Genetic Information Nondiscrimination Act





















































Genetic Information Nondiscrimination Act of 2008
Great Seal of the United States
Long title An act to prohibit discrimination on the basis of genetic information with respect to health insurance and employment.

Acronyms .mw-parser-output .nobold{font-weight:normal}
(colloquial)
 GINA
Enacted by the 110th United States Congress
Effective May 21, 2008
Citations
Public law 110-233
Statutes at Large 122 Stat. 881
Codification
Acts amended
Employee Retirement Income Security Act
Public Health Service Act
Internal Revenue Code of 1986
Social Security Act of 1965
Fair Labor Standards Act
Titles amended
29, 42
U.S.C. sections amended 29 USC §216(e)
29 USC §1132
29 USC §1182
29 USC §1182(b)
29 USC §1191b(d)
42 USC §300gg–1
42 USC §300gg–1(b)
42 USC §300gg–21(b)(2)
42 USC §300gg–22(b)
42 USC §300gg–51 et seq.
42 USC §300gg–61(b)
42 USC §300gg–91
42 USC §300gg–91(d)
42 USC §1395ss
42 USC §1395ss(o)
42 USC §1395ss(s)(2)
Legislative history


  • Introduced in the House of Representatives as H.R. 493 by Louise Slaughter (D-NY) on January 16, 2007


  • Committee consideration by Education and Labor, Energy and Commerce, Subcommittee on Health, and Ways and Means


  • Passed the House on April 25, 2007 (420-3)


  • Passed the Senate on April 24, 2008 (95-0) with amendment


  • House agreed to Senate amendment on May 1, 2008 (414-1)


  • Signed into law by President George W. Bush on May 21, 2008

The Genetic Information Nondiscrimination Act of 2008 (Pub.L. 110–233, 122 Stat. 881, enacted May 21, 2008, GINA, pronounced Jee-na), is an Act of Congress in the United States designed to prohibit some types of genetic discrimination. The act bars the use of genetic information in health insurance and employment: it prohibits group health plans and health insurers from denying coverage to a healthy individual or charging that person higher premiums based solely on a genetic predisposition to developing a disease in the future, and it bars employers from using individuals' genetic information when making hiring, firing, job placement, or promotion decisions.[1] Senator Ted Kennedy called it the "first major new civil rights bill of the new century."[2] The Act contains amendments to the Employee Retirement Income Security Act of 1974[3] and the Internal Revenue Code of 1986.[4]


In 2008, on April 24 H.R. 493 passed the Senate 95-0. The bill was then sent back to the House of Representatives and passed 414-1 on May 1; the lone dissenter was Congressman Ron Paul.[5] President George W. Bush signed the bill into law on May 21, 2008.[6][7]


In 2017, HR 1313[8] was introduced which would let employers demand workers' genetic test results.[9]




Contents






  • 1 Legislative history


  • 2 Arguments for


  • 3 Arguments against


  • 4 See also


  • 5 References


  • 6 External links





Legislative history


In the 104th Congress (1995–1996) several related bills were introduced.[10]



  • The Genetic Privacy and Nondiscrimination Act of 1996, S. 1416: Sen. Mark Hatfield and H.R. 2690: Rep. Clifford Stearns

  • The Genetic Fairness Act of 1996, S. 1600: Sen. Dianne Feinstein

  • The Genetic Information Nondiscrimination in Health Insurance Act of 1995, H.R. 2748: Rep. Louise Slaughter and S. 1694: Sen. Olympia Snowe

  • Genetic Confidentiality and Nondiscrimination Act of 1996, S. 1898: Sen. Pete Domenici


In 1997, the Coalition for Genetic Fairness (CGF) was formed by several patient and civil rights groups to spearhead genetic nondiscrimination legislation on Capitol Hill. The CGF became the primary non-governmental driver of Federal genetic non-discrimination legislation.


In 2003, GINA was introduced as H.R. 1910, by Louise Slaughter, D-NY, and as S. 1053 by Senator Snowe, R-ME.


In 2005, it was proposed as H.R. 1227 by Representative Biggert, R-IL, and as S. 306 by Senator Snowe, R-ME.


The Genetic Information Nondiscrimination Act of 2007 was introduced into the United States House of Representatives as H.R. 493 by Representatives Slaughter, Biggert, Eshoo, and Walden. It passed the House by a 420 - 9 - 3 vote on April 25, 2007.


The same bill was introduced into the United States Senate as S. 358 by Senators Olympia Snowe, Ted Kennedy, Mike Enzi, and Christopher Dodd.[11][12][13][14] On 2008-04-24, the Senate approved the bill 95-0, with five Senators not voting (including presidential candidates McCain, Clinton, and Obama). It had been subject of a "hold" placed by Tom Coburn, M.D., Republican U.S. Senator from Oklahoma.[15]


The bill was then sent back to the House of Representatives and passed 414 - 16 - 1 on May 1, 2008 (the lone dissenter was Congressman Ron Paul). President George W. Bush signed the bill into law on May 21, 2008.[6] The text of the final approved version of GINA is here.


On May 17, 2016, the Equal Employment Opportunity Commission (EEOC) amended various GINA regulations providing further clarification on acceptable workplace wellness programs.[16] The new guidelines are effective on July 16, 2016.[17] The new amendments require that (1) employee wellness programs are voluntary; (2) employers cannot deny health care coverage for non participation, or (3) take adverse employment actions against or coerce employees who do not participate in wellness programs. Additionally, the new GINA regulations cover spousal participation in wellness programs and employers may not ask employees or covered dependents to agree to permit the sale of their genetic information in exchange for participation in wellness plans.[18]



Arguments for


Along with an overview of the topic, the NIH National Human Genome Research Institute states that "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." This point of view thus regards GINA as important for the advancement of personalized medicine.[19]


The Coalition for Genetic Fairness[20] presents some arguments for genetic nondiscrimination. As of 2007, their argument makes the claim that because all humans have genetic anomalies, this would prevent them from accessing medication and health insurance. The Coalition also cites the potential for misuse of genetic information.


The GINA legislation has historically received support from the majority of both Democrats and Republicans, as evidenced by the 420-3 vote in 2007 by the House.



Arguments against


The National Association of Manufacturers, the National Retail Federation, the Society for Human Resource Management, the United States Chamber of Commerce, and other members of the Genetic Information Nondiscrimination in Employment Coalition (GINE) say the proposed legislation is overly broad and are concerned the bills would do little to rectify inconsistent state laws and hence might increase frivolous litigation and/or punitive damages as a result of ambiguous record-keeping and other technical requirements. In addition, they are concerned that it would force employers to offer health plan coverage of all treatments for genetically-related conditions.[21]


Insurance industry representatives argued that they may need genetic information. Without it, more high-risk people would buy insurance, causing rate unfairness.[22]


While GINA has been cited as a strong step forward, some say that the legislation does not go far enough in enabling personal control over genetic testing results.[23] The law does not cover life, disability, or long-term care insurance, which may cause some reluctance to get tested.[22][24]


Some legal scholars have called for the addition of a "disparate impact" theory of action to strengthen GINA as a law.[25]



See also



  • Employment Non-Discrimination Act

  • Genetic discrimination

  • Genealogical DNA test

  • Gattaca

  • Genetic privacy



References





  1. ^ Statement of Administration policy, Executive Office of the President, Office of Management and Budget, April 27, 2007


  2. ^ "Kennedy in support of genetic information nondiscrimination bill". April 24, 2008. Retrieved May 28, 2008..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}


  3. ^ See Act sec. 101.


  4. ^ See Act sec. 103.


  5. ^ "Final Vote Results for Roll Call 234". Clerk of the House of Representatives. May 1, 2008. Retrieved October 26, 2009.


  6. ^ ab Keim, Brandon (May 21, 2008). "Genetic Discrimination by Insurers, Employers Becomes a Crime". Wired.com. Retrieved May 28, 2008.


  7. ^ National Human Genome Research Institute (May 21, 2008). "President Bush Signs the Genetic Information Nondiscrimination Act of 2008". Retrieved Feb 17, 2014.


  8. ^ "H.R.1313 - Preserving Employee Wellness Programs Act". Congress.gov. Retrieved March 12, 2017.


  9. ^ Sharon Begley (March 10, 2017). "The House GOP is pushing a bill that would let employers demand workers' genetic test results". Stat (website). Retrieved March 12, 2017 – via Business Insider.

    Lena H. Sun (March 11, 2017). "To Your Health; Employees who decline genetic testing could face penalties under proposed bill". Washingtonpost.com. Retrieved March 12, 2017.

    American Society of Human Genetics (March 8, 2017). "ASHG opposes H.R.1313, the Preserving Employee Wellness Programs Act; Bill would undermine genetic privacy protections". Eurekalert!. Retrieved March 12, 2017.


  10. ^ Berman JJ, Moore GW, Hutchins GM (1998). "U.S. Senate Bill 422: the Genetic Confidentiality and Nondiscrimination Act of 1997". Diagn Mol Pathol. 7 (4): 192–6. doi:10.1097/00019606-199808000-00002. PMID 9917128.

    "Genetic Nondiscrimination Federal Legislation Archive".


  11. ^ Gene act, Wired magazine


  12. ^ Genetic Information Nondiscrimination Act of 2007, National Human Genome Research Institute, Update as of May 2, 2007


  13. ^ S. 358, (accessed July 28, 2007)


  14. ^ US to outlaw corporate prejudice based on genes, 10:00 06 May 2007, New Scientist Print Edition.


  15. ^ buffalonews.com


  16. ^ Suver, Jami K. (7 June 2016). "EEOC Issues ADA And GINA Rules Applicable To Employer Wellness Programs". The National Law Review. Steptoe & Johnson PLLC. Retrieved 8 June 2016.


  17. ^ "EEOC Issues Final Rules on Employer Wellness Programs". U.S. Equal Employment Opportunity Commission. Retrieved 8 June 2016.


  18. ^ Pak, Yoora; Gregerson, Janice P. (2 June 2016). "EEOC Issues New Guidance on Employee Wellness Programs". The National Law Review. Wilson Elser Moskowitz Edelman & Dicker LLP. ISSN 2161-3362. Retrieved 8 June 2016.


  19. ^ GINA — A big step toward personalized medicine, by David Resnick, Mass Tech High, August 22, 2008.


  20. ^ Coalition for Genetic Fairness


  21. ^ businessinsurance.com
    geneforum.org


  22. ^ ab Kira Peikoff (April 7, 2014). "Fearing Punishment for Bad Genes". NYT. Retrieved March 12, 2017.


  23. ^ Genetic Protections Skimp on Privacy, Says Gene Tester, Wired Science, May 23, 2008


  24. ^ Rob Stein (2012-09-16). "Scientists See Upside And Downside Of Sequencing Their Own Genes". NPR.


  25. ^ Ajunwa, Ifeoma (2015). "Genetic Data and Civil Rights". Harvard Civil Rights-Civil Liberties Law Review. SSRN 2460897.




External links







  • Full text of GINA in its final form from GovTrack

  • National Human Genome Research Institute (NIH)

  • Coalition for Genetic Fairness


  • S. 358, Genetic Information Nondiscrimination Act of 2007


  • S. 976, Genomics and Personalized Medicine Act of 2007

  • Your GINA resource

  • Genetic Alliance


  • Genetic Discrimination Saves Lives - Editorial arguing against the bill.




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