Before Mailing, register your DNA kit at 23andMe online otherwise, your saliva sample will NOT be processed. 23andMe provides the best DNA-based ancestry test kit with the most comprehensive ancestry breakdown and 30+ trait reports. Discover how your DNA ancestry contributes to certain traits and characteristics that make you, you. Easily upgrade to 23andMe's Health + Ancestry Service at any time for an extra cost and receive access to 65 health and wellness reports. See how your DNA breaks out across over 2,750 regions worldwide. Learn about your ancestral origins and see where your ancestors lived 500+ years ago. Travel the world based on your DNA. Find out where your DNA comes from using your ancestry test ? and use that discovery to create the ultimate itinerary. 23andMe's Family Tree is automatically built from your DNA relationships. It?s easy. It?s convenient. It?s just a click away. Opt-in to DNA Relatives to connect with people who share DNA with you - and message them! Discover and meet living DNA relatives from around the world and get a better understanding of your family history. Understand how the migration of our DNA tells the story of your ancestors with the Haplogroups report. This ancestry test kit will help you explore genetic similarities and differences between you and your relatives. Compare genetic similarities and differences between you and your genotyped relatives. See how different ancestries have traveled through generations of your family. Neanderthal Ancestry uncovers how much Neanderthal DNA you inherited and how your Neanderthal composition compares to others. Gain access to over 30+ traits reports, including: Hair (Color, Curliness, Male Bald Spot), Taste & Smell (Sweet vs. Salty, Bitter), Facial Features (Cheek Dimples, Unibrow, Freckles). 23andMe Ancestry Service includes DNA ancestry reports and empowers you to learn more accurately about your ethnicity, genealogy, family lineage, and traits that make you, you!
- WHAT YOU GET: At-home DNA test kit with access to 80+ personalized reports. Our innovative ancestry composition estimates your ancestry to the 0.1% across 2750+ geographic regions. Learn when your most recent ancestors from each population lived. Opt in to find DNA relatives and automatically build your family tree. Find out what makes you unique with personalized traits reports.
- ANCESTRY FEATURES: Dig deeper into your ancestry with the most comprehensive ancestry breakdown. Go back in time with the Ancestry Timeline to gain a clearer picture of where your ancestors lived and when they lived there. Discover your family origins with the Haplogroup feature. Opt-in to DNA Relative Finder to discover and connect with people who share your DNA. The automatic Family Tree feature makes it easy to see your DNA relationships.
- TRAIT REPORTS: Do you have freckles, a taste aversion to cilantro, perfect musical pitch, prefer sweet or salty, have a fear of heights, or get more mosquito bites than others? See what your DNA might have to say about these traits and others from 30+ reports that uncover how your genes make you unique.
- SIMPLE & EASY: DNA-based ancestry test in 3 simple steps, all from home. No blood, no needles. Our at-home saliva collection kit is all you need to send your DNA to the lab. We have made the process as simple as possible. Spit in the provided tube, register your kit using the barcode, and return the saliva sample back to our lab in the pre-paid package. Get results back in 4-5 weeks. Upgrade to our essential Health + Ancestry Service at anytime from your account.
- 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.
- * 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. **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. 23andMe Claim Substantiation for "80% get genetically meaningful health info." Date range: August 2020 - August 2021. Source: 23andMe internal data.
