Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs771386507 0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6