Resource
The Genetic Information Nondiscrimination Act (GINA)
This web resource is a discussion guide for clinicians. It includes background documents, a guide suggesting how and when to talk about GINA with patients, a teaching slide set, and case studies that describe how the law works in a variety of real-world, clinical settings.
This resource was developed by the National Coalition for Health Professional Education in Genetics (NCHPEG), Genetic Alliance, and Johns Hopkins University, and is now hosted by The Jackson Laboratory.
| Type | Website |
| CME Available | No |
| Topic | Ethical, Legal And Social Implications |
| Cost | Free |
| Note | Website with document available |
| Date of Resource |
Genomic Competencies
Experts from the disciplines listed below have tagged this resource as fulfulling genomic competencies.
