Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10491093 17 10978681 intergenic variant T/G snv 0.72 1
rs10737175 1 159750152 intergenic variant T/C snv 0.24 1
rs1125226 8 58506952 downstream gene variant C/A snv 0.54 1
rs11658572 17 10979696 intergenic variant C/T snv 0.58 1
rs1173766 5 32804422 intergenic variant T/C snv 0.57 1
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 1
rs11953630 5 158418394 intergenic variant C/A;T snv 1
rs1327235 20 10988382 intron variant A/G snv 0.46 1
rs1468326 12 748335 upstream gene variant A/C;T snv 1
rs16827043 1 146039555 upstream gene variant C/T snv 0.89 1
rs1979255 4 189396926 intergenic variant C/G snv 0.64 1
rs275646 3 148745735 downstream gene variant T/C snv 0.95 1
rs35530071 17 7659807 downstream gene variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTTT delins 1
rs4267385 17 63506395 intron variant C/T snv 0.61 1
rs4373814 10 18131043 intergenic variant G/C;T snv 1
rs4496877 7 150983418 intergenic variant T/G snv 0.74 1
rs4901474 14 54003019 regulatory region variant C/G;T snv 1
rs4977950 9 24732484 intergenic variant G/C;T snv 1
rs531003 9 110850339 intergenic variant G/C;T snv 1
rs6677719 1 159753330 intergenic variant C/T snv 0.77 1
rs7542235 1.000 0.040 1 196854483 intron variant A/G snv 0.23 1
rs820430 3 27507409 regulatory region variant A/G snv 0.30 1
rs834576 6 44238042 downstream gene variant C/A snv 0.16 1
rs9381299 6 44244130 upstream gene variant T/C snv 0.15 1
rs9899362 17 10977893 intergenic variant A/G;T snv 1