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Who was studied 190,493 European ancestry cases, 582,775 European ancestry controls, 6,378 Hispanic or Latin American cases, 24,270 Hispanic or Latin American controls, 1,702 African American or Afro-Caribbean cases, 59,507 African American or Afro-Caribbean controls, 29,319 East Asian ancestry cases, 183,134 East Asian ancestry controls.
The effect
Each copy of the T allele shifted the measure 0.0195 lower (95% confidence interval 0.013-0.026); p = 1 × 10−9.
How common The T allele had a frequency of about 33% in the people studied.
Where it sits Chromosome X, band Xq12 — in an intron of OPHN1.
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.
rs1410127 is a single position in the genome, in or near the OPHN1 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 rs1410127 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 rs1410127 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 rs1410127 come from?
GWAS Catalog, Nature medicine 2022, PMID:35915156. 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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