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Gut HealthpancreaticEvidence 3Physician review
rs113993960 · CFTR
Risk-Allele Phenotype
CFTR rs113993960 — classified as pathogenic; associated with Cystic fibrosis. This variant has been identified as disease-causing with clinical evidence supporting its pathogenicity.
Reference-Allele Phenotype
Normal CFTR function at this locus, with no elevated genetic risk contribution to Cystic fibrosis from this variant.
Evidence Level
3 — Limited — 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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