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
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46