https://23andme.com

DNA Genetic Testing For Health, Ancestry And More - 23andMe Europe23andMe offers DNA testing with the most comprehensive ancestry breakdown, personalized health insights and more.DNA Genetic Testing For Health, Ancestry And More - 23andMe EuropeSkip to main contentServicesAncestry ServiceThe most comprehensive ancestry breakdown on the market.Health +plus Ancestry ServiceEverything in Ancestry Service, plus a more complete picture of your health with insights from your genetic data.Compare our servicesPrivacySecuritySign inRegister kitHelpJoinOpen MenuClose MenuJoinServicesAncestry ServiceThe most comprehensive ancestry breakdown on the market.Health +plus Ancestry ServiceEverything in Ancestry Service, plus a more complete picture of your health with insights from your genetic data.Compare our servicesPrivacySecuritySign inRegister kitHelpJoinExclusive Offer: Buy one kit, get 20% OFF each additional kit. See cart for details. Buy now Trusted by Experts recognized for ExcellenceAward-winning science that gives you clearer, more actionable insights about you.Best InventionsRecognized for pioneering the direct-to-consumer genetic testing category.Learn moreBrands That MatterHonored for mission-driven impact, cultural resonance, and authenticity.Learn moreEditor’s ChoiceSelected for simplifying personal discovery and empowering meaningful connection.Learn moreOprah’s Favorite ThingsSelected for simplifying personal discovery and empowering meaningful connection.Learn moreOur servicesAncestry ServiceBasic AncestryExplore the unique story written in your DNA, from your global ancestry breakdown out of 4,500+ locations to the relatives who share your genetic legacy.€99 Learn more about Ancestry ServiceHealth +plus Ancestry ServiceBasic Health + AncestryGet personalised genetic insights and tools that can help make it easier for you to take action on your health.€189 Learn more about Health +plus Ancestry ServiceHealth + AncestryFor all the wonder that is you.From the lineage of your distant past to the insights into your future, it’s all coded in your DNA. Unlock it with in-depth ancestry results and foundational genetic health reports.Health Predispositions*WellnessCarrier status*“It never would’ve occurred to me. It just wasn’t a part of our world.”Watch Hilary's StoryGet ahead of what’s aheadUsing insights backed by the latest science, see how your DNA can affect your chances of developing certain health conditions. Your personalised reports break down your genetic data, the science, and potential next steps.The dashboard of youDiscover 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 going forward.For the future of your familyIf you’re thinking of starting a family, you can learn if you're a carrier for genetic variants linked to certain inherited health conditions.Basic Health + AncestryHealth + Ancestry ServiceWhat sets it apart:Genetic health screening for 10+ conditionsSelect FDA-authorised reportsAll Ancestry Service features€189Add to CartImportant test infoLearn MoreAncestry ServiceThere’s more to your story.Understand the larger context of where you come from, breaking down your ancestry to the 0.1%. It's the most comprehensive genetic breakdown on the market, helping you gain a more complete portrait of yourself.Ancestry CompositionAncestry TimelineDNA Relative Finder“I always wanted to know who are my ancestors? Who are the people that made me, me?”Watch Jordan's StoryIf it's worth knowing, it's worth knowing down to the 0.1%Discover where in the world your DNA is from across 4,500+ locations - in some cases, down to the county level.In the grand scheme of youTime hop to gain a clearer picture of where you came from, where your ancestors lived and when they lived there.The family tree that keeps growingFrom close family members to distant branches, you'll be amazed by the myriad of people you could be connected to. Open your world to DNA relatives, old and new.BasicAncestry ServiceWhat sets it apart:4,500+ locations worldwideNeanderthal DNAHaplogroupsFamily Tree€99Add to CartLearn MorePrivacy by designThere is no advanced science that comes before your protection. Read more about our enhanced measures designed to keep your data safe, in any scenario.Learn moreThings you might be wondering:How accurate is 23andMe?23andMe has rigorous standards that ensure high-quality results. Our team of scientists and medical experts use a robust process to develop genetic reports for our customers. Here are specific examples:With one of the largest reference datasets in the world, 23andMe provides customers with one of the most detailed and accurate ancestry breakdowns on the market. Our algorithms make ancestry estimates based on probabilities and they’re generally very accurate, but your results are not set in stone. We are always trying to improve and refine these estimates.Our Genetic Health Risk*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks, Carrier Status*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks, reports meet FDA requirements. This means that each variant in those reports demonstrated >greater than99% accuracy and reproducibility when tested under different laboratory conditions. This article on the accuracy of 23andMe reports provides additional information.How does 23andMe DNA testing work?After you provide a saliva sample, 23andMe uses genotyping to analyse your DNA. This means we look at specific locations in your genome that are known to differ between people. We then turn those results into personalised genetic reports on everything from ancestry composition to traits to genetic health risks. Note that genotyping is different from DNA sequencing, which looks at every letter in a particular stretch of DNA.Who can use 23andMe?Most adults who are able to provide saliva samples can use the 23andMe kit. However there are some considerations that can complicate the DNA accuracy. Check out our Terms of Service for more info on those cases.How do I get my 23andMe reports and how long does it take?To begin, visit www.23andme.com/start. Once you have successfully registered your DNA testing kit, provided a saliva sample and put the kit in the post, you can use the return tracking link available on your profile homepage to track your kit's progress to the lab. Once your sample reaches the lab, it is typically processed within a few weeks, with results then delivered to your secure online account.Do 23andMe DNA test kits expire?We encourage customers to provide their sample before the "Collect saliva by" date on the side of the collection tube. If your sample collection kit is lost or damaged, or if it has expired, please contact customer care to assist you with getting a replacement kit.Why should I choose 23andMe?There are many benefits of DNA testing, including finding relatives, learning whether you have genetic variants you could pass onto your children, and receiving personalised insights into your insights into your health and ancestry. 23andMe Health + Ancestry Service offers 150+ DNA reports that do just that. We're also committed to providing you with a safe place where you can learn about your DNA knowing your privacy is protected. 23andMe has sold 12+ million kits, and with each and every one of those, privacy has been our number one priority. You may learn more about our commitment to privacy hereon our privacy page.Stay in the know.Keep up-to-date with new discoveries and exclusive promotions on our DNA testing kits and services.Please provide consent.I consent to the transfer and validation of my email address in conjunction with this email service. I understand that I may withdraw my consent and unsubscribe at any time.Email addressSign up*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. 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. For important information and limitations regarding each genetic health risk and carrier status report, visit 23andme.com/test-info/ FooterServicesHealth +plus AncestryAncestry ServiceCompanyBlogCareersReporter InquiriesReturn & Refund PolicyCustomer CareSite MapLearnAbout UsHow it WorksSciencePrivacySecurityResearchStoriesGenetics Learning HubBusiness DevelopmentLegalImportant Test InfoTerms of ServicePrivacy StatementData ProtectionFamily ConsiderationsResearch ConsentBiobanking ConsentCookie PolicyCookie SettingsReport a Security IssueDownload AppEurope | ChangeChange locationConnect© 2026 23andMe Research Institute All rights reserved.eneuen-eu1772387761https://23andme.com

Edit your site?

What are you doing?