Standard

Height (standard GWA)

CDC14B · rs7852498

Where this position leads

Condition: Height

rs7852498 Condition: Height Height Condition rs7852498 rs7852498 CDC14B

What the study found

Who was studied 283,749 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.201 higher (95% confidence interval 0.17-0.24); p = 7 × 10−30.

Where it sits Chromosome 9, band 9q22.33 — in an intron of CDC14B.

What each result means

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

Questions about rs7852498

What is rs7852498?

rs7852498 is a single position in the genome, in or near the CDC14B gene. Published research associates it with height (standard gwa). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7852498 linked to?

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

Does having rs7852498 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 rs7852498 come from?

GWAS Catalog, Nature human behaviour 2023, PMID:37106081. 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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Height (standard GWA) (rs7852498). MyGeneLog™. https://www.mygenelog.com/variants/rs7852498

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