Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs11709077 0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs7929543 0.925 0.120 11 49329474 intron variant A/C snv 0.12 2