AllergiesasthmaEvidence 3

rs17780470 · LINC01478

Risk-Allele Phenotype

LINC01478 rs17780470 — associated with Asthma or gastroesophageal reflux disease (MTAG) based on genetic association studies.

Reference-Allele Phenotype

Normal LINC01478 function at this locus, with no elevated genetic risk contribution to Asthma or gastroesophageal reflux disease (MTAG) from this variant.

Evidence Level

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

Cross-References

dbSNP — rs17780470
ClinVar — search rs17780470
NCBI Gene — LINC01478

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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