Root for Your Roots SM
Discover your connections to the world.

23 pairs of chromosomes.
One unique you.

Receive an overview of your DNA through
detailed reports, tools and more.

buy online at these select retailers

For kits purchased at a retail store, there is a required lab fee.

The lab fee is for processing your saliva sample and generating your reports.

Two easy ways to discover you.

Choose what's right for you.

See Full List of Reports

$69 lab fee

Ancestry
Service

Experience your ancestry in a new way! Get a breakdown of your global ancestry by percentages, connect with DNA relatives and more.

recommended

$169 lab fee

Health + Ancestry Service

Get an even more comprehensive understanding of your genetics. Receive 75+ online reports on your ancestry, traits and health - and more.

You can always upgrade to the Health + Ancestry Service at a later time - once you've received your Ancestry reports.

Please note that you can save $25 today by purchasing the Health + Ancestry Service for $100 more.
Or you can add Health reports later for $125.**

Thinking about gifting? You can cover the cost of a lab fee with a gift card.

Saliva Collection

How it works

For kits purchased from a retailer

  1. Pay required lab fee online

    Go online and register your kit using the saliva tube barcode so we know it belongs to you. Choose from our Health + Ancestry or Ancestry services. Pay the required lab fee - $69 for Ancestry and $169 for Health + Ancestry. Our lab will not process your sample and you will not receive your reports until you have registered and your payment is received.

  2. Spit

    Follow kit instructions to spit in the tube provided and mail it back to our lab in the pre-paid package.

  3. Discover

    After we analyze your sample, we will send you an email to let you know your reports are ready in your online account. Log in and start discovering what your DNA says about you.

Hi. Still have questions?

Here are just a few of the things people frequently ask about 23andMe.
If you don't see your question here, get in touch with us.

FAQ

FAQs

*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. Warnings & Limitations: The 23andMe PGS Genetic Health Risk Report for BRCA1/BRCA2 (Selected Variants) is indicated for reporting of the 185delAG and 5382insC variants in the BRCA1 gene and the 6174delT variant in the BRCA2 gene. The report describes if a woman is at increased risk of developing breast and ovarian cancer, and if a man is at increased risk of developing breast cancer or may be at increased risk of developing prostate cancer. The three variants included in this report are most common in people of Ashkenazi Jewish descent and do not represent the majority of BRCA1/BRCA2 variants in the general population. 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. 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/

**Savings based on regular upgrade price of $125. We may offer special discounted upgrades from time to time.

Already have a kit?

Register & pay lab fee

Welcome

Remember, for kits purchased from a retail store:

There is a required lab fee for processing your saliva sample and generating your reports.