Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11074956 0.925 0.160 16 11243864 downstream gene variant G/T snv 0.34 2
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs12979659 0.925 0.160 19 6825021 intron variant T/C snv 0.36 0.28 2
rs13017599 0.882 0.160 2 60937196 non coding transcript exon variant G/A snv 0.25 3
rs13315591 0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs151719 0.925 0.160 6 32936123 non coding transcript exon variant C/T snv 0.72 2
rs17421624 0.925 0.160 6 32098400 intron variant T/C snv 0.25 2
rs212389 0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 4
rs2157051 0.925 0.160 6 32690847 regulatory region variant G/A snv 0.69 2
rs2242665 0.882 0.160 6 31871532 missense variant C/T snv 0.60 0.60 3
rs2524089 0.925 0.160 6 31298745 intron variant G/T snv 0.65 3
rs2524095 0.925 0.160 6 31298340 intron variant A/C snv 0.65 2
rs2546133 0.925 0.160 19 6799666 intron variant T/A;C snv 2
rs2617822 0.925 0.160 19 6801470 intron variant G/A;C snv 2
rs2621383 0.925 0.160 6 32791558 intergenic variant C/A snv 0.65 2
rs2621384 0.925 0.160 6 32791496 intergenic variant C/T snv 0.66 2
rs26232 0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs2736172 0.882 0.160 6 31623121 non coding transcript exon variant C/T snv 0.41 0.29 6
rs2849015 0.925 0.160 6 32231159 intergenic variant G/A snv 0.38 2
rs2857161 0.925 0.160 6 32791520 intergenic variant G/A snv 0.65 2
rs2894249 0.925 0.160 6 32358058 intron variant C/G;T snv 2
rs3093023 0.851 0.160 6 167120802 intron variant G/A snv 0.34 7
rs3129872 0.925 0.160 6 32439376 upstream gene variant A/T snv 0.24 2
rs3129877 0.925 0.160 6 32440820 intron variant G/A snv 0.26 2