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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 2,426 European ancestry cases, 351,961 European ancestry controls.
The effect
The reported allele is T; the catalogue records no effect size
; p = 9 × 10−11.
Where it sits Chromosome 3, band 3p25.1 — between genes, 2 kb from LINC01267.
What each result means
C/CNo copy of the version the research linked to Uveal melanoma. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Uveal melanoma. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Uveal melanoma. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs11707457 is a single position in the genome, in or near the near LINC01267 gene. Published research associates it with uveal melanoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11707457 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 rs11707457 come from?
GWAS Catalog, HGG advances 2025, PMID:40495383. 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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