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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 29,895 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.04 lower; p = 1 × 10−13.
How common The C allele had a frequency of about 78% in the people studied.
Where it sits Chromosome 13, band 13q12.11 — between genes, 12.1 kb from LINC00540.
What each result means
C/CTwo copies of the version the research linked to Ascending aorta distensibility (MTAG). 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 Ascending aorta distensibility (MTAG). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Ascending aorta distensibility (MTAG). This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 35922433 · open access
Questions about rs12863716
What is rs12863716?
rs12863716 is a single position in the genome, in or near the near LINC00540 gene. Published research associates it with ascending aorta distensibility (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12863716 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 rs12863716 come from?
GWAS Catalog, Nature communications 2022, PMID:35922433. 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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