Sensitive

Coronary artery disease

near MAP9 · rs13118820

Where this position leads

Condition: Coronary Artery Disease

rs13118820 Condition: Coronary Artery Disease Coronary Artery Disease Condition rs13118820 rs13118820 near MAP9

What the study found

Who was studied 88,192 cases, 162,544 controls; replicated in 34,541 cases, 261,984 controls.

The effect Each copy of the A allele shifted the measure 0.042 higher (95% confidence interval 0.029-0.055); p = 1 × 10−10.

How common The A allele had a frequency of about 36% in the people studied.

Where it sits Chromosome 4, band 4q32.1 — in an intron of LOC105377505.

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/C One copy of the version the research linked to Coronary artery disease. That is a smaller link than two copies.
C/C 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 rs13118820

What is rs13118820?

rs13118820 is a single position in the genome, in or near the near MAP9 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 rs13118820 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 rs13118820 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 rs13118820 come from?

GWAS Catalog, Circ Res 2017, 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

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 (rs13118820). MyGeneLog™. https://www.mygenelog.com/variants/rs13118820

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