Standard

Height

CPN2 · rs11711157

Where this position leads

Condition: Height

rs11711157 Condition: Height Height Condition rs11711157 rs11711157 CPN2

What the study found

Who was studied 5,314,291 European ancestry, Hispanic or Latin American, East Asian ancestry, African ancestry, South Asian ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0114 higher (95% confidence interval 0.01-0.013); p = 4 × 10−61.

How common The T allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 3, band 3q29 — a missense change in CPN2.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Height — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Height.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Height compared to the general population.
Source

Questions about rs11711157

What is rs11711157?

rs11711157 is a single position in the genome, in or near the CPN2 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 rs11711157 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 rs11711157 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 rs11711157 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 (rs11711157). MyGeneLog™. https://www.mygenelog.com/variants/rs11711157

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