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| How will genetic health insights empower you? |
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Did you know your DNA can play an integral role in your health? In fact, 92% of doctors surveyed say genetics is an important part of a patient’s complete health picture.
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Get 23andMe+ Premium to access 190+ DNA reports, insights and new features throughout the year. Learn about heart health, and conditions including anxiety, depression, and high blood pressure. |
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What you get with your
23andMe+ Premium Membership |
All reports included in our Health + Ancestry Service, plus an annual membership with 45+ exclusive reports and features
to help you stay on top of your health all year long. |
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45+ personalized reports that help you learn about atrial fibrillation, anxiety, depression, insomnia, how you process certain medications**, and more. |
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Just Added Our Health Tracks℠ feature helps you understand how genetics and lifestyle can impact your likelihood of developing certain conditions. |
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Just Added Our Health Action Plan features personalized recommendations, including those for clinical screenings and lab work, based on genetic and non-genetic data. |
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First year membership included (renews at $69/yr) and valid payment method required at kit registration. |
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† Based on 2022 surveys, designed by 23andMe, Medscape, and Material Holdings LLC, of approximately 1,000 doctors and approximately 1,500 patients. Learn more
* Offer is valid for up to 3 of the same service type, placed in a single order on 23andme.com and shipped to a single address. 23andMe+ Premium Membership will auto-renew at regular price of $69/year. Cancel anytime from your Account Settings at least a day before each renewal date. Membership fees are non-refundable. See Membership Terms
for additional details. Discount is automatically applied at checkout. Cannot be combined or used with any other discount, promotion or special pricing and cannot be applied to previous purchases. Offer ends on December 25, 2023.
** 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/.
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