You may not know the language or the culture. But we all share a connection to the countries participating in this summer's tournament, thanks to our DNA.
- Purchase your 23andMe kit
- Discover personal connections to the 32-team field.
- Root for Your Roots!
How it works:
Explore your ancestry's breakdown by region (150+ regions), including East Asia, Sub-Sahara Africa, Europe and more. Discover where your ancestors lived more than 500 years ago!
Discover the origins of your maternal and paternal ancestors and how they migrated around the world over thousands of years.
DNA Relatives allows you to shed new light on your family story by connecting you with 23andMe customers who share your DNA.
Trace your ancestors through generations and discover when different ancestries from your family history were introduced into your DNA.
Health + Ancestry Service
Genetic Health Risks*5+ reports Meets FDA requirements
Carrier Status*40+ reports Meets FDA requirements
Understand your DNA.
*The 23andMe PGS test uses qualitative genotyping to detect select clinically relevant variants in the genomic DNA of adults from saliva for the purpose of reporting and interpreting genetic health risks and reporting carrier status. It is not intended to diagnose any disease. Your ethnicity may affect the relevance of each report and how your genetic health risk results are interpreted. 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. The test is 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, how much of a medication you should take, or determine any treatment. 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, the health of your fetus, or your newborn child's risk of developing a particular disease later in life. For certain conditions, we provide a single report that includes information on both carrier status and genetic health risk.