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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 181,927 Japanese ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0416 higher (95% confidence interval 0.03-0.054); p = 8 × 10−12.
Where it sits Chromosome 20, band 20q13.32 — in the 5′ untranslated region of GNAS.
What each result means
A/ANo copy of the version the research linked to Uric acid levels (1KG-JEWEL7K). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Uric acid levels (1KG-JEWEL7K). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Uric acid levels (1KG-JEWEL7K). That is the strongest link of the three results. A link in a study is not a diagnosis.
Communications biology · 2024 · PMID 39702642 · open access
Questions about rs202213319
What is rs202213319?
rs202213319 is a single position in the genome, in or near the GNAS gene. Published research associates it with uric acid levels (1kg-jewel7k). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs202213319 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 rs202213319 come from?
GWAS Catalog, Communications biology 2024, PMID:39702642. 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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