Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs3129882 0.807 0.240 6 32441753 intron variant G/A snv 0.56 5
rs6903608 0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs2019960 0.925 0.160 8 128180025 intron variant T/C snv 0.27 2