Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs1800472 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 11