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DNA Labs India

SDHAF2 Gene Pheochromocytoma type 5 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

SDHAF2 Gene Pheochromocytoma type 5 NGS Genetic Test

Short Name: SDHAF2 Gene Test

Also known as: SDHAF2 Mutation Test, Pheochromocytoma Type 5 Genetic Test, SDHAF2 Gene Analysis

SDHAF2 Gene Pheochromocytoma type 5 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.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to identify mutations in the SDHAF2 gene for early detection and management of Pheochromocytoma Type 5, facilitating genetic counseling, family screening, and personalized therapeutic interventions.

Test Code
2924
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. Genetic counseling is recommended prior to testing.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm using standard venipuncture techniques.

Step 3

Report Delivery

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

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Understand the test implications through genetic counseling. No fasting required.
2
During the Test:Blood sample collection takes about 10-15 minutes. The process is minimally invasive.
3
After the Test:Results will be available online in 3-4 weeks. Follow-up with a healthcare provider for interpretation.

About This Test

Who Should Get This Test

The purpose of this test is to identify mutations in the SDHAF2 gene for early detection and management of Pheochromocytoma Type 5, facilitating genetic counseling, family screening, and personalized therapeutic interventions.

How to Prepare

  • Ensure proper identification of the patient
  • Use sterile collection equipment
  • Label samples correctly
  • Transport samples at ambient temperature

Doctor's Notes

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

"Early genetic testing for SDHAF2 mutations can guide personalized management and family screening for hereditary pheochromocytoma."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 mL blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture

Sample Stability

Blood samples stable for 7 days at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient sample volume
  • Improper labeling

Understanding Your Results

Results indicate the presence or absence of mutations in the SDHAF2 gene. Positive results suggest a genetic predisposition to Pheochromocytoma Type 5, while negative results may not entirely rule out risk due to other genetic factors.
📊

Positive

Pathogenic mutation detected; increased risk for Pheochromocytoma Type 5. Genetic counseling and further clinical evaluation recommended.

📊

Negative

No pathogenic mutation detected; risk may be lower but not eliminated. Clinical correlation advised.

📊

Variant of Uncertain Significance

Genetic variant found but significance unknown; may require additional testing or family studies.

⚠️ When to Consult a Doctor:

Consult a doctor if you have a family history of pheochromocytoma, experience symptoms like hypertension or palpitations, or receive a positive test result for further management.

Limitations

  • May not detect all genetic variants
  • Requires genetic counseling for interpretation
  • Not a standalone diagnostic tool; clinical correlation needed

Risks & Considerations

  • Minor bruising or discomfort at the blood draw site
  • Rare risk of infection
  • Psychological impact of genetic results

Interfering Factors

  • Poor sample quality
  • Contamination during collection
  • Recent blood transfusions

Compare With Similar Tests

TestSDHAF2 Gene Pheochromocytoma type 5 NGS Genetic TestSDHB Gene TestSDHC Gene TestPheochromocytoma Panel Test
ComparisonSDHAF2 Gene Pheochromocytoma type 5 NGS Genetic TestTests for mutations in SDHB gene, associated with similar adrenal tumors.Focuses on SDHC gene mutations linked to paragangliomas.Comprehensive panel testing multiple genes related to pheochromocytoma.

Frequently Asked Questions

What is the SDHAF2 Gene Pheochromocytoma Type 5 NGS Genetic Test?
It is a genetic test that uses Next Generation Sequencing to detect mutations in the SDHAF2 gene, associated with Pheochromocytoma Type 5, a rare adrenal tumor.
Who should consider this test?
Individuals with a family history of pheochromocytoma, symptoms like hypertension or palpitations, or those diagnosed with adrenal tumors.
What are the symptoms of Pheochromocytoma Type 5?
Symptoms include high blood pressure, headaches, heart palpitations, sweating, anxiety, and tremors, which may occur suddenly.
How is the test performed?
A blood sample or extracted DNA is collected and analyzed using NGS technology to identify mutations in the SDHAF2 gene.
What is the cost of the test?
The cost at DNA Labs India is INR 20,000, with free home sample collection available across India.
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 online bookings in numerous cities across India.
What does a positive result mean?
A positive result indicates a pathogenic mutation in the SDHAF2 gene, increasing the risk for Pheochromocytoma Type 5. Genetic counseling is recommended.
What are the risks of the test?
Risks are minimal, including minor bruising from blood draw. Psychological impact of results may occur, so counseling is advised.
How accurate is the test?
The test uses advanced NGS technology for high accuracy, but no genetic test is 100% definitive. Clinical correlation is important.
Can the test be used for prenatal diagnosis?
This test is not typically used for prenatal diagnosis; consult a genetic counselor for prenatal testing options.
What should I do after receiving the results?
Discuss results with a healthcare provider or genetic counselor for appropriate management, family screening, and follow-up care.
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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