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SDHC Gene Pheochromocytoma type 3 NGS Genetic Test

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SDHC Gene Pheochromocytoma type 3 NGS Genetic Test

Short Name: SDHC Gene Pheochromocytoma Test

Also known as: SDHC Gene Mutation Test, Pheochromocytoma Type 3 Genetic Test

SDHC Gene Pheochromocytoma type 3 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

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

To identify mutations in the SDHC gene for the diagnosis and risk assessment of Pheochromocytoma type 3.

Test Code
2925
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

Genetic counseling recommended. Provide clinical history and family pedigree.

Method: Venipuncture

Step 2

Laboratory Analysis

Blood sample collected via venipuncture in a sterile environment.

Step 3

Report Delivery

Apply pressure to the puncture site. Sample sent to lab for analysis.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling session to discuss test implications and draw family pedigree.
2
During the Test:Blood sample collection via venipuncture.
3
After the Test:Wait for report in 3-4 weeks. Discuss results with genetic counselor or physician.

About This Test

Who Should Get This Test

To identify mutations in the SDHC gene for the diagnosis and risk assessment of Pheochromocytoma type 3.

How to Prepare

  • No fasting required for this test
  • Avoid strenuous activity before sample collection
  • Ensure proper labeling of the sample

Doctor's Notes

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

"Genetic testing for SDHC mutations is crucial for identifying individuals at risk of Pheochromocytoma type 3, enabling proactive management and family screening."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture

Sample Stability

Blood sample stable at room temperature for 24 hours
Extracted DNA stable at -20°C for long-term storage
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results indicate the presence or absence of mutations in the SDHC gene, which are linked to Pheochromocytoma type 3.
📊

No mutation detected

Low risk for Pheochromocytoma type 3, but clinical correlation advised. Continue monitoring if symptoms persist.

📊

Mutation detected

Increased risk for Pheochromocytoma type 3. Further clinical evaluation, genetic counseling, and family screening recommended.

⚠️ When to Consult a Doctor:

If you have symptoms of pheochromocytoma, a family history of the condition, or are diagnosed with an adrenal tumor, consult a doctor for genetic testing.

Limitations

  • ⚠May not detect all types of mutations, such as large deletions
  • ⚠Results should be correlated with clinical findings and family history

Risks & Considerations

  • ●Minor bruising at puncture site
  • ●Rare infection risk
  • ●Emotional impact of results

Interfering Factors

  • ●Hemolyzed samples
  • ●Contaminated DNA
  • ●Recent blood transfusions

Frequently Asked Questions

What is the SDHC Gene Pheochromocytoma type 3 NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the SDHC gene, which are associated with Pheochromocytoma type 3, a rare adrenal cancer.
What is the cost of this test in India?
The cost is INR 20,000 at DNA Labs India, with free home sample collection available across many cities.
How is the test performed?
The test requires a blood sample, which is collected via venipuncture and analyzed using NGS technology to identify SDHC gene mutations.
What are the symptoms of Pheochromocytoma type 3?
Symptoms include high blood pressure, headaches, sweating, heart palpitations, anxiety, weight loss, and abdominal pain due to excess hormone production.
Who should get this test?
Individuals with a family history of pheochromocytoma, symptoms of the condition, or those diagnosed with adrenal tumors should consider this test.
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 across India.
What does a positive result mean?
A positive result indicates a mutation in the SDHC gene, increasing the risk for Pheochromocytoma type 3. Genetic counseling and further evaluation are recommended.
What are the risks of the test?
Risks are minimal and include minor bruising at the puncture site and rare infection risk.
Is genetic counseling required?
Genetic counseling is recommended before and after testing to understand the implications of results and for family planning.
Can this test be used for family screening?
Yes, if a mutation is identified, family members can be tested to assess their risk.
What other tests are related to pheochromocytoma?
Related tests include SDHB, SDHD, VHL, RET, and NF1 gene tests, which are also associated with hereditary cancer syndromes.
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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For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

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