rs8176750
A SNP in the ABO gene on chromosome 9. Its most notable genotype is G;G: common in complete genomics
- Gene
- ABO
- Location
- Chr 9133,255,672 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 5%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs8176750 on the minus strand: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other ABO SNPs
- rs505922C;Cblood type is not O, increased risk for some diseases.Worth knowing
- rs657152A;AA few different minor risk associations; see detailsWorth knowing
- rs1008708453A;AO2 alleles (ABO Type O) may be presentWorth knowing
- rs2519093C;Ccommon/normalTypical
- rs7853989C;CLikely blood group BTypical
- rs8176719-;-likely to be of blood type OTypical
- rs8176740A;ANo summary available.Typical
- rs8176743C;CNo summary available.Typical
Notes
From SNPedia
Notes
This SNP is in the ABO gene, and is therefore potentially useful in determing blood group type, such as through the use of genosets. This particular SNP can be useful in determining whether an ABO type A allele is more specifically an A1 type allele or an A2 type allele. The more common allele (80% of A types on average) is A1, consistent with having a rs8176750(C) allele, with the rarer A2 allele encoded by the deletion form rs8176750(-). This is the key defining characteristic between an A1 and an A2 allele.
Source and license
Adapted from rs8176750 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.