Book contents
- Consumer Genetic Technologies
- Consumer Genetic Technologies
- Copyright page
- Contents
- Contributors
- Acknowledgments
- Introduction
- Part I Consumer Genetic Technologies: Rights, Liabilities, and Other Obligations
- Part II Privacy in the Age of Consumer Genetics
- Part III Tinkering with Ourselves: The Law and Ethics of DIY Genomics
- Part IV Consumer Genetics and Identity
- Introduction to Part IV
- 13 Generational Failures of Law and Ethics
- 14 Precision Medicine and the Resurgence of Race in Genomic Medicine
- 15 Losing Our Minds?
- 16 Investigative Genetic Genealogy and the Problem of Familial Forensic Identification
- Part V The Impact of Genetic Information
14 - Precision Medicine and the Resurgence of Race in Genomic Medicine
from Part IV - Consumer Genetics and Identity
Published online by Cambridge University Press: 27 August 2021
- Consumer Genetic Technologies
- Consumer Genetic Technologies
- Copyright page
- Contents
- Contributors
- Acknowledgments
- Introduction
- Part I Consumer Genetic Technologies: Rights, Liabilities, and Other Obligations
- Part II Privacy in the Age of Consumer Genetics
- Part III Tinkering with Ourselves: The Law and Ethics of DIY Genomics
- Part IV Consumer Genetics and Identity
- Introduction to Part IV
- 13 Generational Failures of Law and Ethics
- 14 Precision Medicine and the Resurgence of Race in Genomic Medicine
- 15 Losing Our Minds?
- 16 Investigative Genetic Genealogy and the Problem of Familial Forensic Identification
- Part V The Impact of Genetic Information
Summary
There is a deep tension at the heart of modern genomics between the idea that science has now proven that there is only one race, the human race versus an enduring concern with genetic variation that might correlate with racial and ethnic categories.This tension shapes how we conceptualize the nature of race, approach problems of health disparities, and formulate related regulatory directives. Recently, this tension has become manifest in the shift from “personalized” to “precision” medicine and the inauguration of the massive “All of Us” initiative from the NIH aiming to enroll one million people into a genomic data base.This chapter will explore this shift and consider the broader ethical, legal, and social implications of reintroducing race (now as a “subpopulation”) at the forefront of biomedical advancement.In the move from “personal” to “precision” medicine, race is being hard-wired into massive data bases as a basic category for structuring biomedical research and practice.Such practices run the risk of reinvigorating dangerous and inaccurate conceptions of race as biological in a manner that could both undermine attempts to address persistent race-based health disparities and fuel pernicious racist ideologies.
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- Information
- Consumer Genetic TechnologiesEthical and Legal Considerations, pp. 186 - 197Publisher: Cambridge University PressPrint publication year: 2021