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AllergiesatopyEvidence 2B
rs189163698 · CCDST
Risk-Allele Phenotype
CCDST rs189163698 — associated with increased risk of atopic dermatitis, a chronic inflammatory skin condition characterized by impaired barrier function and immune dysregulation.
Reference-Allele Phenotype
Normal CCDST function at this locus, with no increased genetic risk contribution from this variant toward atopic dermatitis.
Evidence Level
2B — Moderate — single replicated study 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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