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WT1 Gene Wilms tumor type 1, familial NGS Genetic Test

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WT1 Gene Wilms tumor type 1, familial NGS Genetic Test

Short Name: WT1 Gene NGS Test

Also known as: WT1 Gene Mutation Test, Wilms Tumor Genetic Test

WT1 Gene Wilms tumor type 1, familial 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.

NGS Genetic TestPediatric🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to detect mutations in the WT1 gene for early diagnosis of familial Wilms tumor, assess risk in family members, guide targeted treatment, and support genetic counseling.

Test Code
5516
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)
Step 1

Sample Collection

Genetic counseling is recommended to discuss test implications and family history. No specific preparation is required.

Method: Venipuncture or FTA card collection

Step 2

Laboratory Analysis

A blood sample will be collected by a trained phlebotomist using standard venipuncture or FTA card method.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Avoid heavy lifting with the arm used for collection.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling session to draw a pedigree chart and discuss family history.
2
During the Test:Sample collection and laboratory analysis using NGS technology.
3
After the Test:Report generation, delivery, and follow-up consultation as needed.

About This Test

Who Should Get This Test

The purpose of this test is to detect mutations in the WT1 gene for early diagnosis of familial Wilms tumor, assess risk in family members, guide targeted treatment, and support genetic counseling.

How to Prepare

  • Ensure proper patient identification and labeling
  • Use sterile equipment and follow aseptic techniques
  • Collect sample in appropriate container (EDTA tube or FTA card)
  • Transport sample at ambient room temperature as specified

Doctor's Notes

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

"As an obstetrician-gynecologist, I recommend genetic testing for families with a history of Wilms tumor to assess risk and plan for early intervention, especially in prenatal or pediatric settings."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeVaries
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or FTA card collection

Sample Stability

Blood: Stable for 24-48 hours at room temperature
Extracted DNA: Stable for longer periods if stored properly
FTA card: Stable for years at room temperature
Sample Rejection Criteria:
  • Insufficient sample volume
  • Hemolyzed or contaminated sample
  • Improper labeling or documentation
  • Sample not stored or transported correctly

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the WT1 gene, which is critical for assessing Wilms tumor risk.
📊

Positive (Pathogenic variant detected)

Increased risk for Wilms tumor. Genetic counseling and clinical monitoring are advised.

📊

Negative (No pathogenic variant detected)

No mutation identified, but clinical symptoms may require further investigation. Family risk assessment may still be needed.

📊

Variant of uncertain significance

Further testing or family studies recommended to clarify clinical significance.

⚠️ When to Consult a Doctor:

Consult a geneticist, oncologist, or nephrologist if symptoms persist, family history is positive, or for interpretation of test results and management planning.

Limitations

  • May not detect all types of WT1 gene mutations
  • Results require interpretation by a genetic specialist
  • Not a standalone diagnostic tool; clinical correlation is essential
  • Variant of uncertain significance may require additional testing

Risks & Considerations

  • Minor bruising or discomfort at the blood draw site
  • Rare risk of infection or hematoma
  • Psychological impact of genetic results, mitigated by counseling

Interfering Factors

  • Sample degradation or contamination
  • Technical errors during sequencing
  • Insufficient DNA quantity or quality

Compare With Similar Tests

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ComparisonWT1 Gene Wilms tumor type 1, familial NGS Genetic Test

Frequently Asked Questions

What is the WT1 Gene Wilms Tumor NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the WT1 gene, which is linked to familial Wilms tumor, a type of kidney cancer in children.
Who should consider this test?
Individuals with a family history of Wilms tumor, those showing symptoms like abdominal mass or blood in urine, and family members of affected patients for carrier testing.
How is the test performed?
A blood sample or extracted DNA is collected and analyzed using NGS technology to identify mutations in the WT1 gene.
What is the cost of the test?
The test costs INR 20000, which includes sample collection, testing, and report delivery.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is the test accurate?
NGS is a highly accurate method for detecting genetic mutations, but results should be interpreted in conjunction with clinical findings and genetic counseling.
What are the symptoms of Wilms tumor?
Common symptoms include abdominal pain or swelling, blood in the urine, fever, loss of appetite, nausea, vomiting, and fatigue.
Can this test be done at home?
Yes, DNA Labs India offers free home sample collection for this test across India.
Is genetic counseling required before the test?
Genetic counseling is recommended to understand the implications of the test and to draw a family pedigree chart.
What if the test is positive?
A positive result indicates a pathogenic mutation in the WT1 gene, increasing the risk for Wilms tumor. Consultation with a geneticist or oncologist is advised for further management.
Are there any risks to the test?
The test involves a standard blood draw, which has minimal risks such as bruising or infection at the puncture site.
How do I book the test?
You can book the test online through DNA Labs India's website or contact us via phone or WhatsApp for assistance.
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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Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

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