Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs104895271 0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6