FANCG Gene Fanconi Anemia Type G NGS Genetic DNA Test
Comprehensive Genetic Testing for Fanconi Anemia Type G
The FANCG Gene Fanconi Anemia Type G NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for individuals at risk of Fanconi anemia type G. This sophisticated next-generation sequencing (NGS) test specifically analyzes the FANCG gene to identify mutations that cause this rare inherited disorder affecting bone marrow function and increasing cancer susceptibility.
What Does the FANCG Gene Test Measure?
This advanced genetic test utilizes cutting-edge NGS technology to comprehensively sequence the entire FANCG gene, detecting:
- Point mutations and single nucleotide variants
- Small insertions and deletions
- Copy number variations
- Pathogenic variants affecting DNA repair mechanisms
- Inheritance patterns of FANCG mutations
Who Should Consider This Genetic Test?
This test is recommended for individuals presenting with:
- Unexplained bone marrow failure or aplastic anemia
- Multiple congenital abnormalities including skeletal malformations
- Short stature and abnormal skin pigmentation
- Family history of Fanconi anemia or consanguineous parents
- Increased chromosomal breakage in laboratory testing
- Suspected inherited bone marrow failure syndromes
- Planning for hematopoietic stem cell transplantation
Key Benefits of FANCG Genetic Testing
Undergoing FANCG gene testing provides numerous advantages:
- Accurate Diagnosis: Confirms or rules out Fanconi anemia type G with high precision
- Personalized Treatment: Guides appropriate therapeutic interventions and monitoring
- Family Planning: Provides crucial information for reproductive decisions
- Early Intervention: Enables proactive management of potential complications
- Cancer Risk Assessment: Identifies increased susceptibility to specific cancers
- Genetic Counseling: Supports informed decision-making for affected families
Understanding Your Test Results
Your FANCG gene test results will be carefully interpreted by our genetic specialists:
- Positive Result: Indicates the presence of pathogenic FANCG mutations confirming Fanconi anemia type G diagnosis
- Negative Result: Suggests absence of detectable FANCG mutations but doesn’t completely rule out other forms of Fanconi anemia
- Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
- Carrier Status: Determines if you carry one copy of a mutated FANCG gene
All results include comprehensive genetic counseling to ensure proper understanding and next steps.
Test Details and Pricing
| Test Component | Details |
|---|---|
| Test Name | FANCG Gene Fanconi Anemia Type G 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 testing, we recommend:
- Comprehensive clinical history documentation
- Genetic counseling session with our specialists
- Development of detailed family pedigree chart
- Discussion of testing implications and potential outcomes
- Informed consent process
Nationwide Testing Availability
We proudly offer FANCG genetic testing services across the United States with convenient locations in major cities including:
- New York, NY
- Los Angeles, CA
- Chicago, IL
- Houston, TX
- Phoenix, AZ
- Philadelphia, PA
- San Antonio, TX
- San Diego, CA
- Dallas, TX
- San Jose, CA
Take Control of Your Genetic Health Today
Don’t wait to get the answers you need about Fanconi anemia type G. Our expert genetic team is ready to provide comprehensive testing and support throughout your diagnostic journey.
Call or WhatsApp us now at +1(267) 388-9828 to schedule your FANCG genetic test consultation. Our genetic counselors will guide you through the testing process and answer all your questions about Fanconi anemia type G diagnosis and management.
Book your appointment today and take the first step toward understanding your genetic health with confidence and clarity.

