AllergiesasthmaEvidence 3

rs28510449 · OR7E161P

Risk-Allele Phenotype

OR7E161P rs28510449 — associated with Asthma or chronic rhinosinusitis based on genetic association studies.

Reference-Allele Phenotype

Normal OR7E161P function at this locus, with no elevated genetic risk contribution to Asthma or chronic rhinosinusitis from this variant.

Evidence Level

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

Cross-References

dbSNP — rs28510449
ClinVar — search rs28510449
NCBI Gene — OR7E161P

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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