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Who was studied 15,302 Japanese ancestry cases, 76,014 European and East Asian ancestry cases, 36,140 Japanese ancestry controls, 264,785 European and East Asian ancestry controls.
The effect
Each copy of the T allele carried 1.07 times the odds of Coronary artery disease (95% confidence interval 1.04-1.11); p = 5 × 10−11.
How common The T allele had a frequency of about 16% in the people studied.
Where it sits Chromosome 17, band 17q23.2 — in an intron of BCAS3.
What each result means
C/CNo copy of the version the research linked to Coronary artery disease. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Coronary artery disease. That is a smaller link than two copies.
T/TTwo 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.
Circulation. Genomic and precision medicine · 2020 · PMID 32469254
Questions about rs7214227
What is rs7214227?
rs7214227 is a single position in the genome, in or near the BCAS3 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 rs7214227 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 rs7214227 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 rs7214227 come from?
GWAS Catalog, Circulation. Genomic and precision medicine 2020, PMID:32469254. 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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