rs682632
A SNP in the TEK gene on chromosome 9. Its most notable genotype is C;C: common in complete genomics
- Gene
- TEK
- Location
- Chr 927,183,465 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 2%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs682632 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 7 HapMap populations.
- AverageC;C 98%
- European ancestry (Utah)C;C 92%
- Han Chinese (Beijing)C;C 99%
- Japanese (Tokyo)C;C 100%
- Yoruba (Nigeria)C;C 100%
- Gujarati IndianC;C 97%
- Mexican ancestry (Los Angeles)C;C 98%
- TuscanC;C 97%
Related
Other TEK SNPs
- rs80338908C;Ttendency for multiple cutaneous and mucosal venous malformationsVery important
- rs80338909A;Ctendency for multiple cutaneous and mucosal venous malformationsVery important
- rs387906745A;Gtendency for multiple cutaneous and mucosal venous malformationsVery important
- rs639225A;Acommon in clinvarTypical
Source and license
Adapted from rs682632 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.