AllergiesatopyEvidence 2B

rs185433896 · CCDST

Risk allele: A

Risk-Allele Phenotype

CCDST rs185433896 — associated with increased risk of atopic dermatitis in carriers of the A allele, based on genome-wide association data.

Reference-Allele Phenotype

Normal CCDST function at this locus, with no detected association with elevated atopic dermatitis risk at rs185433896.

Evidence Level

2B — Moderate — single replicated study See methodology for how we grade evidence.

Cross-References

dbSNP — rs185433896
ClinVar — search rs185433896
NCBI Gene — CCDST

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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