Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs10046 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18