After years of research and clinical testing, we have developed non-invasive, accurate blood tests for early detection of cancer. By making cancer prevention routine, we enable everyone to take control of their own health. The more people take our breakthrough blood tests, the more lives we can save. Life over cancer.

Hereditary Cancer Risk Test

Your DNA can determine your risk for cancer.

We test for 25 hereditary cancers using 98 different genes.

Get the most comprehensive, affordable test available.

Knowing your risk can help you be proactive.

Inherited genetic mutations can increase your cancer risk up to 40 times.1, 2, 3 CellMax Life offers the most comprehensive home test - measuring more genes, more affordably than any other test on the market today.

Our Hereditary Cancer Risk Test can help you:


Screen Early

You can work with your doctor on a screening program. This may include starting at a younger age or getting screened more frequently so cancer can be detected early.

Take Precautions

Your doctor may prescribe preventative medication to reduce cancer risk. Individuals at a higher risk for cancer can benefit from taking FDA-approved drugs to lower the chance of developing certain cancers.

Care for Your Family

Your family members can also determine their risk status and take charge of their health. Parents, siblings and children have up to a 50% chance of carrying the same mutation, putting them at increased risk.4

Hereditary cancer runs in families.

Your results can help loved ones manage their health proactively too.

Early cancer detection improves survival rate. 5, 6

How The Test WorksIn 3 simple steps

Purchase your test online and receive a ready-to-use collection kit in the mail.

Step 1

Provide a saliva sample and send to the lab. Pre-paid envelope included.

Step 2

Receive your easy-to-read report in 3 to 4 weeks.

Step 3

Talk to your doctor about a personalized health plan for yourself and your family.

Who is this test for?

  • Healthy individuals who want to know if they are at an increased risk for cancer.
  • Individuals with a family history of cancer:
    • A combination (usually 2 or more) of cancers on the same side of the family.
    • A family member with breast, colorectal, endometrial, and possibly other types of cancers before age 50.
    • A family member with a rare (i.e. triple-negative breast cancer, ovarian cancer) cancer at any age.
  • Individuals in certain ethnic groups (eg., Ashkenazi Jewish) that have an increased risk for certain cancers.
  • Individuals with cancer who want to understand if their cancer was hereditary and if they are at an increased risk for other cancers.

What Does the Test Include

  • A detailed report on the presence of absence of mutations associated with increased cancer risk.
  • Review of test results by board-certified physicians.

Why CellMax Life?

CellMax Life’s Hereditary Cancer Test is the most comprehensive and affordable test for hereditary cancer available on the market today.

Our Comprehensive Cancer Risk Test looks for mutations in – other home tests only look at 30 or fewer genes – giving you more complete information related to 25 hereditary cancers.

Cancer/tumor risks tested:

  • Breast
  • Ovaries
  • Endometrium (Uterine)
  • Myometrium (Uterine)
  • Prostate Gland
  • Stomach
  • Large Bowel & Rectal
  • Lung and Pleura
  • Small Intestines
  • Esophagus
  • Urinary Tract & Bladder
  • Exocrine Pancreas
  • Endocrine Pancreas
  • Kidneys
  • Cervix
  • Skin
  • Bone
  • Thyroid Gland
  • Liver
  • Soft Tissue
  • Misc. Endocrine Glands
  • Blood
  • Head & Neck
  • Central Nervous System
  • Peripheral Nervous System

Testing is performed at our CLIA-certified and CAP-accredited lab in California, conforming to the highest quality standards for clinical testing.


  1. Easton, Douglas F., Deborah Ford, and D. Timothy Bishop. "Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium." American journal of human genetics 56.1 (1995): 265.
  2. Petrucelli, Nancie, Mary B. Daly, and Gerald L. Feldman. "BRCA1 and BRCA2 hereditary breast and ovarian cancer." (2013).
  3. Antoniou A, Pharoah PDP, Narod S, et al. Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies. American Journal of Human Genetics. 2003

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