23andme started out by being a leader in the direct-to-consumer (DTC) genomic testing business. Time Magazine named it the 2008 Invention of the Year![1] It was the first place I tested my own autosomal DNA and that of many family members back in 2011-2012. Originally it had the best cousin matching tools, best ethnicity estimates, and had a well designed interface to examine the health implications in your own genome. Now I recommend to most that they start with Ancestry DNA and then upload that data to several other sites, including Promethease for the medical analysis, although 23andme still tests a wider range of health related genes.
23andme has been in the news this week because its entire board, except its founder, Anne Wojcicki, resigned over her plan to take it private again. It went public in 2021 but has yet to turn a profit and the WSJ reports that it will run out of cash next year [ref WSJ]. However there is at least one company interested in buying it according to a post on the DNA-Newbie list.
How should those of us who have tests there react to this news? Personally I am not worried, mainly because I hardly ever use the site anymore. I have long since downloaded my data and have contacted most of my closer matches. Roberta Estes has done a thorough blog post (click here) explaining how to save your data from 23andme.
The reason I rarely use 23andme is because it no longer allows you to compare your DNA to a relative in a chromosome browser; the feature I liked the best. I now do that at GEDmatch, Family Tree DNA, and MyHeritage. That tool was removed because of a data breach over a year ago where a hacker got lists of Jewish and Chinese testers and posted them for sale on the dark web. The break-in took advantage of users who had the same email and password on multiple sites, some of which had been exposed elsewhere.
Perhaps it is the resulting class action suit that caused part of 23andme’s financial woes. Click here for an article about how that is being settled with users.
My understanding was that the inspiration for the founding of 23andme was that Genia Brin, the mother of the then husband of founder Anne Wojcicki, was diagnosed with Parkinson’s in 1998 [ref michaelfox org]. The focus of 23andme has always been on discovering the genetic basis of various medical issues, not genealogy. However they have been quite supportive of adoptees (click here), since it is helpful to know what issues may lie in your DNA when you have no known family health history.
One way to look at the genetic basis of various diseases is to crowd-source lots of genomes.