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AllergiesasthmaEvidence 3

rs12521097 · P4HA2

Risk-Allele Phenotype

P4HA2 rs12521097 — associated with Asthma and cardiovascular disease based on genetic association studies.

Reference-Allele Phenotype

Normal P4HA2 function at this locus, with no elevated genetic risk contribution to Asthma and cardiovascular disease from this variant.

Evidence Level

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

Cross-References

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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