Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29