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AllergiesatopyEvidence 3
rs2318761 · CIART
Risk-Allele Phenotype
CIART rs2318761 — associated with Atopic dermatitis based on genetic association studies.
Reference-Allele Phenotype
Normal CIART function at this locus, with no elevated genetic risk contribution to Atopic dermatitis from this variant.
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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