SERPINC1 Gene Antithrombin III Deficiency NGS Genetic DNA Test
Comprehensive Genetic Analysis for Thrombophilia Risk Assessment
The SERPINC1 Gene Antithrombin III Deficiency NGS Genetic DNA Test represents a breakthrough in personalized medicine for individuals concerned about hereditary thrombophilia. This advanced diagnostic tool utilizes cutting-edge Next-Generation Sequencing technology to analyze the SERPINC1 gene, which encodes antithrombin III – a crucial natural anticoagulant protein in our blood clotting system.
What Does This Test Measure?
This comprehensive genetic analysis specifically targets the SERPINC1 gene to identify mutations that cause antithrombin III deficiency. The test examines:
- Complete SERPINC1 gene sequencing for point mutations
- Detection of insertions and deletions affecting gene function
- Identification of genetic variants associated with reduced antithrombin activity
- Assessment of hereditary thrombophilia risk factors
Who Should Consider This Test?
This genetic test is particularly recommended for individuals experiencing:
- Unexplained or recurrent venous thromboembolism (VTE)
- Family history of blood clotting disorders
- Thrombosis at unusual sites (cerebral, mesenteric, portal veins)
- Recurrent pregnancy loss or complications
- Blood clots occurring before age 50
- Resistance to standard anticoagulant therapy
- Planning for major surgery with thrombophilia concerns
Clinical Benefits of Genetic Testing
Understanding your genetic predisposition to antithrombin III deficiency provides numerous clinical advantages:
- Personalized Risk Assessment: Determine your individual thrombophilia risk profile
- Proactive Management: Implement preventive measures before clotting events occur
- Family Planning Guidance: Make informed decisions about genetic inheritance patterns
- Treatment Optimization: Tailor anticoagulant therapy based on genetic findings
- Surgical Planning: Prepare appropriate thromboprophylaxis for procedures
- Peace of Mind: Reduce anxiety through comprehensive genetic understanding
Understanding Your Test Results
Your genetic test report will provide detailed information about your SERPINC1 gene status:
- Normal Result: No pathogenic variants detected in the SERPINC1 gene
- Pathogenic Variant Identified: Specific mutation associated with antithrombin deficiency
- Variant of Uncertain Significance: Genetic change requiring further clinical correlation
- Carrier Status: Information about genetic inheritance patterns
All results include comprehensive interpretation by our genetic specialists and recommendations for clinical management.
Test Details and Pricing
| Test Component | Details |
|---|---|
| Test Name | SERPINC1 Gene Antithrombin III Deficiency 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 scheduling your test, we recommend:
- Complete clinical history documentation
- Genetic counseling session to discuss family history
- Development of pedigree chart for affected family members
- Understanding of potential implications and limitations
Nationwide Accessibility
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. Our network of certified collection centers ensures accessible testing regardless of your location.
Take Control of Your Genetic Health
Don’t let uncertainty about hereditary thrombophilia risk affect your quality of life. Our SERPINC1 Gene Antithrombin III Deficiency NGS Genetic DNA Test provides the clarity you need to make informed healthcare decisions. With advanced NGS technology and expert genetic interpretation, you’ll receive comprehensive insights into your genetic predisposition to clotting disorders.
Ready to understand your genetic risk profile? Contact our genetic specialists today to schedule your test or discuss your concerns. Call or WhatsApp us at +1(267) 388-9828 to book your appointment and take the first step toward personalized thrombophilia management.
Our dedicated team of genetic counselors and healthcare professionals are available to answer your questions and guide you through the testing process. Early detection and understanding of genetic risk factors can significantly impact your long-term health outcomes.
