rs201930497
A SNP in the TCHH gene on chromosome 1. Its most notable genotype is A;A: Uncombable hair syndrome
- Gene
- TCHH
- Location
- Chr 1152,112,226 (GRCh38)
- Highest magnitude
- 3.3Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadUncombable hair syndrome
- A;GBadCarrier of an uncombable hair syndrome variant
- G;GGoodcommon/normal
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
Uncombable hair syndrome variant in TCHH gene, c.991C>T or p.Gln331*
A;A
see uncombable hair syndrome
A;G
see uncombable hair syndrome; unaffected unless carrying another related mutation
Source and license
Adapted from rs201930497 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.