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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 33,022 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 6.97 z score lower; p = 3 × 10−12.
How common The A allele had a frequency of about 32% in the people studied.
Where it sits Chromosome 17, band 17q23.3 — between genes, 0.9 kb from CSHL1.
What each result means
A/ATwo copies of the version the research linked to Posterior thigh muscle volume. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Posterior thigh muscle volume. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Posterior thigh muscle volume. This is the starting point the study compared everyone against.
Communications biology · 2022 · PMID 36402844 · open access
Questions about rs2854152
What is rs2854152?
rs2854152 is a single position in the genome, in or near the near CSHL1 gene. Published research associates it with posterior thigh muscle volume. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2854152 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 rs2854152 come from?
GWAS Catalog, Communications biology 2022, PMID:36402844. 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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