Health + Ancestry Service
Health + Ancestry Service
Get personalized genetic insights and tools that can help make it easier for you to take action on your health.
- 150+ personalized reports
- Includes Ancestry + Traits Service
- Includes FDA-authorized reports
- FSA/HSA eligibility♦
There is a lot to consider with genetic testing. We encourage you to review relevant information about Carrier Status* and Genetic Health Risk* reports.
Discover how your DNA can influence your health.
Using insights backed by the latest science, see how your DNA can affect your chances of developing certain health conditions. Your personalized reports break down your genetic data, the science and potential next steps.
10+ reports, including:
(Powered by 23andMe
Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.(Selected Variants)

10+ reports, including:
Type 2 Diabetes (Powered by 23andMe
Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.
Explore how your DNA relates to your lifestyle.
Discover what your DNA has to say about lifestyle factors like diet, exercise, and sleep. Use what you've learned to help you make informed decisions.
5+ reports, including:

5+ reports, including:
Muscle Composition
See what you may pass on to your future children.
If you're thinking of starting a family, find out if you're a carrier for genetic variants linked to certain inherited health conditions.
40+ reports, including:

40+ reports, including:
Cystic Fibrosis
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
As more and more people choose DNA testing for health reasons, they're sharing more and more inspiring stories. These are just a few of the stories of 23andMe customers who used what they learned from their DNA to take a more proactive approach to their health.

Watch Charlie's story
Uncovering a truth

Watch Kristin's story
Taking action
More insights are
on the way.
When you join the 23andMe community, you’re immersing yourself in an exciting world that is constantly evolving. As discoveries are made, you’ll have the opportunity to receive updated and new reports that could give you even more insights, based on your DNA.
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/
♦Based on purchase price of $199. Check with your FSA/HSA administrator or your tax professional for confirmation on the specific requirements for individual eligibility and reimbursement, including usage, procedures and qualifications.
**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 https://permalinks.23andme.com/pdf/pgt_product_info_page_21jan2020.pdf