Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs1689510 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
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
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 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