HNPCC/ LYNCH SYNDROME GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited   
This test analyzes multiple genes associated with Hereditary Non-Polyposis Colorectal Cancer (HNPCC), also known as Lynch Syndrome, using advanced Next Generation Sequencing (NGS) technology. It helps identify genetic mutations that significantly increase the risk of colorectal, endometrial, ovarian, stomach, and other cancers. The test is essential for individuals with a strong family history of cancer or early-onset malignancies. Metropolis Healthcare offers highly accurate sequencing and genetic interpretation to support prevention planning, surveillance strategies, and personalized clinical management

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 18,000.00

Sample Type: EDTA BLOOD

Fasting Not Required


Booking Procedure:
  1. Technician from Metropolis will be assigned for a home sample collection after booking confirmation.
  2. Sample will be collected by our technician at your address at given slot.
  3. You can make the payment to the technician at the time of collection
  4. Your sample will then be transported to the nearest collection center and will be centrifuged before sending to the lab for processing.
  5. Soft copy reports will be sent to your email address within 24 to 48 hours or as per defined TAT for Tests.

Frequently Asked Questions (FAQ's):

What does the HNPCC / Lynch Syndrome Gene Panel detect?
It detects inherited mutations that increase the risk of Lynch Syndrome–related cancers.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses advanced NGS technology to analyze multiple cancer-related genes with high precision.

Who should consider taking this test?
Individuals with a family history of colorectal or endometrial cancer, early cancer onset below age 50, or multiple related cancers.

What type of sample is required?
EDTA blood collected through a routine blood draw.

Is fasting required before this test?
No fasting or special preparation is needed.

How are the results useful clinically?
They help guide cancer surveillance plans, preventive interventions, and family genetic counseling.

How long does Metropolis Healthcare take to provide the report?
Reports are generally available within 2–3 weeks due to detailed sequencing and interpretation.

Can family members also get tested if a mutation is detected?

Yes, cascade testing is recommended for close relatives to assess inherited cancer risk 

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