AllergieseosinophilicEvidence 3

rs1620996 · BOLA2P3

Risk-Allele Phenotype

BOLA2P3 rs1620996 — associated with Eosinophilic esophagitis based on genetic association studies.

Reference-Allele Phenotype

Normal BOLA2P3 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 — rs1620996
ClinVar — search rs1620996
NCBI Gene — BOLA2P3

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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