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SDHA Gene Cardiomyopathy, dilated type 1GG NGS Genetic Test

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SDHA Gene Cardiomyopathy, dilated type 1GG NGS Genetic Test

Short Name: SDHA Cardiomyopathy NGS Test

Also known as: SDHA-related dilated cardiomyopathy, SDHA gene mutation test, SDHA cardiomyopathy genetic analysis

SDHA Gene Cardiomyopathy, dilated type 1GG NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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 pathogenic mutations in the SDHA gene that cause dilated cardiomyopathy type 1GG. It aids in confirming diagnosis, assessing risk for family members, guiding treatment strategies, and facilitating genetic counseling for informed family planning.

Test Code
5211
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
NGS Technology
Step 1

Sample Collection

Provide clinical history and undergo genetic counseling to draw a pedigree chart. No fasting required.

Step 2

Laboratory Analysis

A blood sample will be drawn via venipuncture or a drop collected on an FTA card by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Resume normal activities immediately.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling session to discuss family history and test implications. No special preparation needed.
2
During the Test:Blood sample collection takes about 10-15 minutes. Minimal discomfort from needle prick.
3
After the Test:Resume normal activities. Results available in 3-4 weeks via online portal, email, or WhatsApp.

About This Test

Who Should Get This Test

The purpose of this test is to identify pathogenic mutations in the SDHA gene that cause dilated cardiomyopathy type 1GG. It aids in confirming diagnosis, assessing risk for family members, guiding treatment strategies, and facilitating genetic counseling for informed family planning.

How to Prepare

  • Ensure proper identification and labeling of samples
  • Use sterile equipment for blood collection
  • Store samples at recommended temperatures before transport

Doctor's Notes

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

"Genetic testing for SDHA mutations is vital for identifying hereditary cardiomyopathy risks, especially in families with a history of sudden cardiac death. Early detection allows for proactive management and genetic counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Blood samples stable for 24 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Incorrect labeling or missing patient information

Understanding Your Results

Results indicate the presence or absence of pathogenic SDHA gene mutations. Positive results suggest increased risk for dilated cardiomyopathy, while negative results reduce likelihood but do not eliminate risk entirely.
📊

Positive for pathogenic variant

Confirms genetic predisposition to SDHA cardiomyopathy. Recommend cardiac monitoring, lifestyle modifications, and family screening.

📊

Negative for pathogenic variant

No mutations detected in the SDHA gene. Clinical correlation advised if symptoms persist.

📊

Variant of uncertain significance

Further testing and family studies may be needed for clarity.

⚠️ When to Consult a Doctor:

Consult a cardiologist or genetic specialist if you experience symptoms of cardiomyopathy, have a family history of the condition, or receive a positive test result for guidance on management and family screening.

Limitations

  • May not detect all genetic variants or mutations in non-coding regions
  • Results require interpretation by a genetic counselor or specialist
  • Does not replace clinical diagnosis; must be correlated with symptoms and other tests

Risks & Considerations

  • Minor bruising or pain at blood draw site
  • Psychological stress from test results
  • Risk of misinterpretation without genetic counseling

Interfering Factors

  • Sample contamination during collection or transport
  • Degraded DNA due to improper storage
  • Recent blood transfusions may affect results

Compare With Similar Tests

TestSDHA Gene Cardiomyopathy, dilated type 1GG NGS Genetic TestCardiac MRIEchocardiogramECGComprehensive Cardiomyopathy Panel
ComparisonSDHA Gene Cardiomyopathy, dilated type 1GG NGS Genetic Test

Frequently Asked Questions

What is SDHA gene cardiomyopathy?
It is a rare inherited heart condition caused by mutations in the SDHA gene, leading to dilated cardiomyopathy and potential heart failure.
Who should consider this genetic test?
Individuals with a family history of cardiomyopathy, sudden cardiac death, or symptoms like shortness of breath and fatigue.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to detect SDHA gene mutations.
What is the cost of the test in India?
The test costs INR 20,000, with free home sample collection available across India.
Is fasting required before the test?
No, fasting is not required for this genetic test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do positive results mean?
Positive results indicate a pathogenic SDHA mutation, increasing risk for cardiomyopathy. Consult a doctor for management.
Is genetic testing covered by insurance?
Generally, genetic testing is not covered by health insurance in India. Check with your provider for specifics.
Can this test be done at home?
Yes, free home sample collection is available for online bookings in many cities across India.
What are the symptoms of SDHA cardiomyopathy?
Symptoms include shortness of breath, chest pain, fatigue, leg swelling, irregular heartbeat, and dizziness.
How accurate is the NGS genetic test?
NGS technology is highly accurate for detecting gene mutations, but results should be interpreted by a genetic specialist.
What should I do after receiving results?
Discuss results with a cardiologist or genetic counselor for personalized advice on monitoring and treatment.
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.

LIMS Integration

Your Data Privacy

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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