rs11665084
A SNP in the HRH4 gene on chromosome 18. Its most notable genotype is C;C: common on affy axiom data
- Gene
- HRH4
- Location
- Chr 1824,476,802 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 7%
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 88%
- European ancestry (Utah)C;C 85%
- Han Chinese (Beijing)C;C 92%
- Japanese (Tokyo)C;C 81%
- Yoruba (Nigeria)C;C 99%
- Chinese (Denver)C;C 94%
- Gujarati IndianC;C 94%
- Luhya (Kenya)C;C 98%
- Mexican ancestry (Los Angeles)C;C 71%
- Maasai (Kenya)C;C 84%
- TuscanC;C 78%
Related
Source and license
Adapted from rs11665084 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.