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Who was studied 88,965 European ancestry cases, 685,602 European ancestry controls.
The effect
Each copy of the C allele carried 1.03 times the odds of Asthma or chronic rhinosinusitis (95% confidence interval 1.023-1.045); p = 9 × 10−11.
How common The C allele had a frequency of about 61% in the people studied.
Where it sits Chromosome 16, band 16p11.2 — in an intron of STX1B.
What each result means
C/CTwo copies of the version the research linked to Asthma or chronic rhinosinusitis. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Asthma or chronic rhinosinusitis. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Asthma or chronic rhinosinusitis. This is the starting point the study compared everyone against.
Nature communications · 2025 · PMID 41213931 · open access
Questions about rs7184567
What is rs7184567?
rs7184567 is a single position in the genome, in or near the STX1B gene. Published research associates it with asthma or chronic rhinosinusitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7184567 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 rs7184567 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 rs7184567 come from?
GWAS Catalog, Nature communications 2025, PMID:41213931. 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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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.
Asthma or chronic rhinosinusitis (rs7184567). MyGeneLog™. https://www.mygenelog.com/variants/rs7184567