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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 31,434 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.37 lower (95% confidence interval 0.27-0.47); p = 2 × 10−16.
How common The C allele had a frequency of about 20% in the people studied.
Where it sits Chromosome 3, band 3p14.1 — inside FRMD4B.
What each result means
C/CTwo copies of the version the research linked to Retinal nerve fibre layer (RNFL) thickness. 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 Retinal nerve fibre layer (RNFL) thickness. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Retinal nerve fibre layer (RNFL) thickness. This is the starting point the study compared everyone against.
PLoS genetics · 2021 · PMID 33979322 · open access
Questions about rs62252355
What is rs62252355?
rs62252355 is a single position in the genome, in or near the FRMD4B gene. Published research associates it with retinal nerve fibre layer (rnfl) thickness. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs62252355 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 rs62252355 come from?
GWAS Catalog, PLoS genetics 2021, PMID:33979322. 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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