Standard

Height

GPRIN3 · rs1560489

Where this position leads

Condition: Height

rs1560489 Condition: Height Height Condition rs1560489 rs1560489 GPRIN3

What the study found

Who was studied up to 248,507 non-Hispanic white individuals, up to 68,155 non-Hispanic black individuals, up to 25,847 Hispanic individuals, up to 3,054 Asian ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.12 higher; p = 9 × 10−9.

Where it sits Chromosome 4, band 4q22.1 — in an intron of GPRIN3.

What each result means

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

Questions about rs1560489

What is rs1560489?

rs1560489 is a single position in the genome, in or near the GPRIN3 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 rs1560489 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 rs1560489 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 rs1560489 come from?

GWAS Catalog, American journal of human genetics 2019, PMID:31564439. 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 (rs1560489). MyGeneLog™. https://www.mygenelog.com/variants/rs1560489

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