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Who was studied 19,901 Finnish ancestry cases, 199,208 Finnish ancestry controls.
The effect
The reported allele is G; the catalogue records no effect size
; p = 1 × 10−22.
How common The G allele had a frequency of about 30% in the people studied.
Where it sits Chromosome 5, band 5q22.1 — in an intron of WDR36.
What each result means
A/ANo copy of the version the research linked to Chronic inflammatory sinonasal disease. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Chronic inflammatory sinonasal disease. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Chronic inflammatory sinonasal disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2023 · PMID 36653354 · open access
Questions about rs6884870
What is rs6884870?
rs6884870 is a single position in the genome, in or near the WDR36 gene. Published research associates it with chronic inflammatory sinonasal 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 rs6884870 linked to?
On MyGeneLog this position is linked to Chronic Inflammatory Sinonasal Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs6884870 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 rs6884870 come from?
GWAS Catalog, Nature communications 2023, PMID:36653354. 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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