AllergiesasthmaEvidence 3

rs12551256 · IL33

Risk-Allele Phenotype

IL33 rs12551256 — associated with Asthma (childhood onset) based on genetic association studies.

Reference-Allele Phenotype

Normal IL33 function at this locus, with no elevated genetic risk contribution to Asthma (childhood onset) from this variant.

Evidence Level

3 — Limited — single study or in-vitro See methodology for how we grade evidence.

Cross-References

dbSNP — rs12551256
ClinVar — search rs12551256
NCBI Gene — IL33

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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