AllergiesasthmaEvidence 3

rs111935829 · ORMDL3

Risk-Allele Phenotype

ORMDL3 rs111935829 — associated with Asthma (childhood onset) based on genetic association studies.

Reference-Allele Phenotype

Normal ORMDL3 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 — rs111935829
ClinVar — search rs111935829
NCBI Gene — ORMDL3

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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