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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 2,109 White British ancestry male individuals.
The effect
Each copy of the A allele shifted the measure 910 g higher; p = 5 × 10−9.
Where it sits Chromosome 3, band 3p22.3 — between genes, 16.3 kb from CMTM8.
What each result means
A/ATwo copies of the version the research linked to Gynoid 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 Gynoid lean mass. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Gynoid lean mass. This is the starting point the study compared everyone against.
Frontiers in endocrinology · 2021 · PMID 34239500 · open access
Questions about rs145972737
What is rs145972737?
rs145972737 is a single position in the genome, in or near the near CMTM8 gene. Published research associates it with gynoid 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 rs145972737 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 rs145972737 come from?
GWAS Catalog, Frontiers in endocrinology 2021, PMID:34239500. 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
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Gynoid lean mass (rs145972737). MyGeneLog™. https://www.mygenelog.com/variants/rs145972737