Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7127214 0.807 0.120 11 36322143 intron variant C/G;T snv 6
rs72698115 0.807 0.120 1 154406893 intron variant A/C snv 7.2E-02 6
rs73300638 0.807 0.120 7 28147725 intron variant A/C;G snv 6
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 6
rs7909519 0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02 6
rs79893749 0.807 0.120 3 46212159 intron variant C/T snv 0.10 6
rs114940806 0.882 0.120 1 44093000 intron variant A/G snv 5.4E-02 3
rs1178121 0.882 0.120 7 18723029 intron variant C/A snv 0.31 3
rs12517545 0.882 0.120 5 74384489 intron variant G/A snv 0.13 3
rs1279094 0.882 0.120 9 11706771 intron variant T/C snv 0.43 3
rs1823549 0.882 0.120 1 102682275 intergenic variant T/C snv 0.89 3
rs41291794 0.882 0.120 6 32457985 downstream gene variant A/T snv 7.5E-02 3
rs481331 0.882 0.120 10 42507600 intergenic variant A/T snv 0.80 3
rs72632736 0.882 0.120 1 4389144 intergenic variant A/G snv 4.3E-02 3
rs79575701 0.882 0.120 18 48053250 intron variant C/A;T snv 3
rs864089 0.882 0.120 3 64258442 intron variant T/C snv 0.22 3