• IMPORTANT: There is a lot to consider with genetic testing. Please review important information about Pharmacogenetics**, Carrier Status* and Genetic Health Risk* reports. Before purchasing, review important information at 23andme.com/test-info/pharmacogenetics and 23andme.com/test-info.
• PREMIUM REPORTS & FEATURES: Fuel your health journey with ongoing value. 1-year membership with access to 190+ reports and NEW FEATURES Health TracksSM  and Health Action Plan - recommendations based on genetic and non-genetic data, including blood test data. Receive personalized genetic reports Powered by 23andMe Research on heart health, anxiety, migraine & more. Learn how your DNA may impact the way your body processes certain medications.** Valid payment method required at kit registration.
• PLUS FULL HEALTH + ANCESTRY SERVICE: Learn how genetics can influence your chances of developing certain health conditions.* Find out if you’re a carrier for certain inherited conditions.* Get meaningful DNA insights about your well-being and how it can influence certain lifestyle choices.
• INCLUDES ANCESTRY SERVICE: Discover your ancestry composition & where in the world your DNA is from across 3000+ geographic regions. Research your ancestry faster & more efficiently. Opt-in to DNA Relative Finder to find & connect with people who share your DNA. The automatic Family Tree feature makes it easy to see your DNA relationships. Find out what makes you unique with personalized trait reports including taste and smell, ability to match musical pitch or hatred of the sound of chewing.
• PRIVATE AND PROTECTED: 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 learn and what you want to share. Subject to 23andMe’s Terms of Service at 23andme.com/tos and Privacy Statement at 23andme.com/about/privacy.

23andMe+ Membership

Because you’re never done being healthy, receive an annual membership with 10+ exclusive reports & features throughout the calendar year to keep fueling your health journey.

• Includes everything from our Health + Ancestry kit
• PLUS access to exclusive reports that help you learn about your heart health, how you process certain medications, migraine and more
• Enhanced ancestry features

23andMe+ members get even more insights into their health.

Get our base Health + Ancestry Service with 150+ personalized DNA reports

Plus

Exclusive Access to 10+ premium reports and features throughout the calendar year

Take a look at what you'll get from the start:

Exclusive premium reports only available with 23andMe+

HEART HEALTH

Exclusive DNA insights to stay proactive with your heart health.

Get a better picture of what may be in store for your heart’s health and learn about lifestyle factors and steps that can help you stay healthy. Premium reports Powered by 23andMe Research include:

• High Blood Pressure
• Atrial Fibrillation
• Coronary Artery Disease
• HDL Cholesterol
• LDL Cholesterol

PHARMACOGENETICS**

Get smarter about the prescriptions you’re taking.

Medications don’t always “work” the same way in different bodies. Discover how your genetics could impact the way your body processes certain medications like citalopram and clopidogrel. Share these reports with your doctor to make smarter decisions together.

Plus more exclusive DNA insights to better understand your health.

Get additional reports Powered by 23andMe Research, including:

• Migraine
• Obstructive Sleep Apnea
• Restless Legs Syndrome

One-year Membership access with option to renew. PLUS everything in our Health + Ancestry Service below.

ANCESTRY SERVICE FEATURES

• Ancestry Reports: 50+ reports including: Ancestry Composition, Ancestry Detail Reports, Maternal & Paternal Haplogroups, Neanderthal Ancestry
• DNA Relative Finder: Find and connect with relatives in the 23andMe database who share DNA with you. (opt-in)
• Family Tree: Automatically built from your DNA relationships. It’s easy. It’s convenient. It’s just a click away. (opt-in)
• Traits reports: 30+ traits including: Hair Photobleaching, Freckles, Taste & Smell and more

HEALTH FEATURES

• Health Predisposition reports*: 10+ reports including: Type 2 Diabetes (Powered by 23andMe Research), Late-Onset Alzheimer's Disease Genetic Health Risk Report, Celiac Disease Genetic Health Risk Report
• Carrier Status reports*: 40+ reports including: Cystic Fibrosis, Sickle Cell Anemia, Tay-Sachs Disease
• Wellness reports: 5+ reports including: Deep Sleep, Lactose Intolerance, Genetic Weight

OTHER FEATURES

• Share and compare - Trace DNA through your close family and explore your genetic similarities and differences.
• Our Family Health History Tree lets you easily track, visualize and download your family health history information to share with your doctor.

Before mailing, register your kit at 23andme.com/start otherwise, your sample will NOT be processed.

Frequently Asked Questions

Q: How does the 23andMe kit work?

A: Our service is exclusively online. You'll receive your reports and access to additional features through a password-protected account at 23andme.com. Before Mailing, register your kit at 23andme.com/start otherwise your sample will NOT be processed.

Q: How accurate are the reports?

A: 23andMe is the first and only genetic service available directly to you that includes reports that meet FDA requirements for clinical and scientific validity. All saliva samples are processed in CLIA-certified and CAP-accredited labs.

Q: Why do I need to register my kit?

A: You need to register your kit to link it to your 23andMe account online. Registration connects the barcode on your saliva sample to your account so we know your sample belongs to you. Our lab cannot process your sample if it is not registered.

Q: How does my DNA become a report?

A: We send you a saliva collection kit with instructions. Our CLIA-certified lab extracts DNA from cells in your saliva sample. The lab processes the DNA on a genotyping chip. Your genetic data is analyzed, and we generate your personalized reports.

Q: How is my privacy protected?

A: You choose how your genetic information is used and shared with others. We support the Genetic Information Nondiscrimination Act (GINA) and other similar laws that protect individuals from being discriminated against based on their genetics.

Q: Can I cancel my 23andMe+ membership?

A: Yes. You may cancel your 23andMe+ membership at any time. Please note that 23andMe does not pause or pro-rate memberships. 23andMe+ is non-refundable. If you choose to cancel your membership before the end of your billing cycle, you will retain access to your 23andMe+ until the end of your billing cycle (your membership expiration date). Once your membership period has ended, you will lose access to the reports and features that were provided to you under 23andMe+. You will retain the Health + Ancestry Service reports and features that you had access to prior to purchasing 23andMe+.

Legal Disclaimer

* 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. 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

Membership auto-renews at then-current rate, unless canceled in advance. Once a 23andMe+ membership has ended, customer will lose access to 23andMe+ reports and features; customer will retain access to Health + Ancestry Service reports and features. Terms apply

Before you can use 23andMe and see your reports, you must agree to 23andMe's Terms of Service and Membership Terms at the time of registration of your 23andMe kit. Your use of 23andMe is further subject to 23andMe's Privacy Statement.

For use in the USA only - kits shipped or used outside the US will be invalidated and no refund will be provided. Kits may not be redistributed or resold.

Shipping Note: Shipping to Alaska, Hawaii, PO Boxes, and APO addresses is not available for this item