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Age-related nuclear cataracts

CRYAA · rs11911275

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Age-related nuclear cataracts — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Age-related nuclear cataracts.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Age-related nuclear cataracts compared to the general population.
Source

Questions about rs11911275

What is rs11911275?

rs11911275 is a single position in the genome, in or near the CRYAA gene. Published research associates it with age-related nuclear cataracts. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11911275 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 rs11911275 come from?

GWAS Catalog, Hum Mol Genet 2014, PMID:24951543. 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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