CFTR FULL GENE SEQUENCING, EDTA BLOOD
A genetic test that screens for a range of mutations in the CFTR gene, helping diagnose cystic fibrosis and assess the severity of the condition.
Also known asCystic Fibrosis Extended Mutation Panel Cystic Fibrosis Extended Mutation Panel
Test details
CFTR FULL GENE SEQUENCING, EDTA BLOOD Test in Mangaluru Overview
Preparations
No special preparations needed
Test included
CFTR FULL GENE SEQUENCING, EDTA BLOOD includes 1 parameter
- Cftr Gene Mutations
Frequently Asked Questions
This genetic test screens for multiple CFTR gene mutations that cause cystic fibrosis (CF).
- Individuals with CF symptoms
- Couples planning pregnancy (carrier screening)
- Positive – Presence of CF mutation
- Carrier – One mutated gene, no symptoms
- Negative – No detected mutations (but rare variants may exist)
There is no cure, but targeted therapies help manage symptoms.
Test code
RD1460
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 2 ml |
Specimen stability information
Edta Whole Blood
Collection instructions
Clinical History
Specimen rejection criteria
Test run frequency
Every Day TIME - 10:30
Turn around time
28 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
CFTR FULL GENE SEQUENCING, EDTA BLOOD
Package price
₹32000
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₹32000