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FANCF Gene Fanconi anemia type F NGS Genetic Test

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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.

Next-Generation Sequencing (NGS)All Ages🏠 Home Collection

🩺 Medically Reviewed By

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)
Step 1

Sample Collection

No specific preparation required, but genetic counseling is recommended.

Method: Blood Draw or DNA Extraction

Step 2

Laboratory Analysis

Blood sample will be drawn by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling to discuss implications and family history.
2
During the Test:Blood sample collection for DNA extraction and sequencing.
3
After the Test:Results will be available in 3-4 weeks, followed by genetic counseling.

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 — 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

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodBlood Draw or DNA Extraction
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient sample volume
  • Incorrect sample type

Understanding Your Results

Interpretation of the FANCF Gene Fanconi Anemia Type F NGS Genetic Test results should be done by a qualified geneticist or healthcare provider.
📊

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

⚠️ When to Consult a Doctor:

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

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ComparisonFANCF Gene Fanconi anemia type F NGS Genetic Test

Frequently Asked Questions

What is the FANCF Gene Fanconi Anemia Type F NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to identify mutations in the FANCF gene, which cause Fanconi anemia type F.
Who should take this test?
Individuals with symptoms of Fanconi anemia, a family history of the disorder, or those seeking genetic counseling for carrier status.
What are the symptoms of Fanconi anemia type F?
Symptoms include abnormal skin pigmentation, short stature, bone abnormalities, and increased risk of cancer like leukemia.
How is the test performed?
A blood sample is collected, DNA is extracted, and the FANCF gene is analyzed using NGS technology.
What is the cost of the test?
The test costs INR 20000 at DNA Labs India, including testing, analysis, and genetic counseling.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What do the results mean?
Results indicate the presence or absence of FANCF gene mutations, which help confirm or rule out Fanconi anemia type F.
Is genetic counseling included?
Yes, genetic counseling is included in the test cost to help interpret results and discuss implications.
Can this test detect carrier status?
Yes, it can identify carriers of FANCF mutations, which is important for family planning.
What are the risks of the test?
Risks are minimal, primarily related to blood draw, but results may have psychological impacts.
How accurate is the test?
The test is highly accurate for detecting known FANCF mutations, but interpretation should be done by a geneticist.
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 Data Privacy

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.

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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