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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 460,198 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0335 lower (95% confidence interval 0.028-0.039); p = 2 × 10−38.
How common The T allele had a frequency of about 77% in the people studied.
Where it sits Chromosome 3, band 3q22.1 — in an intron of PLXND1.
What each result means
G/GNo copy of the version the research linked to Body shape phenotype PC2. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Body shape phenotype PC2. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Body shape phenotype PC2. That is the strongest link of the three results. A link in a study is not a diagnosis.
Science advances · 2024 · PMID 38640244 · open access
Questions about rs2811462
What is rs2811462?
rs2811462 is a single position in the genome, in or near the PLXND1 gene. Published research associates it with body shape phenotype pc2. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2811462 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 rs2811462 come from?
GWAS Catalog, Science advances 2024, PMID:38640244. 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.
Body shape phenotype PC2 (rs2811462). MyGeneLog™. https://www.mygenelog.com/variants/rs2811462