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Methylenetetrahydrofolate Reductase MTHFR Factor V F5 Factor II F2 Genetic Test

Original price was: $400.Current price is: $300.

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The MTHFR Factor V F5 Factor II F2 genetic test is a comprehensive screening panel that evaluates key genetic mutations affecting blood clotting and methylation processes. This advanced diagnostic test analyzes three critical genetic factors: MTHFR mutations impacting folate metabolism, Factor V Leiden mutation increasing thrombosis risk, and Factor II (Prothrombin) mutation affecting blood coagulation. Priced at $300 USD, this test provides crucial insights for individuals with personal or family history of blood clots, recurrent miscarriages, or cardiovascular concerns. Results help guide personalized prevention strategies and treatment approaches for improved health outcomes.

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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MTHFR Factor V F5 Factor II F2 Comprehensive Genetic Test

Understanding Your Genetic Health Profile

The MTHFR Factor V F5 Factor II F2 genetic test represents a cutting-edge diagnostic approach to understanding your unique genetic predispositions related to blood clotting disorders and methylation processes. This comprehensive panel provides invaluable insights that can significantly impact your long-term health management and preventive care strategies.

What This Test Measures and Detects

This advanced genetic screening evaluates three critical genetic markers that play essential roles in your body’s biochemical processes:

MTHFR Gene Analysis

  • Detects mutations in the Methylenetetrahydrofolate Reductase gene
  • Identifies variations affecting folate metabolism and homocysteine levels
  • Assesses your body’s ability to process folic acid effectively

Factor V Leiden (F5) Mutation

  • Screens for the most common inherited thrombophilia mutation
  • Evaluates genetic predisposition to abnormal blood clotting
  • Identifies increased risk for deep vein thrombosis and pulmonary embolism

Factor II (Prothrombin) Mutation

  • Tests for the G20210A mutation in the prothrombin gene
  • Assesses genetic factors affecting blood coagulation
  • Identifies additional thrombophilia risk factors

Who Should Consider This Genetic Test

This comprehensive screening is particularly valuable for individuals experiencing specific health concerns or with particular risk factors:

Clinical Indications and Symptoms

  • Personal history of unexplained blood clots or thrombosis
  • Family history of thrombophilia or clotting disorders
  • Recurrent pregnancy loss or fertility challenges
  • Unexplained cardiovascular events at a young age
  • Chronic fatigue, brain fog, or neurological symptoms
  • Planning for surgery or major medical procedures
  • Women considering hormonal contraception or hormone replacement therapy
  • Individuals with elevated homocysteine levels

Benefits of Comprehensive Genetic Testing

Understanding your genetic profile through this advanced screening offers numerous advantages for proactive health management:

Personalized Prevention Strategies

  • Enables targeted prevention measures for blood clot risks
  • Guides appropriate supplementation based on MTHFR status
  • Helps optimize medication choices and dosages
  • Supports informed decisions about surgical procedures

Improved Health Outcomes

  • Facilitates early intervention for potential health risks
  • Provides clarity for unexplained medical conditions
  • Supports reproductive health planning and management
  • Enhances cardiovascular risk assessment and management

Understanding Your Test Results

Your genetic test results will provide detailed information about your specific genetic variations and their potential health implications:

MTHFR Results Interpretation

  • Normal MTHFR: Standard folate metabolism capability
  • Heterozygous Mutation: Reduced enzyme activity requiring nutritional support
  • Homozygous Mutation: Significantly impaired methylation requiring comprehensive management

Factor V and Factor II Results

  • Negative/Normal: No increased genetic risk for thrombophilia
  • Heterozygous Carrier: Moderate increased risk for clotting events
  • Homozygous Mutation: Significantly elevated thrombosis risk requiring careful management

Test Pricing and Details

Test Component Details
Test Name MTHFR Factor V F5 Factor II F2 Genetic Test
Discount Price $300 USD
Regular Price $400 USD
Turnaround Time 3-4 Days
Sample Type Peripheral Blood
Test Components EDTA Vacutainer (2ml)
Testing Method End Point PCR + RFLP

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. Our nationwide network ensures accessible, high-quality genetic testing services for everyone.

Take Control of Your Genetic Health Today

Don’t leave your health to chance. Understanding your genetic predispositions can be the key to preventing serious health complications and optimizing your wellness journey. Our comprehensive MTHFR Factor V F5 Factor II F2 genetic test provides the clarity you need to make informed decisions about your health.

Ready to discover your genetic profile? Call us today at +1(267) 388-9828 to schedule your appointment or book your test online. Our genetic counseling team is available to answer your questions and guide you through the testing process.

Note: This test requires a Doctor’s prescription for most cases. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.