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
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 7
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv 5
rs1063857
VWF
12 6044348 synonymous variant A/G snv 0.31 0.40 4