FANCL Gene Fanconi anemia type L NGS Genetic Test
Short Name: FANCL Gene Fanconi Anemia Type L Test
Also known as: FANCL Gene Sequencing, Fanconi Anemia Type L NGS Test, FANCL Mutation Analysis
FANCL Gene Fanconi anemia type L NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS, Next-Generation Sequencing on Blood, Extracted DNA, or One drop Blood on FTA Card samples. Results in 3-4 weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To diagnose Fanconi anemia type L by detecting mutations in the FANCL gene using advanced NGS technology, aiding in clinical management and genetic counseling.
- Test Code
- 1982
- Price
- ₹20,000
- Sample Type
- Blood, Extracted DNA, or One drop Blood on FTA Card
- Result Time
- 3-4 weeks
- Fasting Required
- No
- Method
- NGS, Next-Generation Sequencing
Sample Collection
Provide clinical history and undergo genetic counseling to draw a pedigree chart of family members affected with Fanconi anemia type L.
Method: Venipuncture or FTA Card
Laboratory Analysis
Standard blood draw or FTA card collection procedures performed by a trained phlebotomist.
Report Delivery
Sample is processed in the lab for DNA extraction and NGS analysis. Handle with care to avoid contamination.
Timeline: 3-4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose Fanconi anemia type L by detecting mutations in the FANCL gene using advanced NGS technology, aiding in clinical management and genetic counseling.
How to Prepare
- Blood sample to be collected in EDTA tube
- FTA card blood drop should be air-dried before packaging
- Label samples accurately with patient details
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is essential for early diagnosis and management of Fanconi anemia type L, particularly in families with a history of the disorder or presenting symptoms like bone marrow failure or physical abnormalities."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Positive (Pathogenic mutation detected)
Confirms diagnosis of Fanconi anemia type L. Clinical correlation and genetic counseling recommended.
Negative (No mutation detected)
No pathogenic variants identified in the FANCL gene. Does not completely rule out Fanconi anemia if other genes are involved.
Variant of Uncertain Significance (VUS)
A variant was detected but its clinical significance is unclear. Further testing or family studies may be needed.
If experiencing symptoms such as persistent fatigue, frequent infections, or physical abnormalities, or if there is a family history of Fanconi anemia, consult a healthcare provider for evaluation and possible testing.
Limitations
- ⚠May not detect all possible variants or mosaicism
- ⚠Requires high-quality DNA sample for accurate results
Risks & Considerations
- ●Minor bruising or pain at the puncture site
- ●Rare risk of infection or dizziness during blood draw
Frequently Asked Questions
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Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
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✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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