Skip to main content
DNA Labs India

INF2 Gene Focal segmental glomerulosclerosis type 5 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

INF2 Gene Focal segmental glomerulosclerosis type 5 NGS Genetic Test

Short Name: INF2 Gene FSGS Type 5 NGS Test

Also known as: INF2 Gene FSGS Test, FSGS Type 5 Genetic Test, INF2 Mutation Analysis

INF2 Gene Focal segmental glomerulosclerosis type 5 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.

Next-Generation Sequencing Genetic Test🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

To identify mutations in the INF2 gene that cause Focal Segmental Glomerulosclerosis Type 5, aiding in diagnosis, treatment planning, and genetic counseling.

Test Code
5392
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)
Step 1

Sample Collection

Consult with a genetic counselor. Provide detailed clinical history and family pedigree. Ensure informed consent is obtained.

Method: Venipuncture

Step 2

Laboratory Analysis

Blood sample collected via venipuncture into an EDTA tube. For FTA card, one drop of blood is applied. Minimal discomfort expected.

Step 3

Report Delivery

Sample is transported to the laboratory under stable conditions. Follow up with your healthcare provider for results and next steps.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling session to discuss implications, benefits, and limitations. Obtain informed consent.
2
During the Test:Sample collection via blood draw; procedure takes about 10-15 minutes.
3
After the Test:Wait for laboratory analysis and report generation. Discuss results with a healthcare provider for management plan.

About This Test

Who Should Get This Test

To identify mutations in the INF2 gene that cause Focal Segmental Glomerulosclerosis Type 5, aiding in diagnosis, treatment planning, and genetic counseling.

How to Prepare

  • No specific fasting required unless advised by physician
  • Bring valid ID and doctor's prescription
  • Inform about any medications or supplements
  • Ensure sample is properly labeled

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Genetic testing for FSGS Type 5 helps in personalized treatment, family screening, and early intervention to prevent kidney failure."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5-10 ml
ContainerEDTA tube for blood
Collection MethodVenipuncture

Sample Stability

Blood sample stable at room temperature for 48 hours
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Incorrect sample container or labeling
  • Contaminated sample

Understanding Your Results

Results indicate the presence or absence of mutations in the INF2 gene associated with FSGS Type 5. Genetic counseling is recommended for interpretation.
Mutation Detected: Confirms genetic etiology of FSGS; consider family testing and targeted management.
No Mutation Detected: Other genetic or non-genetic causes may be explored; clinical evaluation continues.
Variant of Uncertain Significance (VUS): Requires further analysis or family studies; not diagnostic.
⚠️ When to Consult a Doctor:

If you experience symptoms of FSGS such as proteinuria or edema, have a family history of kidney disease, or receive a positive genetic test result, consult a nephrologist or geneticist promptly.

Limitations

  • ⚠May not detect all types of mutations (e.g., large deletions)
  • ⚠Requires interpretation by a qualified geneticist
  • ⚠Not a standalone diagnostic tool; clinical correlation needed

Risks & Considerations

  • ●Minimal risk from blood draw (e.g., bruising, infection)
  • ●Psychological impact of genetic results
  • ●Potential for genetic discrimination; laws may protect against this

Interfering Factors

  • ●Poor sample quality or contamination
  • ●Technical errors in sequencing
  • ●Hemolyzed or degraded DNA samples

Compare With Similar Tests

TestINF2 Gene Focal segmental glomerulosclerosis type 5 NGS Genetic TestSanger Sequencing for INF2 GeneFSGS Comprehensive Gene PanelKidney Biopsy
ComparisonINF2 Gene Focal segmental glomerulosclerosis type 5 NGS Genetic Test

Frequently Asked Questions

What is the INF2 Gene FSGS Type 5 NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the INF2 gene associated with Focal Segmental Glomerulosclerosis Type 5, a kidney disorder.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to sequence the INF2 gene and identify mutations.
What are the symptoms of FSGS?
Symptoms include proteinuria (excess protein in urine), edema (swelling) in legs and feet, high blood pressure, fatigue, and nausea.
Who should consider this test?
Individuals with symptoms of FSGS, a family history of kidney disease, or those diagnosed with FSGS through biopsy may benefit from genetic testing.
What is the cost of the test in India?
The test costs INR 20000 at DNA Labs India, with free home sample collection available across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in numerous cities across India.
What do the results mean?
Results indicate if a mutation in the INF2 gene is detected, which can confirm a genetic cause for FSGS and guide treatment and family counseling.
Are there any risks to the test?
The test involves minimal risks from blood draw, such as bruising. Genetic results may have psychological implications, so counseling is recommended.
How accurate is the NGS technology?
NGS is highly accurate for detecting mutations, with high sensitivity and specificity, but interpretation requires expert analysis.
Can this test be used for prenatal diagnosis?
It may be used in prenatal settings if a familial mutation is known, but genetic counseling is essential to discuss implications.
What should I do after getting the results?
Discuss results with a nephrologist or geneticist to understand implications, plan treatment, and consider family testing if indicated.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

Related Tests

Amyloid Protein Identification Test

₹300,000

CLCNKB Gene Bartter syndrome type 3 NGS Genetic Test

₹20,000

SLC12A7 Gene Bartter syndrome NGS Genetic Test

₹20,000

SLC12A5 Gene Bartter syndrome NGS Genetic Test

₹20,000

SLC12A2 Gene Bartter syndrome NGS Genetic Test

₹20,000

KCNJ1 Gene Bartter syndrome type 2 NGS Genetic Test

₹20,000
For Hospitals & Clinics

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.

LIMS Integration

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.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.