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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 1,004,040 European ancestry individuals, 165,726 East Asian ancestry individuals, 13,842 African American individuals, 13,359 South Asian ancestry individuals, 4,961 Hispanic individuals, 2 individuals; replicated in 417,288 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.00176 lower (95% confidence interval 0.0012-0.0023); p = 5 × 10−11.
How common The T allele had a frequency of about 25% in the people studied.
Where it sits Chromosome 2, band 2q37.1 — in an intron of ARMC9.
What each result means
C/CNo copy of the version the research linked to Estimated glomerular filtration rate (creatinine). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Estimated glomerular filtration rate (creatinine). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Estimated glomerular filtration rate (creatinine). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2021 · PMID 34272381 · open access
Questions about rs16827879
What is rs16827879?
rs16827879 is a single position in the genome, in or near the ARMC9 gene. Published research associates it with estimated glomerular filtration rate (creatinine). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs16827879 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 rs16827879 come from?
GWAS Catalog, Nature communications 2021, PMID:34272381. 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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