Ancestry + Traits Service
Ancestry + Traits Service
The best DNA kit with the most comprehensive ancestry breakdown and 30+ trait reports.
- 80+ personalized reports
- Ancestry percentages (to the 0.1%)
- 2000+ geographic regions
- Health upgrade available
Dig deeper into your ancestry.
It's the most complete genetic breakdown on the market, and the most comprehensive portrait of you yet.
Discover where in the world your DNA is from across 2000+ regions — in some cases, down to the county level.
Expand your knowledge with population-specific reports that offer a granular view of your ancestry background, plus curated content on the history, food and popular travel destinations connected to your ancestry.

Ancestry Composition
Discover where in the world your DNA is from across 2000+ regions — in some cases, down to the county level.
Find your people.
Open your world.
Discover people who share your DNA. From close family members to distant ones, you'll be amazed by the way your DNA relatives connect you to the world.
(optional)
Find your matches. Compare ancestries and traits. Message relatives directly to better understand your family connection.
Automatically built from your DNA relationships. It's easy. It's convenient. It's just a click away.
Compare your results with family and friends to uncover similarities and differences.

DNA Relative Finder (optional)
Find your matches. Compare ancestries and traits. Message relatives directly to better understand your family connection.
Trace your path back thousands of years.
Travel back in time to gain a clearer picture of where you came from, where your ancestors lived and when they lived there.
Learn when your most recent ancestors from each population lived, going back more than 8 generations.
Haplo-what? Discover the origins of your maternal- and paternal-line ancestors (i.e. haplogroups) and how they moved around the world over thousands of years.
Explore your genetic connection to famous historical figures. Nelson Mandela? Marie Antoinette? Alexander Hamilton? They might share a distant ancestor with you.
Travel back 40,000 years and discover how much of your ancestry can be traced back to Neanderthals, and learn more about our human origins.

Ancestry Timeline
Learn when your most recent ancestors from each population lived, going back more than 8 generations.
More insights into what makes you unique.
Our genes are a lot like us: endlessly diverse, endlessly interesting, occasionally weird. Find out what makes you unique, in 30+ personalized reports.
Reports include Hair Photobleaching, Freckles, Skin Pigmentation and more.
Reports include Cilantro Taste Aversion, Sweet vs. Salty, Asparagus Odor Detection and more.
Reports include Photic Sneeze Reflex, Ability to Match Musical Pitch, Misophonia (hatred of the sound of chewing) and more.

Physical Features
Reports include Hair Photobleaching, Freckles, Skin Pigmentation and more.
Choose the service you.
that's right forFeature | Ancestry + Traits Service | Health + Ancestry Service |
---|---|---|
Total reports | 80+ | 150+ |
Ancestry Reports | ||
Family Tree | ||
DNA Relative Finder Opt in to connect and message with people who share DNA with you. | ||
Trait reports 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. | ||
Wellness reports Learn how your genes play a role in your well-being and lifestyle choices. | ||
Family Health History Tree NEW! Easily input, track and download your family health history to share with your healthcare provider. | ||
Pharmacogenetics reports** Discover how your DNA may impact how your body processes certain medications with three new Pharmacogenetics reports. | ||
Enhanced ancestry features Get advanced filtering for DNA Relative Finder and access up to 3500 more DNA relatives. | ||
Ongoing new reports and features Get exclusive new reports and enhanced features automatically delivered throughout the calendar year. |
Putting insights into action
Whether it’s connecting with distant relatives or experiencing the cultures where they’re from, our customers aren’t just loving what they’ve learned. They’re living it!

Watch Angelina's story
Finding peace in her identity

Watch Jordan's story
A pathway to a stronger sense of himself
More insights are
on the way.
Guess what? You're just getting started. As we continue to make discoveries, you'll continue to be able to get more. More specificity. More interactivity. More insights into what makes you, you.
Don’t take our word for it...
Stay in the know.
Keep up-to-date with new discoveries and exclusive promotions on our DNA test kits.
*23andMe health predisposition reports include both reports that meet FDA requirements for genetic health risks and reports which are based on 23andMe research and have not been reviewed by the FDA. The 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. 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/
**23andMe PGS Pharmacogenetics reports: The 23andMe test uses qualitative genotyping to detect 6 variants in 3 genes in the genomic DNA of adults from saliva for the purpose of reporting and interpreting information about the processing of certain therapeutics to inform discussions with a healthcare professional. It does not describe if a person will or will not respond to a particular therapeutic and does not describe the association between detected variants and any specific therapeutic. Results should be confirmed by an independent genetic test that is prescribed by your own healthcare professional before taking any medical action. Warning: Test information should not be used to start, stop, or change any course of treatment and does not test for all possible variants that may affect metabolism or protein function. The PGS test is not a substitute for visits to a healthcare professional. Making changes to your current regimen can lead to harmful side effects or reduced intended benefits of your medication, therefore consult with your healthcare professional before taking any medical action. For a complete list of the 6 variants tested, visit 23andme.com/test-info/pharmacogenetics/