Standard

Height (baseline)

near GRM2 · rs141829833

Where this position leads

Condition: Height

rs141829833 Condition: Height Height Condition rs141829833 rs141829833 near GRM2

What the study found

Who was studied 405,540 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0751 lower (95% confidence interval 0.067-0.084); p = 6 × 10−68.

How common The C allele had a frequency of about 98% in the people studied.

Where it sits Chromosome 3, band 3p21.2 — between genes, 23.5 kb from GRM2.

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 rs141829833

What is rs141829833?

rs141829833 is a single position in the genome, in or near the near GRM2 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 rs141829833 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 rs141829833 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 rs141829833 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) (rs141829833). MyGeneLog™. https://www.mygenelog.com/variants/rs141829833

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