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F9 Gene Hemophilia B NGS Genetic DNA Test

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

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The F9 Gene Hemophilia B NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the F9 gene responsible for Hemophilia B, also known as Christmas disease. This advanced next-generation sequencing test provides precise detection of genetic variations that cause Factor IX deficiency, enabling accurate diagnosis and personalized treatment planning. The test is essential for individuals with bleeding disorders, family history of hemophilia, or those planning pregnancy with known genetic risks. Results help guide clinical management, inform family planning decisions, and provide crucial information for genetic counseling. Available for only $500 USD, this test offers significant savings from the regular $700 price. With branches across all major US cities, we provide accessible genetic testing services with expert interpretation and support.

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F9 Gene Hemophilia B NGS Genetic DNA Test

Comprehensive Genetic Analysis for Hemophilia B Detection

The F9 Gene Hemophilia B NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations responsible for Hemophilia B, a serious inherited bleeding disorder. Utilizing next-generation sequencing technology, this test provides unparalleled accuracy in detecting variations within the F9 gene located on the X chromosome. Hemophilia B, also known as Christmas disease, results from deficiencies in clotting Factor IX and affects approximately 1 in 25,000 male births worldwide. Early and accurate genetic diagnosis is crucial for implementing appropriate treatment strategies and preventing life-threatening bleeding complications.

What Does This Test Measure and Detect?

This comprehensive genetic test specifically analyzes the F9 gene using advanced NGS methodology to identify:

  • Point mutations, deletions, and insertions in the F9 gene
  • Missense, nonsense, and frameshift mutations affecting Factor IX production
  • Regulatory region variations impacting gene expression
  • Inversion mutations commonly associated with severe Hemophilia B
  • Novel genetic variants with potential clinical significance

The test covers all eight exons, seven introns, and regulatory regions of the F9 gene, providing comprehensive mutation detection with over 99% accuracy. This thorough analysis enables precise genotype-phenotype correlation, helping predict disease severity and guide personalized treatment approaches.

Who Should Consider This Genetic Test?

This test is recommended for individuals experiencing:

  • Unexplained prolonged bleeding after injuries or surgeries
  • Frequent spontaneous bleeding into joints and muscles
  • Family history of Hemophilia B or bleeding disorders
  • Abnormal coagulation test results suggesting Factor IX deficiency
  • Women with family history of hemophilia considering pregnancy
  • Newborn males with suspected bleeding disorders
  • Individuals requiring confirmation of Hemophilia B diagnosis

Significant Benefits of Genetic Testing

Undergoing F9 gene testing provides numerous clinical advantages:

  • Accurate Diagnosis: Confirms Hemophilia B with genetic precision
  • Personalized Treatment: Guides appropriate Factor IX replacement therapy
  • Family Planning: Enables informed reproductive decisions
  • Prophylactic Management: Helps prevent bleeding complications
  • Genetic Counseling: Provides basis for comprehensive family risk assessment
  • Early Intervention: Facilitates timely treatment initiation

Understanding Your Test Results

Your genetic test report will provide detailed information about F9 gene mutations:

  • Positive Result: Identifies specific F9 gene mutation confirming Hemophilia B diagnosis
  • Negative Result: No mutation detected, though clinical correlation is essential
  • Variant of Uncertain Significance: Requires additional family studies and clinical evaluation
  • Carrier Status: Identifies females carrying Hemophilia B mutations

All results include comprehensive interpretation by board-certified genetic specialists and hematologists, with recommendations for clinical management and family counseling.

Test Pricing and Availability

Test Name Discount Price Regular Price
F9 Gene Hemophilia B NGS Genetic DNA Test $500 USD $700 USD

Nationwide Testing Accessibility

We maintain comprehensive testing facilities across the United States, with branches in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network ensures convenient access to advanced genetic testing services regardless of your location.

Take Action for Your Health Today

Don’t let uncertainty about genetic bleeding disorders affect your quality of life. Our F9 Gene Hemophilia B NGS Genetic DNA Test provides the definitive answers you need for proper diagnosis and management. With our special discounted price of $500 (regularly $700), now is the perfect time to take control of your genetic health.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take the first step toward comprehensive hemophilia management.

Our team of genetic counselors and hematology specialists is ready to guide you through the testing process, from sample collection to result interpretation and ongoing management recommendations. Early genetic diagnosis can significantly improve treatment outcomes and quality of life for individuals with Hemophilia B.