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description=23andMe is a saliva-based DNA service. We provide genetic reports on your ancestry, family history and help you connect with your DNA relatives.;
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Text of the page (random words):
dna genetic testing for ancestry traits 23andme international skip to main content our service privacy security sign in register kit help join open menu close menu join our service privacy security sign in register kit help join exclusive offer buy one kit get 20 off each additional kit see cart for details buy now find out what your dna says about you and your family see how your dna breaks out across 4 500 locations worldwide with the most comprehensive ancestry breakdown on the market discover relatives from near and far with our dna relative finder share reports with family and friends learn how your dna influences your facial features taste smell and other traits usd 119 add to cart ancestry service there 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 composition ancestry timeline dna relative finder i always wanted to know who are my ancestors who are the people that made me me watch jordan s story if 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 you time 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 growing from 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 basic ancestry service what sets it apart 4 500 locations worldwide neanderthal dna haplogroups family tree usd 119 add to cart learn more privacy by design there 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 more things 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 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 and receiving personalised insights into your insights into your health and ancestry 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 here on 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 address sign 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 footer services ancestry service company blog careers reporter inquiries return refund policy customer care site map learn about us how it works science privacy security research stories business development legal terms of service privacy statement data protection research consent biobanking consent cookie policy cookie settings report a security issue download app international change change location connect 2026 23andme research institute all rights reserved