AllergiesasthmaEvidence 3

rs139210940 · CFAP144P2

Risk-Allele Phenotype

CFAP144P2 rs139210940 — associated with Asthma (moderate or severe) based on genetic association studies.

Reference-Allele Phenotype

Normal CFAP144P2 function at this locus, with no elevated genetic risk contribution to Asthma (moderate or severe) from this variant.

Evidence Level

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

Cross-References

dbSNP — rs139210940
ClinVar — search rs139210940
NCBI Gene — CFAP144P2

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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