Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs10010131 0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246