Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48