Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 13
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs2812208 13 50132951 intron variant G/A;C snv 5
rs6918725 6 126669246 intron variant T/G snv 0.50 4
rs12198986 6 7719826 regulatory region variant G/A snv 0.37 3
rs1890995 1 218431336 intron variant G/A snv 0.33 3
rs7155279 14 92019537 intron variant G/A;T snv 3
rs7753012 6 142424746 intron variant T/G snv 0.50 3