Standard

height (minimum, inv-normal transformed)

RAB3GAP1 · rs115227414

Where this position leads

Condition: Height

rs115227414 Condition: Height Height Condition rs115227414 rs115227414 RAB3GAP1

What the study found

Who was studied 119,012 African American or Afro-Caribbean individuals, 57,810 Hispanic or Latin American individuals, 6,384 East Asian ancestry individuals, 424,306 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0701 higher (95% confidence interval 0.055-0.085); p = 3 × 10−19.

How common The T allele had a frequency of about 95% in the people studied.

Where it sits Chromosome 2, band 2q21.3 — in an intron of RAB3GAP1.

What each result means

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

Questions about rs115227414

What is rs115227414?

rs115227414 is a single position in the genome, in or near the RAB3GAP1 gene. Published research associates it with height (minimum, inv-normal transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs115227414 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 rs115227414 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 rs115227414 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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height (minimum, inv-normal transformed) (rs115227414). MyGeneLog™. https://www.mygenelog.com/variants/rs115227414

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