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Genetic Discrimination
Overview of Genetic Discrimination
While most Americans are optimistic about the use of genetic information to
improve health, many are concerned that genetic information may be used by insurers
to deny, limit or cancel health insurance, and by employers to discriminate
in the workplace. They are worried that some insurers may choose not to insure
people who are healthy but genetically pre-disposed to future disease onset:
such people incur more health-related costs for the insurance company than individuals
who are not predisposed. Similarly, they fear that some employers might only
employ or retain individuals who are not pre-disposed to future disease onset,
since healthy individuals are more productive. Therefore, many lawmakers, scientists
and health advocacy groups believe that there is a need for federal legislation
to prevent genetic discrimination.
We now have that legislation:
Legislation on Genetic Discrimination
Genetic Nondiscrimination Federal Legislation Archive
National Conference of State Legislatures (NCSL) Summaries
of State Genetics Laws
NHGRI Interest in Genetic NonDiscrimination Legislation
Concerns and Activities
Public fears about genetic discrimination mean that many individuals do not participate
in important biomedical research at the NIH. Many patients also refuse genetic
diagnostic tests that help doctors identify and treat diseases: they worry that
they will lose their health insurance if it is proven that they are genetically
pre-disposed to a disease. NHGRI believes that legislation that gives comprehensive
protection against all forms of genetic discrimination is necessary to ensure
that biomedical research continues to advance. Similarly, it believes that such
legislation is necessary so that patients are comfortable availing themselves
to genetic diagnostic tests.
NHGRI Policy Recommendations for Genetic Discrimination in Insurance or Employment
In the mid 1990s, the National Institutes of Health-Department of Energy (NIH-DOE)
Ethical, Legal and Social Implications (ELSI) Working Group and the National
Action Plan on Breast Cancer (NAPBC) [womenshealth.gov] cosponsored workshops on genetic discrimination
in health insurance and the workplace. The findings and recommendations of the
workshops were published in Science. They are the foundation for policy-making
in the Executive branch, and for legislation at both the state and federal level.
Reports On Genetic Discrimination
- An
Analysis from the Secretary's Advisory Committee on Genetics, Health and Society
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- Secretary's
Advisory Comittee on Genetics, Health and Society [od.nih.gov]
A listing of reports and correspondence from the Secretary's Advisory Comittee
on Genetics, Health and Society (SACGHS), 2003-2004.
- Faces
of Genetic Discrimination: How Genetic Discrimination Affects Real People
[nationalpartnership.org] A July 2004 report from the National Partnership for Women & Families
on behalf of the Coalition for Genetic Fairness.
- Genetic Information and the Workplace
A 1998 report by the Departments of Labor, Justice, Health and Human Services,
and the Equal Employment Opportunity Commission.
- Workshop on Genetic Discrimination and the Workplace:
Implications for Employment, Insurance and Privacy
A 1996 workshop report by the Joint Ethical, Legal, and Social Implications
Working Group and the National Action Plan on Breast Cancer.
- Workshop on Genetic Discrimination and Health Insurance
A 1995 workshop report by the Joint Ethical, Legal, and Social Implications
Working Group and the National Action Plan on Breast Cancer.
- Genetic Information and Health Insurance
A 1993 Report by the Insurance Task Force of the Ethical, Legal, and Social
Implications Program Working Group.
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Last Updated: January 27, 2009
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