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COQ8B Gene Nephrotic syndrome type 9 NGS Genetic Test

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COQ8B Gene Nephrotic syndrome type 9 NGS Genetic Test

Short Name: COQ8B Nephrotic Syndrome Type 9 Test

Also known as: COQ8B Gene Nephrotic Syndrome Test, Nephrotic Syndrome Type 9 Genetic Test

COQ8B Gene Nephrotic syndrome type 9 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS (Next-Generation Sequencing) 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.

NGS Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify mutations in the COQ8B gene that cause Nephrotic Syndrome Type 9, aiding in diagnosis, genetic counseling, and treatment planning.

Test Code
2625
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 (Next-Generation Sequencing)
Step 1

Sample Collection

No special preparation required. Provide detailed clinical history and family history during genetic counseling.

Method: Blood Draw

Step 2

Laboratory Analysis

A blood sample will be drawn by a trained phlebotomist using sterile equipment.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding. Keep the area clean.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling is recommended to discuss test implications, benefits, and limitations.
2
During the Test:Sample collection and DNA analysis using NGS technology.
3
After the Test:Report generation, interpretation by a geneticist, and follow-up consultation.

About This Test

Who Should Get This Test

To identify mutations in the COQ8B gene that cause Nephrotic Syndrome Type 9, aiding in diagnosis, genetic counseling, and treatment planning.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection tubes
  • Label samples correctly

Doctor's Notes

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

"This test is crucial for diagnosing genetic causes of nephrotic syndrome and guiding personalized treatment plans."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodBlood Draw

Sample Stability

Blood samples stable at room temperature for 24 hours
Extracted DNA stable at -20°C for long-term storage
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient sample volume
  • Contaminated samples

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the COQ8B gene associated with Nephrotic Syndrome Type 9.
📊

Positive

Pathogenic variant detected, confirming genetic cause of nephrotic syndrome

📊

Negative

No pathogenic variant detected; other genetic or environmental factors may be considered

📊

Variant of uncertain significance

Further testing or family studies may be needed

⚠️ When to Consult a Doctor:

If symptoms persist, worsen, or if there is a family history of kidney disease, consult a nephrologist or geneticist for further evaluation.

Limitations

  • May not detect all genetic variants
  • Requires genetic counseling for interpretation
  • Results should be correlated with clinical findings

Risks & Considerations

  • Minimal risk from blood draw (e.g., bruising, infection)
  • Genetic privacy and psychological impact

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Improper sample handling

Frequently Asked Questions

What is the COQ8B Gene Nephrotic Syndrome Type 9 NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the COQ8B gene, which can cause Nephrotic Syndrome Type 9.
Why is this test recommended?
It is recommended for individuals with symptoms of nephrotic syndrome, such as proteinuria and edema, to identify a genetic cause and guide treatment.
What are the symptoms of Nephrotic Syndrome Type 9?
Symptoms include excessive protein in urine, swelling in legs and ankles, fatigue, loss of appetite, and weight gain.
How is the test performed?
The test involves analyzing a blood or DNA sample using NGS technology to sequence the COQ8B gene.
What sample is required for the test?
A blood sample, extracted DNA, or one drop of blood on an FTA card is required.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What is the cost of the test?
The test costs INR 20,000 at DNA Labs India, with free home sample collection available.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection across many cities in India.
What does a positive result mean?
A positive result indicates a pathogenic mutation in the COQ8B gene, confirming a genetic cause for nephrotic syndrome.
What does a negative result mean?
A negative result means no pathogenic mutation was detected; other causes may need to be investigated.
Are there any risks associated with the test?
Risks are minimal, such as bruising from blood draw, but genetic testing may have psychological implications.
How can I prepare for the test?
No special preparation is needed, but genetic counseling is recommended to understand the test and its implications.
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.

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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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