If you have an opinion about genetic testing and the best way to return those results, the U.S. Food and Drug Administration (FDA) wants to hear it at a daylong...

By Anne Wojcicki After discussion with officials from the Food and Drug Administration today, 23andMe will comply with the FDA’s directive and stop offering new consumers access to health-related genetic...

23andMe was started in 2007 with the belief that consumers have the right to get access to their genetic information and that information can help them live healthier lives. It...

We have received the warning letter from the Food and Drug Administration. We recognize that we have not met the FDA’s expectations regarding timeline and communication regarding our submission. Our...

We at 23andMe hear this question a lot when the topic of personal genetic testing comes up. We each have our own answer, but enterprising PBS NewsHour correspondent Spencer Michaels...

We know from scientific research that, in general, people don’t freak out about the results they get from personal genetic testing. When the results show an increased risk for serious...

Earlier this month Public Health Genomics published a paper by a team of Swiss researchers that reinforces the growing body of work showing consumers’ positive experiences with personal genetic testing....

There are a lot of pie charts, numerical tables and graphs on display this week at the American Society of Human Genetics in San Francisco, but one caught our eye...

We would like to give a little shout-out to Holly Dunsworth, an assistant professor of anthropology at the University of Rhode Island and a blogger, for her thoughtful post “Be...

Editor’s note: This post has been altered from the original. The slides from the presentation have been removed. 23andMe, like many others, believes that individuals have a right to access...