Details: How it works? Provide your saliva sample from home. Mail it back to our lab in the same kit it came in- the postage is prepaid.
You will get access to the following Reports and Tools:
1) Ancestry Composition - See how your DNA breaks out across 150+ populations‡ worldwide. 2) DNA Relatives - Opt-in to connect with people who share DNA with you - and message them. 3) Haplogroups - Trace parts of your ancestry to specific groups of individuals from 1,000+ years ago. 4) Share & Compare - Explore genetic similarities and differences between you and your relatives. 5) Neanderthal Ancestry - Discover if you inherited some Neanderthal DNA.
Get a detailed breakdown of your ancestry from 150+ populations‡ worldwide, see if some of your DNA comes from Neanderthals
Find and connect with new DNA relatives from around the world
Provide a saliva sample using our at-home kit and send it back, results ready in about 6-8 weeks
No additional lab fee required, and you always have the option to upgrade to add health reports for an extra cost
Subject to 23andMe's Terms of Service at 23andme.com/tos and Privacy Statement at 23andme.com/privacy
Legal Disclaimer: ‡ 23andMe's Ancestry Composition update with over 120 additional regions will be coming soon to all 23andMe Customers.
*The 23andMe PGS test uses qualitative genotyping to detect clinically relevant variants in the genomic DNA of adults from saliva collected using an FDA-cleared collection device (Oragene·DX model OGD-500.001) for the purpose of reporting and interpreting genetic health risks and reporting carrier status. It is not intended to diagnose any disease. The relevance of each report may vary based on ethnicity. 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. These reports are 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 or how much of a medication you should take. 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 or anything about the health of your fetus, or your newborn child's risk of developing a particular disease later in life. For Gaucher Disease Type 1, we provide a single report that includes information on both carrier status and genetic health risk.
**This data has undergone a general quality review however only a subset of markers have been individually validated for accuracy. The data from 23andMe's Browse Raw Data feature is suitable only for research, educational, and informational use and not for medical, diagnostic or other use.
***Savings based on regular upgrade price of $125. We may offer special discounted upgrades from time to time.
Before you can use 23andMe and see your reports, you must agree to 23andMe's Terms of Service (23andme.com/tos) at the time of registration of your 23andMe kit. Your use of 23andMe is further subject to 23andMe's Privacy Statement (23andme.com/privacy). 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. Many conditions and traits are influenced by multiple factors. 23andMe reports are intended for informational purposes only and do not diagnose disease or illness.