HTT Gene Huntington disease NGS Genetic Test
Short Name: HTT NGS Test
Also known as: Huntington's Disease Genetic Test, HTT Gene Analysis, Huntington's Disease NGS Panel
HTT Gene Huntington disease 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 The NGS test for Huntington's disease is processed within 21-28 working days from the time of sample receipt at the laboratory.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To detect CAG trinucleotide repeat expansion in the HTT gene for diagnosis and predictive testing of Huntington's disease. DNA Labs India transparently provides raw data, FASTQ, and VCF files along with the conclusive clinical report.
- Test Code
- 4131
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- The NGS test for Huntington's disease is processed within 21-28 working days from the time of sample receipt at the laboratory.
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No special preparation is needed. Please provide a copy of previous medical records or genetic counseling referral, if available.
Method: Venipuncture or FTA card spot
Laboratory Analysis
A trained phlebotomist will collect a blood sample using standard sterile technique. If using FTA card, one drop of blood will be placed on the card.
Report Delivery
You can resume normal activities immediately. No post-procedure restrictions apply.
Timeline: The NGS test for Huntington's disease is processed within 21-28 working days from the time of sample receipt at the laboratory.
Patient Instructions
About This Test
Who Should Get This Test
To detect CAG trinucleotide repeat expansion in the HTT gene for diagnosis and predictive testing of Huntington's disease. DNA Labs India transparently provides raw data, FASTQ, and VCF files along with the conclusive clinical report.
How to Prepare
- Do not fast for this test
- The sample can be collected at any time of the day
- Carry relevant medical history and family pedigree chart
- Ensure patient identification and test requisition form are completed
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Genetic testing for Huntington's disease provides critical information for patient management and family planning."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Clotted or hemolyzed blood
- Inadequate sample quantity
- Unlabeled or mislabeled sample
- Sample received after prolonged transport without proper temperature control
Understanding Your Results
Normal
Clinical action: No increased risk of Huntington's disease. No medical action needed.
Intermediate
Clinical action: The individual will not develop HD but the allele may expand in offspring; genetic counseling is advised.
Reduced Penetrance
Clinical action: There is a risk of developing HD; regular neurological follow-up and genetic counseling recommended.
Full Penetrance
Clinical action: The individual will develop Huntington's disease within their lifetime. Refer to a neurologist and genetic counselor for management and family planning.
If you have a parent or sibling with Huntington's disease, or if you experience symptoms such as uncontrolled movements, mood changes, or difficulty thinking without other cause, consult a neurologist or medical geneticist for genetic testing.
Risks & Considerations
- ●Minor pain or bruising at the blood draw site
- ●Dizziness or lightheadedness during blood collection
- ●Rarely, infection at the puncture site
Interfering Factors
- ●Contamination of blood sample during collection
- ●DNA degradation due to improper storage or transport
- ●Recent allogeneic bone marrow transplantation
- ●Sample mix-up or mislabeling
Frequently Asked Questions
What is the HTT NGS genetic test?
What is the cost of HTT gene testing in India?
What sample is required for this test?
Do I need to fast before the test?
How long does it take to get test results?
What does a normal HTT gene result mean?
What if my test shows a full penetrance allele?
Can predictive testing be done in unaffected individuals?
Is prenatal testing possible for Huntington's disease?
Are there any risks associated with blood sample collection?
Why is genetic counseling needed before this test?
How can I book this test at DNA Labs India?
Related Tests
Angelman Syndrome Test
₹10,000Duchenne / Becker Muscular Dystrophy (DMD / BMD) Gene Mutation Test
₹14,000Episodic Ataxia Type 1 Hotspot Test
₹11,500Episodic Ataxia Comprehensive Profile Hotspot Test
₹16,000Megalencephalic Leukoencephalopathy with Subcortical Cysts Van Der Knaap and Nalband MLC Gene Hotspot Mutation Test
₹7,500Analyzer 18 SMA 18 Test Panel
₹1,755Reference 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.
