A/APublished research associates this genotype with typical/baseline likelihood of Chronic rhinosinusitis — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2019, PMID:30643255)
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Chronic rhinosinusitis. (GWAS Catalog, Nat Genet 2019, PMID:30643255)
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Chronic rhinosinusitis compared to the general population. (GWAS Catalog, Nat Genet 2019, PMID:30643255)
rs34210653 is a single position in the genome, in or near the ALOX15 gene. Published research associates it with 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 rs34210653 linked to?
On MyGeneLog this position is linked to Chronic Rhinosinusitis and the Bitter Taste Receptor. The research behind each link, and its sources, are set out on that condition page.
Does having rs34210653 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 rs34210653 come from?
GWAS Catalog, Nat Genet 2019, PMID:30643255. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.