{{Rsnum
|rsid=8176694
|Chromosome=9
|position=133262243
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ABO
|Gene_s=ABO
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 55.8 | 39.8 | 4.4
| HCB | 91.2 | 8.8 | 0.0
| JPT | 71.7 | 25.7 | 2.7
| YRI | 88.4 | 11.6 | 0.0
| ASW | 68.4 | 28.1 | 3.5
| CHB | 91.2 | 8.8 | 0.0
| CHD | 90.8 | 9.2 | 0.0
| GIH | 72.3 | 24.8 | 3.0
| LWK | 89.0 | 11.0 | 0.0
| MEX | 75.9 | 20.7 | 3.4
| MKK | 81.4 | 17.9 | 0.6
| TSI | 73.5 | 22.5 | 3.9
| 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}}