C/CPublished research associates this genotype with typical/baseline likelihood of Urate levels — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Urate levels.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Urate levels compared to the general population.
Nature genetics · 2021 · PMID 33462484 · open access
Questions about rs34783571
What is rs34783571?
rs34783571 is a single position in the genome, in or near the ABCG2 gene. Published research associates it with urate levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does rs34783571 affect how medicines work?
ABCG2 carries pharmacogenomic findings for Statins. 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 rs34783571 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 rs34783571 come from?
GWAS Catalog, Nat Genet 2021, PMID:33462484. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.