Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10224210
rs10224210
9 1.000 0.040 7 151716108 intron variant T/C snv 0.21 0.700 1.000 2 2016 2017
dbSNP: rs218237
rs218237
6 4 54528005 intergenic variant C/T snv 0.18 0.700 1.000 2 2017 2018
dbSNP: rs4953318
rs4953318
5 2 46127912 intron variant A/C snv 0.43 0.700 1.000 2 2012 2017
dbSNP: rs495828
rs495828
24 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 2 2010 2017
dbSNP: rs833805
rs833805
3 6 44062274 non coding transcript exon variant A/G snv 0.92 0.700 1.000 2 2016 2018
dbSNP: rs855791
rs855791
38 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 0.700 1.000 2 2017 2018
dbSNP: rs10008637
rs10008637
2 4 76492991 intron variant T/A;C snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs1010553
rs1010553
2 1.000 0.080 3 52506757 synonymous variant T/C snv 0.53 0.59 0.700 1.000 1 2016 2016
dbSNP: rs10401969
rs10401969
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.700 1.000 1 2016 2016
dbSNP: rs10495928
rs10495928
5 2 46126027 intron variant A/G snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs10711289
rs10711289
1 3 169450583 intron variant AAA/-;A;AA;AAAA;AAAAA delins 0.700 1.000 1 2016 2016
dbSNP: rs10901252
rs10901252
ABO
3 9 133252613 non coding transcript exon variant G/C snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs10953299
rs10953299
1 7 100645788 intron variant T/C snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs11039436
rs11039436
2 11 47866484 intergenic variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11072566
rs11072566
5 0.925 0.120 15 76001630 intron variant A/G snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs11072567
rs11072567
5 15 76006403 intron variant A/G snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs111843364
rs111843364
1 16 70923707 intron variant G/A snv 3.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs112682076
rs112682076
2 1 10297748 intron variant G/C snv 5.8E-03 0.700 1.000 1 2016 2016
dbSNP: rs114948639
rs114948639
3 2 46066687 intron variant C/T snv 7.2E-03 0.700 1.000 1 2016 2016
dbSNP: rs115986297
rs115986297
3 6 2050557 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs11654074
rs11654074
5 17 59748211 intron variant A/C snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs11665867
rs11665867
1 19 40760574 intron variant A/G snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs11689538
rs11689538
3 2 121238062 intron variant G/C snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs11730623
rs11730623
2 4 69020433 upstream gene variant A/T snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs11760376
rs11760376
2 7 134684558 intron variant A/G snv 1.9E-03 0.700 1.000 1 2016 2016