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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 12,328 European ancestry males, 15,813 European ancestry females.
The effect
Each copy of the A allele shifted the measure 0.08 mg/dl higher (95% confidence interval 0.051-0.105); p = 1 × 10−8.
How common The A allele had a frequency of about 83% in the people studied.
Where it sits Chromosome 10, band 10q21.2 — a synonymous change in SLC16A9.
What each result means
A/ATwo copies of the version the research linked to Uric acid levels. 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 levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Uric acid levels. This is the starting point the study compared everyone against.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs12356193
What is rs12356193?
rs12356193 is a single position in the genome, in or near the SLC16A9 gene. Published research associates it with uric acid levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What do people read about alongside rs12356193?
Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (1 papers), infection and immunity (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs12356193 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 rs12356193 come from?
GWAS Catalog, PLoS Genet 2009, PMID:19503597. 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
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