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FANCL Gene Fanconi anemia type L NGS Genetic Test

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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.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

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
Step 1

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

Step 2

Laboratory Analysis

Standard blood draw or FTA card collection procedures performed by a trained phlebotomist.

Step 3

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

1
Before the Test:Genetic counseling session to discuss test implications and family history.
2
During the Test:Sample collection via blood draw or FTA card.
3
After the Test:Wait for results (3-4 weeks) and follow up with genetic counselor or physician for interpretation.

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 — 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

Sample TypeBlood, Extracted DNA, or One drop Blood on FTA Card
Collection MethodVenipuncture or FTA Card

Understanding Your Results

Results indicate the presence or absence of mutations in the FANCL gene. Interpretation should be done in conjunction with clinical findings and family history.
📊

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.

⚠️ When to Consult a Doctor:

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

What is a FANCL Gene Fanconi Anemia Type L NGS Genetic Test?
It is a genetic test that uses next-generation sequencing to analyze the FANCL gene for mutations causing Fanconi anemia type L, a rare bone marrow disorder.
What are the symptoms of Fanconi anemia type L?
Symptoms include fatigue, weakness, pale skin, slow growth, developmental delays, hand/arm abnormalities, increased infections, and higher cancer risk.
How is Fanconi anemia type L diagnosed?
Diagnosis involves physical examination, blood tests showing low cell counts, and genetic testing like the FANCL NGS test to confirm mutations.
What is the cost of the FANCL gene test?
The test costs INR 20000 at DNA Labs India, with free home sample collection available across India.
Is the test covered by insurance?
Coverage varies by insurance plan. It is advisable to check with your provider directly.
What sample is required for the test?
Blood, extracted DNA, or a blood drop on an FTA card can be used.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in numerous cities across India.
Who should consider getting this test?
Individuals with symptoms of Fanconi anemia, family history of the disorder, or those undergoing genetic counseling for related conditions.
What is NGS technology?
Next-generation sequencing (NGS) is an advanced method for analyzing DNA sequences, allowing for detailed detection of genetic mutations.
Are there any risks associated with the test?
The test involves minimal risks from blood draw, such as bruising or rare infection, but no significant health risks.
How should I prepare for the test?
Provide clinical history and undergo genetic counseling. No fasting is required, but ensure accurate sample labeling.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

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