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Birth weight (winsorised)

CCNE1 · rs61750863

Where this position leads

Condition: Birth Weight

rs61750863 Condition: Birth Weight Birth Weight Condition rs61750863 rs61750863 CCNE1

What the study found

Who was studied 241,168 British ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0726 kg higher (95% confidence interval 0.047-0.098); p = 3 × 10−8.

What each result means

A/A Two copies of the version the research linked to Birth weight (winsorised). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/T One copy of the version the research linked to Birth weight (winsorised). That is a smaller link than two copies.
T/T No copy of the version the research linked to Birth weight (winsorised). This is the starting point the study compared everyone against.
Source

Questions about rs61750863

What is rs61750863?

rs61750863 is a single position in the genome, in or near the CCNE1 gene. Published research associates it with birth weight (winsorised). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs61750863 linked to?

On MyGeneLog this position is linked to Birth Weight. The research behind each link, and its sources, are set out on that condition page.

Does having rs61750863 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 rs61750863 come from?

GWAS Catalog, Diabetologia 2025, PMID:40210729. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Birth weight (winsorised) (rs61750863). MyGeneLog™. https://www.mygenelog.com/variants/rs61750863

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