GENETIC HEALTH REPORTS
First & Only company withMultiple FDA clearances
23andMe pioneered access to genetic information. We weren’t just the first to do it, we are the only direct to consumer company with multiple FDA authorizations for genetic health reports.
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Hindsight
Ancestry
Service
- 4000+ Geographic regions
- Automatic Family Tree Builder
- 30+ Trait reports
- DNA Relative Finder
Foresight
23andMe
Premium™
Year
- Everything in Health plus Ancestry Service, plus:
- 30+ Powered by 23andMe Research reports including heart health, anxiety and skin cancerReports 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.
- Breast Cancer (females only), Prostate Cancer (males only) and Colorectal Cancer (certain ethnicities) - all Powered by 23andMe Research
- Pharmacogenetics reports**Learn about Considerations and Limitations for Pharmacogenetics Reports
- Health Action Plan featurePersonalized and ongoing recommendations based on genetic and non-genetic data.
- Health Tracks featureSMSee how making healthy choices each day can greatly impact your health over time.
- Just Added Historical MatchesSM feature
- Plus new reports and features as more discoveries are made
Supersight
23andMe
Total Health™
Year
- Everything in 23andMeplus Premium, plus:
- Clinical-grade exome sequencing
- Biannual blood tests
- Dedicated virtual consultation with clinicians who are trained in genetics-informed care
- Unlimited messaging with clinicians for ongoing support
- Personalized recommendations based on your results
- Just Added Biological Age featureMonitor how your body is aging physiologically based on key biomarkers and change the trajectory of your health.
‡Our genotyping product detects 250 health-related variants in our Carrier Status and Genetic Health Risk reports. The Exome Sequencing reports detect 50,000+ hereditary disease-causing variants.
Valid payment method required at kit registration. 23andMe+ Total Health is not available to residents of HI, NJ, NY, RI and US territories.
Uncover your historical and ancient relatives.
Explore your link to the past with the new Historical Matches feature and discover your DNA connection to individuals from hundreds or even thousands of years ago.
Learn moreCustomer Stories
Watch Kenzie’s story
Kenzie learning about a BRCA1 variant also meant lifesaving knowledge for her mother.
Watch Melissa’s story
Melissa sharing important DNA insights with her doctor empowered her to take control of an important health risk.
Optimize your health with our most advanced membership.
Detects 200x more hereditary disease-causing variants than our Personal Genome Service reports.‡ Screens for 55+ clinically actionable and under-diagnosed conditions.
‡ Our genotyping product detects 250 health-related variants in our Carrier Status and Genetic Health Risk reports. The Exome Sequencing reports detect 50,000+ hereditary disease-causing variants.Image Description: Phone screen showing the Hereditary Cardiovascular Disease report. Example result is No variants detected (of 44 genes tested) for inherited conditions. TRDN, ACTA2, and MYH11 genes shown.
Track results, optimize and measure progress beyond routine labs. Assess your thyroid, kidney, heart health and more with biomarkers such as Lipoprotein(a) (Lp(a)) and Apolipoprotein B (ApoB).
Image Description: Result for thyroid-stimulating hormone (TSH) test. Example result is Your TSH levels are in the normal range, showing a result of 1.2 mIU/L. TSH helps control the level of thyroid hormones in the blood.
Access to clinicians with training in genetics-informed care. Includes unlimited direct messaging and a dedicated virtual consultation annually.
Image Description: A secure message thread between Zoe and her doctor about her family health history.
190+ personalized genotyping reports with new reports and features delivered throughout the year.
Powered by 23andMe ResearchPremium reports to help you learn more about breast cancer (females only), prostate cancer (males only), colorectal cancer (certain ethnicities) and skin cancer.
Image Description: Phone screen showing Breast Cancer report. Example result is Your genetics are associated with a typical likelihood, showing a likelihood of 8%. Factors included in this report include age, family history, and reproductive history.
**Learn about Considerations and Limitations for Pharmacogenetics Reports
Discover how your DNA may impact the way your body processes certain medications with three Pharmacogenetics reports plus Medication Insights.
Image Description: Phone screen showing Pharmacogenetics reports. These reports test for genetic variants that may influence how you process medications. The examples shown are the CYP2C19 Drug Metabolism report (likely normal metabolizer result) and the DPYD Drug Metabolizer report (likely normal metabolizer).
Receive personalized recommendations, including those for clinical screenings and lab work, based on genetic and non-genetic data.
Image Description: Phone screen showing Health Action Plan displaying three high priority recommendations, including checking your blood and biomarker levels and one daily activity recommendation you can take, like exercising for 3 songs.
Learn what your DNA can tell you about your health and ancestry.
Opt in to easily input, track and download your family health history to share with your healthcare provider.
Image Description: Mobile view of Family Health History Tree for Jaime King, who is pictured as one of three children in a pedigree-style family tree with colorful circles, pictures or initials, and health condition icons for different people in the tree. Parents show heart, lung, and eye icons. Jamie shows heart and lung icons. Button at bottom to "View and download your summary"
*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks
Using insights backed by the latest science, see how your DNA can affect your chances of developing certain health conditions.
Image Description: Phone screen showing Type 2 Diabetes report. Example result is Your genetics are associated with a typical likelihood, showing a likelihood of 37%. Factors included in this report include genetics, age, and ethnicity.
*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks
If you're thinking of starting a family, find out if you're a carrier for genetic variants linked to certain inherited health conditions.
Image Description: Phone screen showing Cystic Fibrosis report. Example result is You do not have the variants we tested; 0 variants detected in the CFTR gene.
The most comprehensive ancestry breakdown on the market with over 4,000 regions.
Discover where in the world your DNA is from across 4000+ regions — in some cases, down to the county level.
Image Description: Ancestry Composition report showing example ancestry breakdown and pie chart, with ancestry from different East Asian regions.
Automatically built from your DNA relationships. It's easy. It's convenient. It's just a click away.
Image Description: Family Tree for Jaime showing her brother, sister and mother.
Opt in to find relatives and compare ancestries or traits. Message relatives directly to better understand your family connection.
Image Description: DNA Relatives example showing list of relatives and map of where those relatives live.
The full line up, lined up.
Use the comparison chart below to find the kit that's right for you
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Ancestry
Health
Know that you are in control of your DNA.
Discovery should never come at the expense of privacy. Your data is encrypted, protected and under your control. You decide what you want to know and what you want to share.
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.)
Frequently asked questions
23andMe has rigorous standards that ensure high-quality results. Our team of scientists and medical experts use a robust process to develop genetic reports for our customers. Here are specific examples:
- With one of the largest reference datasets in the world, 23andMe provides customers with one of the most detailed and accurate ancestry breakdowns on the market. Our algorithms make ancestry estimates based on probabilities and they’re generally very accurate, but your results are not set in stone. We are always trying to improve and refine these estimates.
- Our Genetic Health Risk*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks, Carrier Status*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks, Pharmacogenetics**Learn about Considerations and Limitations for Pharmacogenetics Reports reports meet FDA requirements. This means that each variant in those reports demonstrated greater than99% accuracy and reproducibility when tested under different laboratory conditions. This article on the accuracy of 23andMe reports provides additional information.
After you provide a saliva sample, 23andMe uses genotyping to analyze your DNA. This means we look at specific locations in your genome that are known to differ between people. We then turn those results into personalized genetic reports on everything from ancestry composition to traits to genetic health risks. Note that genotyping is different from DNA sequencing, which looks at every letter in a particular stretch of DNA.
Most adults who are able to provide saliva samples can use the 23andMe kit. However there are some considerations that can complicate the DNA accuracy. Check out our Terms of Service for more info on those cases.
To begin, visit www.23andme.com/start. Once you have successfully registered your DNA testing kit, provided a saliva sample and put the kit in the mail, you can use the return tracking link available on your profile homepage to track your kit's progress to the lab. Once your sample reaches the lab, it is typically processed within a few weeks, with results then delivered to your secure online account.
We encourage customers to provide their sample before the "Collect saliva by" date on the side of the collection tube. If your sample collection kit is lost or damaged, or if it has expired, please contact customer care to assist you with getting a replacement kit.
There are many benefits of DNA testing, including finding relatives, learning whether you have genetic variants you could pass onto your children, and receiving personalized insights into your health and ancestry. 23andMe+ Premium Service offers 190+ DNA reports that do just that. In addition to taking greater control of your own health and digging deeper into your ancestry, you can also opt in to participate in research that could help fuel scientific discoveries that benefit the larger community.
We're also committed to providing you with a safe place where you can learn about your DNA knowing your privacy is protected. 23andMe has sold 12+ million kits, and with each and every one of those, privacy has been our number one priority. You may learn more about our commitment to privacy hereon our privacy page.
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*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/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/test-info/pharmacogenetics/
triangleExome Sequencing and blood testing services are available to eligible customers upon completion of the intake questionnaire that must be reviewed, approved and ordered by a third-party clinician. Exome Sequencing is analyzed by a CLIA- and CAP-accredited laboratory. Blood testing is completed by Quest Diagnostics. All telehealth services are provided in accordance with the Telehealth Terms and Consent to Telehealth.