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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 69,591 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0405 lower (95% confidence interval 0.03-0.051); p = 4 × 10−11.
How common The A allele had a frequency of about 53% in the people studied.
Where it sits Chromosome 8, band 8p21.2 — between genes, 30.4 kb from STC1.
What each result means
A/ATwo copies of the version the research linked to Creatinine levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Creatinine levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Creatinine levels. This is the starting point the study compared everyone against.
Nature communications · 2019 · PMID 31015462 · open access
Questions about rs819196
What is rs819196?
rs819196 is a single position in the genome, in or near the STC1 gene. Published research associates it with creatinine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs819196 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 rs819196 come from?
GWAS Catalog, Nature communications 2019, PMID:31015462. 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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