Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228467 1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs2228468 0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 2
rs2195224 3 42859508 intron variant G/A;C snv 2