Informed Consent & Pretest Counseling Checklist
Informed consent is an important step in the genetic testing process. In addition to being required by some state laws and laboratories, thorough pretest counseling will save you time and increase patient understanding when you discuss genetic testing results with the patient.
Discussion of these key points helps prepare an individual for the potential outcomes and limitations of genetic testing.
- Information about the test
- Purpose of testing
- Description of the disorder that will be tested for
- Ability of test to detect disease
- Potential limitations of testing
- Potential benefits and risks of testing
- See risks and benefits table (below)
- Confidentiality protections
- Genetic discrimination risks and protections
- Potential genetic testing results
- Variant of uncertain significance - may need parental/family testing
- Unanticipated results
- Diagnosis unrelated to patient’s presentation
- Potential sample retention by the lab for internal research
- Privacy protections and access to sample and genetic information
- Cost of genetic testing and insurance preauthorization
- Disclosure of results
- Phone vs. in-person
- Anticipated turn-around time
Benefits, Risks and Limitations of Genetic and Genomic Testing
- Diagnose or identify the cause of an individual’s symptoms
- End search for a diagnosis
- If predictive testing, provide more precise estimates of lifetime risk for disease
- Inform personalized management and treatment
- Enable identification of at-risk relatives
- Identify recurrence risk and inform reproductive decision-making
- Possibility of uncertain variants or unanticipated results
- Possibility of a false negative or not coming to a diagnosis; may not identify all possible pathogenic variants (mutations)
- Possibility of a low- or moderate-penetrance gene or variant without established management guidelines
- If predictive testing, not all patients with a pathogenic variant will go on to develop the disease
- May increase anxiety
- May cause blame, guilt, or secrecy in the family
- Labels a patient with a diagnosis or specific risk, increasing concerns about discrimination
For a discussion guide on the Genetic Information Nondiscrimination Act (GINA), see Genetic Information Nondiscrimination Act (GINA).
For a discussion of informed consent in genetics, see Medline/Genetics Home Reference: What is Informed Consent?
American College of Obstetricians and Gynecologists (2017): Committee Opinion No. 693 Summary: Counseling about Genetic Testing and Communication of Genetic Test Results.
American Society of Clinical Oncology (2015): Policy Statement Update Genetic and Genomic Testing for Cancer Susceptibility
National Comprehensive Cancer Network (v.1.2022): Genetic/Familial High Risk Assessment: Breast, Ovarian and Pancreatic, and Colorectal: Principles of Cancer Risk Assessment and Counseling (free registration required).
Reviewed November 2021