Type
Blood Testing
Duration
15 min
Sample
Blood (venous)
What's included
3 deliverables in this treatment
- Venous blood draw (1 × EDTA)
- Targeted sequencing of 139 CFTR mutations
- Result report with variant interpretation and brief consultation
A genetic screen that checks for 139 common mutations causing cystic fibrosis using a single venous blood draw in an EDTA tube.
About this treatment
The Cystic Fibrosis panel screens for 139 well‑characterized CFTR gene mutations from a venous blood sample (1 × EDTA tube). By detecting carrier status or disease‑causing variants, the test may support family planning and early clinical management. The package provides the blood draw, laboratory sequencing of the targeted mutations, and a clear report outlining any identified variants, together with a short consultation to discuss implications. Ideal for individuals with a family history of cystic fibrosis or those considering carrier testing.
Good to know
- Sample
- Blood (venous) – 1 × EDTA
- Markers
- 139 CFTR mutations
Who is this for?
People with a family history of cystic fibrosis or couples planning pregnancy
About the clinic
Reviews, team and credentials
Independent review links and clinic-reported team information.
2,261 clinic reviews
From independent platforms
Treatment highlights
- Venous blood draw (1 × EDTA)
- Targeted sequencing of 139 CFTR mutations
+1 more item in What's included
1xEDTA. Genetic screen.