Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs7042370 0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11741255 0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs6689858 0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs17885785 0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs36001488 0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs114846446 0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs7100025 0.724 0.240 10 37303610 intron variant G/A snv 0.68 14