C>T" "CLDN14" "NM_001146078:c.-82+16205G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773345543" "This variant is a VUS because it does not have enough information."
494057 "chr21:37866480:C>T" "CLDN14" "NM_001146078:c.-82+16181G>A" "FIVE_PRIME_INTRON" "Benign" "rs2071049" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 168 1322 0.1271 747 1006 0.7425 395 694 0.5692 430 1008 0.4266 362 978 0.3701 2102 5008 0.419728
494058 "chr21:37866486:A>G" "CLDN14" "NM_001146078:c.-82+16175T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs143641368" "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
494059 "chr21:37866520:G>A" "CLDN14" "NM_001146078:c.-82+16141C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs541125957" "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
494060 "chr21:37866528:T>C" "CLDN14" "NM_001146078:c.-82+16133A>G" "FIVE_PRIME_INTRON" "Benign" "rs2071050" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 702 1322 0.531 857 1006 0.8519 503 694 0.7248 742 1008 0.7361 616 978 0.6299 3420 5008 0.682907
494061 "chr21:37866529:G>A" "CLDN14" "NM_001146078:c.-82+16132C>T" "FIVE_PRIME_INTRON" "Benign" "rs148118096" "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 0 1008 0 0 978 0 12 5008 0.00239617
494062 "chr21:37866549:G>A" "CLDN14" "NM_001146078:c.-82+16112C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs140968960" "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
494063 "chr21:37866555:C>T" "CLDN14" "NM_001146078:c.-82+16106G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs184308885" "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
494064 "chr21:37866556:G>A" "CLDN14" "NM_001146078:c.-82+16105C>T" "FIVE_PRIME_INTRON" "Benign" "rs73902544" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 109 1322 0.0825 1 1006 0.001 12 694 0.0173 4 1008 0.004 23 978 0.0235 149 5008 0.0297524
494065 "chr21:37866625:A>G" "CLDN14" "NM_001146078:c.-82+16036T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs552840962" "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
494066 "chr21:37866639:G>A" "CLDN14" "NM_001146078:c.-82+16022C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs190022681" "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
494067 "chr21:37866640:G>A" "CLDN14" "NM_001146078:c.-82+16021C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs759335675" "This variant is a VUS because it does not have enough information."
494068 "chr21:37866652:AAATT>-" "CLDN14" "NM_001146078:c.-82+16009_-82+16015delAATTT" "FIVE_PRIME_INTRON" "Benign" "rs199810181" "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 4 694 0.0058 0 1008 0 0 978 0 35 5008 0.00698882
494069 "chr21:37866675:C>T" "CLDN14" "NM_001146078:c.-82+15986G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs373036959" "This variant is a VUS because it does not have enough information."
494070 "chr21:37866692:C>T" "CLDN14" "NM_001146078:c.-82+15969G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs533827920" "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
494071 "chr21:37866701:G>A" "CLDN14" "NM_001146078:c.-82+15960C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs181282612" "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
494072 "chr21:37866736:A>G" "CLDN14" "NM_001146078:c.-82+15925T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs567051486" "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
494073 "chr21:37866741:C>T" "CLDN14" "NM_001146078:c.-82+15920G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs184709589" "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
494074 "chr21:37866820:A>G" "CLDN14" "NM_001146078:c.-82+15841T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs765325348" "This variant is a VUS because it does not have enough information."
494075 "chr21:37866876:G>A" "CLDN14" "NM_001146078:c.-82+15785C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs144781616" "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
494076 "chr21:37866887:C>A" "CLDN14" "NM_001146078:c.-82+15774G>T" "FIVE_PRIME_INTRON" "Benign" "rs188990197" "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 10 1008 0.0099 0 978 0 11 5008 0.00219649
494077 "chr21:37866888:G>A" "CLDN14" "NM_001146078:c.-82+15773C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs370315825" "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
494078 "chr21:37866907:C>T" "CLDN14" "NM_001146078:c.-82+15754G>A" "FIVE_PRIME_INTRON" "Benign" "rs28688747" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 229 1322 0.1732 1 1006 0.001 5 694 0.0072 0 1008 0 0 978 0 235 5008 0.0469249
494079 "chr21:37866911:C>T" "CLDN14" "NM_001146078:c.-82+15750G>A" "FIVE_PRIME_INTRON" "Benign" "rs113493264" "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
494080 "chr21:37866960:C>T" "CLDN14" "NM_001146078:c.-82+15701G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs763637654" "This variant is a VUS because it does not have enough information."
494081 "chr21:37866980:G>C" "CLDN14" "NM_001146078:c.-82+15681C>G" "FIVE_PRIME_INTRON" "Benign" "rs181471819" "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 6 694 0.0086 1 1008 0.001 0 978 0 8 5008 0.00159744
494082 "chr21:37866987:G>A" "CLDN14" "NM_001146078:c.-82+15674C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs577870218" "This variant is a VUS because it does not have enough information."
494083 "chr21:37866988:A>G" "CLDN14" "NM_001146078:c.-82+15673T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs561344174" "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
494084 "chr21:37866989:C>T" "CLDN14" "NM_001146078:c.-82+15672G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs186416049" "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
494085 "chr21:37867006:G>A" "CLDN14" "NM_001146078:c.-82+15655C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs190862254" "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
494086 "chr21:37867010:A>G" "CLDN14" "NM_001146078:c.-82+15651T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs563828438" "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
494087 "chr21:37867024:A>G" "CLDN14" "NM_001146078:c.-82+15637T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs750989557" "This variant is a VUS because it does not have enough information."
494088 "chr21:37867033:->G" "CLDN14" "NM_001146078:c.-82+15628_-82+15629insC" "FIVE_PRIME_INTRON" "Unknown significance" "rs750659470" "This variant is a VUS because it does not have enough information."
494089 "chr21:37867074:C>T" "CLDN14" "NM_001146078:c.-82+15587G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs756938290" "This variant is a VUS because it does not have enough information."
494090 "chr21:37867075:G>A" "CLDN14" "NM_001146078:c.-82+15586C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs532765051" "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
494091 "chr21:37867088:C>T" "CLDN14" "NM_001146078:c.-82+15573G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs535811662" "This variant is a VUS because it does not have enough information."
494092 "chr21:37867104:A>G" "CLDN14" "NM_001146078:c.-82+15557T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs552588683" "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
494093 "chr21:37867112:C>G" "CLDN14" "NM_001146078:c.-82+15549G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs117300590" "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
494094 "chr21:37867124:C>T" "CLDN14" "NM_001146078:c.-82+15537G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs780759142" "This variant is a VUS because it does not have enough information."
494095 "chr21:37867125:C>T" "CLDN14" "NM_001146078:c.-82+15536G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs138723799" "This variant is a VUS because it does not have enough information."
494096 "chr21:37867126:G>A" "CLDN14" "NM_001146078:c.-82+15535C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545256176" "This variant is a VUS because it does not have enough information."
494097 "chr21:37867135:G>A" "CLDN14" "NM_001146078:c.-82+15526C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs181086068" "This variant is a VUS because it does not have enough information."
494098 "chr21:37867148:A>G" "CLDN14" "NM_001146078:c.-82+15513T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs754216854" "This variant is a VUS because it does not have enough information."
494099 "chr21:37867173:A>G" "CLDN14" "NM_001146078:c.-82+15488T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs185972234" "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
494100 "chr21:37867187:G>C" "CLDN14" "NM_001146078:c.-82+15474C>G" "FIVE_PRIME_INTRON" "Benign" "rs2071051" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 18 1322 0.0136 62 1006 0.0616 32 694 0.0461 309 1008 0.3065 192 978 0.1963 613 5008 0.122404
494101 "chr21:37867208:A>C" "CLDN14" "NM_001146078:c.-82+15453T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs549755200" "This variant is a VUS because it does not have enough information."
494102 "chr21:37867213:C>G" "CLDN14" "NM_001146078:c.-82+15448G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs190878760" "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
494103 "chr21:37867213:C>T" "CLDN14" "NM_001146078:c.-82+15448G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs190878760" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 1 1006 0.001 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
494104 "chr21:37867214:G>A" "CLDN14" "NM_001146078:c.-82+15447C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs141739255" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 3 1006 0.003 2 694 0.0029 0 1008 0 0 978 0 6 5008 0.00119808
494105 "chr21:37867233:C>T" "CLDN14" "NM_001146078:c.-82+15428G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs569471121" "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
494106 "chr21:37867271:C>T" "CLDN14" "NM_001146078:c.-82+15390G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs538866777" "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
494107 "chr21:37867309:G>A" "CLDN14" "NM_001146078:c.-82+15352C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs558568707" "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
494108 "chr21:37867322:C>A" "CLDN14" "NM_001146078:c.-82+15339G>T" "FIVE_PRIME_INTRON" "Benign" "rs9974115" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 688 1322 0.5204 856 1006 0.8509 502 694 0.7233 743 1008 0.7371 612 978 0.6258 3401 5008 0.679113
494109 "chr21:37867340:C>A" "CLDN14" "NM_001146078:c.-82+15321G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs534691175" "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
494110 "chr21:37867353:C>T" "CLDN14" "NM_001146078:c.-82+15308G>A" "FIVE_PRIME_INTRON" "Benign" "rs2071052" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 168 1322 0.1271 746 1006 0.7416 398 694 0.5735 428 1008 0.4246 359 978 0.3671 2099 5008 0.419129
494111 "chr21:37867363:C>T" "CLDN14" "NM_001146078:c.-82+15298G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs146283986" "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
494112 "chr21:37867364:G>A" "CLDN14" "NM_001146078:c.-82+15297C>T" "FIVE_PRIME_INTRON" "Benign" "rs138099367" "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 13 1008 0.0129 0 978 0 13 5008 0.00259585
494113 "chr21:37867391:T>A" "CLDN14" "NM_001146078:c.-82+15270A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs370066632" "This variant is a VUS because it does not have enough information."
494114 "chr21:37867438:C>A" "CLDN14" "NM_001146078:c.-82+15223G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs557532879" "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
494115 "chr21:37867445:G>A" "CLDN14" "NM_001146078:c.-82+15216C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs577366858" "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
494116 "chr21:37867448:A>C" "CLDN14" "NM_001146078:c.-82+15213T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs747020035" "This variant is a VUS because it does not have enough information."
494117 "chr21:37867453:C>A" "CLDN14" "NM_001146078:c.-82+15208G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs183067686" "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
494118 "chr21:37867460:T>C" "CLDN14" "NM_001146078:c.-82+15201A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs559781834" "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
494119 "chr21:37867477:A>C" "CLDN14" "NM_001146078:c.-82+15184T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs528750633" "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
494120 "chr21:37867504:G>A" "CLDN14" "NM_001146078:c.-82+15157C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs188154713" "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
494121 "chr21:37867558:C>T" "CLDN14" "NM_001146078:c.-82+15103G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs374357235" "This variant is a VUS because it does not have enough information."
494122 "chr21:37867559:G>A" "CLDN14" "NM_001146078:c.-82+15102C>T" "FIVE_PRIME_INTRON" "Benign" "rs149461248" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 163 1322 0.1233 1 1006 0.001 10 694 0.0144 4 1008 0.004 23 978 0.0235 201 5008 0.0401358
494123 "chr21:37867569:G>A" "CLDN14" "NM_001146078:c.-82+15092C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs759472829" "This variant is a VUS because it does not have enough information."
494124 "chr21:37867582:G>A" "CLDN14" "NM_001146078:c.-82+15079C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs529648731" "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
494125 "chr21:37867806:C>T" "CLDN14" "NM_001146078:c.-82+14855G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs190746062" "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
494126 "chr21:37867864:C>T" "CLDN14" "NM_001146078:c.-82+14797G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs371217568" "This variant is a VUS because it does not have enough information."
494127 "chr21:37867952:C>G" "CLDN14" "NM_001146078:c.-82+14709G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs569456626" "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
494128 "chr21:37867954:C>G" "CLDN14" "NM_001146078:c.-82+14707G>C" "FIVE_PRIME_INTRON" "Benign" "rs545474009" "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
494129 "chr21:37868006:AGAGAGTGTTCTTACCCCACGAAGTTCTTGTCCACTCAGAACCTC>-" "CLDN14" "NM_001146078:c.-82+14655_-82+14701delGAGGTTCTGAGTGGACAAGAACTTCGTGGGGTAAGAACACTCTCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs765308951" "This variant is a VUS because it does not have enough information."
494130 "chr21:37868009:G>A" "CLDN14" "NM_001146078:c.-82+14652C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs752202809" "This variant is a VUS because it does not have enough information."
494131 "chr21:37868010:A>C" "CLDN14" "NM_001146078:c.-82+14651T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs757993443" "This variant is a VUS because it does not have enough information."
494132 "chr21:37868014:T>A" "CLDN14" "NM_001146078:c.-82+14647A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs777498056" "This variant is a VUS because it does not have enough information."
494133 "chr21:37868015:T>C" "CLDN14" "NM_001146078:c.-82+14646A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs746633973" "This variant is a VUS because it does not have enough information."
494134 "chr21:37868039:A>G" "CLDN14" "NM_001146078:c.-82+14622T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs552381497" "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
494135 "chr21:37868069:G>C" "CLDN14" "NM_001146078:c.-82+14592C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs565751059" "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
494136 "chr21:37868113:G>A" "CLDN14" "NM_001146078:c.-82+14548C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs534872549" "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
494137 "chr21:37868124:T>G" "CLDN14" "NM_001146078:c.-82+14537A>C" "FIVE_PRIME_INTRON" "Benign" "rs58865958" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 264 1322 0.1997 109 1006 0.1083 96 694 0.1383 316 1008 0.3135 254 978 0.2597 1039 5008 0.207468
494138 "chr21:37868138:C>T" "CLDN14" "NM_001146078:c.-82+14523G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs143849495" "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 4 978 0.0041 6 5008 0.00119808
494139 "chr21:37868143:G>T" "CLDN14" "NM_001146078:c.-82+14518C>A" "FIVE_PRIME_INTRON" "Benign" "rs148638188" "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 2 694 0.0029 1 1008 0.001 28 978 0.0286 39 5008 0.00778754
494140 "chr21:37868202:G>A" "CLDN14" "NM_001146078:c.-82+14459C>T" "FIVE_PRIME_INTRON" "Benign" "rs115962362" "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 4 694 0.0058 0 1008 0 0 978 0 35 5008 0.00698882
494141 "chr21:37868210:C>T" "CLDN14" "NM_001146078:c.-82+14451G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs570240528" "This variant is a VUS because it does not have enough information."
494142 "chr21:37868270:G>A" "CLDN14" "NM_001146078:c.-82+14391C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs577305140" "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
494143 "chr21:37868271:G>A" "CLDN14" "NM_001146078:c.-82+14390C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545998977" "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
494144 "chr21:37868299:C>G" "CLDN14" "NM_001146078:c.-82+14362G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs182979469" "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
494145 "chr21:37868361:C>T" "CLDN14" "NM_001146078:c.-82+14300G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs367717954" "This variant is a VUS because it does not have enough information."
494146 "chr21:37868362:G>A" "CLDN14" "NM_001146078:c.-82+14299C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs573359090" "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
494147 "chr21:37868393:T>C" "CLDN14" "NM_001146078:c.-82+14268A>G" "FIVE_PRIME_INTRON" "Benign" "rs117024128" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 46 1006 0.0457 49 694 0.0706 2 1008 0.002 38 978 0.0389 136 5008 0.0271565
494148 "chr21:37868438:C>T" "CLDN14" "NM_001146078:c.-82+14223G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs769110299" "This variant is a VUS because it does not have enough information."
494149 "chr21:37868450:C>T" "CLDN14" "NM_001146078:c.-82+14211G>A" "FIVE_PRIME_INTRON" "Benign" "rs57400206" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 69 1322 0.0522 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 73 5008 0.0145767
494150 "chr21:37868451:G>A" "CLDN14" "NM_001146078:c.-82+14210C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs529634738" "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
494151 "chr21:37868454:T>A" "CLDN14" "NM_001146078:c.-82+14207A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs555402273" "This variant is a VUS because it does not have enough information."
494152 "chr21:37868484:A>G" "CLDN14" "NM_001146078:c.-82+14177T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs375350181" "This variant is a VUS because it does not have enough information."
494153 "chr21:37868486:C>T" "CLDN14" "NM_001146078:c.-82+14175G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs543042229" "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
494154 "chr21:37868488:C>G" "CLDN14" "NM_001146078:c.-82+14173G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs563220312" "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
494155 "chr21:37868494:GA>-" "CLDN14" "NM_001146078:c.-82+14167_-82+14170delTC" "FIVE_PRIME_INTRON" "Unknown significance" "rs531380850" "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
494156 "chr21:37868496:G>A" "CLDN14" "NM_001146078:c.-82+14165C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs368247036" "This variant is a VUS because it does not have enough information."
494157 "chr21:37868551:T>G" "CLDN14" "NM_001146078:c.-82+14110A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs750069769" "This variant is a VUS because it does not have enough information."
494158 "chr21:37868618:C>T" "CLDN14" "NM_001146078:c.-82+14043G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs755372995" "This variant is a VUS because it does not have enough information."
494159 "chr21:37868619:G>C" "CLDN14" "NM_001146078:c.-82+14042C>G" "FIVE_PRIME_INTRON" "Benign" "rs2409819" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 712 1322 0.5386 194 1006 0.1928 172 694 0.2478 392 1008 0.3889 392 978 0.4008 1862 5008 0.371805
494160 "chr21:37868670:G>A" "CLDN14" "NM_001146078:c.-82+13991C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs376895559" "This variant is a VUS because it does not have enough information."
494161 "chr21:37868673:C>T" "CLDN14" "NM_001146078:c.-82+13988G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs368075377" "This variant is a VUS because it does not have enough information."
494162 "chr21:37868674:G>A" "CLDN14" "NM_001146078:c.-82+13987C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs142137979" "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
494163 "chr21:37868720:G>T" "CLDN14" "NM_001146078:c.-82+13941C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs61375055" "This variant is a VUS because it does not have enough information."
494164 "chr21:37868735:A>-" "CLDN14" "NM_001146078:c.-82+13926delT" "FIVE_PRIME_INTRON" "Benign" "rs533656454" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 589 1322 0.4455 651 1006 0.6471 385 694 0.5548 400 1008 0.3968 453 978 0.4632 2478 5008 0.494808
494165 "chr21:37868735:->A" "CLDN14" "NM_001146078:c.-82+13926_-82+13927insT" "FIVE_PRIME_INTRON" "Unknown significance" "rs767260778" "This variant is a VUS because it does not have enough information."
494166 "chr21:37868735:AA>-" "CLDN14" "NM_001146078:c.-82+13926_-82+13929delTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs749923940" "This variant is a VUS because it does not have enough information."
494167 "chr21:37868735:AAA>-" "CLDN14" "NM_001146078:c.-82+13926_-82+13930delTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs763941356" "This variant is a VUS because it does not have enough information."
494168 "chr21:37868813:G>A" "CLDN14" "NM_001146078:c.-82+13848C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs565829104" "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
494169 "chr21:37868816:C>T" "CLDN14" "NM_001146078:c.-82+13845G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs528335806" "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
494170 "chr21:37868817:G>A" "CLDN14" "NM_001146078:c.-82+13844C>T" "FIVE_PRIME_INTRON" "Benign" "rs58192378" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 520 1322 0.3933 84 1006 0.0835 80 694 0.1153 80 1008 0.0794 141 978 0.1442 905 5008 0.180711
494171 "chr21:37868842:C>A" "CLDN14" "NM_001146078:c.-82+13819G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs147376064" "This variant is a VUS because it does not have enough information."
494172 "chr21:37868877:C>G" "CLDN14" "NM_001146078:c.-82+13784G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs368865252" "This variant is a VUS because it does not have enough information."
494173 "chr21:37868921:G>C" "CLDN14" "NM_001146078:c.-82+13740C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs568392791" "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
494174 "chr21:37868944:C>T" "CLDN14" "NM_001146078:c.-82+13717G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs537429418" "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
494175 "chr21:37868945:G>C" "CLDN14" "NM_001146078:c.-82+13716C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs553220426" "This variant is a VUS because it does not have enough information."
494176 "chr21:37868947:C>T" "CLDN14" "NM_001146078:c.-82+13714G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs188047830" "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
494177 "chr21:37868983:A>G" "CLDN14" "NM_001146078:c.-82+13678T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs139064577" "This variant is a VUS because it does not have enough information."
494178 "chr21:37868990:T>A" "CLDN14" "NM_001146078:c.-82+13671A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs201237895" "This variant is a VUS because it does not have enough information."
494179 "chr21:37869030:AGGG>-" "CLDN14" "NM_001146078:c.-82+13631_-82+13636delCCCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs746937873" "This variant is a VUS because it does not have enough information."
494180 "chr21:37869034:AGGGAGGA>-" "CLDN14" "NM_001146078:c.-82+13627_-82+13636delTCCTCCCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs370785055" "This variant is a VUS because it does not have enough information."
494181 "chr21:37869037:G>A" "CLDN14" "NM_001146078:c.-82+13624C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs9980394" "This variant is a VUS because it does not have enough information."
494182 "chr21:37869044:G>C" "CLDN14" "NM_001146078:c.-82+13617C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs113069335" "This variant is a VUS because it does not have enough information."
494183 "chr21:37869045:A>G" "CLDN14" "NM_001146078:c.-82+13616T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs141836490" "This variant is a VUS because it does not have enough information."
494184 "chr21:37869053:G>A" "CLDN14" "NM_001146078:c.-82+13608C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs9980396" "This variant is a VUS because it does not have enough information."
494185 "chr21:37869057:G>A" "CLDN14" "NM_001146078:c.-82+13604C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs577740208" "This variant is a VUS because it does not have enough information."
494186 "chr21:37869061:G>A" "CLDN14" "NM_001146078:c.-82+13600C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs148323543" "This variant is a VUS because it does not have enough information."
494187 "chr21:37869073:G>A" "CLDN14" "NM_001146078:c.-82+13588C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs771109006" "This variant is a VUS because it does not have enough information."
494188 "chr21:37869081:A>G" "CLDN14" "NM_001146078:c.-82+13580T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs113439874" "This variant is a VUS because it does not have enough information."
494189 "chr21:37869082:AGGCAGGG>-" "CLDN14" "NM_001146078:c.-82+13579_-82+13588delCCCTGCCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs375259460" "This variant is a VUS because it does not have enough information."
494190 "chr21:37869085:C>G" "CLDN14" "NM_001146078:c.-82+13576G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs146262177" "This variant is a VUS because it does not have enough information."
494191 "chr21:37869090:->AGGA" "CLDN14" "NM_001146078:c.-82+13571_-82+13572insTCCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs372449159" "This variant is a VUS because it does not have enough information."
494192 "chr21:37869117:G>A" "CLDN14" "NM_001146078:c.-82+13544C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs147733982" "This variant is a VUS because it does not have enough information."
494193 "chr21:37869121:G>A" "CLDN14" "NM_001146078:c.-82+13540C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs373441982" "This variant is a VUS because it does not have enough information."
494194 "chr21:37869127:G>-" "CLDN14" "NM_001146078:c.-82+13534delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs767356237" "This variant is a VUS because it does not have enough information."
494195 "chr21:37869129:G>A" "CLDN14" "NM_001146078:c.-82+13532C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs796927879" "This variant is a VUS because it does not have enough information."
494196 "chr21:37869131:GGG>-" "CLDN14" "NM_001146078:c.-82+13530_-82+13534delCCC" "FIVE_PRIME_INTRON" "Unknown significance" "rs760404924" "This variant is a VUS because it does not have enough information."
494197 "chr21:37869133:G>A" "CLDN14" "NM_001146078:c.-82+13528C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs145780280" "This variant is a VUS because it does not have enough information."
494198 "chr21:37869153:G>A" "CLDN14" "NM_001146078:c.-82+13508C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs375745410" "This variant is a VUS because it does not have enough information."
494199 "chr21:37869165:G>A" "CLDN14" "NM_001146078:c.-82+13496C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs138365409" "This variant is a VUS because it does not have enough information."
494200 "chr21:37869185:A>G" "CLDN14" "NM_001146078:c.-82+13476T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs372760647" "This variant is a VUS because it does not have enough information."
494201 "chr21:37869229:G>A" "CLDN14" "NM_001146078:c.-82+13432C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs796261715" "This variant is a VUS because it does not have enough information."
494202 "chr21:37869317:G>A" "CLDN14" "NM_001146078:c.-82+13344C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs145554784" "This variant is a VUS because it does not have enough information."
494203 "chr21:37869345:G>A" "CLDN14" "NM_001146078:c.-82+13316C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs374442394" "This variant is a VUS because it does not have enough information."
494204 "chr21:37869349:G>A" "CLDN14" "NM_001146078:c.-82+13312C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs367716999" "This variant is a VUS because it does not have enough information."
494205 "chr21:37869357:G>A" "CLDN14" "NM_001146078:c.-82+13304C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs140363006" "This variant is a VUS because it does not have enough information."
494206 "chr21:37869371:G>A" "CLDN14" "NM_001146078:c.-82+13290C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111220558" "This variant is a VUS because it does not have enough information."
494207 "chr21:37869372:G>A" "CLDN14" "NM_001146078:c.-82+13289C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111220557" "This variant is a VUS because it does not have enough information."
494208 "chr21:37869373:G>A" "CLDN14" "NM_001146078:c.-82+13288C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111220559" "This variant is a VUS because it does not have enough information."
494209 "chr21:37869397:G>A" "CLDN14" "NM_001146078:c.-82+13264C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111220599" "This variant is a VUS because it does not have enough information."
494210 "chr21:37869401:G>A" "CLDN14" "NM_001146078:c.-82+13260C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs375910209" "This variant is a VUS because it does not have enough information."
494211 "chr21:37869535:G>A" "CLDN14" "NM_001146078:c.-82+13126C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111449221" "This variant is a VUS because it does not have enough information."
494212 "chr21:37869559:G>A" "CLDN14" "NM_001146078:c.-82+13102C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111730926" "This variant is a VUS because it does not have enough information."
494213 "chr21:37869560:G>A" "CLDN14" "NM_001146078:c.-82+13101C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs112624456" "This variant is a VUS because it does not have enough information."
494214 "chr21:37869561:G>A" "CLDN14" "NM_001146078:c.-82+13100C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111764621" "This variant is a VUS because it does not have enough information."
494215 "chr21:37869689:A>G" "CLDN14" "NM_001146078:c.-82+12972T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs555862578" "This variant is a VUS because it does not have enough information."
494216 "chr21:37869691:G>A" "CLDN14" "NM_001146078:c.-82+12970C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs111454364" "This variant is a VUS because it does not have enough information."
494217 "chr21:37869693:A>G" "CLDN14" "NM_001146078:c.-82+12968T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs370553545" "This variant is a VUS because it does not have enough information."
494218 "chr21:37869709:G>A" "CLDN14" "NM_001146078:c.-82+12952C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs372253766" "This variant is a VUS because it does not have enough information."
494219 "chr21:37869713:A>G" "CLDN14" "NM_001146078:c.-82+12948T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs187059052" "This variant is a VUS because it does not have enough information."
494220 "chr21:37869714:->AGGG" "CLDN14" "NM_001146078:c.-82+12947_-82+12948insCCCT" "FIVE_PRIME_INTRON" "Unknown significance" "rs148689892" "This variant is a VUS because it does not have enough information."
494221 "chr21:37869721:G>A" "CLDN14" "NM_001146078:c.-82+12940C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs192506453" "This variant is a VUS because it does not have enough information."
494222 "chr21:37869728:G>A" "CLDN14" "NM_001146078:c.-82+12933C>T" "FIVE_PRIME_INTRON" "Benign" "rs112090285" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 66 1322 0.0499 0 1006 0 4 694 0.0058 0 1008 0 0 978 0 70 5008 0.0139776
494223 "chr21:37869741:G>A" "CLDN14" "NM_001146078:c.-82+12920C>T" "FIVE_PRIME_INTRON" "Benign" "rs185488918" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 47 1322 0.0356 0 1006 0 0 694 0 0 1008 0 0 978 0 47 5008 0.00938498
494224 "chr21:37869763:C>T" "CLDN14" "NM_001146078:c.-82+12898G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs553199329" "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
494225 "chr21:37869770:G>A" "CLDN14" "NM_001146078:c.-82+12891C>T" "FIVE_PRIME_INTRON" "Benign" "rs79043484" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 160 1322 0.121 1 1006 0.001 9 694 0.013 4 1008 0.004 22 978 0.0225 196 5008 0.0391374
494226 "chr21:37869842:T>A" "CLDN14" "NM_001146078:c.-82+12819A>T" "FIVE_PRIME_INTRON" "Benign" "rs12482492" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 107 1322 0.0809 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 111 5008 0.0221645
494227 "chr21:37869858:C>G" "CLDN14" "NM_001146078:c.-82+12803G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs538090695" "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
494228 "chr21:37869869:C>T" "CLDN14" "NM_001146078:c.-82+12792G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs371385818" "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
494229 "chr21:37869870:G>T" "CLDN14" "NM_001146078:c.-82+12791C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs187620269" "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
494230 "chr21:37869934:C>T" "CLDN14" "NM_001146078:c.-82+12727G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773348335" "This variant is a VUS because it does not have enough information."
494231 "chr21:37869942:C>T" "CLDN14" "NM_001146078:c.-82+12719G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs192574296" "This variant is a VUS because it does not have enough information."
494232 "chr21:37869947:C>T" "CLDN14" "NM_001146078:c.-82+12714G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs563265533" "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
494233 "chr21:37869958:A>T" "CLDN14" "NM_001146078:c.-82+12703T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568998432" "This variant is a VUS because it does not have enough information."
494234 "chr21:37869963:G>C" "CLDN14" "NM_001146078:c.-82+12698C>G" "FIVE_PRIME_INTRON" "Benign" "rs576773515" "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 0 1008 0 0 978 0 12 5008 0.00239617
494235 "chr21:37869976:C>T" "CLDN14" "NM_001146078:c.-82+12685G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs558327009" "This variant is a VUS because it does not have enough information."
494236 "chr21:37869977:G>A" "CLDN14" "NM_001146078:c.-82+12684C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs760797451" "This variant is a VUS because it does not have enough information."
494237 "chr21:37870001:C>T" "CLDN14" "NM_001146078:c.-82+12660G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs545875532" "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
494238 "chr21:37870014:C>T" "CLDN14" "NM_001146078:c.-82+12647G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs559230330" "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
494239 "chr21:37870021:C>T" "CLDN14" "NM_001146078:c.-82+12640G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs778074571" "This variant is a VUS because it does not have enough information."
494240 "chr21:37870027:C>T" "CLDN14" "NM_001146078:c.-82+12634G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs528274208" "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
494241 "chr21:37870034:C>T" "CLDN14" "NM_001146078:c.-82+12627G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs766677646" "This variant is a VUS because it does not have enough information."
494242 "chr21:37870038:C>G" "CLDN14" "NM_001146078:c.-82+12623G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs548442410" "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
494243 "chr21:37870063:T>C" "CLDN14" "NM_001146078:c.-82+12598A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs776261973" "This variant is a VUS because it does not have enough information."
494244 "chr21:37870065:C>T" "CLDN14" "NM_001146078:c.-82+12596G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759409863" "This variant is a VUS because it does not have enough information."
494245 "chr21:37870066:G>A" "CLDN14" "NM_001146078:c.-82+12595C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs539966743" "This variant is a VUS because it does not have enough information."
494246 "chr21:37870071:C>T" "CLDN14" "NM_001146078:c.-82+12590G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs75410964" "This variant is a VUS because it does not have enough information." 0 1322 0 4 1006 0.004 3 694 0.0043 0 1008 0 1 978 0.001 8 5008 0.00159744
494247 "chr21:37870098:C>T" "CLDN14" "NM_001146078:c.-82+12563G>A" "FIVE_PRIME_INTRON" "Benign" "rs117697776" "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 7 694 0.0101 0 1008 0 2 978 0.002 18 5008 0.00359425
494248 "chr21:37870099:G>A" "CLDN14" "NM_001146078:c.-82+12562C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs771119470" "This variant is a VUS because it does not have enough information."
494249 "chr21:37870117:C>T" "CLDN14" "NM_001146078:c.-82+12544G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs575446050" "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
494250 "chr21:37870118:G>A" "CLDN14" "NM_001146078:c.-82+12543C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs746067065" "This variant is a VUS because it does not have enough information."
494251 "chr21:37870133:A>C" "CLDN14" "NM_001146078:c.-82+12528T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs763681117" "This variant is a VUS because it does not have enough information."
494252 "chr21:37870137:C>T" "CLDN14" "NM_001146078:c.-82+12524G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs543413936" "This variant is a VUS because it does not have enough information."
494253 "chr21:37870163:G>T" "CLDN14" "NM_001146078:c.-82+12498C>A" "FIVE_PRIME_INTRON" "Benign" "rs145148988" "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 4 694 0.0058 0 1008 0 0 978 0 35 5008 0.00698882
494254 "chr21:37870173:C>T" "CLDN14" "NM_001146078:c.-82+12488G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs149138138" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 4 1006 0.004 3 694 0.0043 0 1008 0 2 978 0.002 10 5008 0.00199681
494255 "chr21:37870196:T>G" "CLDN14" "NM_001146078:c.-82+12465A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs547066109" "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
494256 "chr21:37870224:C>T" "CLDN14" "NM_001146078:c.-82+12437G>A" "FIVE_PRIME_INTRON" "Benign" "rs566876995" "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
494257 "chr21:37870289:C>T" "CLDN14" "NM_001146078:c.-82+12372G>A" "FIVE_PRIME_INTRON" "Benign" "rs116983832" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 4 1322 0.003 25 1006 0.0249 9 694 0.013 1 1008 0.001 6 978 0.0061 45 5008 0.00898562
494258 "chr21:37870314:T>G" "CLDN14" "NM_001146078:c.-82+12347A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs75590445" "This variant is a VUS because it does not have enough information."
494259 "chr21:37870316:G>T" "CLDN14" "NM_001146078:c.-82+12345C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs79005334" "This variant is a VUS because it does not have enough information."
494260 "chr21:37870386:C>T" "CLDN14" "NM_001146078:c.-82+12275G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs578074686" "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
494261 "chr21:37870390:C>T" "CLDN14" "NM_001146078:c.-82+12271G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs374646008" "This variant is a VUS because it does not have enough information."
494262 "chr21:37870398:A>G" "CLDN14" "NM_001146078:c.-82+12263T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs184854661" "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
494263 "chr21:37870401:C>T" "CLDN14" "NM_001146078:c.-82+12260G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs774144752" "This variant is a VUS because it does not have enough information."
494264 "chr21:37870403:A>G" "CLDN14" "NM_001146078:c.-82+12258T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs538101390" "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
494265 "chr21:37870424:G>A" "CLDN14" "NM_001146078:c.-82+12237C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs558208399" "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
494266 "chr21:37870426:G>A" "CLDN14" "NM_001146078:c.-82+12235C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs367606088" "This variant is a VUS because it does not have enough information."
494267 "chr21:37870432:->GGGATTACAGGCAC" "CLDN14" "NM_001146078:c.-82+12229_-82+12230insGTGCCTGTAATCCC" "FIVE_PRIME_INTRON" "Benign" "rs538838240" "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
494268 "chr21:37870440:A>G" "CLDN14" "NM_001146078:c.-82+12221T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs533611461" "This variant is a VUS because it does not have enough information."
494269 "chr21:37870444:A>G" "CLDN14" "NM_001146078:c.-82+12217T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs551674763" "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
494270 "chr21:37870448:A>T" "CLDN14" "NM_001146078:c.-82+12213T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs545510355" "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
494271 "chr21:37870451:A>T" "CLDN14" "NM_001146078:c.-82+12210T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs570377050" "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
494272 "chr21:37870452:C>T" "CLDN14" "NM_001146078:c.-82+12209G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs531186861" "This variant is a VUS because it does not have enough information."
494273 "chr21:37870458:C>T" "CLDN14" "NM_001146078:c.-82+12203G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs779327659" "This variant is a VUS because it does not have enough information."
494274 "chr21:37870492:T>A" "CLDN14" "NM_001146078:c.-82+12169A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs59126027" "This variant is a VUS because it does not have enough information."
494275 "chr21:37870505:G>T" "CLDN14" "NM_001146078:c.-82+12156C>A" "FIVE_PRIME_INTRON" "Benign" "rs188494171" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
494276 "chr21:37870508:A>G" "CLDN14" "NM_001146078:c.-82+12153T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs541970674" "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
494277 "chr21:37870509:G>T" "CLDN14" "NM_001146078:c.-82+12152C>A" "FIVE_PRIME_INTRON" "Benign" "rs145078249" "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
494278 "chr21:37870518:C>T" "CLDN14" "NM_001146078:c.-82+12143G>A" "FIVE_PRIME_INTRON" "Benign" "rs113585361" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 71 1322 0.0537 109 1006 0.1083 67 694 0.0965 10 1008 0.0099 62 978 0.0634 319 5008 0.0636981
494279 "chr21:37870541:C>T" "CLDN14" "NM_001146078:c.-82+12120G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs550840322" "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
494280 "chr21:37870554:C>G" "CLDN14" "NM_001146078:c.-82+12107G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs772629350" "This variant is a VUS because it does not have enough information."
494281 "chr21:37870562:G>A" "CLDN14" "NM_001146078:c.-82+12099C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs773146857" "This variant is a VUS because it does not have enough information."
494282 "chr21:37870590:C>T" "CLDN14" "NM_001146078:c.-82+12071G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs753109373" "This variant is a VUS because it does not have enough information."
494283 "chr21:37870608:C>T" "CLDN14" "NM_001146078:c.-82+12053G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs758631572" "This variant is a VUS because it does not have enough information."
494284 "chr21:37870622:G>A" "CLDN14" "NM_001146078:c.-82+12039C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs564267825" "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
494285 "chr21:37870641:A>G" "CLDN14" "NM_001146078:c.-82+12020T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs533336036" "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
494286 "chr21:37870648:A>G" "CLDN14" "NM_001146078:c.-82+12013T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs546709960" "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
494287 "chr21:37870684:C>G" "CLDN14" "NM_001146078:c.-82+11977G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs567237145" "This variant is a VUS because it does not have enough information."
494288 "chr21:37870718:A>G" "CLDN14" "NM_001146078:c.-82+11943T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs140357441" "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
494289 "chr21:37870719:C>T" "CLDN14" "NM_001146078:c.-82+11942G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs764717830" "This variant is a VUS because it does not have enough information."
494290 "chr21:37870725:TT>-" "CLDN14" "NM_001146078:c.-82+11936_-82+11939delAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs753650510" "This variant is a VUS because it does not have enough information."
494291 "chr21:37870728:T>C" "CLDN14" "NM_001146078:c.-82+11933A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs752084008" "This variant is a VUS because it does not have enough information."
494292 "chr21:37870773:A>G" "CLDN14" "NM_001146078:c.-82+11888T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs534731201" "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
494293 "chr21:37870779:G>T" "CLDN14" "NM_001146078:c.-82+11882C>A" "FIVE_PRIME_INTRON" "Benign" "rs75541459" "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 2 694 0.0029 0 1008 0 0 978 0 11 5008 0.00219649
494294 "chr21:37870785:C>T" "CLDN14" "NM_001146078:c.-82+11876G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs745903666" "This variant is a VUS because it does not have enough information."
494295 "chr21:37870804:A>C" "CLDN14" "NM_001146078:c.-82+11857T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs776922359" "This variant is a VUS because it does not have enough information."
494296 "chr21:37870823:C>G" "CLDN14" "NM_001146078:c.-82+11838G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs756367620" "This variant is a VUS because it does not have enough information."
494297 "chr21:37870827:T>G" "CLDN14" "NM_001146078:c.-82+11834A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs145413269" "This variant is a VUS because it does not have enough information."
494298 "chr21:37870846:A>T" "CLDN14" "NM_001146078:c.-82+11815T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs780084657" "This variant is a VUS because it does not have enough information."
494299 "chr21:37870849:A>G" "CLDN14" "NM_001146078:c.-82+11812T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs534582116" "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
494300 "chr21:37870867:A>G" "CLDN14" "NM_001146078:c.-82+11794T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs749168070" "This variant is a VUS because it does not have enough information."
494301 "chr21:37870888:A>G" "CLDN14" "NM_001146078:c.-82+11773T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs538103064" "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
494302 "chr21:37870899:C>T" "CLDN14" "NM_001146078:c.-82+11762G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs768334555" "This variant is a VUS because it does not have enough information."
494303 "chr21:37870900:G>A" "CLDN14" "NM_001146078:c.-82+11761C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs759335721" "This variant is a VUS because it does not have enough information."
494304 "chr21:37870905:G>C" "CLDN14" "NM_001146078:c.-82+11756C>G" "FIVE_PRIME_INTRON" "Benign" "rs558409380" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
494305 "chr21:37870908:C>T" "CLDN14" "NM_001146078:c.-82+11753G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs181684861" "This variant is a VUS because it does not have enough information."
494306 "chr21:37870910:T>A" "CLDN14" "NM_001146078:c.-82+11751A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs374968658" "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
494307 "chr21:37870911:G>A" "CLDN14" "NM_001146078:c.-82+11750C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs774310564" "This variant is a VUS because it does not have enough information."
494308 "chr21:37870925:C>T" "CLDN14" "NM_001146078:c.-82+11736G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs534526725" "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
494309 "chr21:37870968:A>G" "CLDN14" "NM_001146078:c.-82+11693T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs184327751" "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
494310 "chr21:37870973:A>T" "CLDN14" "NM_001146078:c.-82+11688T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs571245110" "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
494311 "chr21:37870979:C>T" "CLDN14" "NM_001146078:c.-82+11682G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs541907464" "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
494312 "chr21:37870983:->GTA" "CLDN14" "NM_001146078:c.-82+11678_-82+11679insTAC" "FIVE_PRIME_INTRON" "Unknown significance" "rs775496763" "This variant is a VUS because it does not have enough information."
494313 "chr21:37871010:G>A" "CLDN14" "NM_001146078:c.-82+11651C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs771943966" "This variant is a VUS because it does not have enough information."
494314 "chr21:37871012:G>A" "CLDN14" "NM_001146078:c.-82+11649C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs555540526" "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
494315 "chr21:37871027:C>T" "CLDN14" "NM_001146078:c.-82+11634G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs772735828" "This variant is a VUS because it does not have enough information."
494316 "chr21:37871048:C>T" "CLDN14" "NM_001146078:c.-82+11613G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs575504142" "This variant is a VUS because it does not have enough information." 0 1322 0 1 1006 0.001 0 694 0 2 1008 0.002 0 978 0 3 5008 0.000599042
494317 "chr21:37871066:T>-" "CLDN14" "NM_001146078:c.-82+11595delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs778700015" "This variant is a VUS because it does not have enough information."
494318 "chr21:37871086:G>A" "CLDN14" "NM_001146078:c.-82+11575C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs760111808" "This variant is a VUS because it does not have enough information."
494319 "chr21:37871089:G>T" "CLDN14" "NM_001146078:c.-82+11572C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs544101575" "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
494320 "chr21:37871090:C>T" "CLDN14" "NM_001146078:c.-82+11571G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs148062127" "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
494321 "chr21:37871091:G>A" "CLDN14" "NM_001146078:c.-82+11570C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs540931089" "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 3 978 0.0031 6 5008 0.00119808
494322 "chr21:37871104:C>A" "CLDN14" "NM_001146078:c.-82+11557G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs538872894" "This variant is a VUS because it does not have enough information."
494323 "chr21:37871114:T>C" "CLDN14" "NM_001146078:c.-82+11547A>G" "FIVE_PRIME_INTRON" "Benign" "rs141761574" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 32 1322 0.0242 1 1006 0.001 3 694 0.0043 0 1008 0 0 978 0 36 5008 0.0071885
494324 "chr21:37871118:C>G" "CLDN14" "NM_001146078:c.-82+11543G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs188759404" "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
494325 "chr21:37871118:C>T" "CLDN14" "NM_001146078:c.-82+11543G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs188759404" "This variant is a VUS because it does not have enough information."
494326 "chr21:37871119:G>A" "CLDN14" "NM_001146078:c.-82+11542C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs529257970" "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
494327 "chr21:37871126:G>A" "CLDN14" "NM_001146078:c.-82+11535C>T" "FIVE_PRIME_INTRON" "Benign" "rs56318369" "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 1 694 0.0014 1 1008 0.001 2 978 0.002 9 5008 0.00179712
494328 "chr21:37871128:C>T" "CLDN14" "NM_001146078:c.-82+11533G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs569039231" "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
494329 "chr21:37871130:C>T" "CLDN14" "NM_001146078:c.-82+11531G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs531918781" "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
494330 "chr21:37871133:A>C" "CLDN14" "NM_001146078:c.-82+11528T>G" "FIVE_PRIME_INTRON" "Benign" "rs61592461" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 165 1322 0.1248 1 1006 0.001 4 694 0.0058 0 1008 0 1 978 0.001 171 5008 0.0341454
494331 "chr21:37871137:G>A" "CLDN14" "NM_001146078:c.-82+11524C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs571836062" "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
494332 "chr21:37871159:A>G" "CLDN14" "NM_001146078:c.-82+11502T>C" "FIVE_PRIME_INTRON" "Benign" "rs73380196" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 768 1322 0.5809 3 1006 0.003 37 694 0.0533 0 1008 0 1 978 0.001 809 5008 0.161542
494333 "chr21:37871160:A>G" "CLDN14" "NM_001146078:c.-82+11501T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs554516230" "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
494334 "chr21:37871167:C>T" "CLDN14" "NM_001146078:c.-82+11494G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs150165588" "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 1 978 0.001 3 5008 0.000599042
494335 "chr21:37871171:A>G" "CLDN14" "NM_001146078:c.-82+11490T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs200387491" "This variant is a VUS because it does not have enough information."
494336 "chr21:37871185:T>C" "CLDN14" "NM_001146078:c.-82+11476A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs371833138" "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
494337 "chr21:37871197:G>A" "CLDN14" "NM_001146078:c.-82+11464C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs555478029" "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
494338 "chr21:37871212:G>A" "CLDN14" "NM_001146078:c.-82+11449C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs138411118" "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
494339 "chr21:37871231:T>C" "CLDN14" "NM_001146078:c.-82+11430A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs544308449" "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
494340 "chr21:37871241:A>-" "CLDN14" "NM_001146078:c.-82+11420delT" "FIVE_PRIME_INTRON" "Benign" "rs574751199" "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
494341 "chr21:37871285:C>G" "CLDN14" "NM_001146078:c.-82+11376G>C" "FIVE_PRIME_INTRON" "Benign" "rs149240544" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 35 1322 0.0265 1 1006 0.001 1 694 0.0014 0 1008 0 0 978 0 37 5008 0.00738818
494342 "chr21:37871336:A>G" "CLDN14" "NM_001146078:c.-82+11325T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs756137152" "This variant is a VUS because it does not have enough information."
494343 "chr21:37871343:G>A" "CLDN14" "NM_001146078:c.-82+11318C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs780392705" "This variant is a VUS because it does not have enough information."
494344 "chr21:37871349:A>G" "CLDN14" "NM_001146078:c.-82+11312T>C" "FIVE_PRIME_INTRON" "Benign" "rs79921887" "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 0 694 0 0 1008 0 0 978 0 61 5008 0.0121805
494345 "chr21:37871370:G>A" "CLDN14" "NM_001146078:c.-82+11291C>T" "FIVE_PRIME_INTRON" "Benign" "rs147385815" "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 2 694 0.0029 0 1008 0 0 978 0 15 5008 0.00299521
494346 "chr21:37871375:C>T" "CLDN14" "NM_001146078:c.-82+11286G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs749437237" "This variant is a VUS because it does not have enough information."
494347 "chr21:37871391:A>G" "CLDN14" "NM_001146078:c.-82+11270T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs767021616" "This variant is a VUS because it does not have enough information."
494348 "chr21:37871401:G>T" "CLDN14" "NM_001146078:c.-82+11260C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs541012261" "This variant is a VUS because it does not have enough information."
494349 "chr21:37871427:C>T" "CLDN14" "NM_001146078:c.-82+11234G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs778697831" "This variant is a VUS because it does not have enough information."
494350 "chr21:37871437:G>T" "CLDN14" "NM_001146078:c.-82+11224C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs182166393" "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
494351 "chr21:37871448:A>T" "CLDN14" "NM_001146078:c.-82+11213T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs559840327" "This variant is a VUS because it does not have enough information."
494352 "chr21:37871449:G>A" "CLDN14" "NM_001146078:c.-82+11212C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs747894029" "This variant is a VUS because it does not have enough information."
494353 "chr21:37871483:C>T" "CLDN14" "NM_001146078:c.-82+11178G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs533265842" "This variant is a VUS because it does not have enough information."
494354 "chr21:37871490:G>A" "CLDN14" "NM_001146078:c.-82+11171C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs187243864" "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
494355 "chr21:37871491:C>T" "CLDN14" "NM_001146078:c.-82+11170G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs370074360" "This variant is a VUS because it does not have enough information."
494356 "chr21:37871492:G>A" "CLDN14" "NM_001146078:c.-82+11169C>T" "FIVE_PRIME_INTRON" "Benign" "rs542647533" "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 11 978 0.0112 11 5008 0.00219649
494357 "chr21:37871513:T>C" "CLDN14" "NM_001146078:c.-82+11148A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs190868934" "This variant is a VUS because it does not have enough information."
494358 "chr21:37871515:G>A" "CLDN14" "NM_001146078:c.-82+11146C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs772001057" "This variant is a VUS because it does not have enough information."
494359 "chr21:37871525:G>A" "CLDN14" "NM_001146078:c.-82+11136C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs562558504" "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
494360 "chr21:37871528:C>A" "CLDN14" "NM_001146078:c.-82+11133G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs531685932" "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
494361 "chr21:37871543:T>C" "CLDN14" "NM_001146078:c.-82+11118A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs777629440" "This variant is a VUS because it does not have enough information."
494362 "chr21:37871555:TTTG>-" "CLDN14" "NM_001146078:c.-82+11106_-82+11111delCAAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs750438900" "This variant is a VUS because it does not have enough information."
494363 "chr21:37871573:G>A" "CLDN14" "NM_001146078:c.-82+11088C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs79807401" "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
494364 "chr21:37871586:C>T" "CLDN14" "NM_001146078:c.-82+11075G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs373549774" "This variant is a VUS because it does not have enough information."
494365 "chr21:37871587:G>A" "CLDN14" "NM_001146078:c.-82+11074C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs565298220" "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
494366 "chr21:37871619:C>T" "CLDN14" "NM_001146078:c.-82+11042G>A" "FIVE_PRIME_INTRON" "Benign" "rs743424" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 126 1322 0.0953 540 1006 0.5368 227 694 0.3271 274 1008 0.2718 261 978 0.2669 1428 5008 0.285144
494367 "chr21:37871622:G>A" "CLDN14" "NM_001146078:c.-82+11039C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs776396882" "This variant is a VUS because it does not have enough information."
494368 "chr21:37871626:C>T" "CLDN14" "NM_001146078:c.-82+11035G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs548104585" "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
494369 "chr21:37871630:C>A" "CLDN14" "NM_001146078:c.-82+11031G>T" "FIVE_PRIME_INTRON" "Benign" "rs143229056" "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 1 1008 0.001 3 978 0.0031 22 5008 0.00439297
494370 "chr21:37871640:T>C" "CLDN14" "NM_001146078:c.-82+11021A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs535424570" "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
494371 "chr21:37871650:C>T" "CLDN14" "NM_001146078:c.-82+11011G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs774861396" "This variant is a VUS because it does not have enough information."
494372 "chr21:37871668:C>A" "CLDN14" "NM_001146078:c.-82+10993G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs531247831" "This variant is a VUS because it does not have enough information."
494373 "chr21:37871689:C>A" "CLDN14" "NM_001146078:c.-82+10972G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs768200578" "This variant is a VUS because it does not have enough information."
494374 "chr21:37871758:T>A" "CLDN14" "NM_001146078:c.-82+10903A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs548962240" "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
494375 "chr21:37871804:G>A" "CLDN14" "NM_001146078:c.-82+10857C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs180807250" "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
494376 "chr21:37871822:T>C" "CLDN14" "NM_001146078:c.-82+10839A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs575245554" "This variant is a VUS because it does not have enough information."
494377 "chr21:37871836:G>C" "CLDN14" "NM_001146078:c.-82+10825C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs537497618" "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
494378 "chr21:37871859:G>A" "CLDN14" "NM_001146078:c.-82+10802C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs750964992" "This variant is a VUS because it does not have enough information."
494379 "chr21:37871885:C>G" "CLDN14" "NM_001146078:c.-82+10776G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs147498900" "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
494380 "chr21:37871885:C>T" "CLDN14" "NM_001146078:c.-82+10776G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs147498900" "This variant is a VUS because it does not have enough information."
494381 "chr21:37871886:G>A" "CLDN14" "NM_001146078:c.-82+10775C>T" "FIVE_PRIME_INTRON" "Benign" "rs730265" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 282 1322 0.2133 204 1006 0.2028 81 694 0.1167 81 1008 0.0804 97 978 0.0992 745 5008 0.148762
494382 "chr21:37871924:T>A" "CLDN14" "NM_001146078:c.-82+10737A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs753903315" "This variant is a VUS because it does not have enough information."
494383 "chr21:37871936:C>A" "CLDN14" "NM_001146078:c.-82+10725G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs148586936" "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
494384 "chr21:37871951:C>T" "CLDN14" "NM_001146078:c.-82+10710G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs758875613" "This variant is a VUS because it does not have enough information."
494385 "chr21:37871952:G>A" "CLDN14" "NM_001146078:c.-82+10709C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs553636640" "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
494386 "chr21:37871962:T>C" "CLDN14" "NM_001146078:c.-82+10699A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs567938824" "This variant is a VUS because it does not have enough information."
494387 "chr21:37871964:C>T" "CLDN14" "NM_001146078:c.-82+10697G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs573565160" "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
494388 "chr21:37871976:G>A" "CLDN14" "NM_001146078:c.-82+10685C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs528131867" "This variant is a VUS because it does not have enough information."
494389 "chr21:37871981:T>C" "CLDN14" "NM_001146078:c.-82+10680A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs557433375" "This variant is a VUS because it does not have enough information."
494390 "chr21:37871996:C>T" "CLDN14" "NM_001146078:c.-82+10665G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs143000137" "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
494391 "chr21:37871997:G>A" "CLDN14" "NM_001146078:c.-82+10664C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs546274812" "This variant is a VUS because it does not have enough information."
494392 "chr21:37872004:A>G" "CLDN14" "NM_001146078:c.-82+10657T>C" "FIVE_PRIME_INTRON" "Benign" "rs743425" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 493 1322 0.3729 252 1006 0.2505 134 694 0.1931 88 1008 0.0873 160 978 0.1636 1127 5008 0.22504
494393 "chr21:37872016:T>C" "CLDN14" "NM_001146078:c.-82+10645A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs117744204" "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
494394 "chr21:37872043:C>T" "CLDN14" "NM_001146078:c.-82+10618G>A" "FIVE_PRIME_INTRON" "Benign" "rs73902545" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 41 1322 0.031 9 1006 0.0089 17 694 0.0245 2 1008 0.002 30 978 0.0307 99 5008 0.0197684
494395 "chr21:37872044:G>A" "CLDN14" "NM_001146078:c.-82+10617C>T" "FIVE_PRIME_INTRON" "Benign" "rs369936139" "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 1 1008 0.001 20 978 0.0204 21 5008 0.00419329
494396 "chr21:37872050:C>T" "CLDN14" "NM_001146078:c.-82+10611G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs562028900" "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
494397 "chr21:37872051:G>A" "CLDN14" "NM_001146078:c.-82+10610C>T" "FIVE_PRIME_INTRON" "Benign" "rs151114535" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 11 1322 0.0083 1 1006 0.001 0 694 0 0 1008 0 0 978 0 12 5008 0.00239617
494398 "chr21:37872070:C>T" "CLDN14" "NM_001146078:c.-82+10591G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs185834364" "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
494399 "chr21:37872072:G>T" "CLDN14" "NM_001146078:c.-82+10589C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs746887563" "This variant is a VUS because it does not have enough information."
494400 "chr21:37872090:G>T" "CLDN14" "NM_001146078:c.-82+10571C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs770853469" "This variant is a VUS because it does not have enough information."
494401 "chr21:37872116:T>A" "CLDN14" "NM_001146078:c.-82+10545A>T" "FIVE_PRIME_INTRON" "Benign" "rs2000544" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 643 1322 0.4864 626 1006 0.6223 308 694 0.4438 482 1008 0.4782 545 978 0.5573 2604 5008 0.519968
494402 "chr21:37872178:C>T" "CLDN14" "NM_001146078:c.-82+10483G>A" "FIVE_PRIME_INTRON" "Benign" "rs2000545" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 503 1322 0.3805 604 1006 0.6004 311 694 0.4481 487 1008 0.4831 499 978 0.5102 2404 5008 0.480032
494403 "chr21:37872180:G>C" "CLDN14" "NM_001146078:c.-82+10481C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs769588372" "This variant is a VUS because it does not have enough information."
494404 "chr21:37872193:G>A" "CLDN14" "NM_001146078:c.-82+10468C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs775272893" "This variant is a VUS because it does not have enough information."
494405 "chr21:37872198:G>A" "CLDN14" "NM_001146078:c.-82+10463C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs568719318" "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
494406 "chr21:37872203:C>T" "CLDN14" "NM_001146078:c.-82+10458G>A" "FIVE_PRIME_INTRON" "Benign" "rs117356573" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 3 1322 0.0023 16 1006 0.0159 16 694 0.0231 1 1008 0.001 2 978 0.002 38 5008 0.00758786
494407 "chr21:37872204:G>A" "CLDN14" "NM_001146078:c.-82+10457C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs560733306" "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 0 978 0 3 5008 0.000599042
494408 "chr21:37872214:C>T" "CLDN14" "NM_001146078:c.-82+10447G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs369224232" "This variant is a VUS because it does not have enough information."
494409 "chr21:37872240:T>C" "CLDN14" "NM_001146078:c.-82+10421A>G" "FIVE_PRIME_INTRON" "Benign" "rs8129010" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1025 1322 0.7753 476 1006 0.4732 281 694 0.4049 298 1008 0.2956 325 978 0.3323 2405 5008 0.480232
494410 "chr21:37872241:G>A" "CLDN14" "NM_001146078:c.-82+10420C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs533656852" "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
494411 "chr21:37872250:G>A" "CLDN14" "NM_001146078:c.-82+10411C>T" "FIVE_PRIME_INTRON" "Benign" "rs7276934" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 276 1322 0.2088 669 1006 0.665 264 694 0.3804 323 1008 0.3204 416 978 0.4254 1948 5008 0.388978
494412 "chr21:37872270:T>C" "CLDN14" "NM_001146078:c.-82+10391A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs753863246" "This variant is a VUS because it does not have enough information."
494413 "chr21:37872280:C>T" "CLDN14" "NM_001146078:c.-82+10381G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759602141" "This variant is a VUS because it does not have enough information."
494414 "chr21:37872281:G>A" "CLDN14" "NM_001146078:c.-82+10380C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs190203143" "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
494415 "chr21:37872287:C>T" "CLDN14" "NM_001146078:c.-82+10374G>A" "FIVE_PRIME_INTRON" "Benign" "rs183194583" "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 0 694 0 0 1008 0 0 978 0 17 5008 0.00339457
494416 "chr21:37872288:G>T" "CLDN14" "NM_001146078:c.-82+10373C>A" "FIVE_PRIME_INTRON" "Benign" "rs28491626" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 175 1322 0.1324 240 1006 0.2386 97 694 0.1398 83 1008 0.0823 73 978 0.0746 668 5008 0.133387
494417 "chr21:37872288:G>A" "CLDN14" "NM_001146078:c.-82+10373C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs28491626" "This variant is a VUS because it does not have enough information."
494418 "chr21:37872289:C>T" "CLDN14" "NM_001146078:c.-82+10372G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs576358312" "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
494419 "chr21:37872290:G>A" "CLDN14" "NM_001146078:c.-82+10371C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs578058511" "This variant is a VUS because it does not have enough information."
494420 "chr21:37872294:T>G" "CLDN14" "NM_001146078:c.-82+10367A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs545411286" "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 2 978 0.002 3 5008 0.000599042
494421 "chr21:37872312:T>C" "CLDN14" "NM_001146078:c.-82+10349A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs565217120" "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
494422 "chr21:37872318:T>-" "CLDN14" "NM_001146078:c.-82+10343delA" "FIVE_PRIME_INTRON" "Benign" "rs5843765" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 563 1322 0.4259 590 1006 0.5865 291 694 0.4193 474 1008 0.4702 544 978 0.5562 2462 5008 0.491613
494423 "chr21:37872318:T>A" "CLDN14" "NM_001146078:c.-82+10343A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs369963223" "This variant is a VUS because it does not have enough information."
494424 "chr21:37872332:T>C" "CLDN14" "NM_001146078:c.-82+10329A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs572535089" "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
494425 "chr21:37872352:G>C" "CLDN14" "NM_001146078:c.-82+10309C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs186097791" "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
494426 "chr21:37872376:A>G" "CLDN14" "NM_001146078:c.-82+10285T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs751331087" "This variant is a VUS because it does not have enough information."
494427 "chr21:37872445:G>A" "CLDN14" "NM_001146078:c.-82+10216C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs767051894" "This variant is a VUS because it does not have enough information."
494428 "chr21:37872446:G>T" "CLDN14" "NM_001146078:c.-82+10215C>A" "FIVE_PRIME_INTRON" "Benign" "rs139711899" "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
494429 "chr21:37872447:C>T" "CLDN14" "NM_001146078:c.-82+10214G>A" "FIVE_PRIME_INTRON" "Benign" "rs2000546" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 484 1322 0.3661 578 1006 0.5746 281 694 0.4049 446 1008 0.4425 475 978 0.4857 2264 5008 0.452077
494430 "chr21:37872470:C>T" "CLDN14" "NM_001146078:c.-82+10191G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs544116930" "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
494431 "chr21:37872509:A>G" "CLDN14" "NM_001146078:c.-82+10152T>C" "FIVE_PRIME_INTRON" "Benign" "rs9984472" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 202 1322 0.1528 250 1006 0.2485 112 694 0.1614 83 1008 0.0823 101 978 0.1033 748 5008 0.149361
494432 "chr21:37872514:G>C" "CLDN14" "NM_001146078:c.-82+10147C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs371396976" "This variant is a VUS because it does not have enough information."
494433 "chr21:37872527:T>C" "CLDN14" "NM_001146078:c.-82+10134A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs755684848" "This variant is a VUS because it does not have enough information."
494434 "chr21:37872544:G>A" "CLDN14" "NM_001146078:c.-82+10117C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs531192834" "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
494435 "chr21:37872548:T>C" "CLDN14" "NM_001146078:c.-82+10113A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs374833269" "This variant is a VUS because it does not have enough information."
494436 "chr21:37872549:C>G" "CLDN14" "NM_001146078:c.-82+10112G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs376474025" "This variant is a VUS because it does not have enough information."
494437 "chr21:37872555:C>T" "CLDN14" "NM_001146078:c.-82+10106G>A" "FIVE_PRIME_INTRON" "Benign" "rs117268508" "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 2 694 0.0029 1 1008 0.001 2 978 0.002 13 5008 0.00259585
494438 "chr21:37872560:G>A" "CLDN14" "NM_001146078:c.-82+10101C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs191661786" "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
494439 "chr21:37872564:G>A" "CLDN14" "NM_001146078:c.-82+10097C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs527339352" "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
494440 "chr21:37872567:T>G" "CLDN14" "NM_001146078:c.-82+10094A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs748929741" "This variant is a VUS because it does not have enough information."
494441 "chr21:37872576:G>A" "CLDN14" "NM_001146078:c.-82+10085C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs547102145" "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
494442 "chr21:37872597:G>C" "CLDN14" "NM_001146078:c.-82+10064C>G" "FIVE_PRIME_INTRON" "Benign" "rs73380197" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 327 1322 0.2474 6 1006 0.006 50 694 0.072 176 1008 0.1746 59 978 0.0603 618 5008 0.123403
494443 "chr21:37872611:G>A" "CLDN14" "NM_001146078:c.-82+10050C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs536091433" "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
494444 "chr21:37872630:G>A" "CLDN14" "NM_001146078:c.-82+10031C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs773478159" "This variant is a VUS because it does not have enough information."
494445 "chr21:37872647:C>G" "CLDN14" "NM_001146078:c.-82+10014G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs370614362" "This variant is a VUS because it does not have enough information."
494446 "chr21:37872647:C>T" "CLDN14" "NM_001146078:c.-82+10014G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs370614362" "This variant is a VUS because it does not have enough information."
494447 "chr21:37872648:G>A" "CLDN14" "NM_001146078:c.-82+10013C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs556164356" "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
494448 "chr21:37872660:G>A" "CLDN14" "NM_001146078:c.-82+10001C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs183933541" "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
494449 "chr21:37872706:G>A" "CLDN14" "NM_001146078:c.-82+9955C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs568353874" "This variant is a VUS because it does not have enough information."
494450 "chr21:37872723:T>G" "CLDN14" "NM_001146078:c.-82+9938A>C" "FIVE_PRIME_INTRON" "Benign" "rs76415705" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 9 1322 0.0068 166 1006 0.165 88 694 0.1268 141 1008 0.1399 328 978 0.3354 732 5008 0.146166
494451 "chr21:37872729:T>A" "CLDN14" "NM_001146078:c.-82+9932A>T" "FIVE_PRIME_INTRON" "Benign" "rs78248421" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 13 694 0.0187 0 1008 0 0 978 0 263 5008 0.052516
494452 "chr21:37872730:A>T" "CLDN14" "NM_001146078:c.-82+9931T>A" "FIVE_PRIME_INTRON" "Benign" "rs75266315" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 158 1322 0.1195 13 1006 0.0129 23 694 0.0331 35 1008 0.0347 73 978 0.0746 302 5008 0.0603035
494453 "chr21:37872731:A>T" "CLDN14" "NM_001146078:c.-82+9930T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs541496091" "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
494454 "chr21:37872762:T>G" "CLDN14" "NM_001146078:c.-82+9899A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs13049068" "This variant is a VUS because it does not have enough information."
494455 "chr21:37872772:C>T" "CLDN14" "NM_001146078:c.-82+9889G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs775737243" "This variant is a VUS because it does not have enough information."
494456 "chr21:37872799:G>A" "CLDN14" "NM_001146078:c.-82+9862C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs368276575" "This variant is a VUS because it does not have enough information."
494457 "chr21:37872801:T>G" "CLDN14" "NM_001146078:c.-82+9860A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs13049082" "This variant is a VUS because it does not have enough information."
494458 "chr21:37872806:C>T" "CLDN14" "NM_001146078:c.-82+9855G>A" "FIVE_PRIME_INTRON" "Benign" "rs74732869" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 85 1322 0.0643 0 1006 0 31 694 0.0447 178 1008 0.1766 45 978 0.046 339 5008 0.0676917
494459 "chr21:37872807:G>A" "CLDN14" "NM_001146078:c.-82+9854C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs532253786" "This variant is a VUS because it does not have enough information."
494460 "chr21:37872835:T>G" "CLDN14" "NM_001146078:c.-82+9826A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs575081143" "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
494461 "chr21:37872846:C>T" "CLDN14" "NM_001146078:c.-82+9815G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs13048330" "This variant is a VUS because it does not have enough information."
494462 "chr21:37872847:A>G" "CLDN14" "NM_001146078:c.-82+9814T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs751325379" "This variant is a VUS because it does not have enough information."
494463 "chr21:37872886:T>C" "CLDN14" "NM_001146078:c.-82+9775A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs757065827" "This variant is a VUS because it does not have enough information."
494464 "chr21:37872942:C>T" "CLDN14" "NM_001146078:c.-82+9719G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs377267689" "This variant is a VUS because it does not have enough information."
494465 "chr21:37872967:T>C" "CLDN14" "NM_001146078:c.-82+9694A>G" "FIVE_PRIME_INTRON" "Benign" "rs146820518" "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 2 694 0.0029 0 1008 0 0 978 0 34 5008 0.00678914
494466 "chr21:37872976:C>T" "CLDN14" "NM_001146078:c.-82+9685G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs563747294" "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
494467 "chr21:37872977:G>A" "CLDN14" "NM_001146078:c.-82+9684C>T" "FIVE_PRIME_INTRON" "Benign" "rs532811617" "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 0 1008 0 0 978 0 12 5008 0.00239617
494468 "chr21:37872991:A>C" "CLDN14" "NM_001146078:c.-82+9670T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs546183396" "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
494469 "chr21:37873014:G>A" "CLDN14" "NM_001146078:c.-82+9647C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs564860272" "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
494470 "chr21:37873017:A>G" "CLDN14" "NM_001146078:c.-82+9644T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs550428857" "This variant is a VUS because it does not have enough information."
494471 "chr21:37873018:C>T" "CLDN14" "NM_001146078:c.-82+9643G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568593883" "This variant is a VUS because it does not have enough information."
494472 "chr21:37873019:C>G" "CLDN14" "NM_001146078:c.-82+9642G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs750346638" "This variant is a VUS because it does not have enough information."
494473 "chr21:37873020:G>A" "CLDN14" "NM_001146078:c.-82+9641C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs527330080" "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
494474 "chr21:37873036:T>G" "CLDN14" "NM_001146078:c.-82+9625A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs368731807" "This variant is a VUS because it does not have enough information."
494475 "chr21:37873048:G>A" "CLDN14" "NM_001146078:c.-82+9613C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs755737844" "This variant is a VUS because it does not have enough information."
494476 "chr21:37873056:T>C" "CLDN14" "NM_001146078:c.-82+9605A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs539131247" "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
494477 "chr21:37873102:G>A" "CLDN14" "NM_001146078:c.-82+9559C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs757758726" "This variant is a VUS because it does not have enough information."
494478 "chr21:37873114:C>T" "CLDN14" "NM_001146078:c.-82+9547G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs796891283" "This variant is a VUS because it does not have enough information."
494479 "chr21:37873155:C>T" "CLDN14" "NM_001146078:c.-82+9506G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs567053360" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 1 1008 0.001 0 978 0 4 5008 0.000798722
494480 "chr21:37873216:T>C" "CLDN14" "NM_001146078:c.-82+9445A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs781305859" "This variant is a VUS because it does not have enough information."
494481 "chr21:37873228:A>C" "CLDN14" "NM_001146078:c.-82+9433T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs529820823" "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
494482 "chr21:37873237:C>T" "CLDN14" "NM_001146078:c.-82+9424G>A" "FIVE_PRIME_INTRON" "Benign" "rs11700868" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 309 1322 0.2337 879 1006 0.8738 375 694 0.5403 365 1008 0.3621 576 978 0.589 2504 5008 0.5
494483 "chr21:37873238:G>A" "CLDN14" "NM_001146078:c.-82+9423C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs778566027" "This variant is a VUS because it does not have enough information."
494484 "chr21:37873284:G>A" "CLDN14" "NM_001146078:c.-82+9377C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs569770898" "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
494485 "chr21:37873318:C>A" "CLDN14" "NM_001146078:c.-82+9343G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs747390175" "This variant is a VUS because it does not have enough information."
494486 "chr21:37873330:G>T" "CLDN14" "NM_001146078:c.-82+9331C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs188933334" "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
494487 "chr21:37873336:G>A" "CLDN14" "NM_001146078:c.-82+9325C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs770101361" "This variant is a VUS because it does not have enough information."
494488 "chr21:37873345:G>A" "CLDN14" "NM_001146078:c.-82+9316C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs771321554" "This variant is a VUS because it does not have enough information."
494489 "chr21:37873429:C>T" "CLDN14" "NM_001146078:c.-82+9232G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs377458860" "This variant is a VUS because it does not have enough information."
494490 "chr21:37873466:T>C" "CLDN14" "NM_001146078:c.-82+9195A>G" "FIVE_PRIME_INTRON" "Benign" "rs75211466" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 13 694 0.0187 0 1008 0 0 978 0 263 5008 0.052516
494491 "chr21:37873467:C>T" "CLDN14" "NM_001146078:c.-82+9194G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs60167842" "This variant is a VUS because it does not have enough information."
494492 "chr21:37873471:G>-" "CLDN14" "NM_001146078:c.-82+9190delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs34167760" "This variant is a VUS because it does not have enough information."
494493 "chr21:37873493:T>C" "CLDN14" "NM_001146078:c.-82+9168A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs566070729" "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
494494 "chr21:37873506:G>A" "CLDN14" "NM_001146078:c.-82+9155C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs746351118" "This variant is a VUS because it does not have enough information."
494495 "chr21:37873529:T>C" "CLDN14" "NM_001146078:c.-82+9132A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs192469128" "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
494496 "chr21:37873542:T>G" "CLDN14" "NM_001146078:c.-82+9119A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs555077401" "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
494497 "chr21:37873575:C>T" "CLDN14" "NM_001146078:c.-82+9086G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs574953099" "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
494498 "chr21:37873580:C>T" "CLDN14" "NM_001146078:c.-82+9081G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs60026272" "This variant is a VUS because it does not have enough information."
494499 "chr21:37873623:T>-" "CLDN14" "NM_001146078:c.-82+9038delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs200031186" "This variant is a VUS because it does not have enough information."
494500 "chr21:37873631:TTTTTTTTTTTTTTTTTTTTT>-" "CLDN14" "NM_001146078:c.-82+9030_-82+9052delAAAAAAAAAAAAAAAAAAAAA" "FIVE_PRIME_INTRON" "Benign" "rs567984352" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 852 1322 0.6445 40 1006 0.0398 91 694 0.1311 240 1008 0.2381 133 978 0.136 1356 5008 0.270767
494501 "chr21:37873631:T>-" "CLDN14" "NM_001146078:c.-82+9030delA" "FIVE_PRIME_INTRON" "Unknown significance" "rs58458004" "This variant is a VUS because it does not have enough information."
494502 "chr21:37873631:TTTTTTTTTTTTTTTTTTTTTTT>-" "CLDN14" "NM_001146078:c.-82+9030_-82+9054delAAAAAAAAAAAAAAAAAAAAAAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs202184592" "This variant is a VUS because it does not have enough information."
494503 "chr21:37873658:TTTTTTTTTAG>AAA" "CLDN14" "Unknown significance" "rs762562373" "This variant is a VUS because it does not have enough information."
494504 "chr21:37873668:G>A" "CLDN14" "NM_001146078:c.-82+8993C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs11701484" "This variant is a VUS because it does not have enough information."
494505 "chr21:37873694:A>G" "CLDN14" "NM_001146078:c.-82+8967T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs368609995" "This variant is a VUS because it does not have enough information."
494506 "chr21:37873699:T>A" "CLDN14" "NM_001146078:c.-82+8962A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs539829706" "This variant is a VUS because it does not have enough information."
494507 "chr21:37873699:T>C" "CLDN14" "NM_001146078:c.-82+8962A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs539829706" "This variant is a VUS because it does not have enough information."
494508 "chr21:37873706:T>C" "CLDN14" "NM_001146078:c.-82+8955A>G" "FIVE_PRIME_INTRON" "Benign" "rs77213226" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 250 1322 0.1891 1 1006 0.001 13 694 0.0187 0 1008 0 0 978 0 264 5008 0.0527157
494509 "chr21:37873710:G>A" "CLDN14" "NM_001146078:c.-82+8951C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs56093029" "This variant is a VUS because it does not have enough information."
494510 "chr21:37873718:G>C" "CLDN14" "NM_001146078:c.-82+8943C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs557483043" "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
494511 "chr21:37873733:T>C" "CLDN14" "NM_001146078:c.-82+8928A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs577375477" "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
494512 "chr21:37873740:T>C" "CLDN14" "NM_001146078:c.-82+8921A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs762963245" "This variant is a VUS because it does not have enough information."
494513 "chr21:37873746:C>T" "CLDN14" "NM_001146078:c.-82+8915G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs145453476" "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
494514 "chr21:37873765:G>A" "CLDN14" "NM_001146078:c.-82+8896C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs182828183" "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
494515 "chr21:37873767:G>A" "CLDN14" "NM_001146078:c.-82+8894C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs377312024" "This variant is a VUS because it does not have enough information."
494516 "chr21:37873779:G>A" "CLDN14" "NM_001146078:c.-82+8882C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs56395351" "This variant is a VUS because it does not have enough information."
494517 "chr21:37873816:T>C" "CLDN14" "NM_001146078:c.-82+8845A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs187190036" "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
494518 "chr21:37873821:C>T" "CLDN14" "NM_001146078:c.-82+8840G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs796564885" "This variant is a VUS because it does not have enough information."
494519 "chr21:37873844:G>A" "CLDN14" "NM_001146078:c.-82+8817C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs56178762" "This variant is a VUS because it does not have enough information."
494520 "chr21:37873957:C>A" "CLDN14" "NM_001146078:c.-82+8704G>T" "FIVE_PRIME_INTRON" "Benign" "rs8128673" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 250 1322 0.1891 1 1006 0.001 15 694 0.0216 0 1008 0 0 978 0 266 5008 0.053115
494521 "chr21:37873958:C>A" "CLDN14" "NM_001146078:c.-82+8703G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs761558030" "This variant is a VUS because it does not have enough information."
494522 "chr21:37873968:->ACTC" "CLDN14" "NM_001146078:c.-82+8693_-82+8694insGAGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs763536457" "This variant is a VUS because it does not have enough information."
494523 "chr21:37873986:G>A" "CLDN14" "NM_001146078:c.-82+8675C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs767323993" "This variant is a VUS because it does not have enough information."
494524 "chr21:37873989:A>G" "CLDN14" "NM_001146078:c.-82+8672T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs191702008" "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
494525 "chr21:37874004:G>A" "CLDN14" "NM_001146078:c.-82+8657C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs574101947" "This variant is a VUS because it does not have enough information."
494526 "chr21:37874049:A>C" "CLDN14" "NM_001146078:c.-82+8612T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs529764082" "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
494527 "chr21:37874059:G>T" "CLDN14" "NM_001146078:c.-82+8602C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs183837016" "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
494528 "chr21:37874133:G>A" "CLDN14" "NM_001146078:c.-82+8528C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs563455401" "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
494529 "chr21:37874222:T>-" "CLDN14" "NM_001146078:c.-82+8439delA" "FIVE_PRIME_INTRON" "Benign" "rs34964362" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 504 1322 0.3812 903 1006 0.8976 407 694 0.5865 453 1008 0.4494 681 978 0.6963 2948 5008 0.588658
494530 "chr21:37874222:->T" "CLDN14" "NM_001146078:c.-82+8439_-82+8440insA" "FIVE_PRIME_INTRON" "Unknown significance" "rs796535772" "This variant is a VUS because it does not have enough information."
494531 "chr21:37874222:T>C" "CLDN14" "NM_001146078:c.-82+8439A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs369419320" "This variant is a VUS because it does not have enough information."
494532 "chr21:37874262:C>T" "CLDN14" "NM_001146078:c.-82+8399G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs532246730" "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
494533 "chr21:37874263:G>A" "CLDN14" "NM_001146078:c.-82+8398C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs552442193" "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
494534 "chr21:37874287:C>T" "CLDN14" "NM_001146078:c.-82+8374G>A" "FIVE_PRIME_INTRON" "Benign" "rs145282279" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 13 1006 0.0129 4 694 0.0058 0 1008 0 3 978 0.0031 21 5008 0.00419329
494535 "chr21:37874327:A>G" "CLDN14" "NM_001146078:c.-82+8334T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs756148421" "This variant is a VUS because it does not have enough information."
494536 "chr21:37874342:A>G" "CLDN14" "NM_001146078:c.-82+8319T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs766350277" "This variant is a VUS because it does not have enough information."
494537 "chr21:37874365:C>T" "CLDN14" "NM_001146078:c.-82+8296G>A" "FIVE_PRIME_INTRON" "Benign" "rs116167284" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
494538 "chr21:37874369:A>G" "CLDN14" "NM_001146078:c.-82+8292T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs548574862" "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
494539 "chr21:37874374:T>C" "CLDN14" "NM_001146078:c.-82+8287A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs749032039" "This variant is a VUS because it does not have enough information."
494540 "chr21:37874386:C>T" "CLDN14" "NM_001146078:c.-82+8275G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs568468514" "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
494541 "chr21:37874403:A>C" "CLDN14" "NM_001146078:c.-82+8258T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs533808399" "This variant is a VUS because it does not have enough information."
494542 "chr21:37874417:A>G" "CLDN14" "NM_001146078:c.-82+8244T>C" "FIVE_PRIME_INTRON" "Benign" "rs6517354" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 965 1322 0.73 914 1006 0.9085 462 694 0.6657 594 1008 0.5893 764 978 0.7812 3699 5008 0.738618
494543 "chr21:37874424:G>A" "CLDN14" "NM_001146078:c.-82+8237C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs557216900" "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
494544 "chr21:37874443:T>G" "CLDN14" "NM_001146078:c.-82+8218A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs148267139" "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
494545 "chr21:37874446:G>T" "CLDN14" "NM_001146078:c.-82+8215C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs539675868" "This variant is a VUS because it does not have enough information." 2 1322 0.0015 0 1006 0 0 694 0 1 1008 0.001 0 978 0 3 5008 0.000599042
494546 "chr21:37874450:A>C" "CLDN14" "NM_001146078:c.-82+8211T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs553239483" "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
494547 "chr21:37874484:A>T" "CLDN14" "NM_001146078:c.-82+8177T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs573163700" "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
494548 "chr21:37874491:G>A" "CLDN14" "NM_001146078:c.-82+8170C>T" "FIVE_PRIME_INTRON" "Benign" "rs9680300" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 128 1322 0.0968 15 1006 0.0149 23 694 0.0331 49 1008 0.0486 71 978 0.0726 286 5008 0.0571086
494549 "chr21:37874543:A>C" "CLDN14" "NM_001146078:c.-82+8118T>G" "FIVE_PRIME_INTRON" "Benign" "rs7278181" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 153 1322 0.1157 1 1006 0.001 7 694 0.0101 0 1008 0 0 978 0 161 5008 0.0321486
494550 "chr21:37874585:C>G" "CLDN14" "NM_001146078:c.-82+8076G>C" "FIVE_PRIME_INTRON" "Benign" "rs9979731" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1026 1322 0.7761 914 1006 0.9085 464 694 0.6686 592 1008 0.5873 734 978 0.7505 3730 5008 0.744808
494551 "chr21:37874592:T>C" "CLDN14" "NM_001146078:c.-82+8069A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs746165511" "This variant is a VUS because it does not have enough information."
494552 "chr21:37874629:T>C" "CLDN14" "NM_001146078:c.-82+8032A>G" "FIVE_PRIME_INTRON" "Benign" "rs189003531" "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 0 694 0 0 1008 0 1 978 0.001 7 5008 0.00139776
494553 "chr21:37874662:A>T" "CLDN14" "NM_001146078:c.-82+7999T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs780526004" "This variant is a VUS because it does not have enough information."
494554 "chr21:37874709:T>C" "CLDN14" "NM_001146078:c.-82+7952A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs749438188" "This variant is a VUS because it does not have enough information."
494555 "chr21:37874710:A>T" "CLDN14" "NM_001146078:c.-82+7951T>A" "FIVE_PRIME_INTRON" "Benign" "rs142709818" "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 1 694 0.0014 0 1008 0 0 978 0 35 5008 0.00698882
494556 "chr21:37874717:->G" "CLDN14" "NM_001146078:c.-82+7944_-82+7945insC" "FIVE_PRIME_INTRON" "Unknown significance" "rs149612032" "This variant is a VUS because it does not have enough information."
494557 "chr21:37874770:C>T" "CLDN14" "NM_001146078:c.-82+7891G>A" "FIVE_PRIME_INTRON" "Benign" "rs115286032" "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
494558 "chr21:37874806:C>T" "CLDN14" "NM_001146078:c.-82+7855G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs774488880" "This variant is a VUS because it does not have enough information."
494559 "chr21:37874823:A>G" "CLDN14" "NM_001146078:c.-82+7838T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs552436210" "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
494560 "chr21:37874856:T>C" "CLDN14" "NM_001146078:c.-82+7805A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs146922176" "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
494561 "chr21:37874870:T>C" "CLDN14" "NM_001146078:c.-82+7791A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs528348036" "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
494562 "chr21:37874876:T>G" "CLDN14" "NM_001146078:c.-82+7785A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs548514510" "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
494563 "chr21:37874882:G>T" "CLDN14" "NM_001146078:c.-82+7779C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs34241595" "This variant is a VUS because it does not have enough information."
494564 "chr21:37874975:A>C" "CLDN14" "NM_001146078:c.-82+7686T>G" "FIVE_PRIME_INTRON" "Benign" "rs41513750" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 164 1322 0.1241 15 1006 0.0149 24 694 0.0346 51 1008 0.0506 72 978 0.0736 326 5008 0.0650958
494565 "chr21:37875017:C>T" "CLDN14" "NM_001146078:c.-82+7644G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs527822708" "This variant is a VUS because it does not have enough information."
494566 "chr21:37875072:C>T" "CLDN14" "NM_001146078:c.-82+7589G>A" "FIVE_PRIME_INTRON" "Benign" "rs138023142" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
494567 "chr21:37875126:A>G" "CLDN14" "NM_001146078:c.-82+7535T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs561425218" "This variant is a VUS because it does not have enough information."
494568 "chr21:37875127:T>A" "CLDN14" "NM_001146078:c.-82+7534A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs7283831" "This variant is a VUS because it does not have enough information."
494569 "chr21:37875233:C>T" "CLDN14" "NM_001146078:c.-82+7428G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs551034049" "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
494570 "chr21:37875241:C>T" "CLDN14" "NM_001146078:c.-82+7420G>A" "FIVE_PRIME_INTRON" "Benign" "rs570892984" "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
494571 "chr21:37875256:C>T" "CLDN14" "NM_001146078:c.-82+7405G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs193053857" "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
494572 "chr21:37875265:G>C" "CLDN14" "NM_001146078:c.-82+7396C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs766478173" "This variant is a VUS because it does not have enough information."
494573 "chr21:37875272:C>A" "CLDN14" "NM_001146078:c.-82+7389G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs753820850" "This variant is a VUS because it does not have enough information."
494574 "chr21:37875317:C>A" "CLDN14" "NM_001146078:c.-82+7344G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs553121024" "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
494575 "chr21:37875391:G>A" "CLDN14" "NM_001146078:c.-82+7270C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs573101370" "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
494576 "chr21:37875403:G>C" "CLDN14" "NM_001146078:c.-82+7258C>G" "FIVE_PRIME_INTRON" "Benign" "rs185667675" "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 2 694 0.0029 0 1008 0 0 978 0 13 5008 0.00259585
494577 "chr21:37875458:T>C" "CLDN14" "NM_001146078:c.-82+7203A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs573592210" "This variant is a VUS because it does not have enough information."
494578 "chr21:37875472:C>T" "CLDN14" "NM_001146078:c.-82+7189G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs555678276" "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
494579 "chr21:37875489:T>G" "CLDN14" "NM_001146078:c.-82+7172A>C" "FIVE_PRIME_INTRON" "Benign" "rs143475288" "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
494580 "chr21:37875505:C>T" "CLDN14" "NM_001146078:c.-82+7156G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759007457" "This variant is a VUS because it does not have enough information."
494581 "chr21:37875510:->C" "CLDN14" "NM_001146078:c.-82+7151_-82+7152insG" "FIVE_PRIME_INTRON" "Unknown significance" "rs34333880" "This variant is a VUS because it does not have enough information."
494582 "chr21:37875583:C>A" "CLDN14" "NM_001146078:c.-82+7078G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs764780804" "This variant is a VUS because it does not have enough information."
494583 "chr21:37875618:T>C" "CLDN14" "NM_001146078:c.-82+7043A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs543077870" "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
494584 "chr21:37875622:G>T" "CLDN14" "NM_001146078:c.-82+7039C>A" "FIVE_PRIME_INTRON" "Benign" "rs2226830" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 314 1322 0.2375 892 1006 0.8867 381 694 0.549 365 1008 0.3621 601 978 0.6145 2553 5008 0.509784
494585 "chr21:37875642:A>G" "CLDN14" "NM_001146078:c.-82+7019T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs758076109" "This variant is a VUS because it does not have enough information."
494586 "chr21:37875664:T>C" "CLDN14" "NM_001146078:c.-82+6997A>G" "FIVE_PRIME_INTRON" "Benign" "rs2409820" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1221 1322 0.9236 917 1006 0.9115 477 694 0.6873 591 1008 0.5863 770 978 0.7873 3976 5008 0.79393
494587 "chr21:37875689:T>C" "CLDN14" "NM_001146078:c.-82+6972A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs545917768" "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
494588 "chr21:37875700:G>A" "CLDN14" "NM_001146078:c.-82+6961C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs750845470" "This variant is a VUS because it does not have enough information."
494589 "chr21:37875732:G>T" "CLDN14" "NM_001146078:c.-82+6929C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs559548247" "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
494590 "chr21:37875736:C>G" "CLDN14" "NM_001146078:c.-82+6925G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs528337472" "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
494591 "chr21:37875741:G>A" "CLDN14" "NM_001146078:c.-82+6920C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs542144375" "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
494592 "chr21:37875749:C>T" "CLDN14" "NM_001146078:c.-82+6912G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs561864363" "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
494593 "chr21:37875758:G>A" "CLDN14" "NM_001146078:c.-82+6903C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs139380671" "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
494594 "chr21:37875765:T>G" "CLDN14" "NM_001146078:c.-82+6896A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs532044470" "This variant is a VUS because it does not have enough information."
494595 "chr21:37875767:G>A" "CLDN14" "NM_001146078:c.-82+6894C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs550668100" "This variant is a VUS because it does not have enough information." 1 1322 0.0008 2 1006 0.002 0 694 0 0 1008 0 0 978 0 3 5008 0.000599042
494596 "chr21:37875771:C>T" "CLDN14" "NM_001146078:c.-82+6890G>A" "FIVE_PRIME_INTRON" "Benign" "rs7278261" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1024 1322 0.7746 914 1006 0.9085 464 694 0.6686 592 1008 0.5873 735 978 0.7515 3729 5008 0.744609
494597 "chr21:37875798:A>G" "CLDN14" "NM_001146078:c.-82+6863T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs749777501" "This variant is a VUS because it does not have enough information."
494598 "chr21:37875806:T>C" "CLDN14" "NM_001146078:c.-82+6855A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs533203600" "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
494599 "chr21:37875830:G>A" "CLDN14" "NM_001146078:c.-82+6831C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs377168230" "This variant is a VUS because it does not have enough information."
494600 "chr21:37875838:T>G" "CLDN14" "NM_001146078:c.-82+6823A>C" "FIVE_PRIME_INTRON" "Benign" "rs546696854" "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
494601 "chr21:37875856:C>T" "CLDN14" "NM_001146078:c.-82+6805G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs566712565" "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
494602 "chr21:37875863:T>G" "CLDN14" "NM_001146078:c.-82+6798A>C" "FIVE_PRIME_INTRON" "Benign" "rs7279532" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1024 1322 0.7746 914 1006 0.9085 464 694 0.6686 592 1008 0.5873 736 978 0.7526 3730 5008 0.744808
494603 "chr21:37875907:T>C" "CLDN14" "NM_001146078:c.-82+6754A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs529695733" "This variant is a VUS because it does not have enough information."
494604 "chr21:37875911:T>A" "CLDN14" "NM_001146078:c.-82+6750A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs555616971" "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
494605 "chr21:37875918:T>C" "CLDN14" "NM_001146078:c.-82+6743A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs569484310" "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
494606 "chr21:37875919:G>T" "CLDN14" "NM_001146078:c.-82+6742C>A" "FIVE_PRIME_INTRON" "Benign" "rs57748016" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 183 1322 0.1384 1 1006 0.001 7 694 0.0101 0 1008 0 0 978 0 191 5008 0.038139
494607 "chr21:37875924:C>T" "CLDN14" "NM_001146078:c.-82+6737G>A" "FIVE_PRIME_INTRON" "Benign" "rs149611120" "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 0 694 0 0 1008 0 0 978 0 21 5008 0.00419329
494608 "chr21:37875929:T>G" "CLDN14" "NM_001146078:c.-82+6732A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs576782833" "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
494609 "chr21:37875935:G>A" "CLDN14" "NM_001146078:c.-82+6726C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545907167" "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
494610 "chr21:37875946:A>G" "CLDN14" "NM_001146078:c.-82+6715T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs764608945" "This variant is a VUS because it does not have enough information."
494611 "chr21:37875955:T>G" "CLDN14" "NM_001146078:c.-82+6706A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs144407600" "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
494612 "chr21:37875995:G>T" "CLDN14" "NM_001146078:c.-82+6666C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs573055664" "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
494613 "chr21:37876084:AC>-" "CLDN14" "NM_001146078:c.-82+6577_-82+6580delGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs780871612" "This variant is a VUS because it does not have enough information."
494614 "chr21:37876100:C>T" "CLDN14" "NM_001146078:c.-82+6561G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs369751019" "This variant is a VUS because it does not have enough information."
494615 "chr21:37876183:C>T" "CLDN14" "NM_001146078:c.-82+6478G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs756275093" "This variant is a VUS because it does not have enough information."
494616 "chr21:37876205:T>C" "CLDN14" "NM_001146078:c.-82+6456A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs190569660" "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
494617 "chr21:37876209:A>G" "CLDN14" "NM_001146078:c.-82+6452T>C" "FIVE_PRIME_INTRON" "Benign" "rs181035996" "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 8 694 0.0115 0 1008 0 35 978 0.0358 46 5008 0.0091853
494618 "chr21:37876222:T>A" "CLDN14" "NM_001146078:c.-82+6439A>T" "FIVE_PRIME_INTRON" "Benign" "rs148790454" "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 6 694 0.0086 0 1008 0 1 978 0.001 17 5008 0.00339457
494619 "chr21:37876264:A>G" "CLDN14" "NM_001146078:c.-82+6397T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs185294988" "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
494620 "chr21:37876292:AG>-" "CLDN14" "NM_001146078:c.-82+6369_-82+6372delCT" "FIVE_PRIME_INTRON" "Benign" "rs151185208" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 183 1322 0.1384 1 1006 0.001 7 694 0.0101 0 1008 0 0 978 0 191 5008 0.038139
494621 "chr21:37876387:A>T" "CLDN14" "NM_001146078:c.-82+6274T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs551327123" "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
494622 "chr21:37876394:T>C" "CLDN14" "NM_001146078:c.-82+6267A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs533193119" "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
494623 "chr21:37876409:G>A" "CLDN14" "NM_001146078:c.-82+6252C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs201442200" "This variant is a VUS because it does not have enough information."
494624 "chr21:37876452:C>A" "CLDN14" "NM_001146078:c.-82+6209G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs546684454" "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
494625 "chr21:37876560:C>T" "CLDN14" "NM_001146078:c.-82+6101G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs765044218" "This variant is a VUS because it does not have enough information."
494626 "chr21:37876577:G>A" "CLDN14" "NM_001146078:c.-82+6084C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs570711778" "This variant is a VUS because it does not have enough information."
494627 "chr21:37876592:C>T" "CLDN14" "NM_001146078:c.-82+6069G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs752265186" "This variant is a VUS because it does not have enough information."
494628 "chr21:37876610:C>T" "CLDN14" "NM_001146078:c.-82+6051G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs762357191" "This variant is a VUS because it does not have enough information."
494629 "chr21:37876629:AAAAAC>-" "CLDN14" "NM_001146078:c.-82+6032_-82+6039delGTTTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs373024276" "This variant is a VUS because it does not have enough information."
494630 "chr21:37876707:T>C" "CLDN14" "NM_001146078:c.-82+5954A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs566650622" "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
494631 "chr21:37876708:T>C" "CLDN14" "NM_001146078:c.-82+5953A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs763805329" "This variant is a VUS because it does not have enough information."
494632 "chr21:37876726:G>A" "CLDN14" "NM_001146078:c.-82+5935C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs143596976" "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
494633 "chr21:37876738:T>C" "CLDN14" "NM_001146078:c.-82+5923A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs751183321" "This variant is a VUS because it does not have enough information."
494634 "chr21:37876751:G>C" "CLDN14" "NM_001146078:c.-82+5910C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs549276039" "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
494635 "chr21:37876804:ACCCCCTTTAAAG>-" "CLDN14" "NM_001146078:c.-82+5857_-82+5871delCTTTAAAGGGGGT" "FIVE_PRIME_INTRON" "Unknown significance" "rs774656533" "This variant is a VUS because it does not have enough information."
494636 "chr21:37876806:C>T" "CLDN14" "NM_001146078:c.-82+5855G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs569455396" "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
494637 "chr21:37876837:C>T" "CLDN14" "NM_001146078:c.-82+5824G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs538117021" "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
494638 "chr21:37876857:G>C" "CLDN14" "NM_001146078:c.-82+5804C>G" "FIVE_PRIME_INTRON" "Benign" "rs73380201" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 248 1322 0.1876 1 1006 0.001 13 694 0.0187 0 1008 0 0 978 0 262 5008 0.0523163
494639 "chr21:37876882:C>A" "CLDN14" "NM_001146078:c.-82+5779G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs373258446" "This variant is a VUS because it does not have enough information."
494640 "chr21:37876886:T>G" "CLDN14" "NM_001146078:c.-82+5775A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs570460870" "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
494641 "chr21:37876903:A>G" "CLDN14" "NM_001146078:c.-82+5758T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs539469271" "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
494642 "chr21:37876967:C>T" "CLDN14" "NM_001146078:c.-82+5694G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs553089692" "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
494643 "chr21:37877000:C>T" "CLDN14" "NM_001146078:c.-82+5661G>A" "FIVE_PRIME_INTRON" "Benign" "rs146771544" "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
494644 "chr21:37877002:T>C" "CLDN14" "NM_001146078:c.-82+5659A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs139510490" "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
494645 "chr21:37877038:A>G" "CLDN14" "NM_001146078:c.-82+5623T>C" "FIVE_PRIME_INTRON" "Benign" "rs538699352" "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
494646 "chr21:37877051:C>T" "CLDN14" "NM_001146078:c.-82+5610G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs557343291" "This variant is a VUS because it does not have enough information."
494647 "chr21:37877113:G>A" "CLDN14" "NM_001146078:c.-82+5548C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs575401982" "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
494648 "chr21:37877157:C>A" "CLDN14" "NM_001146078:c.-82+5504G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs754115571" "This variant is a VUS because it does not have enough information."
494649 "chr21:37877179:T>C" "CLDN14" "NM_001146078:c.-82+5482A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs755510443" "This variant is a VUS because it does not have enough information."
494650 "chr21:37877249:T>C" "CLDN14" "NM_001146078:c.-82+5412A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs199620437" "This variant is a VUS because it does not have enough information."
494651 "chr21:37877264:T>C" "CLDN14" "NM_001146078:c.-82+5397A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs544167483" "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
494652 "chr21:37877269:C>T" "CLDN14" "NM_001146078:c.-82+5392G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs569381057" "This variant is a VUS because it does not have enough information."
494653 "chr21:37877287:AA>-" "CLDN14" "NM_001146078:c.-82+5374_-82+5377delTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs770719628" "This variant is a VUS because it does not have enough information."
494654 "chr21:37877310:T>C" "CLDN14" "NM_001146078:c.-82+5351A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs564450415" "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
494655 "chr21:37877341:A>G" "CLDN14" "NM_001146078:c.-82+5320T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs577592745" "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
494656 "chr21:37877385:G>C" "CLDN14" "NM_001146078:c.-82+5276C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs770420747" "This variant is a VUS because it does not have enough information."
494657 "chr21:37877424:A>C" "CLDN14" "NM_001146078:c.-82+5237T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs370280552" "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
494658 "chr21:37877426:TA>-" "CLDN14" "NM_001146078:c.-82+5235_-82+5238delTA" "FIVE_PRIME_INTRON" "Unknown significance" "rs776172724" "This variant is a VUS because it does not have enough information."
494659 "chr21:37877440:A>G" "CLDN14" "NM_001146078:c.-82+5221T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs144335303" "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
494660 "chr21:37877446:C>T" "CLDN14" "NM_001146078:c.-82+5215G>A" "FIVE_PRIME_INTRON" "Benign" "rs6517355" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 231 1322 0.1747 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 243 5008 0.0485224
494661 "chr21:37877446:CAG>TAA" "CLDN14" "Unknown significance" "rs386818303" "This variant is a VUS because it does not have enough information."
494662 "chr21:37877448:G>A" "CLDN14" "NM_001146078:c.-82+5213C>T" "FIVE_PRIME_INTRON" "Benign" "rs6517356" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 231 1322 0.1747 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 243 5008 0.0485224
494663 "chr21:37877463:C>G" "CLDN14" "NM_001146078:c.-82+5198G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs778179936" "This variant is a VUS because it does not have enough information."
494664 "chr21:37877478:T>C" "CLDN14" "NM_001146078:c.-82+5183A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs151058702" "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
494665 "chr21:37877491:G>A" "CLDN14" "NM_001146078:c.-82+5170C>T" "FIVE_PRIME_INTRON" "Benign" "rs6517357" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 232 1322 0.1755 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 244 5008 0.048722
494666 "chr21:37877510:AAG>-" "CLDN14" "NM_001146078:c.-82+5151_-82+5155delCTT" "FIVE_PRIME_INTRON" "Benign" "rs140301525" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 233 1322 0.1762 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 245 5008 0.0489217
494667 "chr21:37877516:T>G" "CLDN14" "NM_001146078:c.-82+5145A>C" "FIVE_PRIME_INTRON" "Benign" "rs551766994" "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
494668 "chr21:37877538:TT>-" "CLDN14" "NM_001146078:c.-82+5123_-82+5126delAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs766971199" "This variant is a VUS because it does not have enough information."
494669 "chr21:37877546:A>G" "CLDN14" "NM_001146078:c.-82+5115T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs369621760" "This variant is a VUS because it does not have enough information."
494670 "chr21:37877582:T>C" "CLDN14" "NM_001146078:c.-82+5079A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs572006295" "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
494671 "chr21:37877592:G>T" "CLDN14" "NM_001146078:c.-82+5069C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs534514358" "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
494672 "chr21:37877594:A>G" "CLDN14" "NM_001146078:c.-82+5067T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs546593358" "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
494673 "chr21:37877607:A>G" "CLDN14" "NM_001146078:c.-82+5054T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs538123657" "This variant is a VUS because it does not have enough information."
494674 "chr21:37877621:T>A" "CLDN14" "NM_001146078:c.-82+5040A>T" "FIVE_PRIME_INTRON" "Benign" "rs4816538" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1210 1322 0.9153 917 1006 0.9115 472 694 0.6801 594 1008 0.5893 768 978 0.7853 3961 5008 0.790935
494675 "chr21:37877636:C>T" "CLDN14" "NM_001146078:c.-82+5025G>A" "FIVE_PRIME_INTRON" "Benign" "rs59408933" "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
494676 "chr21:37877638:G>A" "CLDN14" "NM_001146078:c.-82+5023C>T" "FIVE_PRIME_INTRON" "Benign" "rs116083368" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 125 1322 0.0946 14 1006 0.0139 22 694 0.0317 33 1008 0.0327 71 978 0.0726 265 5008 0.0529153
494677 "chr21:37877651:T>C" "CLDN14" "NM_001146078:c.-82+5010A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs764835088" "This variant is a VUS because it does not have enough information."
494678 "chr21:37877654:A>C" "CLDN14" "NM_001146078:c.-82+5007T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs140844337" "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
494679 "chr21:37877674:C>G" "CLDN14" "NM_001146078:c.-82+4987G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs538071067" "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
494680 "chr21:37877675:C>A" "CLDN14" "NM_001146078:c.-82+4986G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs557750502" "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
494681 "chr21:37877679:G>A" "CLDN14" "NM_001146078:c.-82+4982C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs150133049" "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
494682 "chr21:37877692:->GC" "CLDN14" "NM_001146078:c.-82+4969_-82+4970insGC" "FIVE_PRIME_INTRON" "Unknown significance" "rs760148272" "This variant is a VUS because it does not have enough information."
494683 "chr21:37877693:C>T" "CLDN14" "NM_001146078:c.-82+4968G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs8130520" "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
494684 "chr21:37877727:A>G" "CLDN14" "NM_001146078:c.-82+4934T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs560068667" "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
494685 "chr21:37877813:A>T" "CLDN14" "NM_001146078:c.-82+4848T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs370897490" "This variant is a VUS because it does not have enough information."
494686 "chr21:37877827:G>T" "CLDN14" "NM_001146078:c.-82+4834C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs573738795" "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
494687 "chr21:37877948:A>G" "CLDN14" "NM_001146078:c.-82+4713T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs775286857" "This variant is a VUS because it does not have enough information."
494688 "chr21:37878033:T>A" "CLDN14" "NM_001146078:c.-82+4628A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545577334" "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
494689 "chr21:37878033:T>C" "CLDN14" "NM_001146078:c.-82+4628A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs545577334" "This variant is a VUS because it does not have enough information."
494690 "chr21:37878066:G>T" "CLDN14" "NM_001146078:c.-82+4595C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs762566685" "This variant is a VUS because it does not have enough information."
494691 "chr21:37878085:A>C" "CLDN14" "NM_001146078:c.-82+4576T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs573385677" "This variant is a VUS because it does not have enough information."
494692 "chr21:37878088:G>A" "CLDN14" "NM_001146078:c.-82+4573C>T" "FIVE_PRIME_INTRON" "Benign" "rs76518530" "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 3 694 0.0043 0 1008 0 0 978 0 44 5008 0.00878594
494693 "chr21:37878105:T>C" "CLDN14" "NM_001146078:c.-82+4556A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs531797822" "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
494694 "chr21:37878136:G>T" "CLDN14" "NM_001146078:c.-82+4525C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs551918393" "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
494695 "chr21:37878145:C>T" "CLDN14" "NM_001146078:c.-82+4516G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs188099015" "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
494696 "chr21:37878146:G>A" "CLDN14" "NM_001146078:c.-82+4515C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs527946092" "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
494697 "chr21:37878150:G>A" "CLDN14" "NM_001146078:c.-82+4511C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs141397194" "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
494698 "chr21:37878156:G>A" "CLDN14" "NM_001146078:c.-82+4505C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566464704" "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
494699 "chr21:37878166:A>T" "CLDN14" "NM_001146078:c.-82+4495T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs540804666" "This variant is a VUS because it does not have enough information."
494700 "chr21:37878181:T>C" "CLDN14" "NM_001146078:c.-82+4480A>G" "FIVE_PRIME_INTRON" "Benign" "rs57280430" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 161 1322 0.1218 0 1006 0 30 694 0.0432 177 1008 0.1756 44 978 0.045 412 5008 0.0822684
494701 "chr21:37878198:T>C" "CLDN14" "NM_001146078:c.-82+4463A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs368344883" "This variant is a VUS because it does not have enough information."
494702 "chr21:37878249:T>G" "CLDN14" "NM_001146078:c.-82+4412A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs548779949" "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
494703 "chr21:37878256:T>G" "CLDN14" "NM_001146078:c.-82+4405A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs568966413" "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
494704 "chr21:37878282:A>T" "CLDN14" "NM_001146078:c.-82+4379T>A" "FIVE_PRIME_INTRON" "Benign" "rs59851452" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 232 1322 0.1755 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 244 5008 0.048722
494705 "chr21:37878326:C>A" "CLDN14" "NM_001146078:c.-82+4335G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs561236529" "This variant is a VUS because it does not have enough information."
494706 "chr21:37878331:A>G" "CLDN14" "NM_001146078:c.-82+4330T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs754239570" "This variant is a VUS because it does not have enough information."
494707 "chr21:37878362:A>G" "CLDN14" "NM_001146078:c.-82+4299T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs557502273" "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
494708 "chr21:37878368:C>T" "CLDN14" "NM_001146078:c.-82+4293G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs181301230" "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
494709 "chr21:37878373:T>C" "CLDN14" "NM_001146078:c.-82+4288A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs146931854" "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
494710 "chr21:37878387:G>T" "CLDN14" "NM_001146078:c.-82+4274C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs553698102" "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
494711 "chr21:37878394:C>G" "CLDN14" "NM_001146078:c.-82+4267G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs573930231" "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
494712 "chr21:37878403:T>C" "CLDN14" "NM_001146078:c.-82+4258A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs543044559" "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
494713 "chr21:37878455:C>T" "CLDN14" "NM_001146078:c.-82+4206G>A" "FIVE_PRIME_INTRON" "Benign" "rs79785004" "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 2 694 0.0029 0 1008 0 2 978 0.002 10 5008 0.00199681
494714 "chr21:37878462:T>G" "CLDN14" "NM_001146078:c.-82+4199A>C" "FIVE_PRIME_INTRON" "Benign" "rs57709437" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 161 1322 0.1218 0 1006 0 30 694 0.0432 177 1008 0.1756 44 978 0.045 412 5008 0.0822684
494715 "chr21:37878480:C>T" "CLDN14" "NM_001146078:c.-82+4181G>A" "FIVE_PRIME_INTRON" "Benign" "rs60663524" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 232 1322 0.1755 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 244 5008 0.048722
494716 "chr21:37878498:T>C" "CLDN14" "NM_001146078:c.-82+4163A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs565441344" "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
494717 "chr21:37878504:T>C" "CLDN14" "NM_001146078:c.-82+4157A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs185561730" "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
494718 "chr21:37878574:G>A" "CLDN14" "NM_001146078:c.-82+4087C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs541739828" "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
494719 "chr21:37878576:A>G" "CLDN14" "NM_001146078:c.-82+4085T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs370263405" "This variant is a VUS because it does not have enough information."
494720 "chr21:37878612:C>T" "CLDN14" "NM_001146078:c.-82+4049G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs78869417" "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
494721 "chr21:37878623:G>A" "CLDN14" "NM_001146078:c.-82+4038C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs374579757" "This variant is a VUS because it does not have enough information."
494722 "chr21:37878646:G>A" "CLDN14" "NM_001146078:c.-82+4015C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs778018751" "This variant is a VUS because it does not have enough information."
494723 "chr21:37878653:G>T" "CLDN14" "NM_001146078:c.-82+4008C>A" "FIVE_PRIME_INTRON" "Benign" "rs191663055" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 48 1322 0.0363 0 1006 0 2 694 0.0029 0 1008 0 0 978 0 50 5008 0.00998403
494724 "chr21:37878658:G>A" "CLDN14" "NM_001146078:c.-82+4003C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs548928262" "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
494725 "chr21:37878682:G>A" "CLDN14" "NM_001146078:c.-82+3979C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs368914761" "This variant is a VUS because it does not have enough information."
494726 "chr21:37878709:G>A" "CLDN14" "NM_001146078:c.-82+3952C>T" "FIVE_PRIME_INTRON" "Benign" "rs8127112" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 910 1322 0.6884 916 1006 0.9105 462 694 0.6657 590 1008 0.5853 766 978 0.7832 3644 5008 0.727636
494727 "chr21:37878726:C>T" "CLDN14" "NM_001146078:c.-82+3935G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs531388967" "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
494728 "chr21:37878728:G>A" "CLDN14" "NM_001146078:c.-82+3933C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs551070197" "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
494729 "chr21:37878731:C>T" "CLDN14" "NM_001146078:c.-82+3930G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs183570865" "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
494730 "chr21:37878731:C>A" "CLDN14" "NM_001146078:c.-82+3930G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs183570865" "This variant is a VUS because it does not have enough information."
494731 "chr21:37878750:T>C" "CLDN14" "NM_001146078:c.-82+3911A>G" "FIVE_PRIME_INTRON" "Benign" "rs8127879" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1249 1322 0.9448 917 1006 0.9115 473 694 0.6816 590 1008 0.5853 766 978 0.7832 3995 5008 0.797724
494732 "chr21:37878818:C>T" "CLDN14" "NM_001146078:c.-82+3843G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs553636568" "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
494733 "chr21:37878821:G>C" "CLDN14" "NM_001146078:c.-82+3840C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs567518299" "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
494734 "chr21:37878826:C>T" "CLDN14" "NM_001146078:c.-82+3835G>A" "FIVE_PRIME_INTRON" "Benign" "rs57929193" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 242 5008 0.0483227
494735 "chr21:37878827:G>A" "CLDN14" "NM_001146078:c.-82+3834C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs559796444" "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 1 978 0.001 4 5008 0.000798722
494736 "chr21:37878843:C>A" "CLDN14" "NM_001146078:c.-82+3818G>T" "FIVE_PRIME_INTRON" "Benign" "rs7275699" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 214 1322 0.1619 3 1006 0.003 12 694 0.0173 0 1008 0 35 978 0.0358 264 5008 0.0527157
494737 "chr21:37878874:G>A" "CLDN14" "NM_001146078:c.-82+3787C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs552342190" "This variant is a VUS because it does not have enough information."
494738 "chr21:37878885:A>C" "CLDN14" "NM_001146078:c.-82+3776T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs747929390" "This variant is a VUS because it does not have enough information."
494739 "chr21:37878886:C>A" "CLDN14" "NM_001146078:c.-82+3775G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs543018993" "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
494740 "chr21:37878889:T>C" "CLDN14" "NM_001146078:c.-82+3772A>G" "FIVE_PRIME_INTRON" "Benign" "rs113644645" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 230 1322 0.174 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 242 5008 0.0483227
494741 "chr21:37878893:T>C" "CLDN14" "NM_001146078:c.-82+3768A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs372056477" "This variant is a VUS because it does not have enough information."
494742 "chr21:37878895:A>-" "CLDN14" "NM_001146078:c.-82+3766delT" "FIVE_PRIME_INTRON" "Unknown significance" "rs113812093" "This variant is a VUS because it does not have enough information."
494743 "chr21:37878895:AAAA>-" "CLDN14" "NM_001146078:c.-82+3766_-82+3771delTTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs796365246" "This variant is a VUS because it does not have enough information."
494744 "chr21:37878907:A>G" "CLDN14" "NM_001146078:c.-82+3754T>C" "FIVE_PRIME_INTRON" "Benign" "rs572653099" "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
494745 "chr21:37878911:G>-" "CLDN14" "NM_001146078:c.-82+3750delC" "FIVE_PRIME_INTRON" "Unknown significance" "rs150422128" "This variant is a VUS because it does not have enough information."
494746 "chr21:37878911:G>A" "CLDN14" "NM_001146078:c.-82+3750C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs201667161" "This variant is a VUS because it does not have enough information."
494747 "chr21:37878916:A>G" "CLDN14" "NM_001146078:c.-82+3745T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs758145222" "This variant is a VUS because it does not have enough information."
494748 "chr21:37878964:A>G" "CLDN14" "NM_001146078:c.-82+3697T>C" "FIVE_PRIME_INTRON" "Benign" "rs41378546" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 166 1322 0.1256 1 1006 0.001 9 694 0.013 0 1008 0 1 978 0.001 177 5008 0.0353435
494749 "chr21:37878968:C>T" "CLDN14" "NM_001146078:c.-82+3693G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs746931844" "This variant is a VUS because it does not have enough information."
494750 "chr21:37878979:G>C" "CLDN14" "NM_001146078:c.-82+3682C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs376978682" "This variant is a VUS because it does not have enough information."
494751 "chr21:37878995:T>C" "CLDN14" "NM_001146078:c.-82+3666A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs749209153" "This variant is a VUS because it does not have enough information."
494752 "chr21:37879005:G>T" "CLDN14" "NM_001146078:c.-82+3656C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs770899391" "This variant is a VUS because it does not have enough information."
494753 "chr21:37879015:G>A" "CLDN14" "NM_001146078:c.-82+3646C>T" "FIVE_PRIME_INTRON" "Benign" "rs73382009" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 151 1322 0.1142 1 1006 0.001 5 694 0.0072 0 1008 0 0 978 0 157 5008 0.0313498
494754 "chr21:37879045:C>T" "CLDN14" "NM_001146078:c.-82+3616G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs530390334" "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
494755 "chr21:37879051:T>C" "CLDN14" "NM_001146078:c.-82+3610A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs75596449" "This variant is a VUS because it does not have enough information."
494756 "chr21:37879052:G>A" "CLDN14" "NM_001146078:c.-82+3609C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs543761776" "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
494757 "chr21:37879061:C>T" "CLDN14" "NM_001146078:c.-82+3600G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773859428" "This variant is a VUS because it does not have enough information."
494758 "chr21:37879062:G>A" "CLDN14" "NM_001146078:c.-82+3599C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs761252382" "This variant is a VUS because it does not have enough information."
494759 "chr21:37879072:G>C" "CLDN14" "NM_001146078:c.-82+3589C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs139015899" "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
494760 "chr21:37879104:T>C" "CLDN14" "NM_001146078:c.-82+3557A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs767210531" "This variant is a VUS because it does not have enough information."
494761 "chr21:37879114:A>G" "CLDN14" "NM_001146078:c.-82+3547T>C" "FIVE_PRIME_INTRON" "Benign" "rs113007625" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 226 1322 0.171 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 238 5008 0.047524
494762 "chr21:37879118:C>T" "CLDN14" "NM_001146078:c.-82+3543G>A" "FIVE_PRIME_INTRON" "Benign" "rs9305585" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 906 1322 0.6853 916 1006 0.9105 462 694 0.6657 590 1008 0.5853 764 978 0.7812 3638 5008 0.726438
494763 "chr21:37879153:C>A" "CLDN14" "NM_001146078:c.-82+3508G>T" "FIVE_PRIME_INTRON" "Benign" "rs73382011" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 226 1322 0.171 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 238 5008 0.047524
494764 "chr21:37879238:A>G" "CLDN14" "NM_001146078:c.-82+3423T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs527401539" "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
494765 "chr21:37879260:G>A" "CLDN14" "NM_001146078:c.-82+3401C>T" "FIVE_PRIME_INTRON" "Benign" "rs73382013" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 228 1322 0.1725 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 240 5008 0.0479233
494766 "chr21:37879266:->A" "CLDN14" "NM_001146078:c.-82+3395_-82+3396insT" "FIVE_PRIME_INTRON" "Benign" "rs576157662" "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
494767 "chr21:37879290:G>A" "CLDN14" "NM_001146078:c.-82+3371C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs567354153" "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
494768 "chr21:37879305:T>C" "CLDN14" "NM_001146078:c.-82+3356A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs763585318" "This variant is a VUS because it does not have enough information."
494769 "chr21:37879315:G>A" "CLDN14" "NM_001146078:c.-82+3346C>T" "FIVE_PRIME_INTRON" "Benign" "rs75751422" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 166 1322 0.1256 1 1006 0.001 9 694 0.013 0 1008 0 0 978 0 176 5008 0.0351438
494770 "chr21:37879347:G>C" "CLDN14" "NM_001146078:c.-82+3314C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs769437736" "This variant is a VUS because it does not have enough information."
494771 "chr21:37879416:C>T" "CLDN14" "NM_001146078:c.-82+3245G>A" "FIVE_PRIME_INTRON" "Benign" "rs549850454" "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
494772 "chr21:37879423:->A" "CLDN14" "NM_001146078:c.-82+3238_-82+3239insT" "FIVE_PRIME_INTRON" "Benign" "rs797012537" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 355 1322 0.2685 23 1006 0.0229 30 694 0.0432 56 1008 0.0556 73 978 0.0746 537 5008 0.107228
494773 "chr21:37879423:AA>-" "CLDN14" "NM_001146078:c.-82+3238_-82+3241delTT" "FIVE_PRIME_INTRON" "Benign" "rs796161573" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 235 1322 0.1778 2 1006 0.002 11 694 0.0159 1 1008 0.001 3 978 0.0031 252 5008 0.0503195
494774 "chr21:37879502:A>G" "CLDN14" "NM_001146078:c.-82+3159T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs202203265" "This variant is a VUS because it does not have enough information."
494775 "chr21:37879515:C>T" "CLDN14" "NM_001146078:c.-82+3146G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs374372662" "This variant is a VUS because it does not have enough information."
494776 "chr21:37879548:A>C" "CLDN14" "NM_001146078:c.-82+3113T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs570027397" "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
494777 "chr21:37879556:C>T" "CLDN14" "NM_001146078:c.-82+3105G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs187393396" "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
494778 "chr21:37879613:C>A" "CLDN14" "NM_001146078:c.-82+3048G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs559077234" "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
494779 "chr21:37879614:C>G" "CLDN14" "NM_001146078:c.-82+3047G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs572536939" "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
494780 "chr21:37879616:A>G" "CLDN14" "NM_001146078:c.-82+3045T>C" "FIVE_PRIME_INTRON" "Benign" "rs139550300" "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 22 978 0.0225 31 5008 0.0061901
494781 "chr21:37879617:T>G" "CLDN14" "NM_001146078:c.-82+3044A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs555097341" "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
494782 "chr21:37879622:C>T" "CLDN14" "NM_001146078:c.-82+3039G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs574943321" "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
494783 "chr21:37879644:G>A" "CLDN14" "NM_001146078:c.-82+3017C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs757408395" "This variant is a VUS because it does not have enough information."
494784 "chr21:37879668:G>T" "CLDN14" "NM_001146078:c.-82+2993C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs781518491" "This variant is a VUS because it does not have enough information."
494785 "chr21:37879700:C>T" "CLDN14" "NM_001146078:c.-82+2961G>A" "FIVE_PRIME_INTRON" "Benign" "rs144190098" "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 9 694 0.013 0 1008 0 25 978 0.0256 47 5008 0.00938498
494786 "chr21:37879734:T>C" "CLDN14" "NM_001146078:c.-82+2927A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs572695976" "This variant is a VUS because it does not have enough information."
494787 "chr21:37879783:C>T" "CLDN14" "NM_001146078:c.-82+2878G>A" "FIVE_PRIME_INTRON" "Benign" "rs34494383" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 10 1322 0.0076 98 1006 0.0974 43 694 0.062 0 1008 0 15 978 0.0153 166 5008 0.033147
494788 "chr21:37879784:G>T" "CLDN14" "NM_001146078:c.-82+2877C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs575617501" "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
494789 "chr21:37879787:C>T" "CLDN14" "NM_001146078:c.-82+2874G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs779747983" "This variant is a VUS because it does not have enough information."
494790 "chr21:37879807:A>G" "CLDN14" "NM_001146078:c.-82+2854T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs536625717" "This variant is a VUS because it does not have enough information."
494791 "chr21:37879820:G>T" "CLDN14" "NM_001146078:c.-82+2841C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs749020586" "This variant is a VUS because it does not have enough information."
494792 "chr21:37879844:C>T" "CLDN14" "NM_001146078:c.-82+2817G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs544571628" "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
494793 "chr21:37879877:T>C" "CLDN14" "NM_001146078:c.-82+2784A>G" "FIVE_PRIME_INTRON" "Benign" "rs144296999" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 84 1322 0.0635 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 85 5008 0.0169728
494794 "chr21:37879890:C>T" "CLDN14" "NM_001146078:c.-82+2771G>A" "FIVE_PRIME_INTRON" "Benign" "rs7280851" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 250 1322 0.1891 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 262 5008 0.0523163
494795 "chr21:37879891:G>A" "CLDN14" "NM_001146078:c.-82+2770C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs747720090" "This variant is a VUS because it does not have enough information."
494796 "chr21:37879919:G>T" "CLDN14" "NM_001146078:c.-82+2742C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs547102062" "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
494797 "chr21:37879932:C>T" "CLDN14" "NM_001146078:c.-82+2729G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs369637472" "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
494798 "chr21:37879936:C>A" "CLDN14" "NM_001146078:c.-82+2725G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs773771885" "This variant is a VUS because it does not have enough information."
494799 "chr21:37879937:G>A" "CLDN14" "NM_001146078:c.-82+2724C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs772963388" "This variant is a VUS because it does not have enough information."
494800 "chr21:37879939:G>C" "CLDN14" "NM_001146078:c.-82+2722C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs529890800" "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
494801 "chr21:37879953:T>C" "CLDN14" "NM_001146078:c.-82+2708A>G" "FIVE_PRIME_INTRON" "Benign" "rs7282048" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494802 "chr21:37879957:C>G" "CLDN14" "NM_001146078:c.-82+2704G>C" "FIVE_PRIME_INTRON" "Benign" "rs7280987" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494803 "chr21:37879967:C>T" "CLDN14" "NM_001146078:c.-82+2694G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs775722117" "This variant is a VUS because it does not have enough information."
494804 "chr21:37879968:G>A" "CLDN14" "NM_001146078:c.-82+2693C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs538947773" "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
494805 "chr21:37880039:G>A" "CLDN14" "NM_001146078:c.-82+2622C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs763350491" "This variant is a VUS because it does not have enough information."
494806 "chr21:37880045:G>C" "CLDN14" "NM_001146078:c.-82+2616C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs192292099" "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
494807 "chr21:37880053:C>T" "CLDN14" "NM_001146078:c.-82+2608G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs566081310" "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
494808 "chr21:37880064:AAAAAG>-" "CLDN14" "NM_001146078:c.-82+2597_-82+2604delCTTTTT" "FIVE_PRIME_INTRON" "Unknown significance" "rs763788791" "This variant is a VUS because it does not have enough information."
494809 "chr21:37880104:G>A" "CLDN14" "NM_001146078:c.-82+2557C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs151183351" "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
494810 "chr21:37880134:A>C" "CLDN14" "NM_001146078:c.-82+2527T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs554806239" "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
494811 "chr21:37880139:T>C" "CLDN14" "NM_001146078:c.-82+2522A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs183080063" "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
494812 "chr21:37880142:C>T" "CLDN14" "NM_001146078:c.-82+2519G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs186695083" "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
494813 "chr21:37880148:C>T" "CLDN14" "NM_001146078:c.-82+2513G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs557544852" "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
494814 "chr21:37880152:C>T" "CLDN14" "NM_001146078:c.-82+2509G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs577093140" "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
494815 "chr21:37880153:G>A" "CLDN14" "NM_001146078:c.-82+2508C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs752082155" "This variant is a VUS because it does not have enough information."
494816 "chr21:37880155:G>A" "CLDN14" "NM_001146078:c.-82+2506C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs375799110" "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
494817 "chr21:37880158:A>G" "CLDN14" "NM_001146078:c.-82+2503T>C" "FIVE_PRIME_INTRON" "Benign" "rs7281159" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494818 "chr21:37880163:C>T" "CLDN14" "NM_001146078:c.-82+2498G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs141331966" "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 3 978 0.0031 5 5008 0.000998403
494819 "chr21:37880180:C>T" "CLDN14" "NM_001146078:c.-82+2481G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs145318544" "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 0 978 0 5 5008 0.000998403
494820 "chr21:37880182:C>T" "CLDN14" "NM_001146078:c.-82+2479G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs756298221" "This variant is a VUS because it does not have enough information."
494821 "chr21:37880187:C>T" "CLDN14" "NM_001146078:c.-82+2474G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs560850190" "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
494822 "chr21:37880213:T>C" "CLDN14" "NM_001146078:c.-82+2448A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs529885575" "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
494823 "chr21:37880321:T>G" "CLDN14" "NM_001146078:c.-82+2340A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs549678031" "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
494824 "chr21:37880347:->TT" "CLDN14" "NM_001146078:c.-82+2314_-82+2315insAA" "FIVE_PRIME_INTRON" "Unknown significance" "rs201980392" "This variant is a VUS because it does not have enough information."
494825 "chr21:37880347:G>T" "CLDN14" "NM_001146078:c.-82+2314C>A" "FIVE_PRIME_INTRON" "Benign" "rs7281847" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 215 1322 0.1626 14 1006 0.0139 24 694 0.0346 50 1008 0.0496 67 978 0.0685 370 5008 0.0738818
494826 "chr21:37880347:GA>TT" "CLDN14" "Unknown significance" "rs386818304" "This variant is a VUS because it does not have enough information."
494827 "chr21:37880348:A>T" "CLDN14" "NM_001146078:c.-82+2313T>A" "FIVE_PRIME_INTRON" "Benign" "rs7281449" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 215 1322 0.1626 14 1006 0.0139 24 694 0.0346 50 1008 0.0496 67 978 0.0685 370 5008 0.0738818
494828 "chr21:37880350:C>G" "CLDN14" "NM_001146078:c.-82+2311G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs373720596" "This variant is a VUS because it does not have enough information."
494829 "chr21:37880361:G>A" "CLDN14" "NM_001146078:c.-82+2300C>T" "FIVE_PRIME_INTRON" "Benign" "rs75625017" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 109 1322 0.0825 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 115 5008 0.0229633
494830 "chr21:37880392:T>C" "CLDN14" "NM_001146078:c.-82+2269A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs778859151" "This variant is a VUS because it does not have enough information."
494831 "chr21:37880393:A>G" "CLDN14" "NM_001146078:c.-82+2268T>C" "FIVE_PRIME_INTRON" "Benign" "rs73382016" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 69 1322 0.0522 0 1006 0 6 694 0.0086 0 1008 0 0 978 0 75 5008 0.014976
494832 "chr21:37880407:C>G" "CLDN14" "NM_001146078:c.-82+2254G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs534173653" "This variant is a VUS because it does not have enough information."
494833 "chr21:37880413:C>G" "CLDN14" "NM_001146078:c.-82+2248G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs559063422" "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
494834 "chr21:37880421:A>T" "CLDN14" "NM_001146078:c.-82+2240T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs13048696" "This variant is a VUS because it does not have enough information."
494835 "chr21:37880422:T>G" "CLDN14" "NM_001146078:c.-82+2239A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs13049636" "This variant is a VUS because it does not have enough information."
494836 "chr21:37880428:G>C" "CLDN14" "NM_001146078:c.-82+2233C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs115503911" "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
494837 "chr21:37880440:G>A" "CLDN14" "NM_001146078:c.-82+2221C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs568426744" "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
494838 "chr21:37880449:T>G" "CLDN14" "NM_001146078:c.-82+2212A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs746461517" "This variant is a VUS because it does not have enough information."
494839 "chr21:37880468:T>G" "CLDN14" "NM_001146078:c.-82+2193A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs13049655" "This variant is a VUS because it does not have enough information."
494840 "chr21:37880539:A>G" "CLDN14" "NM_001146078:c.-82+2122T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs770502980" "This variant is a VUS because it does not have enough information."
494841 "chr21:37880636:G>T" "CLDN14" "NM_001146078:c.-82+2025C>A" "FIVE_PRIME_INTRON" "Benign" "rs57161355" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494842 "chr21:37880643:T>C" "CLDN14" "NM_001146078:c.-82+2018A>G" "FIVE_PRIME_INTRON" "Benign" "rs74645646" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 84 1322 0.0635 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 85 5008 0.0169728
494843 "chr21:37880667:G>A" "CLDN14" "NM_001146078:c.-82+1994C>T" "FIVE_PRIME_INTRON" "Benign" "rs147637738" "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
494844 "chr21:37880682:A>T" "CLDN14" "NM_001146078:c.-82+1979T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs769122038" "This variant is a VUS because it does not have enough information."
494845 "chr21:37880703:C>T" "CLDN14" "NM_001146078:c.-82+1958G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs191150813" "This variant is a VUS because it does not have enough information."
494846 "chr21:37880733:C>A" "CLDN14" "NM_001146078:c.-82+1928G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs774808474" "This variant is a VUS because it does not have enough information."
494847 "chr21:37880746:C>A" "CLDN14" "NM_001146078:c.-82+1915G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs539732553" "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
494848 "chr21:37880763:C>G" "CLDN14" "NM_001146078:c.-82+1898G>C" "FIVE_PRIME_INTRON" "Benign" "rs58998624" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 252 1322 0.1906 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 264 5008 0.0527157
494849 "chr21:37880769:T>G" "CLDN14" "NM_001146078:c.-82+1892A>C" "FIVE_PRIME_INTRON" "Benign" "rs57807040" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 252 1322 0.1906 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 264 5008 0.0527157
494850 "chr21:37880774:T>C" "CLDN14" "NM_001146078:c.-82+1887A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs182607231" "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
494851 "chr21:37880803:C>T" "CLDN14" "NM_001146078:c.-82+1858G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs188178670" "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
494852 "chr21:37880810:G>A" "CLDN14" "NM_001146078:c.-82+1851C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs574423202" "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
494853 "chr21:37880813:C>T" "CLDN14" "NM_001146078:c.-82+1848G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773183237" "This variant is a VUS because it does not have enough information."
494854 "chr21:37880825:A>G" "CLDN14" "NM_001146078:c.-82+1836T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs796604382" "This variant is a VUS because it does not have enough information."
494855 "chr21:37880827:G>A" "CLDN14" "NM_001146078:c.-82+1834C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs543508395" "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
494856 "chr21:37880851:T>C" "CLDN14" "NM_001146078:c.-82+1810A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs141989869" "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
494857 "chr21:37880864:G>A" "CLDN14" "NM_001146078:c.-82+1797C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs760798546" "This variant is a VUS because it does not have enough information."
494858 "chr21:37880894:C>A" "CLDN14" "NM_001146078:c.-82+1767G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs532389383" "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
494859 "chr21:37880918:T>A" "CLDN14" "NM_001146078:c.-82+1743A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs546117250" "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
494860 "chr21:37880946:A>G" "CLDN14" "NM_001146078:c.-82+1715T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs766573163" "This variant is a VUS because it does not have enough information."
494861 "chr21:37880948:C>T" "CLDN14" "NM_001146078:c.-82+1713G>A" "FIVE_PRIME_INTRON" "Benign" "rs150081186" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1 1322 0.0008 15 1006 0.0149 9 694 0.013 0 1008 0 7 978 0.0072 32 5008 0.00638978
494862 "chr21:37880954:C>T" "CLDN14" "NM_001146078:c.-82+1707G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs138478891" "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
494863 "chr21:37880976:C>T" "CLDN14" "NM_001146078:c.-82+1685G>A" "FIVE_PRIME_INTRON" "Benign" "rs115661353" "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 3 694 0.0043 0 1008 0 0 978 0 45 5008 0.00898562
494864 "chr21:37881001:G>A" "CLDN14" "NM_001146078:c.-82+1660C>T" "FIVE_PRIME_INTRON" "Benign" "rs59097582" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494865 "chr21:37881034:T>G" "CLDN14" "NM_001146078:c.-82+1627A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs192969801" "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
494866 "chr21:37881055:C>T" "CLDN14" "NM_001146078:c.-82+1606G>A" "FIVE_PRIME_INTRON" "Benign" "rs563002621" "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 18 978 0.0184 19 5008 0.00379393
494867 "chr21:37881063:A>G" "CLDN14" "NM_001146078:c.-82+1598T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs570705294" "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
494868 "chr21:37881068:G>C" "CLDN14" "NM_001146078:c.-82+1593C>G" "FIVE_PRIME_INTRON" "Benign" "rs16994178" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494869 "chr21:37881070:G>A" "CLDN14" "NM_001146078:c.-82+1591C>T" "FIVE_PRIME_INTRON" "Benign" "rs115895502" "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
494870 "chr21:37881096:C>T" "CLDN14" "NM_001146078:c.-82+1565G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs562009124" "This variant is a VUS because it does not have enough information."
494871 "chr21:37881113:G>A" "CLDN14" "NM_001146078:c.-82+1548C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566791163" "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
494872 "chr21:37881174:C>T" "CLDN14" "NM_001146078:c.-82+1487G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs536171153" "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
494873 "chr21:37881183:T>G" "CLDN14" "NM_001146078:c.-82+1478A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs758271871" "This variant is a VUS because it does not have enough information."
494874 "chr21:37881187:A>T" "CLDN14" "NM_001146078:c.-82+1474T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs554222464" "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
494875 "chr21:37881191:G>A" "CLDN14" "NM_001146078:c.-82+1470C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs531830736" "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
494876 "chr21:37881239:G>C" "CLDN14" "NM_001146078:c.-82+1422C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs544469458" "This variant is a VUS because it does not have enough information."
494877 "chr21:37881247:A>G" "CLDN14" "NM_001146078:c.-82+1414T>C" "FIVE_PRIME_INTRON" "Benign" "rs372587843" "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
494878 "chr21:37881266:A>C" "CLDN14" "NM_001146078:c.-82+1395T>G" "FIVE_PRIME_INTRON" "Benign" "rs57440576" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494879 "chr21:37881289:C>T" "CLDN14" "NM_001146078:c.-82+1372G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs577089830" "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
494880 "chr21:37881290:C>T" "CLDN14" "NM_001146078:c.-82+1371G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs377092386" "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
494881 "chr21:37881291:G>A" "CLDN14" "NM_001146078:c.-82+1370C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs559610125" "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
494882 "chr21:37881297:C>T" "CLDN14" "NM_001146078:c.-82+1364G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs781041510" "This variant is a VUS because it does not have enough information."
494883 "chr21:37881306:C>T" "CLDN14" "NM_001146078:c.-82+1355G>A" "FIVE_PRIME_INTRON" "Benign" "rs73382018" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494884 "chr21:37881363:T>C" "CLDN14" "NM_001146078:c.-82+1298A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs542115296" "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
494885 "chr21:37881385:T>C" "CLDN14" "NM_001146078:c.-82+1276A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs561923791" "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
494886 "chr21:37881402:A>G" "CLDN14" "NM_001146078:c.-82+1259T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs769532931" "This variant is a VUS because it does not have enough information."
494887 "chr21:37881403:ATT>-" "CLDN14" "NM_001146078:c.-82+1258_-82+1262delAAT" "FIVE_PRIME_INTRON" "Unknown significance" "rs538397319" "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
494888 "chr21:37881411:C>T" "CLDN14" "NM_001146078:c.-82+1250G>A" "FIVE_PRIME_INTRON" "Benign" "rs73392026" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494889 "chr21:37881424:G>A" "CLDN14" "NM_001146078:c.-82+1237C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs148837464" "This variant is a VUS because it does not have enough information." 3 1322 0.0023 0 1006 0 0 694 0 1 1008 0.001 0 978 0 4 5008 0.000798722
494890 "chr21:37881441:C>T" "CLDN14" "NM_001146078:c.-82+1220G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs536829115" "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
494891 "chr21:37881442:G>C" "CLDN14" "NM_001146078:c.-82+1219C>G" "FIVE_PRIME_INTRON" "Benign" "rs370313437" "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 16 978 0.0164 16 5008 0.00319489
494892 "chr21:37881478:G>A" "CLDN14" "NM_001146078:c.-82+1183C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs546764036" "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
494893 "chr21:37881485:A>C" "CLDN14" "NM_001146078:c.-82+1176T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs567059982" "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
494894 "chr21:37881510:G>A" "CLDN14" "NM_001146078:c.-82+1151C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs535736224" "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
494895 "chr21:37881530:G>C" "CLDN14" "NM_001146078:c.-82+1131C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs555762476" "This variant is a VUS because it does not have enough information."
494896 "chr21:37881537:C>T" "CLDN14" "NM_001146078:c.-82+1124G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs748490693" "This variant is a VUS because it does not have enough information."
494897 "chr21:37881540:C>A" "CLDN14" "NM_001146078:c.-82+1121G>T" "FIVE_PRIME_INTRON" "Benign" "rs915750" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 240 1322 0.1815 897 1006 0.8917 411 694 0.5922 542 1008 0.5377 659 978 0.6738 2749 5008 0.548922
494898 "chr21:37881549:G>T" "CLDN14" "NM_001146078:c.-82+1112C>A" "FIVE_PRIME_INTRON" "Benign" "rs567961502" "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 5 978 0.0051 6 5008 0.00119808
494899 "chr21:37881551:C>A" "CLDN14" "NM_001146078:c.-82+1110G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs537078299" "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
494900 "chr21:37881572:C>T" "CLDN14" "NM_001146078:c.-82+1089G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773769018" "This variant is a VUS because it does not have enough information."
494901 "chr21:37881585:C>T" "CLDN14" "NM_001146078:c.-82+1076G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs557011830" "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
494902 "chr21:37881588:G>C" "CLDN14" "NM_001146078:c.-82+1073C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs541412431" "This variant is a VUS because it does not have enough information."
494903 "chr21:37881596:A>T" "CLDN14" "NM_001146078:c.-82+1065T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs760705413" "This variant is a VUS because it does not have enough information."
494904 "chr21:37881614:G>A" "CLDN14" "NM_001146078:c.-82+1047C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs766420984" "This variant is a VUS because it does not have enough information."
494905 "chr21:37881659:G>A" "CLDN14" "NM_001146078:c.-82+1002C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs576984682" "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
494906 "chr21:37881700:G>A" "CLDN14" "NM_001146078:c.-82+961C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs776640504" "This variant is a VUS because it does not have enough information."
494907 "chr21:37881768:A>T" "CLDN14" "NM_001146078:c.-82+893T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs576557911" "This variant is a VUS because it does not have enough information."
494908 "chr21:37881793:T>C" "CLDN14" "NM_001146078:c.-82+868A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs539540544" "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
494909 "chr21:37881828:C>T" "CLDN14" "NM_001146078:c.-82+833G>A" "FIVE_PRIME_INTRON" "Benign" "rs74476377" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 240 1322 0.1815 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 252 5008 0.0503195
494910 "chr21:37881828:CA>TG" "CLDN14" "Unknown significance" "rs386818305" "This variant is a VUS because it does not have enough information."
494911 "chr21:37881829:A>G" "CLDN14" "NM_001146078:c.-82+832T>C" "FIVE_PRIME_INTRON" "Benign" "rs2298451" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 1252 1322 0.947 917 1006 0.9115 474 694 0.683 594 1008 0.5893 765 978 0.7822 4002 5008 0.799121
494912 "chr21:37881852:C>T" "CLDN14" "NM_001146078:c.-82+809G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs551335319" "This variant is a VUS because it does not have enough information."
494913 "chr21:37881862:C>T" "CLDN14" "NM_001146078:c.-82+799G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs185245318" "This variant is a VUS because it does not have enough information."
494914 "chr21:37881863:G>A" "CLDN14" "NM_001146078:c.-82+798C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs541752534" "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
494915 "chr21:37881892:T>A" "CLDN14" "NM_001146078:c.-82+769A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs752502519" "This variant is a VUS because it does not have enough information."
494916 "chr21:37881930:C>G" "CLDN14" "NM_001146078:c.-82+731G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs758198956" "This variant is a VUS because it does not have enough information."
494917 "chr21:37881932:G>A" "CLDN14" "NM_001146078:c.-82+729C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs562040321" "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
494918 "chr21:37881948:C>A" "CLDN14" "NM_001146078:c.-82+713G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs575531074" "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
494919 "chr21:37881954:C>T" "CLDN14" "NM_001146078:c.-82+707G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs544168582" "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
494920 "chr21:37881955:G>A" "CLDN14" "NM_001146078:c.-82+706C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs564163891" "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
494921 "chr21:37881970:T>C" "CLDN14" "NM_001146078:c.-82+691A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs763978841" "This variant is a VUS because it does not have enough information."
494922 "chr21:37881976:C>G" "CLDN14" "NM_001146078:c.-82+685G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs777517329" "This variant is a VUS because it does not have enough information."
494923 "chr21:37881979:C>T" "CLDN14" "NM_001146078:c.-82+682G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs533209503" "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
494924 "chr21:37881980:G>A" "CLDN14" "NM_001146078:c.-82+681C>T" "FIVE_PRIME_INTRON" "Benign" "rs138983153" "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 0 694 0 0 1008 0 0 978 0 21 5008 0.00419329
494925 "chr21:37881999:T>G" "CLDN14" "NM_001146078:c.-82+662A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs751492663" "This variant is a VUS because it does not have enough information."
494926 "chr21:37882017:C>T" "CLDN14" "NM_001146078:c.-82+644G>A" "FIVE_PRIME_INTRON" "Benign" "rs8133272" "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 1 694 0.0014 0 1008 0 0 978 0 47 5008 0.00938498
494927 "chr21:37882062:T>G" "CLDN14" "NM_001146078:c.-82+599A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs751393777" "This variant is a VUS because it does not have enough information."
494928 "chr21:37882113:C>T" "CLDN14" "NM_001146078:c.-82+548G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs146401233" "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
494929 "chr21:37882114:G>A" "CLDN14" "NM_001146078:c.-82+547C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs549390385" "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
494930 "chr21:37882127:C>T" "CLDN14" "NM_001146078:c.-82+534G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs569568345" "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
494931 "chr21:37882128:G>A" "CLDN14" "NM_001146078:c.-82+533C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs190568675" "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
494932 "chr21:37882134:C>T" "CLDN14" "NM_001146078:c.-82+527G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs193255591" "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
494933 "chr21:37882135:G>A" "CLDN14" "NM_001146078:c.-82+526C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs570471082" "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
494934 "chr21:37882183:G>A" "CLDN14" "NM_001146078:c.-82+478C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs539529282" "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
494935 "chr21:37882211:A>G" "CLDN14" "NM_001146078:c.-82+450T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs553077642" "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
494936 "chr21:37882253:C>G" "CLDN14" "NM_001146078:c.-82+408G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs745315553" "This variant is a VUS because it does not have enough information."
494937 "chr21:37882258:C>T" "CLDN14" "NM_001146078:c.-82+403G>A" "FIVE_PRIME_INTRON" "Benign" "rs73392028" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494938 "chr21:37882329:A>G" "CLDN14" "NM_001146078:c.-82+332T>C" "FIVE_PRIME_INTRON" "Benign" "rs16994180" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 186 1322 0.1407 15 1006 0.0149 23 694 0.0331 50 1008 0.0496 67 978 0.0685 341 5008 0.0680911
494939 "chr21:37882378:A>G" "CLDN14" "NM_001146078:c.-82+283T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs555284938" "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
494940 "chr21:37882389:G>A" "CLDN14" "NM_001146078:c.-82+272C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs748532628" "This variant is a VUS because it does not have enough information."
494941 "chr21:37882428:G>C" "CLDN14" "NM_001146078:c.-82+233C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs772447485" "This variant is a VUS because it does not have enough information."
494942 "chr21:37882441:C>G" "CLDN14" "NM_001146078:c.-82+220G>C" "FIVE_PRIME_INTRON" "Benign" "rs138461948" "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 0 694 0 0 1008 0 0 978 0 21 5008 0.00419329
494943 "chr21:37882493:G>A" "CLDN14" "NM_001146078:c.-82+168C>T" "FIVE_PRIME_INTRON" "Benign" "rs115561324" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
494944 "chr21:37882604:G>A" "CLDN14" "NM_001146078:c.-82+57C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs141848398" "This variant is a VUS because it does not have enough information."
494945 "chr21:37882632:C>G" "CLDN14" "NM_001146078:c.-82+29G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs374382724" "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
494946 "chr21:37882657:C>G" "CLDN14" "NM_001146078:c.-82+4G>C" "FIVE_PRIME_INTRON" "Benign" "rs16994182" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 400 0 1 320 0.003125 1 320 0.003125 0 400 0 5 360 0.0138889 0 200 0 7 2000 0.0035 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494947 "chr21:37882679:AA>-" "CLDN14" "NM_001146078:c.-100_-97delTT" "FIVE_PRIME_EXON" "Unknown significance" "rs59563067" "This variant is a VUS because it does not have enough information."
494948 "chr21:37882683:G>A" "CLDN14" "NM_001146078:c.-104C>T" "FIVE_PRIME_EXON" "Benign" "rs184746529" "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 0 360 0 1 200 0.005 1 2000 0.0005 0 1322 0 0 1006 0 0 694 0 1 1008 0.001 0 978 0 1 5008 0.000199681
494949 "chr21:37882699:T>G" "CLDN14" "NM_001146078:c.-120A>C" "FIVE_PRIME_EXON" "Unknown significance" "rs747570919" "This variant is a VUS because it does not have enough information."
494950 "chr21:37882708:T>G" "CLDN14" "NM_001146078:c.-129A>C" "FIVE_PRIME_EXON" "Benign" "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 4 320 0.0125 0 400 0 0 360 0 5 200 0.025 9 2000 0.0045
494951 "chr21:37882712:C>T" "CLDN14" "NM_001146078:c.-133G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs769191161" "This variant is a VUS because it does not have enough information."
494952 "chr21:37882718:T>G" "CLDN14" "NM_001146078:c.-139A>C" "FIVE_PRIME_EXON" "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
494953 "chr21:37882729:G>A" "CLDN14" "NM_001146078:c.-150C>T" "FIVE_PRIME_EXON" "Benign" "rs57668637" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 0 400 0 1 320 0.003125 1 320 0.003125 0 400 0 5 360 0.0138889 0 200 0 7 2000 0.0035 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494954 "chr21:37882732:T>G" "CLDN14" "NM_001146078:c.-153A>C" "FIVE_PRIME_EXON" "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
494955 "chr21:37882771:G>T" "CLDN14" "NM_001146078:c.-192C>A" "FIVE_PRIME_EXON" "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
494956 "chr21:37882776:C>G" "CLDN14" "NM_001146078:c.-197G>C" "FIVE_PRIME_EXON" "Unknown significance" "rs776693720" "This variant is a VUS because it does not have enough information."
494957 "chr21:37882789:C>A" "CLDN14" "NM_001146078:c.-210G>T" "FIVE_PRIME_EXON" "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
494958 "chr21:37882793:C>T" "CLDN14" "NM_001146078:c.-214G>A" "FIVE_PRIME_EXON" "Unknown significance" "rs529450999" "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
494959 "chr21:37882794:A>G" "CLDN14" "NM_001146078:c.-215T>C" "FIVE_PRIME_EXON" "Unknown significance" "rs543178465" "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
494960 "chr21:37882808:T>G" "CLDN14" "NM_001146078:c.-219-10A>C" "FIVE_PRIME_INTRON" "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
494961 "chr21:37882822:C>T" "CLDN14" "NM_001146078:c.-219-24G>A" "FIVE_PRIME_INTRON" "Benign" "rs79209636" "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 0 694 0 0 1008 0 0 978 0 21 5008 0.00419329
494962 "chr21:37882823:C>T" "CLDN14" "NM_001146078:c.-219-25G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs759552205" "This variant is a VUS because it does not have enough information."
494963 "chr21:37882830:G>C" "CLDN14" "NM_001146078:c.-219-32C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs532000683" "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
494964 "chr21:37882883:C>T" "CLDN14" "NM_001146078:c.-219-85G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs188339414" "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
494965 "chr21:37882901:T>G" "CLDN14" "NM_001146078:c.-219-103A>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs368623238" "This variant is a VUS because it does not have enough information."
494966 "chr21:37882919:A>C" "CLDN14" "NM_001146078:c.-219-121T>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs770058997" "This variant is a VUS because it does not have enough information."
494967 "chr21:37882929:G>A" "CLDN14" "NM_001146078:c.-219-131C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs570456903" "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
494968 "chr21:37882963:T>C" "CLDN14" "NM_001146078:c.-219-165A>G" "FIVE_PRIME_INTRON" "Benign" "rs16994187" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494969 "chr21:37883006:T>A" "CLDN14" "NM_001146078:c.-219-208A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs546360481" "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
494970 "chr21:37883066:A>G" "CLDN14" "NM_001146078:c.-219-268T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs762706172" "This variant is a VUS because it does not have enough information."
494971 "chr21:37883070:C>G" "CLDN14" "NM_001146078:c.-219-272G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs566524669" "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
494972 "chr21:37883080:G>A" "CLDN14" "NM_001146078:c.-219-282C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs763973442" "This variant is a VUS because it does not have enough information."
494973 "chr21:37883088:A>T" "CLDN14" "NM_001146078:c.-219-290T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs564270990" "This variant is a VUS because it does not have enough information."
494974 "chr21:37883102:A>G" "CLDN14" "NM_001146078:c.-219-304T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs371633967" "This variant is a VUS because it does not have enough information."
494975 "chr21:37883131:G>T" "CLDN14" "NM_001146078:c.-219-333C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs150604329" "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
494976 "chr21:37883140:G>A" "CLDN14" "NM_001146078:c.-219-342C>T" "FIVE_PRIME_INTRON" "Benign" "rs76790142" "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 0 694 0 0 1008 0 0 978 0 9 5008 0.00179712
494977 "chr21:37883143:C>T" "CLDN14" "NM_001146078:c.-219-345G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs761817079" "This variant is a VUS because it does not have enough information."
494978 "chr21:37883155:G>A" "CLDN14" "NM_001146078:c.-219-357C>T" "FIVE_PRIME_INTRON" "Benign" "rs2835366" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 225 1322 0.1702 3 1006 0.003 16 694 0.0231 0 1008 0 35 978 0.0358 279 5008 0.0557109
494979 "chr21:37883180:G>A" "CLDN14" "NM_001146078:c.-219-382C>T" "FIVE_PRIME_INTRON" "Benign" "rs537741195" "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
494980 "chr21:37883184:->T" "CLDN14" "NM_001146078:c.-219-386_-219-385insA" "FIVE_PRIME_INTRON" "Unknown significance" "rs36113084" "This variant is a VUS because it does not have enough information."
494981 "chr21:37883256:A>G" "CLDN14" "NM_001146078:c.-219-458T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs750015081" "This variant is a VUS because it does not have enough information."
494982 "chr21:37883276:A>G" "CLDN14" "NM_001146078:c.-219-478T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs768472472" "This variant is a VUS because it does not have enough information."
494983 "chr21:37883278:C>T" "CLDN14" "NM_001146078:c.-219-480G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs773682255" "This variant is a VUS because it does not have enough information."
494984 "chr21:37883344:G>C" "CLDN14" "NM_001146078:c.-219-546C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs557677920" "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
494985 "chr21:37883351:G>A" "CLDN14" "NM_001146078:c.-219-553C>T" "FIVE_PRIME_INTRON" "Benign" "rs73392032" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
494986 "chr21:37883367:C>T" "CLDN14" "NM_001146078:c.-219-569G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs779896600" "This variant is a VUS because it does not have enough information."
494987 "chr21:37883374:C>T" "CLDN14" "NM_001146078:c.-219-576G>A" "FIVE_PRIME_INTRON" "Benign" "rs2835367" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 238 1322 0.18 898 1006 0.8926 412 694 0.5937 540 1008 0.5357 660 978 0.6748 2748 5008 0.548722
494988 "chr21:37883379:C>T" "CLDN14" "NM_001146078:c.-219-581G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs202063448" "This variant is a VUS because it does not have enough information."
494989 "chr21:37883381:A>G" "CLDN14" "NM_001146078:c.-219-583T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs553895365" "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
494990 "chr21:37883385:C>T" "CLDN14" "NM_001146078:c.-219-587G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs200194349" "This variant is a VUS because it does not have enough information."
494991 "chr21:37883410:C>T" "CLDN14" "NM_001146078:c.-219-612G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs149811063" "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
494992 "chr21:37883425:C>T" "CLDN14" "NM_001146078:c.-219-627G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs549628918" "This variant is a VUS because it does not have enough information."
494993 "chr21:37883440:C>A" "CLDN14" "NM_001146078:c.-219-642G>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs771518236" "This variant is a VUS because it does not have enough information."
494994 "chr21:37883445:C>T" "CLDN14" "NM_001146078:c.-219-647G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs754534646" "This variant is a VUS because it does not have enough information."
494995 "chr21:37883456:A>G" "CLDN14" "NM_001146078:c.-219-658T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs530157164" "This variant is a VUS because it does not have enough information."
494996 "chr21:37883563:C>T" "CLDN14" "NM_001146078:c.-219-765G>A" "FIVE_PRIME_INTRON" "Benign" "rs73902549" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 24 1322 0.0182 0 1006 0 0 694 0 0 1008 0 0 978 0 24 5008 0.00479233
494997 "chr21:37883564:G>A" "CLDN14" "NM_001146078:c.-219-766C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs563087475" "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
494998 "chr21:37883569:G>A" "CLDN14" "NM_001146078:c.-219-771C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs117779995" "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
494999 "chr21:37883569:G>T" "CLDN14" "NM_001146078:c.-219-771C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs117779995" "This variant is a VUS because it does not have enough information."
495000 "chr21:37883594:T>A" "CLDN14" "NM_001146078:c.-219-796A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs545693105" "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
495001 "chr21:37883605:C>T" "CLDN14" "NM_001146078:c.-219-807G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs565610062" "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
495002 "chr21:37883606:G>T" "CLDN14" "NM_001146078:c.-219-808C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs771440668" "This variant is a VUS because it does not have enough information."
495003 "chr21:37883612:A>G" "CLDN14" "NM_001146078:c.-219-814T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs528003156" "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
495004 "chr21:37883667:C>T" "CLDN14" "NM_001146078:c.-219-869G>A" "FIVE_PRIME_INTRON" "Benign" "rs2012586" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 686 1322 0.5189 915 1006 0.9095 452 694 0.6513 591 1008 0.5863 764 978 0.7812 3408 5008 0.680511
495005 "chr21:37883698:TA>-" "CLDN14" "NM_001146078:c.-219-900_-219-897delTA" "FIVE_PRIME_INTRON" "Unknown significance" "rs759598038" "This variant is a VUS because it does not have enough information."
495006 "chr21:37883722:G>A" "CLDN14" "NM_001146078:c.-219-924C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs566350041" "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
495007 "chr21:37883774:A>-" "CLDN14" "NM_001146078:c.-219-976delT" "FIVE_PRIME_INTRON" "Unknown significance" "rs758767607" "This variant is a VUS because it does not have enough information."
495008 "chr21:37883788:A>G" "CLDN14" "NM_001146078:c.-219-990T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs746013748" "This variant is a VUS because it does not have enough information."
495009 "chr21:37883794:T>G" "CLDN14" "NM_001146078:c.-219-996A>C" "FIVE_PRIME_INTRON" "Benign" "rs60231729" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 84 1322 0.0635 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 85 5008 0.0169728
495010 "chr21:37883814:T>C" "CLDN14" "NM_001146078:c.-219-1016A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs765232065" "This variant is a VUS because it does not have enough information."
495011 "chr21:37883821:C>T" "CLDN14" "NM_001146078:c.-219-1023G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs531994523" "This variant is a VUS because it does not have enough information."
495012 "chr21:37883847:A>G" "CLDN14" "NM_001146078:c.-219-1049T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs775384607" "This variant is a VUS because it does not have enough information."
495013 "chr21:37883886:T>C" "CLDN14" "NM_001146078:c.-219-1088A>G" "FIVE_PRIME_INTRON" "Benign" "rs16994201" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 215 1322 0.1626 14 1006 0.0139 24 694 0.0346 50 1008 0.0496 67 978 0.0685 370 5008 0.0738818
495014 "chr21:37883912:G>C" "CLDN14" "NM_001146078:c.-219-1114C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs147481384" "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
495015 "chr21:37883928:C>T" "CLDN14" "NM_001146078:c.-219-1130G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs537678882" "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
495016 "chr21:37883941:G>T" "CLDN14" "NM_001146078:c.-219-1143C>A" "FIVE_PRIME_INTRON" "Benign" "rs57608004" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 249 1322 0.1884 1 1006 0.001 11 694 0.0159 0 1008 0 0 978 0 261 5008 0.0521166
495017 "chr21:37883944:T>A" "CLDN14" "NM_001146078:c.-219-1146A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs571174033" "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
495018 "chr21:37883955:C>T" "CLDN14" "NM_001146078:c.-219-1157G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs533848076" "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
495019 "chr21:37883962:A>G" "CLDN14" "NM_001146078:c.-219-1164T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs774211648" "This variant is a VUS because it does not have enough information."
495020 "chr21:37883963:C>G" "CLDN14" "NM_001146078:c.-219-1165G>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs112602257" "This variant is a VUS because it does not have enough information."
495021 "chr21:37883968:G>A" "CLDN14" "NM_001146078:c.-219-1170C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs555160902" "This variant is a VUS because it does not have enough information."
495022 "chr21:37884067:T>C" "CLDN14" "NM_001146078:c.-219-1269A>G" "FIVE_PRIME_INTRON" "Benign" "rs139701779" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 29 1322 0.0219 0 1006 0 1 694 0.0014 0 1008 0 0 978 0 30 5008 0.00599042
495023 "chr21:37884119:T>C" "CLDN14" "NM_001146078:c.-219-1321A>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs573990238" "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
495024 "chr21:37884129:G>A" "CLDN14" "NM_001146078:c.-219-1331C>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs372251418" "This variant is a VUS because it does not have enough information."
495025 "chr21:37884201:T>A" "CLDN14" "NM_001146078:c.-219-1403A>T" "FIVE_PRIME_INTRON" "Unknown significance" "rs536745894" "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
495026 "chr21:37884226:G>C" "CLDN14" "NM_001146078:c.-219-1428C>G" "FIVE_PRIME_INTRON" "Unknown significance" "rs556720327" "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
495027 "chr21:37884274:A>G" "CLDN14" "NM_001146078:c.-219-1476T>C" "FIVE_PRIME_INTRON" "Benign" "rs16994205" "This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005." 171 1322 0.1293 1 1006 0.001 9 694 0.013 0 1008 0 0 978 0 181 5008 0.0361422
495028 "chr21:37884313:A>G" "CLDN14" "NM_001146078:c.-219-1515T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs534259169" "This variant is a VUS because it does not have enough information."
495029 "chr21:37884316:A>T" "CLDN14" "NM_001146078:c.-219-1518T>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs368086450" "This variant is a VUS because it does not have enough information."
495030 "chr21:37884329:A>G" "CLDN14" "NM_001146078:c.-219-1531T>C" "FIVE_PRIME_INTRON" "Unknown significance" "rs760307021" "This variant is a VUS because it does not have enough information."
495031 "chr21:37884331:G>T" "CLDN14" "NM_001146078:c.-219-1533C>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs545581006" "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
495032 "chr21:37884347:C>T" "CLDN14" "NM_001146078:c.-219-1549G>A" "FIVE_PRIME_INTRON" "Unknown significance" "rs765932778" "This variant is a VUS because it does not have enough information."
495033 "chr21:37884377:C>T" "CLDN1