Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 10
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs1924966 0.807 0.080 13 72432915 intergenic variant T/G snv 0.33 6
rs2736108 0.807 0.160 5 1297373 upstream gene variant C/T snv 0.24 6
rs2764736 0.851 0.160 9 25067733 intergenic variant T/C snv 2.4E-02 4
rs1679013 0.882 0.160 9 22206988 intron variant C/A;T snv 0.43 3
rs2270628 0.925 0.120 7 45909971 downstream gene variant C/T snv 0.25 2
rs35597309 0.925 0.120 6 32621489 regulatory region variant G/A snv 4.8E-02 2
rs7578456 1.000 0.080 2 201370625 intergenic variant A/G snv 0.57 2
rs12894364 1.000 0.080 14 37588860 downstream gene variant C/T snv 7.6E-02 1
rs2294750 1.000 0.080 1 10824979 regulatory region variant G/A snv 0.10 1
rs2477137 1.000 0.080 1 17304110 upstream gene variant G/T snv 0.20 1
rs2844695 1.000 0.080 6 30968237 intergenic variant T/C snv 0.28 1
rs2904268 1.000 0.080 20 50433551 upstream gene variant C/A;G snv 1
rs35399661 1.000 0.080 6 32623213 upstream gene variant T/C snv 0.16 1
rs3763338 1.000 0.080 6 28926534 upstream gene variant G/A snv 0.11 1
rs6854472 1.000 0.080 4 89513521 intron variant G/T snv 0.30 1
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1042026
ADH1B
1.000 0.080 4 99307309 3 prime UTR variant T/C snv 0.24 2
rs1614972
ADH1B ; ADH1C
0.925 0.160 4 99336998 intron variant C/T snv 0.38 4
rs1789924
ADH1C
0.925 0.160 4 99353129 upstream gene variant C/G;T snv 5