Genome testing makes it possible to generate very basic knowledge about your biological heritage. Genetics research makes it possible to pinpoint the cause of some hereditary conditions, and in the best cases it is possible to prevent and treat the condition. The results of genome testing can, however, be unclear and knowledge about the genes limited, and it is therefore not always possible to identify any genetic defect causing a hereditary condition in a family.
Genome research can also generate uncertainty and give you knowledge that can be difficult to handle. You should be aware of both the potential benefits and risks of genome testing.
Benefits
Knowledge
Better research
Better treatment
Better public health / public health services
Financial advantages (for the public health services)
Earlier diagnoses
Prevention rather than treatment
Personalised medicine
Risks
Impact on private life
Misuse of information
Informed consent – incomplete or misunderstood information
Scientific uncertainty – false hopes or concerns
Read about ethical dilemmas in genome testing
© FARGEN all rights reserved. Designed and developed by Sansir - Login