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Following FDA OK, 23andMe to Expand Health Prediction

The personal genomics firm is ramping up its suite of disease-related genetic tests.

Written byKerry Grens
| 2 min read

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FLICKR, LEON BROCARDAfter putting a stop in 2013 to 23andMe offering health prediction tests to its consumers, the US Food and Drug Administration (FDA) in February gave the OK for the personal genomics firm to test for one genetic disease. Today (October 21), the company announced it will add 36 additional genetic tests to its health-prediction roster based on expanded FDA approval. The new service will cost $199.

“This isn’t going to get them too far, but maybe it’s a step along the path for them to get rebooted to where they were,” Eric Topol, a genomics professor at the Scripps Research Institute in La Jolla, California, who isn’t affiliated with the company, told The Wall Street Journal.

Nearly two years ago, 23andMe was asked to cease its health and disease tests over concerns about their accuracy. Since then it has only provided ancestry information. In February, the FDA gave the green light to test whether customers are a carrier for Bloom Syndrome. The company’s latest offerings include carrier tests for cystic fibrosis and sickle cell anemia.

“Part of what we tried to do over the last two years is take advantage of ...

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Meet the Author

  • kerry grens

    Kerry served as The Scientist’s news director until 2021. Before joining The Scientist in 2013, she was a stringer for Reuters Health, the senior health and science reporter at WHYY in Philadelphia, and the health and science reporter at New Hampshire Public Radio. Kerry got her start in journalism as a AAAS Mass Media fellow at KUNC in Colorado. She has a master’s in biological sciences from Stanford University and a biology degree from Loyola University Chicago.

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