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APOA2 Gene Apolipoprotein A-II Deficiency Genetic Test

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

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The APOA2 Gene Apolipoprotein A-II Deficiency NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the APOA2 gene responsible for Apolipoprotein A-II deficiency. This advanced Next-Generation Sequencing (NGS) test provides crucial insights into metabolic disorders affecting lipid metabolism and cardiovascular health. The test is particularly valuable for individuals with family history of early-onset cardiovascular disease, abnormal lipid profiles, or unexplained metabolic conditions. Results help guide personalized treatment strategies and preventive healthcare measures. The test costs $500 USD with a regular price of $700 USD, offering significant savings for comprehensive genetic assessment. Turnaround time is 3-4 weeks using blood, extracted DNA, or blood spot samples.

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APOA2 Gene Apolipoprotein A-II Deficiency NGS Genetic DNA Test

Comprehensive Genetic Analysis for Metabolic Health

The APOA2 Gene Apolipoprotein A-II Deficiency NGS Genetic DNA Test represents a cutting-edge diagnostic approach to identifying genetic mutations associated with Apolipoprotein A-II deficiency. This specialized test utilizes Next-Generation Sequencing (NGS) technology to provide comprehensive analysis of the APOA2 gene, offering crucial insights into metabolic disorders that impact cardiovascular health and lipid metabolism.

What This Advanced Genetic Test Measures

This sophisticated genetic screening test specifically targets and analyzes the APOA2 gene, which encodes Apolipoprotein A-II – a crucial component of high-density lipoprotein (HDL) particles. The test detects:

  • Point mutations and single nucleotide variants in the APOA2 gene
  • Insertions and deletions affecting gene function
  • Structural variations impacting protein production
  • Genetic markers associated with impaired lipid metabolism
  • Variants linked to cardiovascular disease risk

Who Should Consider APOA2 Genetic Testing?

This comprehensive genetic assessment is particularly recommended for individuals experiencing:

  • Family history of early-onset cardiovascular disease
  • Unexplained abnormal lipid profiles
  • Persistent metabolic disorders without clear diagnosis
  • Multiple family members with similar metabolic conditions
  • Early signs of atherosclerosis or vascular complications
  • Unexplained low HDL cholesterol levels

Clinical Indications and Symptoms

Patients presenting with symptoms such as premature coronary artery disease, xanthomas, or abnormal lipid panels should consider this test. Individuals with family members diagnosed with Apolipoprotein A-II deficiency or related metabolic disorders benefit significantly from genetic screening.

Significant Benefits of APOA2 Genetic Testing

  • Early Detection: Identify genetic predisposition before symptom onset
  • Personalized Treatment: Develop targeted therapeutic strategies
  • Family Planning: Make informed reproductive decisions
  • Preventive Care: Implement proactive health management
  • Accurate Diagnosis: Confirm suspected metabolic disorders
  • Risk Assessment: Evaluate cardiovascular disease probability

Understanding Your Genetic Test Results

Your APOA2 gene test results will provide comprehensive information about your genetic status:

Positive Result Interpretation

A positive result indicates the presence of pathogenic variants in the APOA2 gene. This confirms Apolipoprotein A-II deficiency and provides essential information for developing personalized management strategies, including dietary modifications, lifestyle adjustments, and targeted medical interventions.

Negative Result Significance

A negative result suggests the absence of known pathogenic variants in the APOA2 gene. However, this doesn’t completely rule out other genetic or environmental factors contributing to metabolic disorders. Further evaluation may be recommended based on clinical presentation.

Variant of Uncertain Significance (VUS)

Some results may identify genetic variants with unclear clinical significance. In such cases, ongoing monitoring and periodic re-evaluation are recommended as scientific understanding evolves.

Test Pricing and Details

Test Feature Details
Test Name APOA2 Gene Apolipoprotein A-II 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 and Preparation

Before undergoing APOA2 genetic testing, patients should complete:

  • Comprehensive clinical history documentation
  • Genetic counseling session with certified genetic counselor
  • Development of detailed family pedigree chart
  • Discussion of potential outcomes and implications
  • Informed consent process

Nationwide Availability Across USA

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, and San Jose. Our network of certified genetic testing facilities ensures accessible, reliable service nationwide.

Take Control of Your Metabolic Health Today

Don’t wait to gain crucial insights into your genetic health. The APOA2 Gene Apolipoprotein A-II Deficiency NGS Genetic DNA Test provides essential information for managing metabolic disorders and cardiovascular risk. Our team of genetic specialists is ready to guide you through the testing process and help interpret your results.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your APOA2 genetic test. Take the first step toward personalized metabolic health management and comprehensive genetic understanding.