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

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

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
SpecimenVacutainerVolume
Edta Whole BloodLavender Vacutainer2 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

32000