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We’re all about real science, real data and genetic insights that positively impact customers’ lives.
eating a healthier
Know your genes.
Own your health.
Learn how genetics can influence your chances of developing certain health conditions.
Thinking of starting a family? Find out if you are a carrier for certain inherited conditions.
Discover what your DNA has to say about your well-being, and how your genes can influence certain lifestyle choices.
Know your personal story, in a whole new way.
Discover where in the world your DNA is from across 1500+ regions — in some cases down to the county level.
Automatically built from your DNA relationships. It’s easy. It’s convenient. It’s just a click away.
Connect with relatives, known and new, near and far, when you opt in to DNA Relatives. Compare ancestries and traits, then send messages to relatives directly to better understand your family connections.
Learn when your most recent ancestors from each population lived, going back over 8 generations.
Know what makes you, you. Explore your traits.
Discover what makes you unique. With reports like hair photobleaching and freckles, learn how your DNA can influence your physical features.
Cilantro: is it delicious, or soapy? See what your DNA might have to say about your taste and smell preferences.
Endlessly fascinating and occasionally weird. With genetic testing, you can discover how DNA might affect your ability to match a musical pitch, or even whether you hate the sound of chewing.
Three paths. One
|Feature||Ancestry + Traits Service||Health + Ancestry Service||VIP Health + Ancestry Service|
Ancestry + Traits
|DNA Relative Finder|
Opt in to connect and message with people who share DNA with you.
Learn how your DNA influences your facial features, taste, smell and other traits.
|Health Predisposition reports*|
Learn how your genetics can influence your chances of developing certain health conditions.
|Carrier Status reports*|
If you are starting a family, find out if you are a carrier for certain inherited conditions.
Learn how your genes play a role in your well-being and lifestyle choices.
Overnight shipping, priority lab processing, premium customer support and a personalized, 30-minute Ancestry results walkthrough.†
Know you're making a difference.
When you opt in to participate in our research, you join forces with millions of other people contributing to science. Your participation could help lead to discoveries that may one day make an impact on your own health, the health of your family and ultimately, people around the world. (Look at you go.)
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*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. Warnings & Limitations: The 23andMe PGS Genetic Health Risk Report for BRCA1/BRCA2 (Selected Variants) is indicated for reporting of the 185delAG and 5382insC variants in the BRCA1 gene and the 6174delT variant in the BRCA2 gene. The report describes if a woman is at increased risk of developing breast and ovarian cancer, and if a man is at increased risk of developing breast cancer or may be at increased risk of developing prostate cancer. The three variants included in this report are most common in people of Ashkenazi Jewish descent and do not represent the majority of BRCA1/BRCA2 variants in the general population. This report does not include variants in other genes linked to hereditary cancers and the absence of variants included in this report does not rule out the presence of other genetic variants that may impact cancer risk. The PGS test is not a substitute for visits to a healthcare professional for recommended screenings or appropriate follow-up. Results should be confirmed in a clinical setting before taking any medical action. For important information and limitations regarding each genetic health risk and carrier status report, visit 23andme.com/test-info/
†Priority lab processing, premium customer support and 30-minute phone Ancestry results walkthrough are valid for 1 year from the date of purchase.