Gene Knowledge Graph
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Sensitive

Coronary artery disease

KIAA1462 · rs9337951

Where this position leads

Condition: Coronary Artery Disease

rs9337951 Condition: Coronary Artery Disease Coronary Artery Disease Condition rs9337951 rs9337951 KIAA1462

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Coronary artery disease compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Coronary artery disease.
G/G Published research associates this genotype with typical/baseline likelihood of Coronary artery disease — no copies of the reported risk allele.
Source
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease
van der Harst P, Verweij N
Circulation research · 2018 · PMID 29212778 · open access

Questions about rs9337951

What is rs9337951?

rs9337951 is a single position in the genome, in or near the KIAA1462 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 rs9337951 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 rs9337951 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 rs9337951 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.

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