Standard

Height

TC2N · rs759232

Where this position leads

Condition: Height

rs759232 Condition: Height Height Condition rs759232 rs759232 TC2N

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 A allele shifted the measure 0.0263 higher (95% confidence interval 0.025-0.028); p = 4 × 10−193.

How common The A allele had a frequency of about 15% in the people studied.

Where it sits Chromosome 14, band 14q32.12 — in an intron of TC2N.

What each result means

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

Questions about rs759232

What is rs759232?

rs759232 is a single position in the genome, in or near the TC2N 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 rs759232 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 rs759232 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 rs759232 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 (rs759232). MyGeneLog™. https://www.mygenelog.com/variants/rs759232

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