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MYH6 Gene Cardiomyopathy, dilated type 1EE NGS Genetic Test

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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.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

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)
Step 1

Sample Collection

No specific preparation required. Provide clinical history and family pedigree during genetic counseling.

Method: Blood draw or FTA card

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or one drop on FTA card by trained phlebotomist.

Step 3

Report Delivery

Sample labeled and transported to lab under stable conditions. Avoid hemolysis.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Understand the test purpose and implications. Provide informed consent and family medical history during genetic counseling.
2
During the Test:Sample collection is quick and minimally invasive, typically taking a few minutes.
3
After the Test:Results are available in 3-4 weeks. Genetic counseling will help interpret findings and plan next steps.

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 — 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 TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodBlood draw or FTA card

Sample Stability

Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improper labeling or documentation
  • Contaminated samples

Understanding Your Results

Results from the MYH6 Gene Cardiomyopathy NGS Genetic Test indicate the presence or absence of pathogenic variants in the MYH6 gene. Positive results confirm genetic predisposition to dilated cardiomyopathy type 1EE, while negative results suggest no known mutations, though other genetic or non-genetic factors may be involved.
📊

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.

⚠️ When to Consult a Doctor:

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?
MYH6 gene cardiomyopathy is a genetic disorder caused by mutations in the MYH6 gene, leading to dilated cardiomyopathy type 1EE, where the heart becomes enlarged and weakened.
How is the NGS Genetic Test performed?
The test uses Next Generation Sequencing to analyze the MYH6 gene from a blood or DNA sample, identifying mutations associated with cardiomyopathy.
What are the symptoms of MYH6 gene cardiomyopathy?
Symptoms include shortness of breath, fatigue, chest pain, swelling in legs and ankles, and rapid or irregular heartbeat.
Who should consider this genetic test?
Individuals with a family history of dilated cardiomyopathy, unexplained heart symptoms, or those seeking genetic counseling for at-risk conditions.
What is the cost of the MYH6 Gene Cardiomyopathy NGS Genetic Test?
The test costs INR 20,000 at DNA Labs India, with 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 fasting required before the test?
No, fasting is not required for this genetic test.
What sample types are accepted?
Blood, extracted DNA, or one drop of blood on an FTA card are accepted samples.
What do the test results mean?
Results indicate the presence or absence of pathogenic variants in the MYH6 gene. Positive results confirm genetic predisposition, while negative results suggest no known mutations.
Can this test be used for prenatal testing?
Yes, in families with known MYH6 mutations, prenatal or preconception testing may be considered after genetic counseling.
Is genetic counseling included with the test?
Yes, DNA Labs India provides genetic counseling to help interpret results and discuss implications for patients and families.
How accurate is the NGS Genetic Test?
NGS technology offers high accuracy for detecting genetic variants, but results should be correlated with clinical findings and interpreted by healthcare professionals.
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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