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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 33,483 Japanese ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.058 lower (95% confidence interval 0.04-0.076); p = 8 × 10−11.
How common The C allele had a frequency of about 60% in the people studied.
Where it sits Chromosome 22, band 22q12.1 — in an intron of ZNRF3.
What each result means
A/ANo copy of the version the research linked to Axial length. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Axial length. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Axial length. That is the strongest link of the three results. A link in a study is not a diagnosis.
Ophthalmology science · 2022 · PMID 36246171 · open access
Questions about rs4823003
What is rs4823003?
rs4823003 is a single position in the genome, in or near the ZNRF3 gene. Published research associates it with axial length. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4823003 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 rs4823003 come from?
GWAS Catalog, Ophthalmology science 2022, PMID:36246171. 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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