Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62