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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 85,750 European ancestry middle-aged adult individuals.
The effect
Each copy of the A allele shifted the measure 0.0707 lower (95% confidence interval 0.049-0.092); p = 8 × 10−11.
How common The A allele had a frequency of about 31% in the people studied.
Where it sits Chromosome 10, band 10q22.1 — in an intron of ADAMTS14.
What each result means
A/ATwo copies of the version the research linked to Appendicular lean mass. 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 Appendicular lean mass. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Appendicular lean mass. This is the starting point the study compared everyone against.
American journal of human genetics · 2019 · PMID 31761296
Questions about rs34616741
What is rs34616741?
rs34616741 is a single position in the genome, in or near the ADAMTS14 gene. Published research associates it with appendicular lean mass. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs34616741 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 rs34616741 come from?
GWAS Catalog, American journal of human genetics 2019, PMID:31761296. 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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Quoting this page
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Appendicular lean mass (rs34616741). MyGeneLog™. https://www.mygenelog.com/variants/rs34616741