F9 Gene Hemophilia B NGS Genetic Test
Short Name: Hemophilia B NGS Test
Also known as: Factor IX Deficiency Test, Hemophilia B Genetic Test, F9 Gene Sequencing
F9 Gene Hemophilia B 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 diagnose Hemophilia B by detecting mutations in the F9 gene, identify carriers, guide treatment decisions, and support genetic counseling for family planning.
- Test Code
- 5589
- 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
Clinical history and genetic counseling recommended. Ensure informed consent is obtained.
Method: Blood Draw
Laboratory Analysis
Standard blood draw procedure performed by a trained phlebotomist.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Sample is processed for genetic analysis.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose Hemophilia B by detecting mutations in the F9 gene, identify carriers, guide treatment decisions, and support genetic counseling for family planning.
How to Prepare
- Provide detailed clinical history and family pedigree
- Genetic counseling session recommended prior to testing
- Blood sample drawn using sterile technique
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This genetic test is essential for accurate diagnosis of Hemophilia B, allowing for tailored treatment strategies and informed family planning decisions."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Positive
Pathogenic variant detected, confirming diagnosis of Hemophilia B or carrier status.
Negative
No pathogenic variants detected, reducing likelihood of Hemophilia B, but clinical correlation is advised.
Variant of Uncertain Significance
Genetic variant identified but clinical significance unknown; further testing and counseling recommended.
If symptoms of bleeding disorders are present, family history of Hemophilia B, or for carrier testing and family planning.
Risks & Considerations
- ●Minor bruising at puncture site
- ●Rare risk of infection
Frequently Asked Questions
What is the F9 Gene Hemophilia B NGS Genetic Test?
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Can this test detect carriers of Hemophilia B?
What is the difference between Hemophilia A and B?
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Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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