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Stable angina pectoris

GOLGA6GP · rs11072799

What the study found

Who was studied 17,894 European ancestry cases, 325,132 European ancestry controls, 18,833 East Asian ancestry cases, 146,214 East Asian ancestry controls.

The effect Each copy of the T allele shifted the measure 0.0753 lower (95% confidence interval 0.058-0.093); p = 7 × 10−17.

Where it sits Chromosome 15, band 15q25.1 — in a non-coding transcript of GOLGA6GP.

What each result means

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

Questions about rs11072799

What is rs11072799?

rs11072799 is a single position in the genome, in or near the GOLGA6GP gene. Published research associates it with stable angina pectoris. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11072799 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 rs11072799 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Stable angina pectoris (rs11072799). MyGeneLog™. https://www.mygenelog.com/variants/rs11072799

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