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MIB1 Gene Left ventricular noncompaction 7 NGS Genetic Test

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MIB1 Gene Left ventricular noncompaction 7 NGS Genetic Test

Short Name: MIB1 Gene LVNC NGS Test

Also known as: Left Ventricular Noncompaction 7 Genetic Test, MIB1 Gene LVNC NGS Analysis

MIB1 Gene Left ventricular noncompaction 7 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

To diagnose and predict the risk of left ventricular noncompaction (LVNC) by analyzing genetic variations in the MIB1 gene and associated genes using NGS technology.

Test Code
5261
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

Clinical history and genetic counseling session required to draw a pedigree chart.

Method: Venipuncture

Step 2

Laboratory Analysis

Standard blood draw procedure using sterile equipment.

Step 3

Report Delivery

Sample is labeled and sent to the laboratory for analysis.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling recommended to understand implications and family history.
2
During the Test:Blood sample collection via venipuncture.
3
After the Test:Wait for report in 3-4 weeks; follow-up with genetic counselor or cardiologist.

About This Test

Who Should Get This Test

To diagnose and predict the risk of left ventricular noncompaction (LVNC) by analyzing genetic variations in the MIB1 gene and associated genes using NGS technology.

How to Prepare

  • Ensure proper sample labeling
  • Use sterile collection tubes
  • Avoid hemolysis during blood draw

Doctor's Notes

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

"This test is crucial for early diagnosis and management of LVNC, especially in families with a history of heart conditions. It helps in risk assessment and guiding treatment plans."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 mL blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture

Sample Stability

Blood: 24 hours at room temperature
DNA: stable for years when stored properly
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient volume
  • Improper labeling

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the MIB1 gene and associated genes linked to LVNC.
📊

Negative

No pathogenic variants detected; reduced genetic risk for LVNC.

📊

Positive

Pathogenic variants detected; increased risk for LVNC, requiring clinical evaluation.

📊

Variant of Uncertain Significance

Genetic variant found but clinical significance unknown; further testing may be needed.

⚠️ When to Consult a Doctor:

If symptoms persist, family history of LVNC, or if genetic counseling is recommended based on test results.

Limitations

  • May not detect all genetic variants
  • Results require clinical correlation

Risks & Considerations

  • Minimal risk from blood draw, such as bruising or infection

Interfering Factors

  • Sample contamination
  • Degraded DNA

Compare With Similar Tests

TestMIB1 Gene Left ventricular noncompaction 7 NGS Genetic Test
ComparisonMIB1 Gene Left ventricular noncompaction 7 NGS Genetic TestImaging test for heart structure; genetic test provides underlying cause.Detailed heart imaging; genetic test identifies genetic predisposition.Measures electrical activity; genetic test assesses genetic risk.

Frequently Asked Questions

What is the MIB1 Gene Left Ventricular Noncompaction 7 NGS Genetic Test?
It is a genetic test that analyzes the MIB1 gene and other genes associated with left ventricular noncompaction (LVNC) using NGS technology to diagnose and predict risk.
Who should consider this test?
Individuals with a family history of LVNC, symptoms like fatigue or shortness of breath, or those seeking diagnostic confirmation for suspected LVNC.
What are the symptoms of LVNC?
Common symptoms include fatigue, weakness, shortness of breath, chest pain, irregular heartbeat, dizziness, and fainting.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to detect genetic variants in the MIB1 gene and associated genes.
What is the cost of the test?
The test costs INR 20,000 at DNA Labs India, with free home sample collection available across India.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings in numerous cities across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result indicates the presence of pathogenic genetic variants, increasing the risk for LVNC, and requires clinical evaluation.
Can this test be used for prenatal diagnosis?
Yes, the test can be used for carrier testing and prenatal diagnosis in families with a history of LVNC.
Is the test covered by insurance?
Coverage varies; it is not typically covered by government schemes like PMJAY, but check with private insurance providers.
What is the accuracy of the test?
The test uses advanced NGS technology for high accuracy, but results should be interpreted in conjunction with clinical findings.
How do I prepare for the test?
No fasting is required. Provide clinical history and undergo genetic counseling before sample collection.
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 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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