What is Genetic Variation?
With the advancement of molecular biomedical science, our understanding of cancer has deepened, and many cancers have now been linked to genetic mutations. The decoding of the human genome marks the beginning of a new era in the diagnosis, prevention, and treatment of diseases. In the case of cancer, genetic differences play a significant role in disease incidence, clinical symptoms, and treatment responses. Therefore, early detection of potential genetic mutations can provide an opportunity to identify the disease early and treat it promptly. 
If your genetic test results indicate that you are in a high-risk group for certain diseases, it may make you more susceptible to developing certain conditions, but this does not necessarily mean you will develop the disease. This is because your gene expression is not fixed and can vary based on your environment, lifestyle, and dietary habits. With the help of doctors and healthcare providers, you can plan an appropriate health management strategy, which is essential for maintaining good health.

Why Test for Cancer Risk Genes?
According to the latest cancer registration report from the National Health Service, cancer has been the leading cause of death in Taiwan since 1982. In 2015, 105,000 people were newly diagnosed with cancer, and 46,000 people died from it, meaning one in every three people dies from cancer. Therefore, screening for hereditary cancer genes, understanding your cancer risk, and undergoing routine tests for early diagnosis and treatment are crucial.

What is Hereditary Cancer?
Cancer is caused by errors in the cell replication process, leading to abnormal cell growth that forms tumors. Some of these proliferating cells may invade other tissues, causing more severe symptoms. Cancer can be classified into two types: sporadic cancer (non-hereditary) and hereditary cancer. Sporadic cancer is caused by a variety of factors such as the environment, diet, lifestyle, and aging, and accounts for approximately 90-95% of all cancer cases. Hereditary cancer accounts for about 5-10% of cancer cases and is caused by genetic abnormalities that increase the risk of developing cancer. Numerous genetic variations associated with hereditary cancer have been identified in current research.

Cancer Risk Gene Screening Eligibility

• Adults aged 18 and older
• Individuals who want to understand if they have hereditary cancer gene mutations
• Individuals with at least two family members diagnosed with the same type of cancer
• Individuals with a family member diagnosed with cancer before the age of 50

The important information provided by Cancer Genomics^® is as follows

• Understand potential genetic predispositions
  Specific gene polymorphisms may influence the development of diseases.
• Cancer Prevention
  Of the factors that trigger cancer, 20-34% are related to genetic abnormalities, while approximately 80% of cancer occurrences are linked to environmental factors and diet. By reducing sources of carcinogens and factors that accelerate cancer progression in daily life, improvements in diet and lifestyle can significantly help prevent cancer. In fact, being mindful in everyday life can make cancer prevention achievable.
• Risk Reduction
  Through dietary habits, environmental factors, lifestyle changes, nutritional supplements, and medical advice, you can optimize the expression of your genetic potential.
• Follow-up Assessment
  Based on potential biochemical imbalances and clinical needs, related follow-up tests will be provided.