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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 A allele shifted the measure 0.113 lower (95% confidence interval 0.082-0.144); p = 8 × 10−13.
Where it sits Chromosome 7, band 7q31.2 — between genes, 8.4 kb from ST7.
What each result means
A/ATwo 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.
A/GOne copy of the version the research linked to Dupuytren's disease. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Dupuytren's disease. This is the starting point the study compared everyone against.
Nature communications · 2024 · PMID 38172110 · open access
Questions about rs38896
What is rs38896?
rs38896 is a single position in the genome, in or near the near ST7 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 rs38896 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 rs38896 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 rs38896 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.
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