Source: GWASDB ×
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
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 3
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 2
rs8176720
ABO
9 133257486 synonymous variant T/A;C;G snv 0.40 0.40 1