Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32