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Height

CDH12 · rs13164873

Where this position leads

Condition: Height

rs13164873 Condition: Height Height Condition rs13164873 rs13164873 CDH12

What the study found

Who was studied 293,593 African ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0346 higher (95% confidence interval 0.025-0.044); p = 6 × 10−13.

How common The A allele had a frequency of about 14% in the people studied.

Where it sits Chromosome 5, band 5p14.3 — in an intron of CDH12.

What each result means

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

Questions about rs13164873

What is rs13164873?

rs13164873 is a single position in the genome, in or near the CDH12 gene. Published research associates it with height. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs13164873 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 rs13164873 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 rs13164873 come from?

GWAS Catalog, Nature 2022, PMID:36224396. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

Height (rs13164873). MyGeneLog™. https://www.mygenelog.com/variants/rs13164873

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