Standard

Height

USP44 · rs3812813

Where this position leads

Condition: Height

rs3812813 Condition: Height Height Condition rs3812813 rs3812813 USP44

What the study found

Who was studied 235,398 non-Hispanic white ancestry individuals, 63,898 non-Hispanic black ancestry individuals, 24,497 Hispanic American ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.02 higher; p = 8 × 10−12.

Where it sits Chromosome 12, band 12q22 — a missense change in USP44.

What each result means

C/C No copy of the version the research linked to Height. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Height. That is a smaller link than two copies.
T/T 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.
Source

Questions about rs3812813

What is rs3812813?

rs3812813 is a single position in the genome, in or near the USP44 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 rs3812813 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 rs3812813 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 rs3812813 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 (rs3812813). MyGeneLog™. https://www.mygenelog.com/variants/rs3812813

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