Personal Health Information, Data Sharing, Privacy & Security
How do you control where your DNA data resides and how it is shared online?
An assessment of the article from Bloomberg
Subjective:
It is the assessment from this article that at this time it is very difficult to understand and control who has access to your genetic data. There are not enough privacy protections in relation to what companies who analyze your genetic data are then able to do with that data after they have gathered it.
Objective:
Currently the primary legislation that helps to protect consumer's privacy in relation to their genetic data is called the Genetic Information Nondiscrimination Act.
Assessment:
One of the key concerns for consumers is whether insurance companies and related payers might potentially get access to that information and be able to increase premiums based on possible risk factors identified within someone's genetic code.
This article at Kaiser Health News seems to indicate that there are some real concerns that we should be aware of: "In general, long-term-care insurers can indeed use genetic test results when they decide whether to offer you coverage. The federal Genetic Information Nondiscrimination Act prohibits health insurers from asking for or using your genetic information to make decisions about whether to sell you health insurance or how much to charge. But those rules don’t apply to long-term-care, life or disability insurance.
When you apply for long-term-care insurance, the insurer may review your medical records and ask you questions about your health history and that of your family. It’s all part of the underwriting process to determine whether to offer you a policy and how much to charge."
Plan:
Before participating in Direct to Consumer Genetic Testing be sure to read that company's policies about who they might potentially share that data with beyond you.
Examples of these types of companies include:
- 23andMe
- Counsyl
- Gene by Gene
- Laboratory Corporation of America
- MyMedLab
- Mapmygenome India
- Positive Bioscience
- Quest Diagnostics, Inc
Documents to download
- GINAhelp(.pdf, 233.56 KB)
More links
- An article from Bloomberg titled, "Glaring Gap Seen in DNA Privacy Pledges by 23andMe, Ancestry"Genetic-testing companies that have decoded the DNA of millions just introduced new guidelines to protect data privacy. But those best practices failed to address a major concern: what happens to customers’ data that is shared for research with pharmaceutical giants, academics and others, often for a profit.
- In-Depth: Consumer genomics furthers healthcare foothold but privacy, resource concerns persistA link to the original article in Mobile Health News: In the last few years consumer genomics has grown in both its offerings and legitimacy. The industry that was once best known for telling clients if they were Italian or Hungarian is now securing its foothold within the healthcare space.
- Deleting Your Online DNA Data Is Brutally DifficultA link to the original article on Bloomberg News
- The Genetic Information Nondiscrimination Act of 2008 (GINA) The Genetic Information Nondiscrimination Act of 2008 (GINA) is a federal law that protects individuals from genetic discrimination in health insurance and employment. Genetic discrimination is the misuse of genetic information.
- A link to the Kaiser Health News article explaining How Genetic Tests Muddy Your Odds Of Getting A Long-Term-Care Policy This is a response to the question of Can getting a genetic test interfere with being able to buy long-term-care insurance in the future? If you do get a plan, can the insurer drop you after you find out the results of a genetic test?