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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 58,406 Korean ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0125 higher (95% confidence interval 0.0094-0.0156); p = 4 × 10−14.
Where it sits Chromosome 7, band 7p22.3 — between genes, 6.8 kb from UNCX.
What each result means
C/CNo copy of the version the research linked to Blood urea nitrogen levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Blood urea nitrogen levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Blood urea nitrogen levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Kidney research and clinical practice · 2024 · PMID 37919891 · open access
Questions about rs11762900
What is rs11762900?
rs11762900 is a single position in the genome, in or near the near UNCX gene. Published research associates it with blood urea nitrogen levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11762900 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 rs11762900 come from?
GWAS Catalog, Kidney research and clinical practice 2024, PMID:37919891. 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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