Cases in Precision Medicine: Concerns About Privacy and Discrimination After Genomic Sequencing.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 31060048.
- Also identified by DOI 10.7326/M18-2666 and PMC identifier 6715527.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Patients and research participants have indicated that privacy of their genetic test results is an important concern, particularly with respect to insurance coverage. Internists and other physicians whose patients ask about legal protections for information generated by genome sequencing for clinical purposes can provide both reassurance and caution. Protections for medical information in general, as well as laws in some states that provide additional safeguards for genetic data, should reassure patients that this information will remain private. Patients themselves will need to weigh the risks versus the benefits of generating genomic data in deciding whether to undergo exome sequencing.
Medical subject headings
- Genetic Counseling
- Genetic Privacy
- Genetic Testing
- Genomics
- Precision Medicine
- Prejudice