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Who was studied 180,129 European ancestry cases, 180,709 European ancestry controls.
The effect
Each copy of the A allele carried 1.07 times the odds of Allergic disease (asthma, hay fever or eczema) (95% confidence interval 1.05-1.08); p = 4 × 10−14.
How common The A allele had a frequency of about 91% in the people studied.
Where it sits Chromosome 11, band 11q13.5 — between genes, 1.9 kb from LINC02757.
What each result means
A/ATwo copies of the version the research linked to Allergic disease (asthma, hay fever or eczema). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Allergic disease (asthma, hay fever or eczema). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Allergic disease (asthma, hay fever or eczema). This is the starting point the study compared everyone against.
Nature genetics · 2017 · PMID 29083406 · open access
Questions about rs11236814
What is rs11236814?
rs11236814 is a single position in the genome, in or near the WNT11 gene. Published research associates it with allergic disease (asthma, hay fever or eczema). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11236814 linked to?
On MyGeneLog this position is linked to Asthma. The research behind each link, and its sources, are set out on that condition page.
Does having rs11236814 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 rs11236814 come from?
GWAS Catalog, Nature genetics 2017, PMID:29083406. 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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Allergic disease (asthma, hay fever or eczema) (rs11236814). MyGeneLog™. https://www.mygenelog.com/variants/rs11236814