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CYP1A2 Gene Cytochrome P450 Deficiency Genetic Test

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

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The CYP1A2 Gene Cytochrome P450 Deficiency NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the CYP1A2 gene responsible for cytochrome P450 enzyme deficiencies. This comprehensive test helps determine individual variations in drug metabolism capabilities, particularly affecting how your body processes common medications like caffeine, antidepressants, antipsychotics, and certain pain relievers. Using Next-Generation Sequencing (NGS) technology, the test provides detailed insights into your metabolic profile, enabling healthcare providers to optimize medication dosages and reduce adverse drug reactions. Individuals experiencing unexpected medication side effects, poor treatment response, or with family history of metabolic disorders should consider this test. Results are typically available within 3-4 weeks from blood, extracted DNA, or FTA card samples. The test is priced at $500 USD (regularly $700) and includes genetic counseling to help interpret your results and create a personalized treatment plan.

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CYP1A2 Gene Cytochrome P450 Deficiency NGS Genetic DNA Test

Understanding CYP1A2 Gene Testing

The CYP1A2 Gene Cytochrome P450 Deficiency NGS Genetic DNA Test represents a breakthrough in personalized medicine, offering crucial insights into how your body metabolizes medications and environmental substances. This advanced genetic analysis examines the CYP1A2 gene, which encodes one of the most important cytochrome P450 enzymes responsible for metabolizing approximately 15% of commonly prescribed drugs.

What Does This Test Measure?

This comprehensive NGS-based test specifically identifies genetic variations and mutations in the CYP1A2 gene that affect cytochrome P450 enzyme function. The test detects:

  • Single nucleotide polymorphisms (SNPs) affecting enzyme activity
  • Gene deletions or duplications impacting metabolic capacity
  • Specific mutations that classify individuals as poor, intermediate, extensive, or ultra-rapid metabolizers
  • Genetic markers influencing caffeine metabolism and drug clearance rates

Who Should Consider This Test?

This genetic test is particularly valuable for individuals experiencing:

  • Unexpected adverse reactions to common medications
  • Poor response to standard drug therapies
  • Family history of medication sensitivity or metabolic disorders
  • Chronic conditions requiring multiple medications
  • History of caffeine sensitivity or intolerance
  • Planning to start new long-term medication regimens

Clinical Indications and Symptoms

Patients with the following symptoms may benefit from CYP1A2 testing:

  • Severe side effects from antidepressants, antipsychotics, or pain medications
  • Difficulty tolerating caffeine-containing products
  • Unexpected drug toxicity at standard doses
  • Poor therapeutic response despite adequate dosing
  • Family history of cytochrome P450 deficiencies

Benefits of CYP1A2 Genetic Testing

Undergoing CYP1A2 genetic testing provides numerous clinical advantages:

  • Personalized Medication Dosing: Enables healthcare providers to tailor drug dosages based on your metabolic profile
  • Reduced Adverse Reactions: Helps prevent medication side effects and toxicity
  • Improved Treatment Outcomes: Increases the likelihood of successful therapy by matching drugs to your metabolic capacity
  • Cost-Effective Healthcare: Reduces trial-and-error prescribing and associated healthcare costs
  • Enhanced Safety: Identifies potential drug interactions before they become problematic

Understanding Your Test Results

Your CYP1A2 genetic test results will classify you into one of four metabolic phenotypes:

  • Poor Metabolizer: Significantly reduced enzyme activity requiring lower drug doses
  • Intermediate Metabolizer: Moderate enzyme activity with potential need for dose adjustments
  • Extensive Metabolizer: Normal enzyme activity suitable for standard dosing
  • Ultra-Rapid Metabolizer: Increased enzyme activity potentially requiring higher doses for therapeutic effect

Our genetic counseling team will provide comprehensive interpretation of your results and create a personalized report for your healthcare provider, including specific medication recommendations and dosing guidelines.

Test Details and Pricing

Test Component Details
Test Name CYP1A2 Gene Cytochrome P450 Deficiency NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 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 the CYP1A2 genetic test, patients should provide:

  • Complete clinical history relevant to medication responses
  • Participation in a genetic counseling session
  • Family pedigree chart documenting relatives with cytochrome P450 deficiencies or medication sensitivities
  • Current medication list and history of drug reactions

Nationwide Availability

We have testing facilities conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our nationwide network ensures accessible genetic testing services for patients throughout the country.

Take Control of Your Medication Safety

Don’t leave your medication responses to chance. The CYP1A2 Gene Cytochrome P450 Deficiency NGS Genetic DNA Test provides the scientific foundation for personalized, safer medication management. Our advanced NGS technology delivers accurate, comprehensive results that can transform your healthcare experience.

Ready to optimize your medication therapy? Book your CYP1A2 genetic test today by calling our dedicated healthcare line at +1(267) 388-9828 or schedule your appointment online. Take the first step toward personalized medicine and enhanced treatment safety.