CD96 Gene C syndrome NGS Genetic Test
Short Name: CD96 Gene C Syndrome Test
Also known as: TIGIT deficiency, C Syndrome
CD96 Gene C syndrome 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.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of the CD96 Gene C Syndrome NGS Genetic Test is to identify mutations in the CD96 gene that cause this rare immune disorder. It aids in accurate diagnosis, guides treatment decisions, and helps in genetic counseling for affected families.
- Test Code
- 5687
- 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)
Sample Collection
Provide clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected with CD96 Gene C Syndrome.
Method: Venipuncture
Laboratory Analysis
Standard blood collection via venipuncture; alternatively, use extracted DNA or one drop of blood on an FTA card.
Report Delivery
Sample is processed and analyzed in the laboratory; results are reviewed by genetic experts.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the CD96 Gene C Syndrome NGS Genetic Test is to identify mutations in the CD96 gene that cause this rare immune disorder. It aids in accurate diagnosis, guides treatment decisions, and helps in genetic counseling for affected families.
How to Prepare
- No fasting required
- Provide detailed clinical and family history
- Genetic counseling recommended before testing
- Ensure proper sample labeling and handling
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Genetic testing for CD96 Gene C Syndrome is crucial for early diagnosis and management of this rare immune disorder. Consult a genetic counselor for personalized advice and family planning."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or contaminated sample
- Insufficient sample volume
- Incorrect or missing patient information
Understanding Your Results
No pathogenic variants detected
Normal result; CD96 Gene C Syndrome unlikely based on genetic analysis.
Pathogenic variants detected
Abnormal result; confirms CD96 Gene C Syndrome. Consult a geneticist for management.
If symptoms such as recurrent infections, autoimmune issues, or delayed growth persist or worsen, consult a geneticist, immunologist, or pediatrician for further evaluation and management.
Limitations
- ⚠May not detect all genetic variants or mutations
- ⚠Requires interpretation by a genetic counselor or specialist
- ⚠Not a standalone diagnostic tool for all immune disorders
Risks & Considerations
- ●Minor bruising at the blood draw site
- ●Rare risk of infection
- ●Possible fainting during collection
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
- ●Incorrect sample type or handling
Frequently Asked Questions
What is CD96 Gene C Syndrome?
What are the common symptoms of CD96 Gene C Syndrome?
How is CD96 Gene C Syndrome diagnosed?
What is the cost of the CD96 Gene C Syndrome NGS Genetic Test?
Is home sample collection available for this test?
How long does it take to get the test results?
What does a positive test result mean?
Can this test be performed on children?
Is genetic counseling required before the test?
What are the risks associated with the test?
How accurate is the NGS genetic test for CD96 Gene C Syndrome?
What should I do if I test positive for CD96 Gene C Syndrome?
Related Tests
Amino Acids Qualitative Two Dimensional Urine Test
₹1,439Succinylacetone Urine Test
₹5,000RXFP2 Gene Cryptorchidism NGS Genetic Test
₹20,000EFNB1 Gene Craniofrontonasal syndrome NGS Genetic Test
₹20,000MNX1 Gene Currarino syndrome NGS Genetic Test
₹20,000FGFR1 Gene Craniosynostosis, FGFR1 related 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.
