rs3118536
A SNP in the RXRA gene on chromosome 9. Its most notable genotype is C;C.
- Gene
- RXRA
- Location
- Chr 9134,416,616 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 16%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 10 HapMap populations.
- AverageC;C 71%
- European ancestry (Utah)C;C 72%
- Han Chinese (Beijing)C;C 61%
- Japanese (Tokyo)C;C 66%
- Yoruba (Nigeria)C;C 100%
- African ancestry (Southwest US)C;C 83%
- Chinese (Denver)C;C 62%
- Gujarati IndianC;C 52%
- Mexican ancestry (Los Angeles)C;C 59%
- Maasai (Kenya)C;C 97%
- TuscanC;C 62%
Related
Notes
From SNPedia
Notes
Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat. Vitamin d pathway genes, diet, and risk of renal cell carcinoma.
Source and license
Adapted from rs3118536 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.