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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 2,466 Black/admixed ancestry individuals; replicated in up to 1,653 European, Hispanic, Asian or Black individuals.
The effect
Each copy of the T allele shifted the measure 0.968 higher (95% confidence interval 0.74-1.2); p = 1 × 10−16.
Where it sits Chromosome 3, band 3p21.2 — between genes, 1 kb from RRP9.
What each result means
C/CNo copy of the version the research linked to N-acetyl-L-glutamine levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to N-acetyl-L-glutamine levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to N-acetyl-L-glutamine levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2022 · PMID 35995766 · open access
Questions about rs139627801
What is rs139627801?
rs139627801 is a single position in the genome, in or near the near RRP9 gene. Published research associates it with n-acetyl-l-glutamine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs139627801 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 rs139627801 come from?
GWAS Catalog, Nature communications 2022, PMID:35995766. 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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