Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62574565
ABO
9 133252872 non coding transcript exon variant G/A snv 0.24 1
rs58081338
ABO
9 133252942 non coding transcript exon variant T/C;G snv 1
rs62574567
ABO
9 133253034 non coding transcript exon variant C/G snv 0.27 1
rs7857390
ABO
9 133253159 non coding transcript exon variant A/G snv 0.67 2
rs12554336
ABO
9 133253276 non coding transcript exon variant A/G snv 0.27 1
rs12554339
ABO
9 133253350 non coding transcript exon variant A/C snv 0.25 1
rs10901253
ABO
9 133253385 non coding transcript exon variant T/C snv 0.27 1
rs11244052
ABO
9 133253738 non coding transcript exon variant C/A snv 0.25 1
rs11244053
ABO
9 133253973 non coding transcript exon variant A/G snv 0.27 1
rs4962114
ABO
9 133254224 non coding transcript exon variant G/A snv 0.27 1
rs4962116
ABO
9 133254329 non coding transcript exon variant G/A snv 0.27 1
rs8176748
ABO
9 133255902 missense variant C/A;T snv 4.0E-06; 0.27 2
rs8176742
ABO
9 133256050 synonymous variant C/T snv 0.24 0.22 1
rs7873635
ABO
9 133256625 intron variant T/C;G snv 1
rs8176726
ABO
9 133257221 intron variant C/T snv 0.25 1
rs8176715
ABO
9 133257761 intron variant T/A;C snv 1
rs8176714
ABO
9 133257791 intron variant G/A snv 0.26 4
rs4962040
ABO
9 133258141 intron variant G/A snv 0.67 1
rs641959
ABO
9 133258308 intron variant A/C snv 0.29 4
rs641943
ABO
9 133258323 intron variant A/G snv 0.29 4
rs514708
ABO
9 133258352 intron variant C/T snv 0.29 4
rs626035
ABO
9 133259603 intron variant T/G snv 0.28 4
rs547495
ABO
9 133259604 intron variant T/C snv 0.28 1
rs8176702
ABO
9 133260743 intron variant G/A snv 1
rs2073826
ABO
9 133261560 intron variant G/A;C;T snv 1