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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 219,768 East Asian ancestry individuals, 677,373 European ancestry individuals, 132,182 individuals.
The effect
Each copy of the T allele shifted the measure 0.0181 higher (95% confidence interval 0.014-0.023); p = 5 × 10−15.
Where it sits Chromosome 20, band 20q11.22 — in an intron of NCOA6.
What each result means
C/CNo copy of the version the research linked to Serum urate levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Serum urate levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Serum urate levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2024 · PMID 38658550 · open access
Questions about rs6119524
What is rs6119524?
rs6119524 is a single position in the genome, in or near the NCOA6 gene. Published research associates it with serum urate levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs6119524 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 rs6119524 come from?
GWAS Catalog, Nature communications 2024, PMID:38658550. 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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