Is it possible that there is an ulterior motive to the FDA restricting at-home self-testing testing from 23andme? If people are allowed to learn about and act

Is it possible that there is an ulterior motive to the FDA restricting at-home self-testing testing from 23andme? If people are allowed to learn about and act on their genetic risk factors, is it possible that certain medical practices stand to lose a lot of money? Is it possible that cheap preventive care could replace expensive procedures/drugs that you are forced to purchase later, once your diseases become unmanageable? I find it very strange, and incredibly hard to believe that the risk of people overreacting from their medical information outweighs the positive impacts of having the knowledge.