Hereditary Cancer Panel Test
Short Name: HCP
Also known as: Cancer Risk Panel, Hereditary Cancer Genetic Test, Multi-Gene Cancer Panel
Hereditary Cancer Panel Test test available at DNA Labs India for ₹18,000. Uses Next-Generation Sequencing (NGS) on Blood samples. Results in Results are typically available within 10-14 business days after the sample reaches the laboratory.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 15, 2026
Overview
The purpose of the Hereditary Cancer Panel is to identify inherited genetic mutations that increase an individual's susceptibility to developing certain types of cancer. This information is crucial for individuals with a strong family history of cancer, those diagnosed with cancer at a young age, or those with multiple cancers in the family. The test helps in risk stratification, guiding clinical management such as enhanced surveillance, prophylactic surgeries, or chemoprevention. It also provides valuable information for family members who may be at risk, enabling cascade testing and early intervention.
- Test Code
- 6453
- CPT Code
- 81432
- ICD Code
- Z15.09
- Price
- ₹18,000
- Sample Type
- Blood
- Result Time
- Results are typically available within 10-14 business days after the sample reaches the laboratory.
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No special preparation is required. However, it is recommended to bring any previous genetic test results or family history documentation.
Method: Venipuncture
Laboratory Analysis
A blood sample will be drawn from a vein in your arm. The procedure is quick and minimally invasive.
Report Delivery
You may resume normal activities immediately. A small bruise or soreness at the puncture site is normal and resolves quickly.
Timeline: Results are typically available within 10-14 business days after the sample reaches the laboratory.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the Hereditary Cancer Panel is to identify inherited genetic mutations that increase an individual's susceptibility to developing certain types of cancer. This information is crucial for individuals with a strong family history of cancer, those diagnosed with cancer at a young age, or those with multiple cancers in the family. The test helps in risk stratification, guiding clinical management such as enhanced surveillance, prophylactic surgeries, or chemoprevention. It also provides valuable information for family members who may be at risk, enabling cascade testing and early intervention.
How to Prepare
- No fasting required
- Inform the lab if you have had a blood transfusion or bone marrow transplant
- Wear comfortable clothing with easy access to the arm
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"Early identification of hereditary cancer syndromes allows for tailored surveillance and risk-reduction strategies, potentially reducing cancer mortality in high-risk families."
Last medically reviewed: September 15, 2026
Test Parameters & Specifications
Sample Stability
- Clotted sample
- Hemolyzed sample
- Incorrect labeling
- Sample received after 7 days without proper storage
Understanding Your Results
Pathogenic variant detected
Increased risk for associated cancer(s). Clinical management and family testing recommended.
Likely pathogenic variant detected
High likelihood of increased risk. Similar management as pathogenic variant.
Variant of Uncertain Significance (VUS)
Insufficient evidence to determine risk. Additional testing or family studies may be needed.
No pathogenic variant detected
No known hereditary cancer mutation found. Risk may still exist based on family history.
Consult your physician or genetic counselor if you receive a positive result (pathogenic or likely pathogenic variant) to discuss surveillance and prevention options. Also, consult if you have a VUS to understand its implications.
Limitations
- ⚠This test does not detect all possible genetic causes of cancer
- ⚠Variants of uncertain significance (VUS) may be reported, which require further investigation
- ⚠Negative results do not eliminate the risk of cancer entirely
- ⚠Results should be interpreted in the context of personal and family history
Risks & Considerations
- ●Psychological impact of learning about increased cancer risk
- ●Potential for variants of uncertain significance (VUS) causing anxiety
- ●Risk of genetic discrimination (though limited by laws in some countries)
Interfering Factors
- ●Recent blood transfusion (within 7 days) may dilute DNA
- ●Bone marrow transplantation can affect results
- ●Clotted or hemolyzed samples may cause test failure
- ●Certain medications or supplements are not known to interfere with genetic testing
Compare With Similar Tests
| Test | Hereditary Cancer Panel | Hereditary Cancer Panel | BRCA1/BRCA2 Only |
|---|---|---|---|
| Comparison | Hereditary Cancer Panel |
Frequently Asked Questions
What is the Hereditary Cancer Panel test?
Who should take this test?
How is the test performed?
Do I need to fast before the test?
How long does it take to get results?
What does a positive result mean?
What is a Variant of Uncertain Significance (VUS)?
Is genetic counseling included?
Can this test detect all types of cancer?
Will my insurance cover the cost?
Is home sample collection available?
How accurate is the test?
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Reference 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.
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