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
rs79105258 12 111280427 intron variant C/A;T snv 23
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs2294915 1.000 0.040 22 43945024 intron variant C/G;T snv 5