CFTR Single Gene
Sequence variants and/or copy number variants (deletions/duplications) within the CFTR gene will be detected with >99% sensitivity. Variants classified as unknown significance (VUS), likely pathogenic, or pathogenic will be reported. Benign and likely benign variants are generally not reported. Reflex to clinical exome ("All-in-One") and whole exome ("Whole-in-One") is available by request.
|CPT Code||81220, 81221, 81222, 81223|