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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 0.026-0.051); p = 1 × 10−9.
How common The A allele had a frequency of about 27% in the people studied.
Where it sits Chromosome 10, band 10q24.33 — between genes, 3.2 kb from LOC102724351.
What each result means
A/ATwo 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/GOne copy of the version the research linked to Coronary artery disease. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Coronary artery disease. This is the starting point the study compared everyone against.
Circulation research · 2018 · PMID 29212778 · open access
Questions about rs4918072
What is rs4918072?
rs4918072 is a single position in the genome, in or near the near STN1 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 rs4918072 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 rs4918072 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 rs4918072 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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