Help Dad stay at the
top of his dad game.
With personalized DNA insights,
he can take even greater control
of his health.
Offer ends June 20
Offer ends June 20
basic: Ancestry +
- 2000+ Geographic regions
- Automatic Family Tree Builder
- 30+ Trait reports
- DNA Relative Finder
- Learn more about Ancestry +
essential: Health +
- Everything in Basic, plus…
- 60+ health reports and features including:
- Health Predisposition reports*
- Wellness reports
- Carrier Status reports*
- Includes FDA-authorized reports
- Family Health History Tree
- Learn more about Health +
Ancestry ServiceImportant test info
- Everything in Essential, plus…
- Instant access to exclusive reports and features, including:
- Heart Health reports
- Pharmacogenetics reports (how you process certain medications) **
- Migraine report (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.
- Obstructive Sleep Apnea report (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.
- Plus new reports and features as more discoveries are made
- Learn more about 23andMe
MembershipImportant test info
Hi, we're 23andMe. We're all about real science, real data and genetic insights that can help make it easier for you to take action on your health.
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 2000+ 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.
Choose the service
|Feature||Ancestry + Traits Service||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.
|Family Health History Tree|
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.
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.)
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 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 and does not describe the association between detected variants and any specific 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. Results for SLCO1B1 and 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 Pharmacogenetics reports, visit 23andme.com/test-info/pharmacogenetics/