Pending an FDA decision, genetic testing companies will no longer offers customers access to health or persona trait reports. Even though the Terms of Service specifically state "Genetic research is not comprehensive", users "should not change [their] health behaviors solely on the basis of information", and "Services are for research, informational, and educational use only", we should have access to own personal information if we request it. Why should this be any different from our diagnosis on Medical Records that a physician provides based on their 'experience' and training?
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