LAMA5 Gene Focal segmental glomerulosclerosis, LAMA5 related NGS Genetic Test
Short Name: LAMA5 Gene FSGS NGS Test
Also known as: LAMA5 Gene Test for FSGS, FSGS Genetic Panel, Laminin Alpha-5 Mutation Analysis
LAMA5 Gene Focal segmental glomerulosclerosis, LAMA5 related NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) 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 identify mutations in the LAMA5 gene associated with Focal Segmental Glomerulosclerosis, enabling early diagnosis, personalized treatment, and family risk assessment.
- Test Code
- 5394
- 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
- Next-Generation Sequencing (NGS)
Sample Collection
No specific preparation required. Provide clinical history and family pedigree chart during genetic counseling.
Method: Venipuncture or FTA Card
Laboratory Analysis
Blood sample collected via venipuncture or one drop on FTA card by trained phlebotomist.
Report Delivery
Apply pressure to the puncture site. Store sample as per instructions for stability.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the LAMA5 gene associated with Focal Segmental Glomerulosclerosis, enabling early diagnosis, personalized treatment, and family risk assessment.
How to Prepare
- Ensure proper identification of patient
- Use sterile collection tubes
- Label samples correctly
- Transport at ambient temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for LAMA5 mutations can aid in early diagnosis, personalized treatment, and family counseling for FSGS patients."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed samples
- Insufficient volume
- Improper labeling
- Contaminated samples
Understanding Your Results
Pathogenic variant detected
Confirms genetic basis for FSGS; consider family screening and tailored management.
No pathogenic variant detected
LAMA5 mutations unlikely; evaluate other genetic or non-genetic factors.
Variant of uncertain significance
Further testing or clinical correlation needed.
Consult a nephrologist if symptoms persist, worsen, or if genetic counseling is needed for family planning.
Limitations
- ⚠May not detect all genetic variants
- ⚠Results require clinical correlation
- ⚠Does not rule out other causes of FSGS
Risks & Considerations
- ●Minimal risk from blood draw: bruising, infection, or discomfort
Interfering Factors
- ●Poor sample quality
- ●Contaminated DNA
- ●Hemolyzed blood samples
Frequently Asked Questions
What is the LAMA5 Gene FSGS NGS Genetic Test?
Why is this test recommended?
What sample is required for the test?
Is fasting required before the test?
How long does it take to get results?
What is the cost of the test?
Is home sample collection available?
What do the results mean?
Can this test diagnose FSGS definitively?
Are there any risks associated with the test?
How should I prepare for the test?
Is the test covered by insurance?
Related Tests
Amyloid Protein Identification Test
₹300,000CLCNKB Gene Bartter syndrome type 3 NGS Genetic Test
₹20,000SLC12A7 Gene Bartter syndrome NGS Genetic Test
₹20,000SLC12A5 Gene Bartter syndrome NGS Genetic Test
₹20,000SLC12A2 Gene Bartter syndrome NGS Genetic Test
₹20,000KCNJ1 Gene Bartter syndrome type 2 NGS Genetic Test
₹20,000Reference 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.
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.
Book Your Test
Enter your details and we'll connect you within 15 minutes.
