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FANCM Gene Fanconi anemia type M NGS Genetic Test

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FANCM Gene Fanconi anemia type M NGS Genetic Test

Short Name: FANCM Gene Test

Also known as: Fanconi Anemia Complementation Group M, FANCM Mutation Test, FANCM Gene Analysis

FANCM Gene Fanconi anemia type M 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 Reports available in 3 to 4 weeks via online portal, email, or WhatsApp.. Free home collection in 300+ cities across India.

Next-Generation Sequencing (NGS)All ages, typically diagnosed in childhood🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Fanconi anemia type M by identifying pathogenic mutations in the FANCM gene using NGS technology. This test helps in early detection, risk assessment, and management planning for affected individuals and their families.

Test Code
1987
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Reports available in 3 to 4 weeks via online portal, email, or WhatsApp.
Fasting Required
Yes
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Provide detailed clinical history and family pedigree as part of genetic counseling.

Method: Venipuncture for blood or saliva swab

Step 2

Laboratory Analysis

Sample collection follows standard phlebotomy or saliva collection protocols.

Step 3

Report Delivery

Apply pressure to the puncture site if blood drawn. Store samples as instructed for transport.

Timeline: Reports available in 3 to 4 weeks via online portal, email, or WhatsApp.

Patient Instructions

1
Before the Test:Genetic counseling and informed consent are required prior to testing.
2
During the Test:Sample collection as per standard procedures; no special preparation needed during the test.
3
After the Test:Follow-up with healthcare provider to discuss results and implications.

About This Test

Who Should Get This Test

To diagnose Fanconi anemia type M by identifying pathogenic mutations in the FANCM gene using NGS technology. This test helps in early detection, risk assessment, and management planning for affected individuals and their families.

How to Prepare

  • Use sterile collection tubes
  • Label samples with patient details
  • Transport at ambient temperature (15-30°C)
  • Avoid hemolysis during blood draw

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Genetic testing for FANCM mutations is crucial for early diagnosis and management of Fanconi anemia type M. I recommend this test for families with a history of the disorder or individuals showing symptoms like bone marrow failure or developmental delays."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required
ContainerSterile blood collection tube or FTA card
Collection MethodVenipuncture for blood or saliva swab

Sample Stability

Blood: Store at 2-8°C for up to 24 hours
DNA: Stable at -20°C for long-term storage
FTA card: Room temperature for extended periods
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient volume
  • Improperly labeled or contaminated samples
  • Expired sample stability

Understanding Your Results

Results from the FANCM Gene Test are interpreted in the context of clinical findings, family history, and other diagnostic tests.
📊

Negative for FANCM mutations associated with Fanconi anemia type M; clinical correlation advised

📊

Confirms diagnosis of Fanconi anemia type M; genetic counseling recommended for family members

📊

Further testing, family studies, or functional assays may be needed for classification

⚠️ When to Consult a Doctor:

If symptoms of Fanconi anemia (e.g., bone marrow failure, developmental delays) are present or if there is a family history of the disorder, consult a geneticist or hematologist promptly.

Limitations

  • May not detect all types of genetic variants
  • Variants of uncertain significance (VUS) may be reported
  • Does not rule out other genetic conditions or environmental factors

Risks & Considerations

  • Minimal risk from blood draw (e.g., bruising, infection)
  • Emotional impact of genetic results on patients and families

Interfering Factors

  • Inadequate sample quality
  • Hemolyzed blood samples
  • DNA degradation
  • Technical errors during sequencing

Compare With Similar Tests

TestFANCM Gene Fanconi anemia type M NGS Genetic TestFANCA Gene TestChromosomal Breakage TestWhole Exome Sequencing
ComparisonFANCM Gene Fanconi anemia type M NGS Genetic TestTargets a different gene for Fanconi anemia types A, the most common formFunctional assay for Fanconi anemia, not gene-specificBroader genetic analysis, may identify other causes of similar symptoms

Frequently Asked Questions

What is Fanconi anemia type M?
Fanconi anemia type M is a rare genetic disorder caused by mutations in the FANCM gene, leading to impaired DNA repair and symptoms like bone marrow failure and increased cancer risk.
What causes Fanconi anemia type M?
It is caused by pathogenic mutations in the FANCM gene, inherited in an autosomal recessive pattern.
How is Fanconi anemia type M diagnosed?
Diagnosis involves genetic testing, such as the FANCM Gene NGS Test, along with clinical evaluation and family history analysis.
What does the FANCM Gene Test involve?
The test uses Next-Generation Sequencing to analyze the FANCM gene for mutations from a blood or saliva sample.
What are the symptoms of Fanconi anemia type M?
Symptoms include bone marrow failure, developmental delays, abnormal skin pigmentation, and a higher risk of cancers like leukemia.
How accurate is the NGS Genetic Test?
NGS is highly accurate for detecting mutations, but clinical correlation is essential for interpretation.
What is the cost of the test?
The FANCM Gene Fanconi Anemia Type M NGS Genetic Test costs INR 20,000, which includes sample collection and counseling.
Is home sample collection available?
Yes, free home sample collection is offered across India for online bookings.
How long does it take to get results?
Reports are typically available in 3 to 4 weeks after sample collection.
Who should get this test?
Individuals with symptoms of Fanconi anemia, a family history of the disorder, or those undergoing genetic counseling.
What is the difference between NGS and other genetic tests?
NGS allows simultaneous analysis of multiple genes with high sensitivity, while other tests like Sanger sequencing focus on single genes.
Can this test be used for prenatal diagnosis?
Prenatal testing may be possible if a familial mutation is known, but consult a genetic counselor for options.
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.

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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