Genetic Data Privacy Solutions in the GDPR

Kristi Harbord
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引用次数: 4

Abstract

The intersection of healthcare and technology is a rapidly growing area. One thriving field at this intersection involves obtaining, processing, and storing genetic data. While the benefits have been great, genetic information can reveal a great deal about individuals and their families. And the information that can be conveyed from genetic data appears limitless and is constantly growing and changing. Many entities have begun storing, processing, and sharing genetic data on a very large scale. This creates many privacy concerns that the current regulatory framework does not account for. The line between patient data and consumer data is blurred; many entities are interested in obtaining genetic data with varied interests. In the direct-to-consumer genetic testing market, consumers pay to send private companies their DNA samples in exchange for a trivial amount of information about their ancestry and health risks. But health data obtained and processed by a company are subjected to far less stringent privacy regulations than health data obtained and processed at a doctor’s office or hospital. This Comment summarizes some of the current genetic privacy problems in United States laws and examines the EU’s recently adopted GDPR for a possible solution. A GDPR-style regulation could provide more consistency, give individuals more control, and protect against future unknown uses.
GDPR中的基因数据隐私解决方案
医疗保健和技术的交叉是一个快速发展的领域。在这个交叉领域,一个蓬勃发展的领域涉及获取、处理和存储基因数据。虽然好处是巨大的,但遗传信息可以揭示个人及其家庭的很多信息。从基因数据中可以传递的信息似乎是无限的,并且是不断增长和变化的。许多实体已经开始大规模地存储、处理和共享遗传数据。这就产生了许多当前监管框架没有考虑到的隐私问题。患者数据和消费者数据之间的界限是模糊的;许多实体都有兴趣获得不同兴趣的遗传数据。在直接面向消费者的基因检测市场上,消费者花钱将自己的DNA样本寄给私人公司,以换取有关其祖先和健康风险的少量信息。但是,公司获取和处理的健康数据受到的隐私法规远不如医生办公室或医院获取和处理的健康数据严格。本评论总结了目前美国法律中的一些基因隐私问题,并研究了欧盟最近通过的GDPR,以寻求可能的解决方案。gdpr式的监管可以提供更多的一致性,给个人更多的控制权,并防止未来未知的用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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