Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs1232880706 0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs66527965 0.763 0.240 17 50193038 missense variant C/A;T snv 31
rs760805 0.776 0.240 1 24925432 intron variant A/T snv 0.42 9
rs180177038 0.851 0.200 7 140778007 missense variant C/G;T snv 4