G6PD Gene Favism, susceptibility to NGS Genetic Test
Short Name: G6PD Gene Favism Test
Also known as: G6PD deficiency, Favism
G6PD Gene Favism, susceptibility to NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To detect mutations in the G6PD gene for accurate diagnosis of Favism susceptibility, enabling targeted management and family planning.
- Test Code
- 1993
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 weeks
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
Genetic counseling session to discuss clinical history and draw a family pedigree chart for Favism susceptibility assessment.
Method: Venipuncture or FTA card
Laboratory Analysis
Standard blood draw from a vein or one drop on FTA card; minimal discomfort expected.
Report Delivery
Apply pressure to the site to prevent bruising; resume normal activities unless advised otherwise.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To detect mutations in the G6PD gene for accurate diagnosis of Favism susceptibility, enabling targeted management and family planning.
How to Prepare
- Provide a detailed family and clinical history before testing
- Use sterile equipment for blood collection
- Ensure proper labeling of samples with patient information
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early detection of G6PD mutations through NGS testing helps in managing Favism susceptibility, preventing hemolytic crises, and guiding family planning decisions."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Mutation detected
Confirms G6PD deficiency susceptibility; management strategies should be implemented.
No mutation detected
No genetic predisposition to Favism; clinical correlation advised if symptoms persist.
Carrier status
Individual carries one mutated allele; may pass it to offspring but may not exhibit severe symptoms.
Consult a healthcare provider if you experience symptoms like jaundice, dark urine, or unexplained anemia, or if you have a family history of G6PD deficiency.
Risks & Considerations
- ●Minor bruising or discomfort at the needle site
- ●Rare risk of infection or bleeding
- ●Emotional impact of genetic results
Frequently Asked Questions
What is G6PD gene favism?
What are the common symptoms of G6PD deficiency?
How is G6PD deficiency diagnosed?
What is NGS genetic testing for G6PD?
What does the G6PD NGS genetic test involve?
How long does it take to get results for the G6PD genetic test?
What is the cost of the G6PD NGS genetic test in India?
Is home collection available for this test?
Who should consider getting a G6PD genetic test?
Are there any risks associated with the G6PD genetic test?
How should I interpret the results of the G6PD genetic test?
Can G6PD deficiency be treated or managed?
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