This document discusses several data breaches that have exposed the personal information of millions of individuals. It also discusses how over 12 million Americans have shared their DNA data with companies like 23andMe and AncestryDNA. While this can help medical research, it also raises privacy concerns about potential genetic discrimination and challenges with informed consent. The document provides recommendations for patients, practitioners, and stakeholders to help address these privacy challenges through practices like informing patients, limiting data use, ensuring accountability, and identifying risks.