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MUTYH Gene Familial adenomatous polyposis type 2 NGS Genetic Test

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MUTYH Gene Familial adenomatous polyposis type 2 NGS Genetic Test

Short Name: MUTYH Gene FAP Type 2 NGS Test

Also known as: Familial Adenomatous Polyposis Type 2, MUTYH-associated polyposis, FAP Type 2

MUTYH Gene Familial adenomatous polyposis type 2 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS, Next-Generation Sequencing on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in Results are typically available within 3 to 4 weeks after sample collection.. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the MUTYH Gene FAP Type 2 NGS Genetic Test is to identify pathogenic mutations in the MUTYH gene, enabling early diagnosis of Familial Adenomatous Polyposis Type 2. This facilitates proactive medical management, including regular screening, preventive measures, and informed decision-making to reduce the risk of colorectal cancer.

Test Code
2872
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Results are typically available within 3 to 4 weeks after sample collection.
Fasting Required
No
Method
NGS, Next-Generation Sequencing
Step 1

Sample Collection

No specific preparation is required. Ensure to provide accurate clinical and family history information.

Method: Blood draw or saliva sample

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm, or a saliva sample may be collected using a kit. For FTA card, a drop of blood is applied.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Resume normal activities unless advised otherwise.

Timeline: Results are typically available within 3 to 4 weeks after sample collection.

Patient Instructions

1
Before the Test:Consult with a genetic counselor or doctor to discuss the test's implications, benefits, and limitations. Provide detailed family medical history.
2
During the Test:The test involves a simple blood draw or saliva sample collection. The process is quick and minimally invasive.
3
After the Test:Wait for results as per the turnaround time. Discuss findings with a healthcare provider to understand next steps, including screening or treatment options.

About This Test

Who Should Get This Test

The purpose of the MUTYH Gene FAP Type 2 NGS Genetic Test is to identify pathogenic mutations in the MUTYH gene, enabling early diagnosis of Familial Adenomatous Polyposis Type 2. This facilitates proactive medical management, including regular screening, preventive measures, and informed decision-making to reduce the risk of colorectal cancer.

How to Prepare

  • Bring a valid ID and doctor's prescription if available
  • Inform the phlebotomist of any bleeding disorders or medications
  • For saliva collection, avoid eating or drinking 30 minutes prior

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Genetic testing for MUTYH mutations is essential for individuals with a family history of FAP type 2 to guide personalized screening, surveillance, and preventive strategies to reduce cancer risk."

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 saliva sample

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results from the MUTYH Gene FAP Type 2 NGS Genetic Test indicate the presence or absence of mutations in the MUTYH gene. A positive result confirms a genetic predisposition to FAP type 2, while a negative result suggests no detected mutations, though clinical correlation is essential.
📊

Pathogenic mutation detected in the MUTYH gene, confirming diagnosis of FAP type 2. Increased risk for colorectal cancer. Recommend genetic counseling, regular colonoscopies, and possible surgical consultation.

Result type: Positive

📊

No pathogenic mutations detected. However, clinical symptoms may warrant further evaluation. Does not entirely rule out FAP type 2 if strong family history exists.

Result type: Negative

📊

A genetic variant was found, but its clinical significance is unknown. Requires periodic re-evaluation and genetic counseling.

Result type: Variant of Uncertain Significance (VUS)

⚠️ When to Consult a Doctor:

Consult a doctor immediately if you test positive for a MUTYH mutation, have symptoms of FAP type 2, or have a family history of the condition. Regular follow-ups are crucial for monitoring and management.

Limitations

  • May not detect all types of MUTYH gene mutations, such as large deletions or duplications
  • Results require interpretation by a genetic counselor or healthcare provider
  • False negatives are possible but rare with NGS technology
  • Does not replace clinical evaluation or other diagnostic tests like colonoscopy

Risks & Considerations

  • Minimal risks from blood draw, such as bruising or infection at the puncture site
  • Psychological impact of genetic results, addressed through counseling
  • No significant risks from saliva collection

Interfering Factors

  • Sample contamination or degradation
  • Insufficient DNA quantity or quality
  • Recent blood transfusions may affect results
  • Technical errors in sequencing or analysis

Compare With Similar Tests

TestMUTYH Gene Familial adenomatous polyposis type 2 NGS Genetic TestAPC Gene Test for FAP Type 1Comprehensive Colorectal Cancer PanelColonoscopy Screening
ComparisonMUTYH Gene Familial adenomatous polyposis type 2 NGS Genetic TestDetects mutations in the APC gene, which causes FAP type 1. MUTYH test is specific for FAP type 2, an autosomal recessive condition.Includes multiple genes associated with hereditary colorectal cancer, providing broader analysis but at higher cost.A diagnostic procedure to visualize polyps, not a genetic test. Genetic testing identifies underlying mutations for risk assessment.

Frequently Asked Questions

What is the MUTYH Gene FAP Type 2 NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the MUTYH gene, which causes Familial Adenomatous Polyposis Type 2, a condition increasing colorectal cancer risk.
Who should consider this test?
Individuals with a family history of FAP type 2, symptoms like abdominal pain or rectal bleeding, or those with multiple colorectal polyps should consider this test.
How is the test performed?
The test requires a blood or saliva sample, which is analyzed in a laboratory using NGS technology to identify MUTYH gene mutations.
What does a positive result mean?
A positive result indicates a pathogenic mutation in the MUTYH gene, confirming FAP type 2 diagnosis and increased cancer risk, necessitating regular screening and possible intervention.
What if the test is negative?
A negative result means no mutations were detected, but clinical symptoms may require further evaluation. It does not completely rule out FAP type 2 if family history is strong.
How accurate is the NGS Genetic Test?
NGS technology is highly accurate for detecting mutations, but no test is 100% foolproof. Results should be interpreted by a genetic counselor.
What is the cost of the test?
The test costs INR 20,000, which includes sample collection, analysis, and report delivery. Home collection is available across India.
Is the test covered by insurance?
Some insurance plans may cover genetic testing, but it is not guaranteed. Check with your provider for specific coverage details.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Are there any risks associated with the test?
The test involves minimal risks from blood draw, such as bruising. Psychological impacts are managed through genetic counseling.
Can I get home sample collection?
Yes, DNA Labs India offers free home sample collection for online bookings across numerous cities in India.
What should I do after receiving results?
Discuss results with a healthcare provider or genetic counselor to understand implications, plan screening, and consider treatment options if necessary.
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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