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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 6,125 Icelandic ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.235 higher; p = 2 × 10−28.
Where it sits Chromosome 2, band 2q13 — inside ANAPC1.
What each result means
A/ATwo copies of the version the research linked to Corneal endothelial cell size variation coefficient. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Corneal endothelial cell size variation coefficient. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Corneal endothelial cell size variation coefficient. This is the starting point the study compared everyone against.
Nature communications · 2019 · PMID 30894546 · open access
Questions about rs201205018
What is rs201205018?
rs201205018 is a single position in the genome, in or near the ANAPC1 gene. Published research associates it with corneal endothelial cell size variation coefficient. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs201205018 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 rs201205018 come from?
GWAS Catalog, Nature communications 2019, PMID:30894546. 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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