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
rs11466334 1.000 0.080 19 41341832 intron variant G/A snv 5.9E-03 2.4E-02 1