Tag: CLIA


October 22, 2012

23andMe Supports Better Access to Health Records

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The Genetic Alliance, a nonprofit health advocacy organization, is asking for support to expand people’s right to their own health information by giving them direct access to their clinical laboratory test results. 23andMe supports this position and several of our employees are signing-on to a letter the [...]

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November 4, 2011

Support Your Right to Access Your Clinical Lab Results

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Giving people access to their genetic information is what we are about at 23andMe. We believe that it is not just a fundamental right, but, as with access to all of your health records, it is vital to making informed decisions about your wellbeing. That is why 23andMe is so encouraged by statements coming [...]

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April 1, 2008

Sorry for the Delay: A Message from 23andMe Founders Anne Wojcicki and Linda Avey

The 23andMe Blog

Linda AveySome customers who recently ordered our Personal Genome Service™ have had to wait more than the usual four to six weeks after spitting to get their genetic information. We know that it can be frustrating to wait when you are curious about what your genome holds, so we would like to apologize and [...]

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