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Who was studied 60,653 European ancestry cases, 804,329 European ancestry controls; replicated in 387,407 European ancestry cases, 2,517,257 European ancestry controls.
The effect
Each copy of the C allele carried 0.95 times the odds of Atopic dermatitis (95% confidence interval 0.94-0.96); p = 3 × 10−26.
How common The C allele had a frequency of about 10% in the people studied.
Where it sits Chromosome 11, band 11q13.5 — between genes, 1.9 kb from LINC02757.
What each result means
C/CTwo copies of the version the research linked to Atopic dermatitis. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Atopic dermatitis. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Atopic dermatitis. This is the starting point the study compared everyone against.
Nature communications · 2023 · PMID 37794016 · open access
Questions about rs11236813
What is rs11236813?
rs11236813 is a single position in the genome, in or near the near LINC02757 gene. Published research associates it with atopic dermatitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11236813 linked to?
On MyGeneLog this position is linked to Atopic Dermatitis. The research behind each link, and its sources, are set out on that condition page.
Does having rs11236813 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 rs11236813 come from?
GWAS Catalog, Nature communications 2023, PMID:37794016. 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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