Standard

Height

CALCB · rs11023392

Where this position leads

Condition: Height

rs11023392 Condition: Height Height Condition rs11023392 rs11023392 CALCB

What the study found

Who was studied 455,180 Hispanic or Latin American individuals.

The effect Each copy of the A allele shifted the measure 0.0227 higher (95% confidence interval 0.016-0.03); p = 2 × 10−10.

How common The A allele had a frequency of about 11% in the people studied.

Where it sits Chromosome 11, band 11p15.2 — inside CALCB.

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 rs11023392

What is rs11023392?

rs11023392 is a single position in the genome, in or near the CALCB 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 rs11023392 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 rs11023392 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 rs11023392 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 (rs11023392). MyGeneLog™. https://www.mygenelog.com/variants/rs11023392

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