Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs35188965 5 1104823 intron variant C/G;T snv 12
rs150813342 9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs8176685
ABO
9 133263363 intron variant CACCACTACGCC/- delins 4