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
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27