Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10893872 0.882 0.120 11 128455658 downstream gene variant T/C snv 0.44 4
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs148314165 0.925 0.160 6 137908902 intergenic variant T/- delins 2.0E-02 3
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs200820567 0.882 0.160 6 137908903 intergenic variant T/A snv 2.0E-02 4
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14