Sensitive

Coronary artery disease

UNC5C · rs3775058

Where this position leads

Condition: Coronary Artery Disease

rs3775058 Condition: Coronary Artery Disease Coronary Artery Disease Condition rs3775058 rs3775058 UNC5C

What the study found

Who was studied up to 122,733 cases, up to 424,528 controls.

The effect Each copy of the A allele shifted the measure 0.0386 higher (95% confidence interval 0.025-0.052); p = 8 × 10−9.

How common The A allele had a frequency of about 23% in the people studied.

Where it sits Chromosome 4, band 4q22.3 — in an intron of UNC5C.

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/T One copy of the version the research linked to Coronary artery disease. That is a smaller link than two copies.
T/T 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 rs3775058

What is rs3775058?

rs3775058 is a single position in the genome, in or near the UNC5C 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 rs3775058 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 rs3775058 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 rs3775058 come from?

GWAS Catalog, Circulation research 2018, PMID:29212778. 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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Coronary artery disease (rs3775058). MyGeneLog™. https://www.mygenelog.com/variants/rs3775058

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