Standard

height (minimum, inv-normal transformed)

near ZNF619P1 · rs17172639

Where this position leads

Condition: Height

rs17172639 Condition: Height Height Condition rs17172639 rs17172639 near ZNF619P1

What the study found

Who was studied 424,306 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0842 lower (95% confidence interval 0.076-0.093); p = 1 × 10−82.

How common The G allele had a frequency of about 89% in the people studied.

Where it sits Chromosome 7, band 7p12.3 — between genes, 19.9 kb from ZNF619P1.

What each result means

A/A No copy of the version the research linked to height (minimum, inv-normal transformed). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to height (minimum, inv-normal transformed). That is a smaller link than two copies.
G/G 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 rs17172639

What is rs17172639?

rs17172639 is a single position in the genome, in or near the near ZNF619P1 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 rs17172639 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 rs17172639 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 rs17172639 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 (minimum, inv-normal transformed) (rs17172639). MyGeneLog™. https://www.mygenelog.com/variants/rs17172639

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