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
Experience your ancestry in a new way! Get a breakdown of your global ancestry by percentages, connect with DNA relatives and more.
$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.
Thinking about gifting? You can cover the cost of a lab free with a gift card.
How it works
For kits purchased from a retailer
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.
Follow kit instructions to spit in the tube provided and mail it back to our lab in the pre-paid package.
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.
Our service is exclusively online. You'll receive your reports through a password-protected account at 23andme.com, and you'll have access to additional web-based tools and features.
In order to receive reports and participate in the service, you need to have a valid email address that allows you to send and receive messages. You also need access to a computer or mobile device that connects to the Internet.
You need to register your kit in order to link it to your 23andMe account online. Registration connects the barcode on your saliva sample to your account so we know your sample belongs to you. Our lab cannot process your sample if it is not registered.
Your saliva contains DNA from cells in your mouth. The saliva collection kit you purchase will come with instructions for providing your sample.
Our CLIA-certified lab extracts DNA from cells in your saliva sample. Then the lab processes the DNA on a genotyping chip that reads hundreds of thousands of locations in your genome.
Your genetic data is analyzed, and we generate your personalized reports based on well-established scientific and medical research.
23andMe offers two Personal Genetic Services: Health + Ancestry and Ancestry. Both services require submitting a saliva sample using our saliva collection kit that you send to the lab for analysis.
Our Health + Ancestry Service provides insights on your genetic health risks*, carrier status*, traits, wellness and ancestry. We analyze, compile and distill the information extracted from your DNA into 75+ reports you can access online and share with family and friends. See full list of reports offered.
Our Ancestry Service helps you understand who you are, where your DNA comes from and your family story. We analyze, compile and distill your DNA information into reports on your Ancestry Composition, Maternal & Paternal Haplogroups, Neanderthal Ancestry, Your DNA Family and provide a DNA Relatives tool to enable you to connect with relatives who share similar DNA.
If you have the Health + Ancestry Service you have access to the full 23andMe experience. If you only have the Ancestry Service, you can easily upgrade to the Health + Ancestry Service for $125 which gives you access to all 75+ reports on ancestry, traits and health. You are eligible to upgrade once you have received your Ancestry reports. To upgrade, log in to your 23andMe account and navigate to the Settings page. You will receive immediate access to your new health reports.
You may save up to $25 if you purchase the $199 Health + Ancestry Service instead of the $99 Ancestry Service as the fee for adding health reports later is $125 ($224 total). We may offer special discounted upgrades from time to time.
There is a special process for kits purchased from a retailer. In order to receive the 23andMe service with a kit that has been purchased from a retailer, payment of an additional lab fee must be made at the time the kit is registered online at 23andMe.com/start.
One suggestion is that you provide the additional funds for the lab fee as part of the gift, perhaps by including a gift card in the amount of the lab fee.
There is a special process for kits purchased from a retailer. You will need to pay an additional lab fee. This has to be paid at the time the kit is registered online at 23andMe.com/start and cannot be prepaid by the gift giver.
To receive a refund for the cost of the kit, $29.99 plus applicable taxes, you must return your kit to the retailer from which you purchased it. Please consult the refund policy of the retailer to determine if your kit is eligible to receive a refund. Refunds for the kit are only available through the retailer.
To receive a refund for the lab fee, you must fill out our online refund form. We cannot issue a refund if (i) you request a refund more than 30 days after the payment of your lab fee was processed; or (ii) our laboratory had begun processing your saliva sample prior to your request for refund. The refund form can be found on the 23andMe Help Center, found at customercare.23andme.com.
You choose how your genetic information is used and shared with others. We tell you how those choices are implemented and how we collect, use and disclose your information.
- We will not share your individual-level information with any third party without your explicit consent
- We support the Genetic Information Nondiscrimination Act (GINA) and other similar laws that protect individuals from being discriminated against based on their genetics and will not provide your information or results to employers or health insurance companies
- We have guidelines and policies in place to protect the personal information of children as well as incapacitated or deceased individuals
- We do not provide information to law enforcement unless we are required to comply with a valid subpoena or a court-ordered request
*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. The Celiac Disease genetic health risk report (i) is indicated for reporting of the rs2187668 variant in the HLA-DQA1 gene, which tags the HLA-DQ2.5 haplotype; and the rs7454108 variant near the HLA-DQB1 gene, which tags the HLA-DQ8 haplotype, (ii) describes if a person has variants associated with a higher risk of developing celiac disease. (iii) The variants included in this test are most common and best studied in people of European descent. The Late-onset Alzheimer's Disease genetic health risk report is indicated for reporting of the ε4 variant in the APOE gene and describes if a person has a variant associated with an increased risk of developing late-onset Alzheimer's disease. The ε4 variant included in this report is found and has been studied in many ethnicities. Detailed risk estimates have been studied the most in people of European descent. The Parkinson's Disease genetic health risk report (i) is indicated for reporting of the G2019S variant in the LRRK2 gene, and the N370S variant in the GBA gene, (ii) describes if a person has variants associated with an increased risk of developing Parkinson's disease, and (iii) is most relevant for people of European, Ashkenazi Jewish, and North African Berber descent. The Cystic Fibrosis carrier status report is indicated for the detection of 28 variants in the CFTR gene and is most relevant for people of Ashkenazi Jewish, European, and Hispanic/Latino descent. The Sickle Cell Anemia carrier status report is indicated for the detection of the HbS variant in the HBB gene and is most relevant for people of African descent. The carrier status reports related to hereditary hearing loss consist of two tests – one indicated for the detection of two variants in the GJB2 gene which is most relevant for people of Ashkenazi Jewish and European descent, and one indicated for the detection of six variants in the SLC26A4 gene.
**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
Your DNA can tell you about your family history. Reports include: Ancestry Composition, Haplogroups, Neanderthal Ancestry, Your DNA Family
Find and connect with relatives in the 23andMe database who share DNA with you.
Learn how your genetics can influence your risk for certain diseases. Example reports include: Celiac Disease, Late-Onset Alzheimer's Disease, Parkinson's Disease
If you are starting a family, find out if you are a carrier for an inherited condition. Example reports include: Cystic Fibrosis, Sickle Cell Anemia, Hereditary Hearing Loss
Learn how your genes play a role in your well-being and lifestyle choices. Example reports include: Deep Sleep, Lactose Intolerance, Genetic Weight
Explore what makes you unique, from food preferences to physical features. Example reports include: Male Bald Spot, Sweet vs. Salty, Unibrow
Your DNA can tell you about your family history. Reports include: Ancestry Composition, Maternal & Paternal Haplogroups, Neanderthal Ancestry, Your DNA Family