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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 112,262 Japanese ancestry individuals; replicated in 36,276 Japanese ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.116 higher (95% confidence interval 0.094-0.138); p = 8 × 10−26.
Where it sits Chromosome 4, band 4p16.1 — in an intron of SLC2A9.
What each result means
A/ATwo copies of the version the research linked to Uric acid x sex interaction. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Uric acid x sex interaction. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Uric acid x sex interaction. This is the starting point the study compared everyone against.
rs12507330 is a single position in the genome, in or near the SLC2A9 gene. Published research associates it with uric acid x sex interaction. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12507330 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 rs12507330 come from?
GWAS Catalog, Nature 2026, PMID:41606330. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Uric acid x sex interaction (rs12507330). MyGeneLog™. https://www.mygenelog.com/variants/rs12507330