Sensitive

Carpal tunnel syndrome

TTLL5 · rs72725608

Where this position leads

Condition: Carpal Tunnel Syndrome

rs72725608 Condition: Carpal Tunnel Syndrome Carpal Tunnel Syndrome Condition rs72725608 rs72725608 TTLL5

What the study found

Who was studied 48,843 European ancestry cases, 1,190,837 European ancestry controls.

The effect The reported allele is C; the catalogue records no effect size ; p = 4 × 10−12.

How common The C allele had a frequency of about 4% in the people studied.

Where it sits Chromosome 14, band 14q24.3 — inside TTLL5.

What ClinVar records

Classification Benign; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2026-02-02. ClinVar record 1170254 NM_015072.5(TTLL5):c.2388-12T>C

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

C/C Two copies of the version the research linked to Carpal tunnel syndrome. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Carpal tunnel syndrome. That is a smaller link than two copies.
T/T No copy of the version the research linked to Carpal tunnel syndrome. This is the starting point the study compared everyone against.
Source

Questions about rs72725608

What is rs72725608?

rs72725608 is a single position in the genome, in or near the TTLL5 gene. Published research associates it with carpal tunnel syndrome. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs72725608 linked to?

On MyGeneLog this position is linked to Carpal Tunnel Syndrome. The research behind each link, and its sources, are set out on that condition page.

Does having rs72725608 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs72725608 come from?

GWAS Catalog, Nature communications 2022, PMID:35332129. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Carpal tunnel syndrome (rs72725608). MyGeneLog™. https://www.mygenelog.com/variants/rs72725608

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