rs6094752
A SNP in the NCOA3 gene on chromosome 20. Its most notable genotype is C;C: common on affy axiom data
- Gene
- NCOA3
- Location
- Chr 2047,627,680 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 3%
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 90%
- European ancestry (Utah)C;C 96%
- Han Chinese (Beijing)C;C 98%
- Japanese (Tokyo)C;C 99%
- Yoruba (Nigeria)C;C 83%
- African ancestry (Southwest US)C;C 84%
- Gujarati IndianC;C 85%
- Luhya (Kenya)C;C 88%
- Mexican ancestry (Los Angeles)C;C 95%
- Maasai (Kenya)C;C 85%
- TuscanC;C 90%
Related
Notes
From SNPedia
Notes
NPAS2 and PER2 are linked to risk factors of the metabolic syndrome. CLOCK is suggested to associate with comorbid alcohol use and depressive disorders.
Source and license
Adapted from rs6094752 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.