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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 0.442 lower (95% confidence interval 0.3-0.58); p = 4 × 10−10.
Where it sits Chromosome 4, band 4q21.1 — in an intron of SHROOM3.
What each result means
C/CNo copy of the version the research linked to Estimated glomerular filtration rate. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Estimated glomerular filtration rate. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Estimated glomerular filtration rate. 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 rs10029777
What is rs10029777?
rs10029777 is a single position in the genome, in or near the SHROOM3 gene. Published research associates it with estimated glomerular filtration rate. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10029777 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 rs10029777 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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