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Who was studied 768 Korean ancestry cases, 19,999 Korean ancestry controls.
The effect
Each copy of the C allele carried 2.28 times the odds of Coronary artery disease in dyslipidemia (95% confidence interval 1.724-3.01899999999999); p = 8 × 10−9.
How common The C allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 9, band 9q22.2 — in an intron of LINC03062.
What each result means
C/CTwo copies of the version the research linked to Coronary artery disease in dyslipidemia. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Coronary artery disease in dyslipidemia. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Coronary artery disease in dyslipidemia. This is the starting point the study compared everyone against.
Journal of translational medicine · 2021 · PMID 33632238 · open access
Questions about rs79166762
What is rs79166762?
rs79166762 is a single position in the genome, in or near the LINC03062 gene. Published research associates it with coronary artery disease in dyslipidemia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs79166762 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 rs79166762 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 rs79166762 come from?
GWAS Catalog, Journal of translational medicine 2021, PMID:33632238. 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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Coronary artery disease in dyslipidemia (rs79166762). MyGeneLog™. https://www.mygenelog.com/variants/rs79166762