Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 20
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs2303428 0.776 0.240 2 47476361 splice region variant T/A;C;G snv 4.0E-06; 0.12 9
rs771386507 0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6