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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 40,028 European or unknown ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0711 higher (95% confidence interval 0.056-0.087); p = 2 × 10−19.
How common The C allele had a frequency of about 83% in the people studied.
Where it sits Chromosome 10, band 10q23.33 — in an intron of PLCE1.
What each result means
C/CTwo copies of the version the research linked to Descending aorta strain. 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 Descending aorta strain. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Descending aorta strain. This is the starting point the study compared everyone against.
Journal of the American College of Cardiology · 2023 · PMID 37019578
Questions about rs79958663
What is rs79958663?
rs79958663 is a single position in the genome, in or near the PLCE1 gene. Published research associates it with descending aorta strain. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs79958663 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 rs79958663 come from?
GWAS Catalog, Journal of the American College of Cardiology 2023, PMID:37019578. 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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