{{Rsnum
|rsid=574347
|Chromosome=9
|position=133260255
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ABO
|Gene_s=ABO
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 5.3 | 46.0 | 48.7
| HCB | 8.0 | 37.2 | 54.7
| JPT | 6.2 | 46.9 | 46.9
| YRI | 9.5 | 44.9 | 45.6
| ASW | 10.5 | 52.6 | 36.8
| CHB | 8.0 | 37.2 | 54.7
| CHD | 6.4 | 44.0 | 49.5
| GIH | 3.0 | 34.7 | 62.4
| LWK | 10.0 | 47.3 | 42.7
| MEX | 12.1 | 53.4 | 34.5
| MKK | 4.5 | 35.9 | 59.6
| TSI | 7.8 | 29.4 | 62.7
| HapMapRevision=28
}}This SNP is a variant in the [[ABO]] gene, and is therefore potentially useful in determining [[ABO blood group]], such as through the use of [[genosets]].

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}