Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 42
rs3184504 0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67 31
rs2476601 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 22
rs6679677 0.679 0.250 1 113761186 intergenic variant C/A snp 8.2E-02 18
rs4676410 0.715 0.214 2 240624322 intron variant G/A snp 0.26 15
rs12598357 0.724 0.214 16 28329624 intergenic variant A/G snp 0.45 14
rs2836882 0.724 0.214 21 39094644 regulatory region variant G/A snp 0.23 14
rs7731626 0.715 0.214 5 56148856 intron variant G/A snp 0.29 14
rs12928404 0.724 0.214 16 28835925 splice region variant T/C snp 0.44 0.45 14
rs602662 0.715 0.250 19 48703728 missense variant G/A snp 0.40 0.45 14
rs706778 0.699 0.286 10 6056986 intron variant C/T snp 0.47 14
rs4246905 0.724 0.214 9 114790969 missense variant T/A,C snp 0.76 0.79 14
rs10822050 0.724 0.214 10 62679011 intergenic variant T/C snp 0.35 13
rs12232497 0.707 0.250 17 39883866 intergenic variant T/C snp 0.36 13
rs12863738 0.724 0.214 X 136949968 intron variant C/T snp 0.16 13
rs1332099 0.724 0.214 10 99538694 regulatory region variant T/C,G snp 0.55; 3.2E-05 13
rs2075184 0.724 0.214 2 102464132 intergenic variant T/C snp 0.79 13
rs2738774 0.724 0.214 20 63637985 G/A,C snp 0.26 13
rs2807264 0.724 0.214 X 136583619 intergenic variant C/A snp 0.77 13
rs34884278 0.724 0.214 1 172869708 intron variant C/T snp 0.64 13
rs36051895 0.724 0.214 9 4981866 intergenic variant G/T snp 0.26 13
rs62131887 0.724 0.214 19 10476920 C/T snp 0.37 13
rs7100025 0.724 0.214 10 37303610 intron variant G/A snp 0.69 13
rs755374 0.724 0.214 5 159402286 intron variant C/T snp 0.29 13
rs7660520 0.724 0.214 4 182824168 intergenic variant G/A,C snp 0.31 13