As GINA is Signed Into Law, Most Predict Great Gains, But Some See Shortcomings, Others Find a Mixed Bag
By John T. Aquino,
The Bureau of National Affairs
| 06. 05. 2008
[Quotes CGS's Marcy Darnovsky]
President Bush May 21 signed into law the Genetic Information
Nondiscrimination Act, which prohibits employers, health plans, and
insurers from discriminating against individuals on the basis of
genetic information. The new law was applauded by lawmakers of both
parties and by health-related groups. After the signing, however, some
individuals and organizations, while acknowledging up-front benefits,
began to suggest that, long term, the new law might lead to loss of
privacy and threaten biopharmaceutical research and intellectual
property. Others discounted those fears, predicting the industries
will be strengthened not harmed.
The Genetic Information Nondiscrimination Act (GINA), which was
introduced in Congress six times in various forms over the last 12
years and passed twice by the Senate but not by the House of
Representatives, was approved unanimously by the Senate April 24 and
on a vote of 414-1 by the House May 1 (2 LSLR 373, 5/9/08). The new
law (Pub. L. No. 110-233) aims to eliminate any fear of discrimination
by those who undergo genetic testing and thus encourage people to have
these potentially beneficial tests. The law amends the...
Related Articles
By Annika Inampudi, Science | 08.01.2025
In June, Sara* received a message asking whether she wanted to continue to participate in a massive, multicenter research project led by scientists at Aarhus University in Denmark. The iPsych study, the message said, had sequenced her genetic data from...
The Center for Genetics and Society is delighted to recommend the current edition of GMWatch Review – Number 589. UK-based GMWatch, a long-standing ally, was founded in 1998 by Jonathan Matthews as an independent organization seeking to counter the enormous corporate political power and propaganda of the GMO industry and its supporters. Matthews and Claire Robinson are its directors and managing editors.
CGS works to ensure that social justice, equity, human rights, and democratic governance are front...
By Katherine Drabiak, Journal of Medical Ethics Forum | 08.07.2025
Adapted from Mitochondrial DNA at
National Human Genome Research Institute
Recently, media outlets around the world have been reporting on children born from pronuclear genome transfer (sometimes called “3-parent IVF,” “mitochondrial donation” or “mitochondrial replacement therapy”) at Newcastle Fertility Center...
By Annika Inampudi, Science | 07.10.2025
Before a baby in the United States reaches a few days old, doctors will run biochemical tests on a few drops of their blood to catch certain genetic diseases that need immediate care to prevent brain damage or other serious...