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NIPA1 Gene SPG6 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

NIPA1 Gene SPG6 NGS Genetic Test

Short Name: SPG6 Genetic Test

Also known as: SPG6 Genetic Test, NIPA1 Gene Mutation Test

NIPA1 Gene SPG6 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) Genetic TestAll ages, with symptoms often beginning in early adulthood🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Spastic Paraplegia Type 6 (SPG6) by identifying pathogenic mutations in the NIPA1 gene through advanced NGS technology.

Test Code
1812
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 session to draw a family pedigree and obtain clinical history. No fasting required.

Method: Venipuncture for blood or DNA extraction

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or DNA extracted from provided sample.

Step 3

Report Delivery

Sample processed and analyzed using NGS; reports delivered in 3 to 4 weeks.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Schedule a genetic counseling session and provide clinical history. No special preparation needed.
2
During the Test:Blood sample collection takes about 10-15 minutes.
3
After the Test:Results available online or via email/WhatsApp in 3 to 4 weeks.

About This Test

Who Should Get This Test

To diagnose Spastic Paraplegia Type 6 (SPG6) by identifying pathogenic mutations in the NIPA1 gene through advanced NGS technology.

How to Prepare

  • Provide a blood sample or extracted DNA
  • Use sterile containers
  • Follow home collection guidelines if applicable

Doctor's Notes

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

"Early genetic testing for SPG6 is vital for managing symptoms and family planning. Consult a genetic counselor to interpret results and discuss care options."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required for testing
ContainerSterile tube or FTA card
Collection MethodVenipuncture for blood or DNA extraction

Sample Stability

Blood samples stable at room temperature for 48 hours
DNA extracts stable at -20°C for long-term storage
Sample Rejection Criteria:
  • Hemolyzed or contaminated samples
  • Insufficient sample volume

Understanding Your Results

Results indicate presence or absence of mutations in the NIPA1 gene associated with SPG6. Positive results confirm diagnosis; negative results may require further investigation if symptoms persist.
Consult the genetic counseling report for mutation details
Discuss implications with a healthcare provider
Consider family genetic testing for risk assessment
⚠️ When to Consult a Doctor:

If symptoms such as leg stiffness, walking difficulties, or bladder/bowel issues persist, or if there is a family history of SPG6.

Limitations

  • Test only detects mutations in the NIPA1 gene; other SPG-related genes are not covered
  • Results may require confirmation with additional testing

Risks & Considerations

  • Minor bruising or discomfort at the blood draw site
  • Minimal risk of infection

Interfering Factors

  • Contaminated DNA sample
  • Improper sample storage

Frequently Asked Questions

What is SPG6?
Spastic Paraplegia Type 6 (SPG6) is a rare genetic disorder affecting the nervous system, causing progressive muscle stiffness and weakness in the legs.
How is SPG6 diagnosed?
SPG6 is diagnosed through genetic testing, specifically the NIPA1 Gene SPG6 NGS Genetic Test, which analyzes DNA for mutations in the NIPA1 gene.
What are the symptoms of SPG6?
Symptoms include progressive muscle stiffness and weakness in the legs, difficulty walking, muscle spasms, and bladder or bowel problems.
What is the cost of the NIPA1 Gene SPG6 NGS Genetic Test?
The test costs INR 20000 at DNA Labs India, which includes genetic testing, counseling, and result interpretation.
What sample is required for the test?
A blood sample, extracted DNA, or one drop of blood on an FTA card is required.
Is fasting required before the test?
No, fasting is not required for this genetic test.
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 online bookings across India.
Who should consider this test?
Individuals with symptoms of SPG6, those with a family history of the disorder, or as recommended by a neurologist or genetic counselor.
What does a positive result mean?
A positive result confirms the presence of NIPA1 gene mutations associated with SPG6, aiding in diagnosis and management.
Can this test be used for family planning?
Yes, genetic counseling based on test results can help assess risks for family members and guide reproductive decisions.
Is the test available in multiple cities?
Yes, the test is available in numerous cities across India, including Mumbai, Delhi, Bangalore, and others, with home collection services.
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 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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