Our DNA is made up of many genes, each with a specific function. Every gene can exist in different versions, called gene variants. While most variants are harmless and contribute to natural differences between individuals, some variants can increase the risk of developing cancer.
What is Hereditary Cancer Testing?
- Certain variants (such as BRCA1 and BRCA2) are strongly linked to specific cancers like breast and ovarian cancer.
- Others increase the risk of multiple cancer types because they affect fundamental processes involved in how cells become cancerous.
Having a cancer-related variant does not mean you will definitely develop cancer. It simply means your risk is higher than average. Environmental and lifestyle factors, such as smoking, diet, exercise, and sun exposure, also play a significant role in cancer development.
Overall, it is estimated that 5โ10% of cancers are linked to inherited genetic variants.
Hereditary cancer testing looks for these variants to determine whether you have an increased genetic risk. This information can empower individuals to make proactive lifestyle choices, join risk management programmes, and access more frequent screening for earlier detection.
Value of Hereditary cancer Testing
Hereditary cancer testing provides several benefits:
What Hereditary Cancer Panels do we offer?
Partnering with Your Clinic to Enhance Patient Care
Source Genomics provides clinics and healthcare providers with access to novel biomarker-driven tests across multiple cancer types. Partnering with us will enable access to:
Our accredited hereditary cancer testing services support clinicians in identifying patients with an increased genetic risk, allowing for earlier intervention, targeted screening, and informed family counselling. Get in touch today to find out how you can provide your patients with advanced hereditary cancer testing and clear, actionable results.