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TNNI3 Gene Cardiomyopathy Familial Hypertrophic Type 7 NGS Genetic DNA Test

Original price was: $700.Current price is: $500.

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The TNNI3 Gene Cardiomyopathy Familial Hypertrophic Type 7 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the TNNI3 gene associated with familial hypertrophic cardiomyopathy type 7. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to provide accurate detection of genetic variations that can lead to abnormal thickening of the heart muscle. The test is essential for individuals with family history of cardiomyopathy, unexplained cardiac symptoms, or those planning pregnancy with known genetic risk factors. Results help guide treatment decisions, inform family planning, and enable proactive cardiac monitoring. The test is available for $500 USD and provides results within 3-4 weeks using blood, extracted DNA, or blood spot samples.

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TNNI3 Gene Cardiomyopathy Familial Hypertrophic Type 7 NGS Genetic DNA Test

Understanding TNNI3 Gene Cardiomyopathy Testing

The TNNI3 Gene Cardiomyopathy Familial Hypertrophic Type 7 NGS Genetic DNA Test represents a breakthrough in cardiovascular genetic diagnostics. This advanced test specifically targets mutations in the TNNI3 gene, which encodes cardiac troponin I—a crucial protein responsible for regulating heart muscle contraction. When mutations occur in this gene, they can lead to familial hypertrophic cardiomyopathy type 7, a serious inherited heart condition characterized by abnormal thickening of the heart muscle walls.

What Does This Test Detect?

Our comprehensive NGS-based test identifies specific genetic variations in the TNNI3 gene that are known to cause familial hypertrophic cardiomyopathy type 7. The test examines:

  • Point mutations in the TNNI3 gene coding regions
  • Small insertions and deletions affecting protein function
  • Genetic variants associated with impaired cardiac muscle contraction
  • Inheritance patterns of cardiomyopathy risk factors

Who Should Consider TNNI3 Genetic Testing?

This test is particularly important for individuals experiencing or at risk for:

  • Family History: Individuals with relatives diagnosed with hypertrophic cardiomyopathy
  • Unexplained Symptoms: Patients experiencing chest pain, palpitations, or shortness of breath without clear cause
  • Abnormal Cardiac Findings: Those with unexplained heart murmurs or abnormal echocardiogram results
  • Family Planning: Couples with family history of cardiomyopathy considering pregnancy
  • Young Athletes: Individuals participating in competitive sports with family cardiac history

Clinical Symptoms and Indicators

Common symptoms that may indicate the need for TNNI3 genetic testing include:

  • Chest pain during physical activity
  • >Shortness of breath with exertion

  • Heart palpitations or irregular heartbeat
  • Dizziness or fainting spells
  • Fatigue during normal activities
  • Family history of sudden cardiac death

Benefits of TNNI3 Genetic Testing

Undergoing TNNI3 genetic testing provides numerous advantages for patients and their families:

  • Early Detection: Identify genetic risk before symptoms develop
  • Family Screening: Enable testing of at-risk family members
  • Personalized Treatment: Guide medication choices and lifestyle recommendations
  • Reproductive Planning: Inform decisions about family planning and prenatal testing
  • Proactive Monitoring: Establish appropriate cardiac surveillance schedules
  • Peace of Mind: Reduce uncertainty about genetic risk status

Understanding Your Test Results

Your TNNI3 genetic test results will fall into one of several categories:

  • Positive Result: A known disease-causing mutation was identified, confirming genetic predisposition to familial hypertrophic cardiomyopathy type 7
  • Negative Result: No known disease-causing mutations were found, significantly reducing but not eliminating cardiomyopathy risk
  • Variant of Uncertain Significance: A genetic change was detected whose clinical significance is currently unknown
  • No Mutation Detected: No genetic variations were identified in the TNNI3 gene

All results are accompanied by comprehensive genetic counseling to ensure proper interpretation and appropriate next steps. Our genetic specialists will help you understand what your results mean for your health and your family.

Test Information and Pricing

Test Details Information
Test Name TNNI3 Gene Cardiomyopathy Familial Hypertrophic Type 7 NGS Genetic DNA Test
Regular Price $700 USD
Discount Price $500 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next-Generation Sequencing (NGS) Technology

Pre-Test Requirements

Before undergoing TNNI3 genetic testing, patients should provide:

  • Complete clinical history including cardiac symptoms and family medical background
  • Participation in genetic counseling session to create detailed family pedigree chart
  • Documentation of affected family members with cardiomyopathy or related conditions
  • Current cardiac evaluation results if available

Nationwide Testing Availability

We proudly offer TNNI3 genetic testing services across the United States with convenient locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art laboratories ensure consistent, high-quality results regardless of your location.

Take Control of Your Cardiac Health Today

Don’t let uncertainty about genetic heart conditions affect your quality of life. The TNNI3 Gene Cardiomyopathy test provides crucial information that can guide your healthcare decisions and protect your family’s future. Our team of cardiovascular genetics specialists is ready to support you through every step of the testing process.

Ready to schedule your TNNI3 genetic test? Contact us today at +1(267) 388-9828 to book your appointment or speak with our genetic counseling team. Take the first step toward understanding your genetic heart health with confidence and clarity.