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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 344,052 European ancestry individuals, 148,767 East Asian ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.013 higher (95% confidence interval 0.0093-0.0167); p = 2 × 10−11.
Where it sits Chromosome X, band Xp22.33 — in an intron of PRKX.
What each result means
C/CTwo 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.
C/TOne copy of the version the research linked to Blood urea nitrogen levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Blood urea nitrogen levels. This is the starting point the study compared everyone against.
rs7879951 is a single position in the genome, in or near the PRKX 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 rs7879951 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 rs7879951 come from?
GWAS Catalog, Nature genetics 2021, PMID:34594039. 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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