Standard

height (mean, inv-normal transformed)

near CCDC17 · rs77131772

Where this position leads

Condition: Height

rs77131772 Condition: Height Height Condition rs77131772 rs77131772 near CCDC17

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, 424,305 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0274 higher (95% confidence interval 0.021-0.034); p = 4 × 10−15.

How common The T allele had a frequency of about 31% in the people studied.

Where it sits Chromosome 1, band 1p34.1 — between genes, 1 kb from CCDC17.

What each result means

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

Questions about rs77131772

What is rs77131772?

rs77131772 is a single position in the genome, in or near the near CCDC17 gene. Published research associates it with height (mean, 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 rs77131772 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 rs77131772 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 rs77131772 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

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 (mean, inv-normal transformed) (rs77131772). MyGeneLog™. https://www.mygenelog.com/variants/rs77131772

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