Which category of professionals does the NSGC code of ethics address in relation to genetic counseling?

The NSGC code of ethics is specifically designed to guide the practice of genetic counselors, ensuring that they uphold the highest standards of professional conduct in their interactions with patients. This code addresses the responsibilities genetic counselors have to their patients, including maintaining confidentiality, obtaining informed consent, and providing accurate and clear information regarding genetic testing and its implications.

The focus on patients within the NSGC code of ethics reflects the primary role of genetic counselors as advocates for individuals undergoing genetic evaluation. It emphasizes the importance of respecting patient autonomy and ensuring their needs are prioritized in the genetic counseling process. In this way, the code serves as a foundation for ethical practice within the field, aiming to protect and empower those seeking genetic services.

While other choices, like public health officials, insurance companies, and research institutions, are relevant stakeholders in the broader context of genetics, they are not the primary focus of the NSGC code of ethics. Instead, their roles may intersect with genetic counseling in varying ways, but the ethical guidelines specifically address the direct relationship between genetic counselors and their patients.