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Who was studied 34,541 cases, 261,984 controls; replicated in 88,192 cases, 162,544 controls.
The effect
Each copy of the A allele shifted the measure 0.079 higher (95% confidence interval 0.061-0.097); p = 6 × 10−20.
How common The A allele had a frequency of about 15% in the people studied.
Where it sits Chromosome 4, band 4q31.22 — between genes, 14.5 kb from PRMT5P1.
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/TOne copy of the version the research linked to Coronary artery disease. That is a smaller link than two copies.
T/TNo 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 rs17612693
What is rs17612693?
rs17612693 is a single position in the genome, in or near the near PRMT5P1 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 rs17612693 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 rs17612693 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 rs17612693 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.
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