Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs7675998 0.827 0.360 4 163086668 intergenic variant A/G;T snv 5
rs9502893 0.827 0.120 6 1339954 intergenic variant C/G;T snv 5
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs1517037 0.882 0.120 18 59211042 intergenic variant C/T snv 0.23 3
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 3
rs7503953 0.882 0.320 17 6238357 intergenic variant A/C snv 0.81 3
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs9543325 0.882 0.200 13 73342491 regulatory region variant C/G;T snv 3
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs6001516 0.925 0.120 22 39248198 intron variant C/T snv 6.1E-02 2
rs9573163 0.925 0.120 13 73334709 regulatory region variant C/G;T snv 2
rs1447826 1.000 0.120 3 74669607 intergenic variant T/A;C;G snv 1
rs2172905 1.000 0.120 6 170019278 regulatory region variant C/T snv 0.30 1
rs2903018 1.000 0.120 19 29164379 intergenic variant G/A;T snv 1
rs199976573
ABCG2
0.925 0.120 4 88132618 missense variant C/T snv 6.4E-05 5.6E-05 4
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs150495372
ADH1B
0.925 0.120 4 99313834 missense variant C/T snv 3.7E-04 3
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12