Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 20
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 2
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 1