Goodyear /
Northern Arizona
Tucson /
Southern Arizona
At Arizona Oncology, we provide leading-edge, comprehensive cancer care for patients with cancer and blood disorders, but we believe prevention and early detection are just as important.
Genetic testing for cancer is a cutting-edge technology that allows doctors to identify whether a person has inherited mutations in certain genes that may increase their risk of developing cancer. This type of testing is particularly useful for individuals who have a family history of cancer or who have already been diagnosed with cancer.
Our partnership with the US Oncology Genetic Risk Evaluation and Testing (GREAT) Program sets us apart as one of the leading organizations in cancer genetics. This program outlines and incorporates best practices in genetic testing and counseling for individuals who may be at higher risk of developing cancer.
Genetic testing can save lives, bring peace of mind, and help you safeguard your health. At Arizona Oncology, we offer personalized cancer-risk assessment with a certified genetic counselor who will evaluate your family history and provide knowledgeable guidance about cancer risk, detection, and prevention. If you decide that genetic testing is right for you, your counselor will also help you interpret the results of your testing and make a plan for next steps. Genetic counseling is available at our locations throughout Arizona.
UNDERSTANDING GENETIC TESTING
Genetic testing is the process of using medical tests to look for specific changes (variants/mutations) in a person’s genes when they have features of a hereditary condition.
WHO SHOULD CONSIDER GENETIC TESTING
Approximately 5-10% of cancers are inherited. Changes in a particular gene can be passed down from a parent and are associated with a higher lifetime risk of cancer.
INSURANCE COVERAGE
A cancer genetics appointment is billed to insurance the same as any appointment to a specialist. Coverage for any additional tests varies by insurance company.
GENETIC TESTING FAQS
Genetic testing is the process of using medical tests to look for changes (variants previously called mutations) in a person’s genes or chromosomes.
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