AllergiesasthmaEvidence 3

rs4952375 · HNRNPA1P57

Risk-Allele Phenotype

HNRNPA1P57 rs4952375 — associated with Asthma with severe exacerbations based on genetic association studies.

Reference-Allele Phenotype

Normal HNRNPA1P57 function at this locus, with no elevated genetic risk contribution to Asthma with severe exacerbations from this variant.

Evidence Level

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

Cross-References

dbSNP — rs4952375
ClinVar — search rs4952375
NCBI Gene — HNRNPA1P57

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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