Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
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
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
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
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
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
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs11817689 1.000 0.120 10 63164457 downstream gene variant T/C snv 0.13 1