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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 29,580 European ancestry individuals, 14,462 Asian ancestry individuals; replicated in 88,218 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.008 mm higher; p = 2 × 10−19.
How common The A allele had a frequency of about 60% in the people studied.
Where it sits Chromosome 10, band 10q24.1 — between genes, 4.1 kb from FRAT1.
What each result means
A/ATwo copies of the version the research linked to Corneal curvature. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/COne copy of the version the research linked to Corneal curvature. That is a smaller link than two copies.
C/CNo copy of the version the research linked to Corneal curvature. This is the starting point the study compared everyone against.
Communications biology · 2020 · PMID 32193507 · open access
Questions about rs10786330
What is rs10786330?
rs10786330 is a single position in the genome, in or near the near FRAT1 gene. Published research associates it with corneal curvature. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10786330 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 rs10786330 come from?
GWAS Catalog, Communications biology 2020, PMID:32193507. 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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