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Height

DET1 · rs13835

Where this position leads

Condition: Height

rs13835 Condition: Height Height Condition rs13835 rs13835 DET1

What the study found

Who was studied 472,730 East Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0211 lower (95% confidence interval 0.015-0.027); p = 4 × 10−11.

How common The A allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 15, band 15q26.1 — in the 3′ untranslated region of DET1.

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

Questions about rs13835

What is rs13835?

rs13835 is a single position in the genome, in or near the DET1 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 rs13835 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 rs13835 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 rs13835 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 (rs13835). MyGeneLog™. https://www.mygenelog.com/variants/rs13835

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