Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34