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Birth weight (winsorised)

KCNQ1 · rs60056002

Where this position leads

Condition: Birth Weight

rs60056002 Condition: Birth Weight Birth Weight Condition rs60056002 rs60056002 KCNQ1

What the study found

Who was studied 241,168 British ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.017 kg higher (95% confidence interval 0.012-0.022); p = 3 × 10−10.

What each result means

C/C No copy of the version the research linked to Birth weight (winsorised). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Birth weight (winsorised). That is a smaller link than two copies.
T/T 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.
Source

Questions about rs60056002

What is rs60056002?

rs60056002 is a single position in the genome, in or near the KCNQ1 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 rs60056002 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 rs60056002 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 rs60056002 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) (rs60056002). MyGeneLog™. https://www.mygenelog.com/variants/rs60056002

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