Sensitive

Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease)

NOS3 · rs3918226

Where this position leads

Condition: Coronary Artery Disease

rs3918226 Condition: Coronary Artery Disease Coronary Artery Disease Condition rs3918226 rs3918226 NOS3

What each result means

C/C No copy of the version the research linked to Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs3918226

What is rs3918226?

rs3918226 is a single position in the genome, in or near the NOS3 gene. Published research associates it with coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart 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 rs3918226 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 rs3918226 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 rs3918226 come from?

GWAS Catalog, Nat Genet 2017, PMID:28714975. 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 (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) (rs3918226). MyGeneLog™. https://www.mygenelog.com/variants/rs3918226

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