Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs7100025 0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs1250563 0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs1689510 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs117372389 0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs4869313 0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
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
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs6689858 0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs7042370 0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14