Hereditary Cancer Gene Panel

Also referred as

Predictive Cancer Risk Test

For men & women

Starts at:

₹8360

Know more about this test

The Hereditary Cancer Gene Panel is a genetic test that checks for inherited changes in multiple genes that may increase the risk of cancers such as breast, ovarian, colorectal, prostate, pancreatic, and thyroid cancers. It helps doctors guide early detection, preventive care, and personalized health decisions for you and your family.

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Blood

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Understanding Hereditary Cancer Gene Panel

Hereditary cancers are caused by inherited mutations in specific genes that can be passed from one generation to another. The Hereditary Cancer Gene Panel is a comprehensive blood test that evaluates multiple genes at once to assess inherited cancer risk. It can help detect various types of genetic changes such as single nucleotide variants (SNVs), small insertions or deletions (INDELs), and copy number variations (CNVs). These changes can indicate a higher risk of developing cancer.

This panel is particularly useful for individuals with a strong family history of cancer, especially if multiple family members, including younger individuals, are affected. Understanding these genetic risks allows doctors to recommend proactive steps, including early cancer screening, lifestyle modifications, and personalized monitoring.

The Hereditary Cancer Gene Panel helps in evaluating the risk for a wide range of cancers, including breast, ovarian, pancreatic, prostate, colorectal, thyroid, renal, skin, endocrine, gynecological, nervous system cancers, as well as paragangliomas and Li-Fraumeni syndrome. By identifying these risks early, patients and healthcare providers can take preventive measures and make informed treatment and lifestyle decisions.

For this test, it is important to submit the clinical history, histopathology report, previous test results, and a doctor’s prescription at the time of sample collection. The Tata 1mg consolidated Test Requisition Form (TRF) must also be duly filled and submitted.

Lab test results may vary across different laboratories. Abnormal test results require an expert interpretation. Therefore, never try to self-medicate at home based solely on these results, and always consult a doctor for proper understanding of the test results.

Note: Genetic counseling can be provided. If interested, please send the request to this email id: [email protected]

What does Hereditary Cancer Gene Panel measure?

The Hereditary Cancer Gene Panel detects inherited (germline) mutations in multiple genes linked to an increased risk of hereditary cancers. By analyzing these genes, the test identifies genetic alterations that may raise susceptibility to cancers such as breast, ovarian, pancreatic, prostate, colorectal, thyroid, renal, endocrine, and gynecological cancers. Using Next-Generation Sequencing (NGS), it accurately detects single nucleotide variants (SNVs), small insertions or deletions (INDELs), and copy number variations (CNVs). The results provide a comprehensive genetic profile that helps doctors assess hereditary cancer risk, plan personalized screening and prevention strategies, guide treatment decisions for patients with existing cancers, and offer genetic counseling to at-risk family members.

Test Information is reviewed by: Dr. Swati Gupta (Anand), MBBS, MD Lab Medicine and written by Dr. Lipika Khurana, BDS, PGDHHM . The test details are for information purpose only. Consult a doctor before taking any test. Last updated on: 7th Apr 2026

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Hereditary Cancer Gene Panel test price for other cities

Price in	Hyderabad	Rs. 8360
Price in	Bangalore	Rs. 8360
Price in	Mumbai	Rs. 8360
Price in	Pune	Rs. 8360
Price in	Chennai	Rs. 8360

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Easy online booking

Search for tests and packages, book your preferred time slot and enter your address for seamless at-home lab tests.

Live tracking of phlebotomist

Track our trained phlebotomist's real time location for seamless sample collection.

Safe Sample Collection

Our phlebotomists follow strict safety protocols to collect samples safely at home and on time.

Sample received at lab

Samples are transported securely to our accredited labs with world-class machines for testing by qualified experts.

Quick, Doctor-Verified Reports

Get doctor-approved reports via email and WhatsApp, with options for doctor follow-ups and AI insights.

FAQs related to Hereditary Cancer Gene Panel

What is the Hereditary Cancer Gene Panel?

This is a genetic test that examines multiple genes to assess your inherited risk of developing certain types of cancer. It helps identify mutations that may increase susceptibility to cancers such as breast, ovarian, pancreatic, prostate, colorectal, thyroid, renal, endocrine, and gynecological cancers.

Who should get this test?

This panel is recommended for individuals with a strong family history of cancer, particularly when multiple family members are affected. It is also suitable for people who were diagnosed with cancer at a young age or who have multiple primary cancers. Additionally, those who want to understand their inherited cancer risks for personal or family planning purposes can benefit from this test.

How is the Hereditary Cancer Gene Panel performed?

A phlebotomist will clean your skin using an antiseptic alcohol cotton swab or wipe and take blood samples from your vein using a needle. The blood sample will be stored safely and transported to the laboratory for analysis.

Do I need to fast before taking the Hereditary Cancer Gene Panel?

No fasting is required for this test. You can schedule it at your convenience without avoiding food or water beforehand.

Is there any risk associated with the Hereditary Cancer Gene Panel?

No, the Hereditary Cancer Gene Panel is generally safe with minimal risks. However, you may feel slight discomfort during blood sample collection but chances of serious complications are extremely rare.

What types of genetic changes does this panel detect?

The panel detects: Single nucleotide variants (SNVs); Small insertions or deletions (INDELs); and Copy number variations (CNVs).

What do abnormal results mean?

Abnormal results may indicate the presence of inherited mutations that increase your risk of certain cancers. These results can guide your doctor in planning early screening, preventive strategies, treatment decisions, and genetic counseling for family members.

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