Sensitive

Dupuytren's disease

DUXA · rs11672486

Where this position leads

Condition: Dupuytren's Disease

rs11672486 Condition: Dupuytren's Disease Dupuytren's Disease Condition rs11672486 rs11672486 DUXA

What the study found

Who was studied 11,320 European ancestry cases, 47,023 European ancestry controls; replicated in 3,248 European ancestry cases, 197,724 European ancestry controls.

The effect Each copy of the T allele shifted the measure 0.302 higher (95% confidence interval 0.27-0.34); p = 5 × 10−60.

Where it sits Chromosome 19, band 19q13.43 — in an intron of DUXA.

What each result means

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

Questions about rs11672486

What is rs11672486?

rs11672486 is a single position in the genome, in or near the DUXA gene. Published research associates it with dupuytren's disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11672486 linked to?

On MyGeneLog this position is linked to Dupuytren's Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs11672486 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 rs11672486 come from?

GWAS Catalog, Nature communications 2024, PMID:38172110. 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.

Dupuytren's disease (rs11672486). MyGeneLog™. https://www.mygenelog.com/variants/rs11672486

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