Casandra
Casandra Test Code QD79758Version 1 (DRAFT)
Performing Lab
Cystic Fibrosis Complete Rare Variant Analysis, Entire Gene Sequence
Also known as: CF Complete™, CF Rare Mutation Analysis, CF Sequencing, CFTR Gene Sequencing, Cystic Fibrosis Entire Gene Sequencing
Clinical Use
Order TestUse
This test is appropriate when there is a strong likelihood of cystic fibrosis and the variant is not detected in the general cystic fibrosis variant panel and familial variants are unknown.
Special Instructions
Not provided.
Limitations
Not provided.
Test Details
Methodology
NGS
Biomarkers
CFTR
GeneSNV/Indel • Mutation • Categorical (e.g., Positive / Negative / Indeterminate)
LOINC Codes
Order Codes
- 21654-9
Result Turnaround Time
Not provided.
Related Documents
For more information, please review the documents below
Specimen Requirements
Specimen
Whole Blood
Volume
Not provided
Minimum Volume
Not provided