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F2 Gene Dysprothrombinemia NGS Genetic DNA Test

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

-29%

The F2 Gene Dysprothrombinemia NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the prothrombin gene (F2) using Next-Generation Sequencing technology. This advanced test detects genetic variations responsible for dysprothrombinemia, a rare inherited bleeding disorder affecting blood clotting function. The test provides crucial information for individuals with unexplained bleeding tendencies, abnormal coagulation test results, or family history of clotting disorders. At $500 USD, this specialized genetic analysis offers precise mutation detection, enabling accurate diagnosis, personalized treatment planning, and informed family decisions. Our state-of-the-art NGS methodology ensures high sensitivity and specificity in identifying both common and rare F2 gene variants.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
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F2 Gene Dysprothrombinemia NGS Genetic DNA Test

Comprehensive Genetic Analysis for Blood Clotting Disorders

The F2 Gene Dysprothrombinemia NGS Genetic DNA Test represents a cutting-edge diagnostic approach to identifying inherited bleeding disorders through advanced genetic sequencing technology. This specialized test focuses on the prothrombin gene (F2), which plays a critical role in the blood coagulation cascade. Dysprothrombinemia refers to genetic mutations that impair prothrombin function, leading to abnormal bleeding tendencies and compromised clot formation.

What Does This Test Measure?

Our comprehensive NGS-based analysis detects specific mutations within the F2 gene that are responsible for dysprothrombinemia. The test examines:

  • Point mutations affecting prothrombin structure and function
  • Insertions and deletions within the F2 gene coding regions
  • Splice site mutations impacting protein production
  • Regulatory region variations affecting gene expression
  • Both known pathogenic variants and novel mutations

Who Should Consider This Test?

This genetic test is particularly recommended for individuals experiencing:

  • Unexplained bleeding episodes or easy bruising
  • Abnormal coagulation test results (prolonged PT/PTT)
  • Family history of bleeding disorders or dysprothrombinemia
  • Recurrent miscarriages or pregnancy complications
  • Pre-surgical evaluation for bleeding risk assessment
  • Children with developmental bleeding symptoms
  • Individuals with known F2 gene mutations in their family

Clinical Benefits of Genetic Testing

Undergoing the F2 Gene Dysprothrombinemia NGS Genetic DNA Test provides numerous advantages:

  • Accurate Diagnosis: Precise identification of specific F2 gene mutations
  • Personalized Treatment: Tailored management strategies based on genetic findings
  • Family Planning: Informed reproductive decisions and genetic counseling
  • Early Intervention: Proactive management of bleeding risks
  • Comprehensive Risk Assessment: Understanding inheritance patterns and family risks
  • Medical Guidance: Collaboration with hematologists for optimal care

Understanding Your Test Results

Our genetic specialists provide comprehensive interpretation of your F2 gene analysis:

  • Positive Result: Identifies specific F2 gene mutation(s) confirming dysprothrombinemia diagnosis
  • Negative Result: No pathogenic F2 mutations detected, though other bleeding disorders may require investigation
  • Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation
  • Carrier Status: Determines if you carry one copy of a mutated gene

All results include detailed explanations and recommendations for follow-up care with your hematologist.

Test Pricing and Availability

Test Name Discount Price Regular Price
F2 Gene Dysprothrombinemia NGS Genetic DNA Test $500 USD $700 USD

Nationwide Testing Availability

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more cities. Our network of certified collection centers ensures accessible genetic testing services nationwide.

Advanced Testing Methodology

Our laboratory utilizes state-of-the-art Next-Generation Sequencing (NGS) technology, providing:

  • High-throughput parallel sequencing for comprehensive gene analysis
  • Superior sensitivity and specificity in mutation detection
  • Simultaneous analysis of multiple genetic regions
  • Quality-controlled bioinformatics pipeline for accurate variant calling
  • CLIA-certified laboratory standards ensuring reliable results

Sample Collection and Processing

We offer flexible sample collection options to accommodate patient needs:

  • Blood Sample: Standard venipuncture collection
  • Extracted DNA: For patients with previously isolated DNA
  • FTA Card: Convenient single blood drop collection

Turnaround Time: 3 to 4 weeks from sample receipt

Pre-Test Requirements

To ensure optimal testing outcomes, we recommend:

  • Comprehensive clinical history documentation
  • Genetic counseling session for pedigree analysis
  • Discussion of testing implications with healthcare provider
  • Informed consent process understanding benefits and limitations

Take Control of Your Genetic Health Today

Don’t let uncertainty about bleeding disorders affect your quality of life. Our F2 Gene Dysprothrombinemia NGS Genetic DNA Test provides the clarity and answers you need for informed healthcare decisions. With our discounted price of $500 USD and nationwide availability, comprehensive genetic testing has never been more accessible.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take the first step toward understanding your genetic predisposition to bleeding disorders.

Our dedicated team of genetic counselors and hematology specialists are ready to guide you through the testing process and help you interpret your results for optimal health management.