Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2229094 0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 17