Standard

Height

PIP4K2A · rs4747443

Where this position leads

Condition: Height

rs4747443 Condition: Height Height Condition rs4747443 rs4747443 PIP4K2A

What the study found

Who was studied 235,398 non-Hispanic white ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.018 higher; p = 3 × 10−9.

How common The A allele had a frequency of about 39% in the people studied.

Where it sits Chromosome 10, band 10p12.2 — in an intron of PIP4K2A.

What each result means

A/A Two copies of the version the research linked to Height. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/C One copy of the version the research linked to Height. That is a smaller link than two copies.
C/C No copy of the version the research linked to Height. This is the starting point the study compared everyone against.
Source

Questions about rs4747443

What is rs4747443?

rs4747443 is a single position in the genome, in or near the PIP4K2A 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 rs4747443 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 rs4747443 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 rs4747443 come from?

GWAS Catalog, PLoS genetics 2022, PMID:35653334. 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 (rs4747443). MyGeneLog™. https://www.mygenelog.com/variants/rs4747443

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