AllergiesrhinitisEvidence 3

rs11236795 · EMSY

Risk-Allele Phenotype

EMSY rs11236795 — associated with ICD10 J30: Vasomotor and allergic rhinitis based on genetic association studies.

Reference-Allele Phenotype

Normal EMSY function at this locus, with no elevated genetic risk contribution to ICD10 J30: Vasomotor and allergic rhinitis from this variant.

Evidence Level

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

Cross-References

dbSNP — rs11236795
ClinVar — search rs11236795
NCBI Gene — EMSY

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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