rs495828
A SNP on chromosome 9. Its most notable genotype is G;G: common/normal
- Gene
- None listed
- Location
- Chr 9133,279,294 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageG;G 71%
- European ancestry (Utah)G;G 63%
- Han Chinese (Beijing)G;G 71%
- Japanese (Tokyo)G;G 55%
- Yoruba (Nigeria)G;G 74%
- African ancestry (Southwest US)G;G 77%
- Chinese (Denver)G;G 72%
- Gujarati IndianG;G 75%
- Luhya (Kenya)G;G 75%
- Mexican ancestry (Los Angeles)G;G 78%
- Maasai (Kenya)G;G 81%
- TuscanG;G 63%
Notes
From SNPedia
Notes
A common variant of the ABO gene protects against hypertension in a Spanish population. Pharmacogenetic predictors of angiotensin-converting enzyme inhibitor-induced cough: the role of ACE, ABO, and BDKRB2 genes. Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.
Source and license
Adapted from rs495828 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.