University of Delaware
Education & Human Development

Center for Disabilities Studies

Quick Links
  • Quick Links
    • Programs at CDS
    • Contacts at CDS
    • CDS Opportunities
    • Our Annual Report
    • Upcoming Events
    • Close
Make a Gift to the center
  
Make a Gift to the center
Main Menu
  • Home
  • Who We Are
    • Our Mission
    • Our Core Connections
    • Our Funding
    • CDS by the Numbers
    • Our Team
    • Our Advisory Council
    • Support CDS
  • What We Do
    • At a Glance
    • Assistive Technology
    • K-12 Education
    • University Education
    • Transitions to Adulthood
    • Autism Initiatives
    • Health & Wellness
    • Advocacy
  • Publications
    • Our Annual Report
    • Peer-Reviewed Research
    • Book and Chapter Citations
    • Posters and Presentations
    • CDS Reports
    • The delAware
    • AT Messenger
  • Videos & Slideshows
    • About CDS
    • Advocacy
    • Assistive Technology
    • Education
    • Employment
    • Events
    • Health and Wellness
  • Blog
    • Inclusion Blog
  • News
    • From CDS
    • Outside CDS
    • Opportunities at CDS

No Insurance Discrimination Based on Genetics

Posted on June 27, 2019

No Insurance Discrimination Based on Genetics

An act to amend Title 18 of the Delaware Code relating to genetics-based discrimination

Synopsis:

S.B. 144 would fill a loophole in the federal Genetic Information Nondiscrimination Act of 2008, which sought to limit insurers’ use of genetic test data to deny consumers insurance coverage. As it is worded, the law only applies to health insurance providers. It does not cover non-health insurance, meaning that insurers offering disability or long-term care plans, for example, are not subject to the anti-discrimination mandate. S.B. 144 would extend the same protection to non-health insurance. It would also prohibit genetic test results being sent directly to insurance companies without the consumer’s written consent. S.B. 144 would not completely bar insurance companies from using consumers’ genetic information. It allows insurance companies to take test results into consideration when they are “reasonably related to anticipated claims experience.” Nevertheless, insurers have expressed concern about tightening genetic discrimination laws, as it will decrease their ability to identify and deny consumers they deem too risky to underwrite.

Sen. Stephanie Hansen
Sen. Stephanie Hansen
S.B. 144 lead sponsor

Supporters:

Sens. Hansen (D), Delcollo (R), Ennis (D), Lockman (D), Poore (D), Sokola (D); Reps. Bentz (D), Baumbach (D), Brady (D), Chukwuocha (D), Heffernan (D), Kowalko (D), Longhurst (D), Osienski (D), Seigfried (D), Spiegelman (R); Insurance Commissioner Trinidad Navarro, Governor’s Advisory Council for Exceptional Citizens, League of Women Voters.

Opponents:

Northwestern Mutual and other large insurance providers.

Links to Additional Resources:

  • S.B. 144
  • Genetic Information Nondiscrimination Act of 2008
  • WDMR: “Lawmakers seek to keep genetic results out of insurance companies’ hands”
  • U.S. National Library of Medicine: “Can the results of direct-to-consumer genetic testing affect my ability to get insurance?”
  • The Atlantic: “The loopholes in the law prohibiting genetic discrimination”

Center for Disabilities Studies

461 Wyoming Road

Newark, DE 19716

Phone: 302-831-6974

TDD: 302-831-4689

UD
  • UD Twitter
  • UD Facebook
  • UD Instagram
  • UD YouTube
  • UD Pinterest
  • UD Linkedin
©2025 University of Delaware
Comments
Legal Notices
Accessibility Notice