AllergiesasthmaEvidence 3

rs912051 · PCDH8P1

Risk-Allele Phenotype

PCDH8P1 rs912051 — associated with Asthma or irritable bowel syndrome (MTAG) based on genetic association studies.

Reference-Allele Phenotype

Normal PCDH8P1 function at this locus, with no elevated genetic risk contribution to Asthma or irritable bowel syndrome (MTAG) from this variant.

Evidence Level

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

Cross-References

dbSNP — rs912051
ClinVar — search rs912051
NCBI Gene — PCDH8P1

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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