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 23
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
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
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 17
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
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
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
rs11087784 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 10
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 10
rs11610543 0.776 0.080 12 42740389 intergenic variant A/G;T snv 10
rs116353863 0.776 0.080 6 31042408 regulatory region variant T/C snv 2.2E-02 10
rs12149163 0.776 0.080 16 86305709 upstream gene variant T/C snv 0.49 10
rs12447408 0.776 0.080 16 86218938 downstream gene variant G/A snv 0.21 10
rs12514517 0.776 0.080 5 40279974 intergenic variant G/A snv 0.21 10
rs12672022 0.776 0.080 7 45096824 downstream gene variant T/C snv 0.13 10
rs12708491 0.776 0.080 15 32700635 downstream gene variant G/A snv 0.33 10