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Corneal endothelial cell size variation coefficient

near BLID · rs76561503

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 each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Corneal endothelial cell size variation coefficient compared to the general population. (GWAS Catalog, Nat Commun 2019, PMID:30894546)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Corneal endothelial cell size variation coefficient. (GWAS Catalog, Nat Commun 2019, PMID:30894546)

T/T Published research associates this genotype with typical/baseline likelihood of Corneal endothelial cell size variation coefficient — no copies of the reported risk allele. (GWAS Catalog, Nat Commun 2019, PMID:30894546)

Source: GWAS Catalog, Nat Commun 2019, PMID:30894546

Questions about rs76561503

What is rs76561503?

rs76561503 is a single position in the genome, in or near the near BLID gene. Published research associates it with corneal endothelial cell size variation coefficient. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs76561503 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 rs76561503 come from?

GWAS Catalog, Nat Commun 2019, PMID:30894546. 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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