PT - JOURNAL ARTICLE AU - A W Cappelen AU - O F Norheim AU - B Tungodden TI - Genomics and equal opportunity ethics AID - 10.1136/jme.2007.021162 DP - 2008 May 01 TA - Journal of Medical Ethics PG - 361--364 VI - 34 IP - 5 4099 - http://jme.bmj.com/content/34/5/361.short 4100 - http://jme.bmj.com/content/34/5/361.full SO - J Med Ethics2008 May 01; 34 AB - Genomics provides information on genetic susceptibility to diseases and new possibilities for interventions which can fundamentally alter the design of fair health policies. The aim of this paper is to explore implications of genomics from the perspective of equal opportunity ethics. The ideal of equal opportunity requires that individuals are held responsible for some, but not all, factors that affect their health. Informational problems, however, often make it difficult to implement the ideal of equal opportunity in the context of healthcare. In this paper, examples are considered of how new genetic information may affect the way individual responsibility for choice is assigned. It is also argued that genomics may result in relocation of the responsibility cut by providing both new information and new technology. Finally, how genomics may affect healthcare policies and the market for health insurance is discussed.