MYH6 Gene Cardiomyopathy, dilated type 1EE NGS Genetic Test
Short Name: MYH6 Cardiomyopathy NGS Test
Also known as: MYH6-related dilated cardiomyopathy, MYH6 gene mutation test, Cardiomyopathy genetic panel
MYH6 Gene Cardiomyopathy, dilated type 1EE 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.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of the MYH6 Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the MYH6 gene associated with dilated cardiomyopathy type 1EE. This aids in confirming diagnosis, assessing genetic risk, informing treatment decisions, and facilitating family screening to prevent complications.
- Test Code
- 5209
- 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)
Sample Collection
No specific preparation required. Provide clinical history and family pedigree during genetic counseling.
Method: Blood draw or FTA card
Laboratory Analysis
Blood sample collected via venipuncture or one drop on FTA card by trained phlebotomist.
Report Delivery
Sample labeled and transported to lab under stable conditions. Avoid hemolysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the MYH6 Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the MYH6 gene associated with dilated cardiomyopathy type 1EE. This aids in confirming diagnosis, assessing genetic risk, informing treatment decisions, and facilitating family screening to prevent complications.
How to Prepare
- Ensure proper patient identification
- Use sterile equipment for blood draw
- For FTA card, apply one drop of blood and air-dry
- Store samples at recommended temperature
- Transport to lab within specified timeframe
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Early genetic testing for MYH6 mutations can guide personalized treatment and family screening, improving outcomes in dilated cardiomyopathy."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Improper labeling or documentation
- Contaminated samples
Understanding Your Results
Pathogenic Variant Detected
Confirms genetic cause of cardiomyopathy. Recommend clinical management, family screening, and genetic counseling.
Likely Pathogenic Variant Detected
High probability of genetic association. Further clinical evaluation and family testing advised.
Variant of Uncertain Significance (VUS)
Insufficient evidence for pathogenicity. Monitor clinically and consider reanalysis with new data.
No Pathogenic Variants Detected
MYH6 mutations not identified. Consider other genetic or environmental factors. Clinical correlation recommended.
Consult a cardiologist or genetic specialist if you experience symptoms like shortness of breath, fatigue, chest pain, or have a family history of cardiomyopathy. After testing, discuss results with a healthcare provider for personalized management.
Limitations
- ⚠May not detect all genetic variants, including large deletions or duplications
- ⚠Results require clinical correlation and genetic counseling
- ⚠Variants of uncertain significance may need further investigation
Risks & Considerations
- ●Minimal physical risks from blood draw, such as bruising or infection
- ●Psychological impact of genetic results, requiring counseling support
- ●Potential for uncertain results leading to anxiety
Interfering Factors
- ●Poor sample quality or insufficient DNA
- ●Contamination during sample collection or processing
- ●Technical limitations of NGS in detecting certain variant types
Frequently Asked Questions
What is MYH6 gene cardiomyopathy?
How is the NGS Genetic Test performed?
What are the symptoms of MYH6 gene cardiomyopathy?
Who should consider this genetic test?
What is the cost of the MYH6 Gene Cardiomyopathy NGS Genetic Test?
How long does it take to get results?
Is fasting required before the test?
What sample types are accepted?
What do the test results mean?
Can this test be used for prenatal testing?
Is genetic counseling included with the test?
How accurate is the NGS Genetic Test?
Related Tests
MMC (Maternal Myopathy with Cardiomyopathy) Mutation Detection Test
₹11,500LPA Gene Coronary artery disease, susceptibility to NGS Genetic Test
₹20,000ITIH4 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test
₹20,000PPP1R17 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test
₹20,000APOA1 Gene Hypoalphalipoproteinemia NGS Genetic Test
₹20,000GJC2 Gene Lymphedema, hereditary, type IC NGS Genetic Test
₹20,000Reference 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.
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.
Book Your Test
Enter your details and we'll connect you within 15 minutes.
