Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs3027012 1 159204333 5 prime UTR variant C/T snv 0.13 3