23andMe Health + Ancestry Service: Personal Genetic DNA Test
Explore How Your DNA Relates to Your Lifestyle with 150+ Reports on Ancestry, Trait, Health Predisposition, Carrier Status & Wellness
Description
IMPORTANT
Before Mailing, register your DNA test kit at 23andMe online otherwise, your saliva sample will NOT be processed.
There is a lot to consider with genetic testing. Please review important information about Carrier Status and Genetic Health Risk reports. Before purchasing, review important information at 23andme.com/test-info.
Customers must be 18+ years old to purchase.
Dig Deeper Into Your Ancestry and Take Action on Your Health
23andMe Health + Ancestry Service features over 150 personalized genetic insights that can help make it easier for you to take action on your health. Using insights backed by the latest science, see how DNA can affect your chances of developing certain health conditions. Wellness reports can help you discover what your DNA has to say about lifestyle factors like diet, exercise, and sleep. And if you're thinking of starting a family, our Carrier Status reports can tell you if you're a carrier for genetic variants linked to certain inherited health conditions.
23andMe's Health + Ancestry Service provides genetic testing
10+ Health Predisposition reports, including:
- Type 2 Diabetes (Powered by 23andMe Research)
- Late-Onset Alzheimer's Disease
- Celiac Disease
45+ Carrier Status reports, including:
- Cystic Fibrosis
- Sickle Cell Anemia
- Tay-Sachs Disease
5+ Wellness reports, including:
- Deep Sleep
- Lactose Intolerance
- Genetic Weight
50+ Personalized DNA ancestry reports
- Ancestry Composition
- Ancestry Detail Reports
- Maternal & Paternal Haplogroups
- Neanderthal Ancestry
30+ Trait reports
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Opt-in to Family Tree
Opt-in to find and connect with relatives in the 23andMe database who share DNA with you. 23andMe automatically generates your family tree for you. Get a visualization of your genetic relatives who have opted-in to the 23andMe DNA Relatives feature.
Who Appears in your 23andMe Family Tree?
- Close relatives (third cousins or closer) who have been genotyped by 23andMe and opted into DNA Relatives will appear automatically.
- Anyone you manually add to your family tree from your match list.
3 Simple Steps: All from home. No blood. No needles. Just a small saliva sample.
- SPIT: Follow kit instructions to spit in the tube provided — all from home.
- REGISTER: Register your saliva collection tube using the barcode so we know it belongs to you
- RETURN: Mail it back to the 23andMe lab in the pre-paid package.
Your reports will be ready in about 4-5 weeks on average. We will send you an email to let you know your reports are ready in your online account. Log in and start discovering what your DNA says about you.
What you get
- At-home DNA test kit
- Access to Health + Ancestry Service that can help give you a more complete picture of your health with insights from your genetic data.
- Personalized genetic insights and tools can help make it easier for you to take action on your health.
- Includes FDA-authorized reports and full access to our Ancestry Service.
Specs
Specs
- Kit: Health + Ancestry Service
- Dimensions: 1.3"H x 6.5"L x 5.0"W
- Weight: 4.8oz
- Color: multi
- Materials: plastic
- Size: one size
- Restrictions: for ages 18+
Includes
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Saliva collection kit for DNA sample submission
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. Visit 23andMe for important test information.
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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. Visit 23andMe for important Pharmacogenetics information.
- Before you can use the 23andMe services and see your reports, you must agree to 23andMe's Terms of Service and 23andMe’s Privacy Statement at the time of registration of your 23andMe kit. For use in the USA only - kits shipped or used outside the US will be invalidated and no refund will be provided.
Shipping
- Ships to Contiguous US
- Free Shipping
- Expected Delivery: Jan 10 - Jan 19
Terms
- All sales final.