root for
your roots
Football connects us to the world, and so does our DNA. Explore your connections.
Ancestry Composition
Like football, your DNA may have global roots.

Explore your ancestry's breakdown by region (1000+ regions), including East Asia, Sub-Sahara Africa, Europe and more. Discover where your ancestors lived more than 500 years ago!

Ancestry Composition Map
There's no diving in football, but you can dive deeper into your ancestry.

Discover the origins of your maternal and paternal ancestors and how they migrated around the world over thousands of years.

DNA Relatives
Find DNA relatives across the globe or across the stadium.

DNA Relatives allows you to shed new light on your family story by connecting you with 23andMe customers who share your DNA.

DNA Relatives Map
Ancestry Timeline
Learn when your ancestors entered the game — that is, your family line.

Trace your ancestors through generations and discover when different ancestries from your family history were introduced into your DNA.

Got goals? Get insights.
23andMe's Health + Ancestry Service gives you 125+ reports that offer insights into your health, traits and more. Got a health- or lifestyle-related goal? A better understanding of your DNA could help you hit it.

Health + Ancestry Service


35+ reports

Genetic Health Risks*

5+ reports Meets FDA requirements


5+ reports

Carrier Status*

40+ reports Meets FDA requirements


25+ reports
23andMe DNA test kit
Know more about your body.
Understand your DNA.
Health +
Ancestry Service
Important Test Info

*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.