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ALK Gene Neuroblastoma type 3, susceptibility to, familial NGS Genetic Test

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ALK Gene Neuroblastoma type 3, susceptibility to, familial NGS Genetic Test

Short Name: ALK Neuroblastoma NGS

Also known as: ALK gene mutation test, Familial neuroblastoma genetic test, ALK NGS panel

ALK Gene Neuroblastoma type 3, susceptibility to, familial 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 Reports are typically delivered within 3 to 4 weeks after sample receipt.. Free home collection in 300+ cities across India.

NGSPediatric🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to identify germline mutations in the ALK gene that predispose to familial neuroblastoma type 3. It aids in confirming diagnosis in symptomatic individuals, presymptomatic testing in at-risk family members, and reproductive risk assessment.

Test Code
5862
CPT Code
81479
ICD Code
Z15.09
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Reports are typically delivered within 3 to 4 weeks after sample receipt.
Fasting Required
No
Method
Next Generation Sequencing (NGS)
Step 1

Sample Collection

No fasting required. A genetic counseling session is recommended prior to testing to discuss implications.

Method: Venipuncture or FTA card spot

Step 2

Laboratory Analysis

Blood sample is drawn by a trained phlebotomist. For FTA card, a drop of blood is placed on the card and allowed to dry.

Step 3

Report Delivery

No special precautions. Resume normal activities.

Timeline: Reports are typically delivered within 3 to 4 weeks after sample receipt.

Patient Instructions

1
Before the Test:No special preparation. Genetic counseling is recommended.
2
During the Test:A blood sample is collected. The procedure is quick and minimally invasive.
3
After the Test:You can resume normal activities immediately. Results will be shared after analysis.

About This Test

Who Should Get This Test

The purpose of this test is to identify germline mutations in the ALK gene that predispose to familial neuroblastoma type 3. It aids in confirming diagnosis in symptomatic individuals, presymptomatic testing in at-risk family members, and reproductive risk assessment.

How to Prepare

  • Use EDTA tube for blood collection
  • For FTA card, apply one drop of blood to each circle
  • Label the sample with patient ID and date
  • Transport at ambient temperature

Doctor's Notes

Reviewed by — MBBS, MD (General Medicine) · Reg. No. 8052

"Early identification of ALK mutations in familial neuroblastoma can guide surveillance and targeted therapy decisions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume2-3 ml blood or 1 FTA card spot
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or FTA card spot

Sample Stability

Blood in EDTA24 hours
Blood in EDTA72 hours
Extracted DNA6 months
FTA card1 year
Sample Rejection Criteria:
  • Hemolyzed blood sample
  • Clotted blood sample
  • Insufficient quantity
  • Improperly labeled sample
  • Sample received after prolonged transit without proper storage

Understanding Your Results

The test report will indicate whether a pathogenic or likely pathogenic variant in the ALK gene was identified. If a variant is found, it confirms the genetic susceptibility to neuroblastoma type 3. A negative result reduces but does not eliminate the risk, as other genes may be involved.
📊

Positive (Pathogenic variant detected)

Confirms genetic susceptibility to familial neuroblastoma type 3. Recommend regular clinical surveillance and family testing.

📊

Negative (No pathogenic variant detected)

No evidence of ALK-related familial neuroblastoma. However, other genetic causes may exist.

📊

Variant of Uncertain Significance (VUS)

A genetic variant was found but its clinical significance is unknown. Further testing of family members may help clarify.

⚠️ When to Consult a Doctor:

Consult a pediatric oncologist or clinical geneticist if you have a family history of neuroblastoma, or if your child shows symptoms such as abdominal swelling, bone pain, or unexplained fever.

Limitations

  • This test detects mutations in the ALK gene only; other genes associated with neuroblastoma are not analyzed.
  • Variant of uncertain significance (VUS) may be reported; further family studies may be needed.
  • Somatic mutations (tumor-only) are not detected by this germline test.
  • Regulatory regions and deep intronic variants may not be covered by NGS.

Risks & Considerations

  • Minimal risk of bruising or infection at the blood draw site
  • Psychological impact of genetic results
  • Potential for incidental findings

Interfering Factors

  • Contaminated or degraded DNA sample
  • Insufficient sample quantity
  • Recent blood transfusion (may dilute DNA)
  • Bone marrow transplantation (may cause chimerism)

Compare With Similar Tests

TestALK Gene Neuroblastoma type 3, susceptibility to, familial NGS Genetic TestALK Gene Single Site AnalysisNeuroblastoma Comprehensive PanelChromosomal Microarray (CMA)
ComparisonALK Gene Neuroblastoma type 3, susceptibility to, familial NGS Genetic Test

Frequently Asked Questions

What is the cost of the ALK Gene Neuroblastoma Type 3 NGS test?
The test costs INR 20000 at DNA Labs India, with free home sample collection.
What sample is required for this test?
Blood or extracted DNA or one drop of blood on an FTA card.
How long does it take to get results?
Reports are typically available within 3 to 4 weeks.
Is fasting required before the test?
No, fasting is not required.
Who should consider this test?
Individuals with a family history of neuroblastoma type 3 or known ALK mutations.
What does a positive result mean?
A positive result indicates a pathogenic ALK mutation, confirming susceptibility to familial neuroblastoma.
Can this test detect all neuroblastoma genes?
No, it only analyzes the ALK gene. Other genes may be involved.
Is genetic counseling included?
Yes, a genetic counseling session is part of the test process.
What is the turnaround time?
3 to 4 weeks.
Is home sample collection available?
Yes, free home sample collection is available across India.
What is the CPT code for this test?
The CPT code is 81479 (unlisted molecular pathology procedure).
Are there any risks associated with the test?
Only minimal risks from blood draw, such as bruising or infection.
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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