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Who was studied 14,296 European ancestry individuals; replicated in 5,698 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.254 lower (95% confidence interval 0.21-0.3); p = 7 × 10−31.
How common The A allele had a frequency of about 94% in the people studied.
Where it sits Chromosome 10, band 10q23.33 — in an intron of CYP2C9.
What each result means
A/ATwo copies of the version the research linked to X-21849 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/COne copy of the version the research linked to X-21849 levels. That is a smaller link than two copies.
C/CNo copy of the version the research linked to X-21849 levels. This is the starting point the study compared everyone against.
Nature medicine · 2022 · PMID 36357675 · open access
Questions about rs9332217
What is rs9332217?
rs9332217 is a single position in the genome, in or near the CYP2C9 gene. Published research associates it with x-21849 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does rs9332217 affect how medicines work?
CYP2C9 carries pharmacogenomic findings for Acenocoumarol and phenprocoumon, NSAIDs, Phenytoin and fosphenytoin, Siponimod, Statins, Sulfonylureas, Warfarin. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.
Does having rs9332217 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 rs9332217 come from?
GWAS Catalog, Nature medicine 2022, PMID:36357675. 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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