BMP1 Gene Osteogenesis imperfecta type 13 NGS Genetic Test
Short Name: BMP1 OI Type 13 NGS Test
Also known as: BMP1-related Osteogenesis Imperfecta, OI Type 13
BMP1 Gene Osteogenesis imperfecta type 13 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 Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To detect mutations in the BMP1 gene for the diagnosis of Osteogenesis Imperfecta Type 13, enabling early intervention and management.
- Test Code
- 5089
- 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 of patient and genetic counseling session to draw a pedigree chart of family members affected with OI.
Method: Blood Draw or Cheek Swab
Laboratory Analysis
Blood draw from vein or cheek swab collection following standard procedures.
Report Delivery
Sample labeled and transported to lab under ambient room temperature for processing.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To detect mutations in the BMP1 gene for the diagnosis of Osteogenesis Imperfecta Type 13, enabling early intervention and management.
How to Prepare
- Use sterile equipment
- Avoid hemolysis in blood samples
- Follow FTA card instructions if applicable
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Early genetic diagnosis of OI Type 13 allows for proactive management to reduce fracture risk and improve quality of life."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Contaminated or hemolyzed samples
- Improper labeling
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of OI Type 13; genetic counseling recommended.
No pathogenic variant detected
OII Type 13 unlikely; consider other genetic or clinical causes.
Variant of uncertain significance
Further testing or family studies may be needed.
If symptoms such as frequent fractures, blue sclera, or hearing loss are present, or if there is a family history of OI.
Limitations
- ⚠May not detect all genetic variants
- ⚠Results require clinical correlation
Risks & Considerations
- ●Minor bruising or discomfort from blood draw
- ●Minimal risk of infection
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
Frequently Asked Questions
What is the BMP1 Gene Osteogenesis Imperfecta Type 13 NGS Genetic Test?
Why is this test recommended?
What are the symptoms of OI Type 13?
How is the test performed?
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How long does it take to get results?
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Is home sample collection available?
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₹7,000Reference 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.
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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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