Standard

Height (baseline)

near RPTN · rs11582331

Where this position leads

Condition: Height

rs11582331 Condition: Height Height Condition rs11582331 rs11582331 near RPTN

What the study found

Who was studied 405,540 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.00863 lower (95% confidence interval 0.0056-0.0117); p = 2 × 10−8.

How common The C allele had a frequency of about 78% in the people studied.

Where it sits Chromosome 1, band 1q21.3 — between genes, 2.4 kb from RPTN.

What each result means

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

Questions about rs11582331

What is rs11582331?

rs11582331 is a single position in the genome, in or near the near RPTN gene. Published research associates it with height (baseline). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11582331 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 rs11582331 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 rs11582331 come from?

GWAS Catalog, Nature communications 2025, PMID:40374629. 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 (baseline) (rs11582331). MyGeneLog™. https://www.mygenelog.com/variants/rs11582331

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