|Important: This article is applicable to customers located in the United States who purchased the 23andMe Ancestry Service. The 23andMe Ancestry Service was introduced on September 21, 2016.|
If you purchased the 23andMe® Ancestry Service, you have the ability to add reports on traits, wellness, genetic health risk* and carrier status* from within your 23andMe account. Following the analysis of your sample at our laboratory, an Upgrade button will be displayed on the Carrier Status, Genetic Health Risk, Traits, and Wellness pages accessible through your list of reports. The new reports will be accessible in your account immediately upon purchasing an upgrade.
The $125 upgrade fee is non-refundable and we are unable to revoke access to these reports once purchased.
You can view a full list of reports here.
*The 23andMe PGS test uses qualitative genotyping to detect clinically relevant variants in the genomic DNA of adults from saliva collected using an FDA-cleared collection device (Oragene·DX model OGD-500.001) for the purpose of reporting and interpreting genetic health risks and reporting carrier status. It is not intended to diagnose any disease. The relevance of each report varies based on ethnicity. Each genetic health risk report describes if a person has variants associated with a higher risk of developing a disease, but does not describe a person’s overall risk of developing the disease. These reports are not intended to tell you anything about your current state of health, or to be used to make medical decisions, including whether or not you should take a medication or how much of a medication you should take. Our carrier status reports can be used to determine carrier status, but cannot determine if you have two copies of any genetic variant. These carrier reports are not intended to tell you anything about your risk for developing a disease in the future or anything about the health of your fetus, or your newborn child's risk of developing a particular disease later in life. For Gaucher Disease Type 1, we provide a single report that includes information on both carrier status and genetic health risk.