Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10880213 12 41955239 intron variant G/A snv 0.50 1
rs115403343 5 39591500 intergenic variant T/C snv 1.1E-02 1
rs116760613 1 51025037 intergenic variant G/A snv 1.8E-02 1
rs11720938 3 66756404 intergenic variant T/C snv 0.16 1
rs11745300 5 34504563 intergenic variant C/G snv 0.40 1
rs11989898 8 126476785 intron variant A/G snv 0.18 1
rs13069000 3 66748526 regulatory region variant C/G snv 0.15 1
rs142177694 3 66767117 intergenic variant G/A;C;T snv 1
rs162185 6 133905009 intergenic variant T/C snv 0.39 1
rs2033149 10 58504981 intergenic variant A/T snv 0.53 1
rs2383531 1 186760269 intergenic variant G/A snv 0.95 1
rs2395811 7 106986584 regulatory region variant C/A;G snv 1
rs271679 17 49908065 intergenic variant C/G snv 0.65 1
rs271681 17 49908833 intergenic variant G/A snv 0.56 1
rs283558 6 51076754 intergenic variant T/C snv 0.54 1
rs300132 6 166003730 intergenic variant G/A;C;T snv 1
rs300143 6 166007639 regulatory region variant A/G snv 0.48 1
rs35451331 10 93082289 downstream gene variant G/A;T snv 1
rs4498196 4 3746115 intergenic variant A/C;G snv 0.39 1
rs4811741 20 56712343 TF binding site variant A/G snv 0.58 1
rs55914958 7 101594473 intergenic variant C/T snv 0.35 1
rs7327286 13 73139310 intergenic variant G/A snv 0.79 1
rs7834797 8 23902022 intergenic variant G/A snv 0.56 1
rs7931938 11 111336380 regulatory region variant G/A snv 0.41 1
rs819195 8 23885024 intergenic variant T/C snv 0.40 1