Inherited variants.
Personal & family context.
Blood sample
Discuss inherited testingInherited & reproductive testing
Explore carrier screening for family planning and inherited BRCA1/2 testing for personal and family cancer history.
For individuals, couples and donor programmes.
Explore carrier screeningA specific genetic question in the context of your personal and family history.
Understand BRCA1/2 testingThe test
A blood test for inherited BRCA1/2 variants. A pathogenic or likely pathogenic finding may inform treatment, cancer-risk assessment and further testing for relatives. Discuss whether testing is appropriate and what the results mean with your clinician and a genetic counsellor.
Two different questions
Tumour BRCA analysis belongs to the cancer portfolio. A tumour finding may require separate testing to establish whether it is inherited.
Blood sample
Discuss inherited testingTumour tissue
Tumour testingBlood for germline BRCA1/2 testing
Germline BRCA1/2 testing examines inherited variants in a blood sample. It can inform cancer-risk assessment and medical management. Discuss the implications for you and your family with your doctor and a genetic counsellor.
Collection and transport requirements are confirmed before the blood draw.
Your guide to testingTumour profiling does not replace inherited-risk testing. Some findings may prompt an additional germline test. To assess inherited BRCA1/2 risk, your doctor may recommend a separate test and genetic counselling.
The cost and reporting time depend on the selected test and performing laboratory. Before testing begins, we provide the exact quotation and expected reporting time. The quotation specifies the analysis, sample preparation and interpretation included, plus any collection or transport charges. We clarify when the reporting period starts and whether sample review or additional preparation could affect it.
Talk to Epicheck
We will clarify the appropriate analysis, sample requirements, cost and reporting time.
Contact our team