rs3176134
A SNP in the THBD gene on chromosome 20. Its most notable genotype is C;C: common in clinvar
- Gene
- THBD
- Location
- Chr 2023,047,500 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- FamilyTreeDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3176134 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageC;C 92%
- Han Chinese (Beijing)C;C 79%
- Japanese (Tokyo)C;C 84%
- Yoruba (Nigeria)C;C 99%
- Chinese (Denver)C;C 79%
- Gujarati IndianC;C 96%
- Luhya (Kenya)C;C 97%
- Mexican ancestry (Los Angeles)C;C 97%
- Maasai (Kenya)C;C 96%
- TuscanC;C 99%
Related
Source and license
Adapted from rs3176134 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.