Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs79105258 12 111280427 intron variant C/A;T snv 23