rs2276307
A SNP in the HTR3B gene on chromosome 11. Its most notable genotype is A;A.
- Gene
- HTR3B
- Location
- Chr 11113,933,165 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). 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.
- AverageA;A 69%
- European ancestry (Utah)A;A 61%
- Han Chinese (Beijing)A;A 74%
- Japanese (Tokyo)A;A 50%
- Yoruba (Nigeria)A;A 84%
- African ancestry (Southwest US)A;A 74%
- Chinese (Denver)A;A 76%
- Gujarati IndianA;A 48%
- Luhya (Kenya)A;A 88%
- Mexican ancestry (Los Angeles)A;A 69%
- Maasai (Kenya)A;A 72%
- TuscanA;A 62%
Related
Source and license
Adapted from rs2276307 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.