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BBS10 Gene Bardet-Biedl syndrome type 10 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

BBS10 Gene Bardet-Biedl syndrome type 10 NGS Genetic Test

Short Name: BBS10 Gene Test

Also known as: BBS10 gene sequencing, Bardet-Biedl syndrome type 10 genetic test, BBS10 NGS test

BBS10 Gene Bardet-Biedl syndrome type 10 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 (NGS)🏠 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 diagnose Bardet-Biedl Syndrome Type 10 by detecting pathogenic mutations in the BBS10 gene using Next-Generation Sequencing (NGS) technology.

Test Code
5370
CPT Code
81479
ICD Code
Q87.8
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

Genetic counseling recommended to discuss test implications and family history.

Method: Venipuncture

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or one drop on FTA card.

Step 3

Report Delivery

Sample transported to lab under ambient conditions for NGS analysis.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review recommended.
2
During the Test:Blood sample collection for DNA extraction and NGS analysis.
3
After the Test:Results available in 3-4 weeks with genetic counseling for interpretation.

About This Test

Who Should Get This Test

To diagnose Bardet-Biedl Syndrome Type 10 by detecting pathogenic mutations in the BBS10 gene using Next-Generation Sequencing (NGS) technology.

How to Prepare

  • Provide clinical history of patient
  • Conduct genetic counseling session to draw pedigree chart of affected family members
  • Ensure proper sample labeling and handling

Doctor's Notes

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

"This test is essential for confirming Bardet-Biedl Syndrome Type 10, enabling early intervention, genetic counseling, and family planning. It helps in managing symptoms like vision loss, obesity, and kidney issues."

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 blood or as required
ContainerEDTA tube or FTA card
Collection MethodVenipuncture

Sample Stability

Blood: 7 days at 2-8°C
FTA card: Stable at room temperature for years
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient sample volume
  • Incorrect container

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the BBS10 gene. Positive results confirm Bardet-Biedl Syndrome Type 10, while negative results may require further testing if symptoms persist.
📊

Pathogenic variant detected

Confirms diagnosis of Bardet-Biedl Syndrome Type 10. Genetic counseling and management recommended.

📊

No pathogenic variants detected

BBS10 gene mutations not found. Consider other genetic causes or clinical evaluation.

📊

Variant of uncertain significance

Further testing or family studies may be needed for clarification.

⚠️ When to Consult a Doctor:

If symptoms such as vision loss, obesity, kidney issues, or extra digits are present, or if there is a family history of Bardet-Biedl Syndrome.

Limitations

  • ⚠May not detect all types of mutations (e.g., large deletions)
  • ⚠Results require interpretation by a genetic counselor

Risks & Considerations

  • ●Minimal physical risk from blood draw
  • ●Psychological impact of genetic results

Interfering Factors

  • ●Sample contamination
  • ●Degraded DNA
  • ●Incorrect sample collection

Frequently Asked Questions

What is the BBS10 Gene Bardet-Biedl Syndrome Type 10 NGS Genetic Test?
It is a genetic test using Next-Generation Sequencing to detect mutations in the BBS10 gene, which causes Bardet-Biedl Syndrome Type 10.
Why is this test recommended?
It is recommended for individuals with symptoms like vision loss, obesity, kidney abnormalities, or a family history of Bardet-Biedl Syndrome.
What is the cost of the test?
The cost is INR 20,000, which includes home sample collection and genetic counseling.
How is the sample collected?
A blood sample is collected via venipuncture or one drop on an FTA card, with home collection available.
Is fasting required for this test?
No, fasting is not required.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What do the results mean?
Results indicate if pathogenic mutations in the BBS10 gene are detected, confirming the diagnosis.
Is genetic counseling included?
Yes, genetic counseling is included to help interpret results and provide guidance.
Can this test be done at home?
Yes, home sample collection is available across India.
What are the risks of the test?
Risks are minimal, mainly related to blood draw, but psychological impact of results should be considered.
Is the test covered by insurance?
Coverage depends on the insurance provider; check with your insurer for details.
What should I do after receiving results?
Consult a genetic counselor or healthcare professional for interpretation and management advice.
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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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.

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