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10th Annual International Clinical Cancer Genetics and Genomics Conference sponsored by University of Chicago Genetics in Clinical Cancer Care: Controversies, Insights & Scalable Solutions April 22

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How to fill out genetics in clinical cancer

01

Obtain detailed family history including any cancer diagnoses and ages of onset

02

Refer patient to genetic counselor for risk assessment and genetic testing recommendations

03

Collect genetic testing samples (blood, saliva, etc.) as needed

04

Review genetic test results with patient and provide appropriate counseling and management recommendations

Who needs genetics in clinical cancer?

01

Individuals with a strong family history of cancer

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Patients with a personal history of early onset cancers

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Individuals with multiple primary cancers

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What is genetics in clinical cancer?

Genetics in clinical cancer refers to the study of how genes and genetic variations contribute to the development and progression of cancer.

Who is required to file genetics in clinical cancer?

Healthcare providers, researchers, and laboratories involved in the diagnosis and treatment of cancer patients are required to file genetics in clinical cancer.

How to fill out genetics in clinical cancer?

Genetics in clinical cancer can be filled out by providing detailed information about the patient's genetic profile, family history of cancer, and any genetic testing results.

What is the purpose of genetics in clinical cancer?

The purpose of genetics in clinical cancer is to help healthcare providers better understand the genetic factors that contribute to cancer development, identify patients at risk, and tailor treatment plans accordingly.

What information must be reported on genetics in clinical cancer?

Information such as genetic mutations, family history of cancer, genetic test results, and treatment plans must be reported on genetics in clinical cancer.

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