Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs3850625 1 201047168 missense variant G/A snv 0.12 8.9E-02 3
rs7024579 9 136208567 3 prime UTR variant C/A;T snv 3
rs2301343 2 40453009 intron variant T/G snv 0.22 2