Give the most personal gift you can give — DNA discovery.
Three amazing gifts. Choose the one that's right for your friends and family.
Basic Ancestry
For the one who wants to start their DNA journey with a deep dive into their ancestry.
Give them a comprehensive portrait of where in the world their DNA is from.
- Ancestry percentages (to the 0.1%)
- 4,500+ geographic regions
- DNA Relative Finder
- Health upgrade available
- †The most comprehensive ancestry breakdown on the market
Premium Ancestry
Unlock hyper-local origins, ancient ancestral connections, and our most advanced family history tools.
Give them an annual membership for the dedicated family historian.
- 4,500+ geographic regions
- DNA Relative Finder
- Family Tree
- Historical Matches
- Reconstructed Ancestors
- Advanced Filters and Clustering Tools for DNA Relatives
- New historical matches and features are added throughout the year.
- Valid payment method required at kit registration
Premium Ancestry + Health
For the one who’s never done being healthy.
Give them an annual membership that includes access to new premium reports and features throughout the year.
- Includes everything from our Premium Ancestry kit
- 65+ health reports and features
- Wellness reports
- Health Predisposition reports*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks for them to see how their DNA can affect their chances of developing certain health conditions.
- Carrier Status reports*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks to find out if they're a carrier for genetic variants linked to certain inherited health conditions.
- PLUS access to exclusive reports that help them learn about their heart health, how they process certain medications**Learn about Considerations and Limitations for Pharmacogenetics Reports, migraine, and more
- Our Health TracksSM lets them see how making healthy choices each day can greatly impact their health over time.
- Health Action Plan gives them personalized and ongoing recommendations based on genetic and non-genetic data.
- Our Historical MatchesSM feature helps you uncover your historical and ancient relatives, linking you to the past.
- Enhanced ancestry features
- Valid payment method required at kit registration
Premium Ancestry + Total Health
For the one who wants our most advanced health membership yet.
Give them a membership that focuses ongoing prevention and early detection.
- Includes everything in Premium Ancestry + Health
- Exome sequencing and interpretations of 100+ genes linked to 55+ conditions
- Biannual blood testing with analysis of 55+ blood biomarkers.
- Genetics-informed clinical care, including a virtual clinical consultation and unlimited messaging
- Premium Ancestry + Total Health is not available to residents of HI, NJ, NY, RI and US territories.
- Valid payment method required at kit registration
The full line up, lined up.
Use the comparison chart below to find the kit that's right for you
| Features |
|---|
Ancestry
| Features | |||
|---|---|---|---|
Ancestry reports See where your DNA is from out of 4,500+ regions worldwide. | |||
Family Tree Automatically discover and map family connections with your DNA-powered tree. | |||
Basic DNA Relative Finder Connect with DNA relatives in the 23andMe database. | |||
Advanced DNA Relative Finder Connect with up to 5000 DNA relatives and sort them by ancestry, lineage, and more using advanced filters. | |||
DNA Relatives Clustering Automatically organize your matches into visual groups to instantly see how different branches of your family connect. | |||
Advanced DNA Comparison Map shared segments across all chromosomes to see exactly how you and your matches are related. | |||
Deeper heritage insights Explore distant connections to groups with shared languages, migrations, and more. | |||
Historical Matches Discover if you share DNA with historical icons like Beethoven, Vikings, and more. | |||
Reconstructed Ancestors Fill in the gaps in your family tree by reconstructing ancestors from your DNA. | |||
Parental Inheritance See which parts of your DNA came from each parent, even if they haven’t tested with 23andMe. |
Health
| Features | |||
|---|---|---|---|
Genetic health screening Deeper insights on your chances of developing certain diseases. | |||
Carrier Status** Learn if you carry genetic variants for inherited health conditions. | |||
Additional health reports Access to new health insights as they are developed. | |||
Pharmacogenetics reports*** Learn how your DNA affects how your body processes certain medications. | |||
Family Health History Tree Track and download your family health history to share with your healthcare provider. | |||
Health Tracks See how making healthy choices each day can impact your health over time. | |||
Blood panel analysis Key biomarkers translated into your personalized biological age for actionable insights. | Add-on | Add-on | Add-on |
Traits
| Features | |||
|---|---|---|---|
Trait Insights Discover how your DNA shapes 30+ everyday quirks like your bald spot, sweet vs. salty preference, unibrow, and more. |
Frequently asked questions
Standard, Expedited, and Express shipping methods are available. Standard and Expedited orders are shipped through USPS. Express orders are shipped through FedEx Standard Overnight. Here are expected delivery timeframes from the date of shipment:
- Standard: delivery within 3-6 business days
- Expedited: delivery within 2-3 business days
- Express: delivery within 1-2 business days
Reports will be available through a secure, online account at 23andme.org in approximately 3-4 weeks.
Stay in the know
Your DNA has more to tell you.
Keep up to date with new discoveries and exclusive promotions on our DNA testing kits and member services.
By subscribing you agree to our Privacy Statement. Unsubscribe anytime.
Includes FDA-authorized genetic health reports
Bank-grade encryption. You control your data.
Analyzed in CLIA-certified U.S. labs
14M+ people have explored their DNA
**The 23andMe PGS test includes health predisposition and carrier status reports. 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 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 44 variants in the BRCA1 and BRCA2 genes. The report describes if a person's genetic result is associated with an increased risk of developing breast cancer and ovarian cancer and may be associated with an increased risk for prostate cancer, pancreatic cancer, and potentially other cancers. The variants included in this report do not represent the majority of the BRCA1/BRCA2 variants in people of most ethnicities. 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. This report is for over-the-counter use by adults over the age of 18, and provides genetic information to inform discussions with a healthcare professional. 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/shop/test-info/
***23andMe PGS Pharmacogenetics reports: The 23andMe test uses qualitative genotyping to detect 3 variants in the CYP2C19 gene, 2 variants in the DPYD gene and 1 variant in the SLCO1B1 gene 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. Our CYP2C19 Pharmacogenetics report provides certain information about variants associated with metabolism of some therapeutics and provides interpretive drug information regarding the potential effect of citalopram and clopidogrel therapy. Our SLCO1B1 Pharmacogenetics report provides certain information about variants associated with the processing of some therapeutics and provides interpretive drug information regarding the potential effect of simvastatin therapy. Our DPYD Pharmacogenetics report does not describe the association between detected variants and any specific therapeutic. Results for DPYD and certain CYP2C19 results should be confirmed by an independent genetic test prescribed by your own healthcare provider 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 important information and limitations regarding Pharmacogenetic reports, visit 23andme.com/shop/test-info/pharmacogenetics/