AllergieseosinophilicEvidence 3

rs8041227 · LINC03034

Risk-Allele Phenotype

LINC03034 rs8041227 — identified as a genetic risk factor for Eosinophilic esophagitis, based on genome-wide association studies and clinical evidence.

Reference-Allele Phenotype

Normal LINC03034 function at this locus, with no elevated genetic risk contribution to Eosinophilic esophagitis from this variant.

Evidence Level

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

Cross-References

dbSNP — rs8041227
ClinVar — search rs8041227
NCBI Gene — LINC03034

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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