Sale!

Glucose-6-Phosphate Dehydrogenase (G6PD) Full Length Gene Sequence Analysis

Original price was: $1,250.Current price is: $938.

-25%

The Glucose-6-Phosphate Dehydrogenase (G6PD) Full Length Gene Sequence Analysis is a comprehensive genetic test that examines the entire G6PD gene to identify mutations responsible for G6PD deficiency. This specialized diagnostic tool utilizes advanced Sanger sequencing technology to detect genetic variations that can lead to hemolytic anemia when exposed to certain medications, foods, or infections. The test is particularly important for individuals with family history of G6PD deficiency, those experiencing unexplained hemolytic episodes, or people planning to take medications known to trigger G6PD-related complications. Results provide crucial information for personalized medical management and preventive care strategies. This test is available for $938 USD with comprehensive genetic counseling included.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
Guaranteed Safe Checkout

Glucose-6-Phosphate Dehydrogenase (G6PD) Full Length Gene Sequence Analysis

Understanding G6PD Genetic Testing

The Glucose-6-Phosphate Dehydrogenase (G6PD) Full Length Gene Sequence Analysis represents a cutting-edge approach to diagnosing G6PD deficiency, one of the most common enzyme deficiencies worldwide affecting over 400 million people globally. This comprehensive genetic examination provides unparalleled insights into your genetic makeup, enabling precise identification of mutations within the G6PD gene located on the X chromosome.

What Does This Test Measure?

This advanced diagnostic test employs Sanger sequencing methodology to analyze the complete coding region of the G6PD gene, spanning approximately 13 kilobases. The test specifically detects:

  • Point mutations affecting enzyme function
  • Small insertions and deletions disrupting gene expression
  • Genetic variants associated with varying degrees of enzyme deficiency
  • Mutations affecting protein structure and catalytic activity
  • Genetic markers predicting disease severity and clinical manifestations

Who Should Consider G6PD Genetic Testing?

This comprehensive genetic analysis is recommended for individuals experiencing:

  • Unexplained episodes of hemolytic anemia following medication exposure
  • Family history of G6PD deficiency or related hemolytic disorders
  • Neonatal jaundice without clear underlying cause
  • Planned use of medications known to trigger hemolysis in G6PD-deficient individuals
  • Recurrent anemia episodes following infection or stress
  • Individuals from ethnic backgrounds with high G6PD deficiency prevalence
  • Pre-surgical screening for anesthesia risk assessment

Clinical Indications and Symptoms

Patients presenting with symptoms including dark urine, fatigue, rapid heart rate, shortness of breath, abdominal pain, or jaundice following exposure to oxidative stressors should consider this genetic evaluation. The test is particularly valuable for individuals planning international travel to malaria-endemic regions where antimalarial medications may be required.

Benefits of G6PD Full Gene Sequence Analysis

  • Precise Diagnosis: Provides definitive genetic confirmation of G6PD deficiency
  • Personalized Medicine: Enables tailored medication and treatment plans
  • Preventive Care: Identifies triggers to avoid future hemolytic crises
  • Family Planning: Offers genetic counseling for inheritance patterns
  • Comprehensive Assessment: Detects both common and rare genetic variants
  • Long-term Management: Supports ongoing healthcare decision-making

Understanding Your Test Results

Your G6PD genetic test results will provide detailed information about specific mutations identified in your G6PD gene. Results typically fall into several categories:

Normal Results

No pathogenic mutations detected indicates normal G6PD enzyme function. However, clinical correlation with enzyme activity levels may be recommended for comprehensive assessment.

Pathogenic Variants

Identification of known disease-causing mutations confirms G6PD deficiency diagnosis. The specific mutation identified can provide insights into expected clinical severity and management requirements.

Variants of Uncertain Significance

Some genetic changes may have unknown clinical significance. In such cases, additional family studies or functional testing may be recommended to determine clinical relevance.

Test Pricing and Details

Test Component Details
Test Name Glucose-6-Phosphate Dehydrogenase (G6PD) Full Length Gene Sequence Analysis
Discount Price $938 USD
Regular Price $1,250 USD
Turnaround Time 2-3 weeks
Sample Type Peripheral blood / Amniotic Fluid / Chorionic villi / Cord blood
Testing Method Sanger Sequencing
Test Components Sterile container / Sterile Normal Saline Container / EDTA Vacutainer (2ml)

Pre-Test Instructions

The Glucose-6-Phosphate Dehydrogenase (G6PD) full length gene sequence analysis requires a Doctor’s prescription for most cases. However, prescription requirements do not apply for surgical preparation, pregnancy-related testing, or individuals planning international travel. Our genetic counselors are available to discuss testing indications and provide comprehensive pre-test education.

Nationwide Testing Availability

We provide comprehensive genetic testing services across all major cities in the United States, including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, Austin, Jacksonville, Fort Worth, Columbus, San Francisco, and many more locations. Our network of certified collection centers ensures convenient access to this advanced genetic testing.

Book Your G6PD Genetic Test Today

Take control of your genetic health with our comprehensive G6PD full gene sequence analysis. Our team of genetic specialists and certified phlebotomists are ready to assist you with convenient scheduling and professional sample collection. For appointments, genetic counseling, or additional information about this vital genetic test, contact our dedicated healthcare team.

Call or WhatsApp: +1(267) 388-9828

Schedule your appointment today to receive the definitive genetic insights needed for personalized medical management and preventive healthcare planning. Our commitment to excellence in genetic testing ensures you receive accurate, reliable results with comprehensive clinical interpretation and ongoing support.