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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 25,235 Finnish ancestry cases, 199,208 Finnish ancestry controls.
The effect
The reported allele is G; the catalogue records no effect size
; p = 3 × 10−9.
How common The G allele had a frequency of about 44% in the people studied.
Where it sits Chromosome 11, band 11q13.5 — between genes, 21.7 kb from LINC02757.
What each result means
A/ANo copy of the version the research linked to Sinonasal disease. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Sinonasal disease. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to 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 rs10160518
What is rs10160518?
rs10160518 is a single position in the genome, in or near the near LINC02757 gene. Published research associates it with sinonasal disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10160518 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 rs10160518 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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