Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs2228467 1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8