FANCF Gene Fanconi anemia type F NGS Genetic Test
Also known as: FANCF Gene Mutation Analysis, Fanconi Anemia Type F Genetic Test
FANCF Gene Fanconi anemia type F NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The primary purpose of the FANCF Gene Fanconi Anemia Type F NGS Genetic Test is to detect mutations in the FANCF gene that lead to Fanconi anemia type F. This helps in confirming the diagnosis, assessing carrier status, and informing treatment and management plans.
- Test Code
- 4679
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No specific preparation required, but genetic counseling is recommended.
Method: Blood Draw or DNA Extraction
Laboratory Analysis
Blood sample will be drawn by a trained phlebotomist.
Report Delivery
Apply pressure to the puncture site to prevent bleeding.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
The primary purpose of the FANCF Gene Fanconi Anemia Type F NGS Genetic Test is to detect mutations in the FANCF gene that lead to Fanconi anemia type F. This helps in confirming the diagnosis, assessing carrier status, and informing treatment and management plans.
How to Prepare
- Ensure proper identification of the patient
- Use sterile equipment
- Label samples correctly
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Early genetic testing for FANCF mutations is crucial for timely diagnosis and management of Fanconi anemia type F, especially in families with a history of the disorder."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
- Hemolyzed sample
- Insufficient sample volume
- Incorrect sample type
Understanding Your Results
Pathogenic mutation detected
Confirms diagnosis of Fanconi anemia type F
No pathogenic mutation detected
Fanconi anemia type F is less likely, but clinical correlation is needed
Variant of uncertain significance
Further testing or family studies may be required
If you have symptoms of Fanconi anemia or a family history, consult a geneticist or hematologist for evaluation and testing.
Limitations
- ⚠May not detect all types of mutations
- ⚠Results require interpretation by a geneticist
- ⚠Does not rule out other genetic disorders
Risks & Considerations
- ●Minimal risk from blood draw
- ●Potential for psychological impact from results
Interfering Factors
- ●Poor sample quality
- ●Contamination during processing
- ●Technical errors in sequencing
Compare With Similar Tests
| Test | FANCF Gene Fanconi anemia type F NGS Genetic Test | FANCA Gene Test | Chromosomal Breakage Test |
|---|---|---|---|
| Comparison | FANCF Gene Fanconi anemia type F NGS Genetic Test |
Frequently Asked Questions
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