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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 0.0183 lower (95% confidence interval 0.012-0.024); p = 4 × 10−9.
Where it sits Chromosome 2, band 2p16.1 — in an intron of LINC01122.
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/TOne copy of the version the research linked to A body shape index. That is a smaller link than two copies.
T/TNo 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 rs2052246
What is rs2052246?
rs2052246 is a single position in the genome, in or near the LINC01122 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 rs2052246 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 rs2052246 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 (rs2052246). MyGeneLog™. https://www.mygenelog.com/variants/rs2052246