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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 31,135 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.53 lower (95% confidence interval 0.39-0.67); p = 3 × 10−16.
How common The G allele had a frequency of about 18% in the people studied.
Where it sits Chromosome 12, band 12q22 — in an intron of NTN4.
What each result means
C/CNo copy of the version the research linked to Photoreceptor cell layer thickness phenotypes (MTAG). This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Photoreceptor cell layer thickness phenotypes (MTAG). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Photoreceptor cell layer thickness phenotypes (MTAG). That is the strongest link of the three results. A link in a study is not a diagnosis.
PLoS genetics · 2023 · PMID 36848389 · open access
Questions about rs76629482
What is rs76629482?
rs76629482 is a single position in the genome, in or near the NTN4 gene. Published research associates it with photoreceptor cell layer thickness phenotypes (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs76629482 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 rs76629482 come from?
GWAS Catalog, PLoS genetics 2023, PMID:36848389. 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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