Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 12
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 12
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 11
rs4813802 0.776 0.080 20 6718948 regulatory region variant T/G snv 0.28 11
rs6063514 0.776 0.080 20 50438781 intergenic variant C/T snv 0.42 11
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11