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DNA Labs India

Comprehensive Hereditary Cancer Panel (154 Genes) Test

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Comprehensive Hereditary Cancer Panel (154 Genes) Test

Also known as: Hereditary Cancer Panel, 154 Gene Cancer Test

Comprehensive Hereditary Cancer Panel (154 Genes) Test test available at DNA Labs India for ₹36,000. Uses Next-Generation Sequencing (NGS) on Peripheral Blood samples. Results in 4-6 weeks. Free home collection in 300+ cities across India.

Next-Generation Sequencing (NGS) TestAdults🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify genetic mutations associated with hereditary cancer syndromes for risk assessment and preventive care.

Test Code
2978
Price
₹36,000
Sample Type
Peripheral Blood
Result Time
4-6 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Comprehensive Hereditary Cancer Panel (154 genes) can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Method: Venipuncture

Step 2

Laboratory Analysis

Standard blood draw procedure using venipuncture with EDTA vacutainer.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Keep the sample cool as indicated.

Timeline: 4-6 weeks

Patient Instructions

1
Before the Test:Obtain a doctor's prescription if required. Inform about any medications or health conditions.
2
During the Test:Blood sample collection via venipuncture.
3
After the Test:Monitor the puncture site for any adverse effects. Await results in 4-6 weeks.

About This Test

Who Should Get This Test

To identify genetic mutations associated with hereditary cancer syndromes for risk assessment and preventive care.

How to Prepare

  • Use EDTA vacutainer (2ml)
  • Keep sample cool with cool pack
  • Ensure proper labeling

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"As an obstetrician-gynecologist, I recommend this test for patients with a family history of breast or ovarian cancer to assess genetic risk and inform screening and prevention strategies."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypePeripheral Blood
Sample Volume2 ml
ContainerEDTA Vacutainer (2ml)
Collection MethodVenipuncture
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient volume
  • Improper labeling

Understanding Your Results

Results indicate the presence or absence of genetic mutations linked to hereditary cancer risk.
Detected: Mutation found, indicating increased cancer risk
Not Detected: No mutation found, but risk may still exist based on family history
Variant of Uncertain Significance: Mutation found but clinical significance unknown
⚠️ When to Consult a Doctor:

If results indicate a genetic mutation or variant of uncertain significance, consult a genetic counselor or oncologist for further guidance.

Limitations

  • May not detect all genetic mutations
  • Variants of uncertain significance may require further testing

Risks & Considerations

  • Bruising at puncture site
  • Rare infection risk
  • Minimal discomfort

Interfering Factors

  • Sample quality issues
  • Contamination during collection

Frequently Asked Questions

What is the Comprehensive Hereditary Cancer Panel?
It is a genetic test that analyzes 154 genes to identify mutations associated with hereditary cancer syndromes.
Who should consider this genetic test?
Individuals with a family history of cancer, early-onset cancer, multiple primary cancers, or rare cancer types.
How is the test performed?
The test uses Next-Generation Sequencing (NGS) on a peripheral blood sample.
What sample is required?
A 2 ml peripheral blood sample collected in an EDTA vacutainer.
How long does it take to get results?
Results are typically available within 4-6 weeks.
What does a positive result mean?
A positive result indicates a genetic mutation that increases cancer risk, requiring further consultation.
What if the result is negative?
A negative result means no mutations were detected, but cancer risk may still exist based on other factors.
Are there any risks associated with the test?
Risks are minimal and include bruising or infection at the blood draw site.
Is genetic counseling included?
Yes, genetic counseling is included in the test cost to help interpret results.
How much does the test cost?
The test costs INR 36000, which includes sample collection and counseling.
Is the test covered by insurance?
Coverage depends on the insurance provider; check with your insurer for details.
Where can I get this test done?
DNA Labs India offers home sample collection across numerous cities in India. Book online for convenience.
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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LIMS Integration

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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