Add a service below.

Update quantity

  • Health + Ancestry: Buy one, get 10% off each additional kit
  • Ancestry
    0
  • Health + Ancestry
    0
  • Total
    $0.00
OR
OR
OR
  • Total (0)
    $0.00

Accepted payment methods

PayPal MasterCard Discover American Express Visa Apple Pay
Secure Server
Tell me more
Tell me more
OR
OR
OR
Loading

Order Details

  • Results should take 2-4 weeks, but processing times may vary.
  • Ships from warehouse in 1-2 business days.
  • Standard and Express shipping methods are available.
  • You will have 12 months from the date of purchase to use your kit.
  • Shipping and processing times may vary due to high volume.

  • Intended for sale and use in the US only. The resale of our kits is prohibited. 23andMe can only guarantee services and provide support for kits purchased directly through our website, www.23andme.com, or through one of our authorized resellers. Learn more

    Kits purchased on any external website, such as Craigslist, or eBay, among others, may not be authentic or functional. To protect our customers and prevent privacy and billing issues, 23andMe routinely deactivates the barcode and genotyping chips for kits that are attempted to be resold by unauthorized resellers.

Helpful Links

×

Great News!

You've been upgraded to our Health + Ancestry Service at no additional cost since the service you selected (Health Lite + Ancestry Service) is currently unavailable. Please note that you will receive all 90+ reports, but you can opt out of receiving your Carrier Status* and Genetic Health Risk* reports. We encourage you to review relevant information about Carrier Status* and Genetic Health Risk* reports in the link below.

Important Test Info

The price of your 23andMe Health + Ancestry kit has been updated to $199.

*The 23andMe PGS 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.