Sanger Sequencing Single Variant Test
Comprehensive Genetic Mutation Analysis
The Sanger Sequencing Single Variant Test represents the gold standard in targeted genetic analysis, providing definitive confirmation of specific genetic mutations with exceptional accuracy. This advanced molecular diagnostic technique enables healthcare providers to precisely identify known genetic variants that may be responsible for inherited disorders, offering crucial insights for diagnosis, treatment planning, and genetic counseling.
What Does This Test Detect?
This specialized test focuses on detecting specific single nucleotide variants (SNVs) and small insertions or deletions in targeted genetic regions. Using the established Sanger sequencing methodology, the test provides:
- Precise identification of known pathogenic mutations
- Confirmation of familial genetic variants
- Detection of single base pair changes
- Analysis of small genetic insertions and deletions
- Verification of specific genetic markers
Who Should Consider This Test?
This targeted genetic analysis is particularly valuable for individuals with:
- Family history of specific genetic disorders
- Clinical symptoms suggesting known genetic conditions
- Previous genetic testing indicating potential mutations
- Need for confirmation of carrier status for specific variants
- Requirements for prenatal genetic testing of known familial mutations
- Suspected inherited metabolic disorders
- Neurological conditions with genetic components
Key Benefits of Sanger Sequencing
- Unmatched Accuracy: Gold-standard methodology with >99.9% accuracy rate
- Targeted Analysis: Focused examination of specific genetic regions of interest
- Clinical Validation: Results supported by extensive clinical research
- Treatment Guidance: Informs personalized treatment strategies
- Family Planning: Provides crucial information for genetic counseling
- Cost-Effective: Affordable targeted testing compared to broader panels
Understanding Your Test Results
Your Sanger Sequencing Single Variant Test results will provide clear, actionable information:
- Positive Result: Confirms the presence of the specific genetic variant being tested
- Negative Result: Indicates the targeted mutation was not detected
- Inconclusive Result: May require additional testing or alternative methods
All results are accompanied by detailed interpretation from our board-certified genetic specialists, explaining the clinical significance and potential implications for your health management.
Test Pricing Information
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $350 |
| Regular Price | $500 |
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 network of certified collection centers ensures accessible genetic testing services nationwide.
Schedule Your Genetic Analysis Today
Take the first step toward understanding your genetic health with our comprehensive Sanger Sequencing Single Variant Test. Our experienced genetic counselors and molecular diagnostics specialists are ready to assist you with:
- Pre-test genetic counseling
- Convenient sample collection
- Expert result interpretation
- Post-test consultation and guidance
Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or to speak with our genetic specialists about whether this test is right for you. Our team is available to answer your questions and help you navigate your genetic health journey with confidence and clarity.
Turnaround Time: Samples accepted daily by 9 AM | Reports delivered within 30 working days
Sample Requirements: 10 mL (5 mL minimum) whole blood from 2 Lavender Top (EDTA) tubes. Ship refrigerated. DO NOT FREEZE. Duly filled Sanger Sequencing Test Requisition Form (Form 38) is mandatory.
