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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 186,825 British ancestry men.
The effect
Each copy of the C allele shifted the measure 0.0196 lower (95% confidence interval 0.013-0.027); p = 2 × 10−8.
Where it sits Chromosome 6, band 6q23.1 — in an intron of L3MBTL3.
What each result means
C/CTwo copies of the version the research linked to A body shape index. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to A body shape index. That is a smaller link than two copies.
G/GNo copy of the version the research linked to A body shape index. This is the starting point the study compared everyone against.
Scientific reports · 2021 · PMID 34021172 · open access
Questions about rs10499172
What is rs10499172?
rs10499172 is a single position in the genome, in or near the L3MBTL3 gene. Published research associates it with a body shape index. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10499172 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 rs10499172 come from?
GWAS Catalog, Scientific reports 2021, PMID:34021172. 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.
A body shape index (rs10499172). MyGeneLog™. https://www.mygenelog.com/variants/rs10499172