23andMe DNA Health Test Kit - Personalized Genetic Reports for Health Predispositions, Carrier Status & Wellness Insights - FSA/HSA Eligible - Home DNA Testing for Ancestry & Health Screening (Ideal for Family Health Planning & Preventive Care)

Compare Health-only Service Add to Cart Ancestry Service Add to Cart Health-only Service Add to Cart Health + Ancestry Service Add to Cart Customer Reviews 4.0 out of 5 stars 1,455 4.6 out of 5 stars 36,599 4.0 out of 5 stars 1,455 4.6 out of 5 stars 36,925 Price $149.00$149.00 $99.00$99.00 $149.00$149.00 $199.00$199.00 Total Reports 65+ 80+ 65+ 150+ Ancestry and Traits reports ✘ ✔ ✘ ✔ Family Tree ✘ ✔ ✘ ✔ DNA Relative Finder ✘ ✔ ✘ ✔ Health Predisposition reports* ✔ ✘ ✔ ✔ Carrier Status reports* ✔ ✘ ✔ ✔ Wellness reports ✔ ✘ ✔ ✔ Family Health History Tree ✘ ✘ ✘ ✔ FDA-authorized reports ✔ ✘ ✔ ✔ FSA/HSA eligible 100% — 100% Partially Product Description: 23andMe's Health Service is FSA & HSA eligible. Get personalized genetic insights that can help you take more informed actions on your health, today and in the future. Before Mailing, register your kit at 23andMe online, otherwise your sample will NOT be processed. Does not include ancestry or trait reports. Option to add Ancestry Service is not available at this time. Over 65 health reports and features, including: Health Predisposition* reports and Wellness and Carrier Status* reports. Includes FDA-authorized reports. Not all DNA tests, at-home testing kits, or ancestry testing kits are reimbursable. 23andMe's Health Service may be fully eligible for FSA and HSA reimbursement. HEALTH FEATURES: 10+ Health Predisposition reports* including: Type 2 Diabetes (Powered by 23andMe Research), Late-Onset Alzheimer's Disease, Celiac Disease 23andMe Health Service can help give you a more complete picture of your health with insights from your genetic data. Discover how your DNA can influence your health. Using insights backed by the latest science, see how your DNA can affect your chances of developing certain health conditions. Your personalized reports break down your genetic data, the science and potential next steps. 45+ Carrier Status reports* including: Cystic Fibrosis, Sickle Cell Anemia, Tay-Sachs Disease See what you may pass on to your future children. If you're thinking of starting a family, find out if you're a carrier for genetic variants linked to certain inherited health conditions. 5+ Wellness reports including: Deep Sleep, Lactose Intolerance, Genetic Weight Explore how your DNA relates to your lifestyle. Discover what your DNA has to say about lifestyle factors like diet, exercise, and sleep. Use what you've learned to help you make informed decisions. At-home DNA test kit. Personalized genetic insights and tools that can help make it easier for you to take action on your health. 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 the 23andMe Type 2 Diabetes health predisposition report which is based on 23andMe research and has not been reviewed by 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. Warnings & Limitations: The 23andMe PGS Genetic Health Risk Report for BRCA1/BRCA2 (Selected Variants) is indicated for reporting of 44 variants in the BRCA1 and BRCA2 genes. The report describes if a person's genetic result is associated with an increased risk of developing breast cancer and ovarian cancer and may be associated with an increased risk for prostate cancer, pancreatic cancer, and potentially other cancers. The variants included in this report do not represent the majority of the BRCA1/BRCA2 variants in people of most ethnicities. 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. This report is for over-the-counter use by adults over the age of 18, and provides genetic information to inform discussions with a healthcare professional. 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. Visit 23andMe for important test information. Before you can use 23andMe services and see your reports, you must agree to 23andMe's Terms of Service and 23andMe’s Privacy Statement at the time of kit registration. For use in the USA only - kits shipped or used outside the US will be invalidated and no refund will be provided.