rs299284
A SNP in the HMMR gene on chromosome 5. Its most notable genotype is C;C: common on affy axiom data
- Gene
- HMMR
- Location
- Chr 5163,469,644 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 8%
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 11 HapMap populations.
- AverageC;C 87%
- European ancestry (Utah)C;C 71%
- Han Chinese (Beijing)C;C 99%
- Japanese (Tokyo)C;C 98%
- Yoruba (Nigeria)C;C 84%
- African ancestry (Southwest US)C;C 77%
- Chinese (Denver)C;C 98%
- Gujarati IndianC;C 89%
- Luhya (Kenya)C;C 89%
- Mexican ancestry (Los Angeles)C;C 86%
- Maasai (Kenya)C;C 94%
- TuscanC;C 69%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
breast cancer *rs10515860 [odds ratio (OR; AA/GG), 0.85; 95% confidence interval (CI), 0.65-1.12; P(trend) = 0.9], *rs299290 [OR (CC/TT), 1.00; 95% CI, 0.87-1.15; P(trend) = 0.7], *rs3756648 (rs7712023) [OR (TT/CC), 0.93; 95% CI, 0.84-1.02; P(trend) = 0.1], *rs299284 [OR (TT/CC), 1.01; 95% CI, 0.76-1.35; P(trend) = 0.5], and *rs13183712 [OR (TT/GG), 1.04; 95% CI, 0.88-1.23; P(trend) = 0.6].
Source and license
Adapted from rs299284 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.