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PRKAG2 Gene Cardiomyopathy, familial hypertrophic type 6 NGS Genetic Test

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PRKAG2 Gene Cardiomyopathy, familial hypertrophic type 6 NGS Genetic Test

Also known as: Familial hypertrophic cardiomyopathy type 6, FHC6, PRKAG2-related cardiomyopathy

PRKAG2 Gene Cardiomyopathy, familial hypertrophic type 6 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 Pasupathy Arumugam

Dr Pasupathy Arumugam

Consultant Pathologist · Reg: 21521

Last reviewed: September 7, 2026

Overview

To detect mutations in the PRKAG2 gene associated with familial hypertrophic cardiomyopathy type 6 for diagnosis, risk assessment, and family planning.

Test Code
5233
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.

Step 2

Laboratory Analysis

Blood sample collected by a trained phlebotomist.

Step 3

Report Delivery

Sample sent to laboratory for analysis. Reports available in 3-4 weeks.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling and informed consent required.
2
During the Test:Blood sample collection.
3
After the Test:Sample processing and analysis. Report generation.

About This Test

Who Should Get This Test

To detect mutations in the PRKAG2 gene associated with familial hypertrophic cardiomyopathy type 6 for diagnosis, risk assessment, and family planning.

How to Prepare

  • Fast for 8-12 hours if required, but not specified for this test.
  • Bring identification and prescription if available.

Doctor's Notes

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

"As a physician, I recommend genetic testing for individuals with a family history of cardiomyopathy to enable early intervention and informed family planning."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Room temperature
Refrigerated
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient sample volume
  • Improperly labeled sample

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the PRKAG2 gene.
📊

No pathogenic variant detected

Low risk for PRKAG2-related cardiomyopathy, but clinical correlation advised.

📊

Pathogenic variant detected

Diagnosis of PRKAG2 gene cardiomyopathy confirmed. Genetic counseling and cardiac monitoring recommended.

⚠️ When to Consult a Doctor:

If you have symptoms of cardiomyopathy or a family history of the condition, consult a cardiologist or geneticist.

Limitations

  • ⚠This test only detects mutations in the PRKAG2 gene; other genes associated with cardiomyopathy are not covered.
  • ⚠Results should be interpreted in conjunction with clinical findings and family history.

Risks & Considerations

  • ●Minimal risk from blood draw: bruising, infection.
  • ●Psychological impact of genetic results.

Compare With Similar Tests

TestPRKAG2 Gene Cardiomyopathy, familial hypertrophic type 6 NGS Genetic TestEchocardiogramECG
ComparisonPRKAG2 Gene Cardiomyopathy, familial hypertrophic type 6 NGS Genetic TestImaging test for heart structure, not genetic.Records electrical activity, not specific for genetic mutations.

Frequently Asked Questions

What is PRKAG2 gene cardiomyopathy?
PRKAG2 gene cardiomyopathy is a rare form of familial hypertrophic cardiomyopathy caused by mutations in the PRKAG2 gene, leading to heart muscle abnormalities.
How is the NGS genetic test performed?
The test uses next-generation sequencing to analyze the PRKAG2 gene from a blood or DNA sample.
What is the cost of the test in India?
The test costs INR 20000 at DNA Labs India.
Is home sample collection available?
Yes, free home collection is available for online bookings across India.
How long does it take to get the results?
Reports are typically available in 3 to 4 weeks.
What do the test results mean?
Results indicate whether pathogenic mutations in the PRKAG2 gene are detected, which can confirm diagnosis or assess risk.
Is genetic counseling recommended?
Yes, genetic counseling is advised before and after testing to understand implications and for family planning.
Can this test be used for prenatal diagnosis?
It may be used in certain cases, but consultation with a geneticist is necessary.
Are there any risks associated with the test?
The test involves a blood draw, which has minimal risks like bruising. Psychological impact of results should be considered.
How accurate is the NGS test?
NGS is highly accurate for detecting gene mutations, but results should be correlated with clinical findings.
What should I do if I test positive?
Consult a cardiologist for management and consider family screening.
Is the test covered by insurance?
Coverage depends on your insurance plan; check with your provider.
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

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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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