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AllergieseosinophilicEvidence 3
rs191051238 · CCNY
Risk allele: C
Risk-Allele Phenotype
CCNY rs191051238 — associated with increased risk of eosinophilic esophagitis in carriers of the C allele, based on genome-wide association meta-analysis evidence.
Reference-Allele Phenotype
Normal CCNY function at this locus, with no detected association with increased eosinophilic esophagitis risk at rs191051238.
Evidence Level
3 — Limited — single study or in-vitro See methodology for how we grade evidence.
Cross-References
Informational only
This page summarizes population-level evidence about a genetic variant. It is not a diagnosis. Your individual risk depends on your full genome, lifestyle, environment, and family history. Consult a healthcare provider for personalized medical advice.
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