rs387906745
A SNP in the TEK gene on chromosome 9. Its most notable genotype is A;G: tendency for multiple cutaneous and mucosal venous malformations
- Gene
- TEK
- Location
- Chr 927,212,764 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadtendency for multiple cutaneous and mucosal venous malformations
- G;GGoodcommon in clinvar
On SNPedia: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs387906745, also known as c.2744G>A, Arg915His and R915H, represents a mutation in the TEK gene on chromosome 9. The rare minor allele for this SNP is reported to cause Multiple cutaneous and mucosal venous malformations.
A;G
see rs387906745
Source and license
Adapted from rs387906745 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.