Sensitive

Coronary artery disease

GABBR1 · rs29266

Where this position leads

Condition: Coronary Artery Disease

rs29266 Condition: Coronary Artery Disease Coronary Artery Disease Condition rs29266 rs29266 GABBR1

What the study found

Who was studied 190,493 European ancestry cases, 582,775 European ancestry controls.

The effect The reported allele is A; the catalogue records no effect size ; p = 1 × 10−9.

Where it sits Chromosome 6, band 6p22.1 — in an intron of GABBR1.

What each result means

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

Questions about rs29266

What is rs29266?

rs29266 is a single position in the genome, in or near the GABBR1 gene. Published research associates it with coronary artery disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs29266 linked to?

On MyGeneLog this position is linked to Coronary Artery Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs29266 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 rs29266 come from?

GWAS Catalog, Nature medicine 2022, PMID:35915156. 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.

Coronary artery disease (rs29266). MyGeneLog™. https://www.mygenelog.com/variants/rs29266

← See all variants