AllergiesasthmaEvidence 4

rs1396407521 · CCL11

Risk-Allele Phenotype

CCL11 rs1396407521 — associated with increased risk of inherited susceptibility to asthma in carriers of the risk allele.

Reference-Allele Phenotype

Normal CCL11 function at this locus, with no identified increased genetic risk for asthma susceptibility at this position.

Evidence Level

4 — Preliminary See methodology for how we grade evidence.

Cross-References

dbSNP — rs1396407521
ClinVar — search rs1396407521
NCBI Gene — CCL11

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.

Want to know your status at rs1396407521?

Upload your DNA file — Atlagene checks this variant and 700+ others across 21 health categories.

Get Started Free