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Find out what your DNA says about your health, traits and ancestry.

meets fda requirements

Genetic Health Risks*

Learn how your genetics can influence your risk for certain diseases.

  • 5+ reports including:
  • Celiac Disease
  • Late-Onset Alzheimer's Disease
  • Parkinson's Disease
  • sample report

Ancestry

Discover where your DNA is from out of 31 populations worldwide - and more.

  • 5 reports including:
  • Ancestry Composition
  • Maternal & Paternal Haplogroups
  • Neanderthal Ancestry
  • sample report

Wellness

Learn how your genes play a role in your well-being and lifestyle choices.

  • 5+ reports including:
  • Deep Sleep
  • Lactose Intolerance
  • Genetic Weight
  • sample report
meets fda requirements

Carrier Status*

If you are starting a family, find out if you are a carrier for certain inherited conditions.

  • 40+ reports including:
  • Cystic Fibrosis
  • Sickle Cell Anemia
  • Hereditary Hearing Loss
  • sample report

Traits

Learn how your DNA influences your facial features, taste, smell and other traits.

  • 15+ reports including:
  • Hair Loss
  • Sweet vs. Salty
  • Unibrow
  • sample report

Check out our newest report — Genetic Weight.

learn more

There is a lot to consider with genetic testing. We encourage you to review relevant information about Carrier Status* and Genetic Health Risk* reports on the Test Information page.

important test info
Genetic Trait Report

Genetic Health Risk reports*

5+ reports

Genetic Health Risk reports provide information about whether you carry genetic markers associated with risks for certain health conditions. They are not for diagnosis. Factors like lifestyle, environment and genetic markers not covered by this test can also play a role. These reports provide you with more insights to be the best possible advocate – for you.

    Reports include*
  • Celiac Disease
  • Late-Onset Alzheimer's Disease lock
  • Parkinson's Disease lock
  • See all reports
See sample report

Ancestry reports

5 reports

Your DNA comes from all of your ancestors. In your DNA, we can find genetic traces of where your ancestors lived throughout history.

You also share DNA with people around the world today. You can choose to connect with them through our DNA Relative database. You can continue to find new relatives as our database of more than one million customers grows over time. Learn more.

See sample report
Ancestry Report
Genetic Wellness Report

Wellness reports

5+ reports

When it comes to your wellbeing, your DNA is one part of the story that also includes your environment and lifestyle.

Find out how your DNA relates to your caffeine consumption, lactose digestion and your muscle type.

See sample report

Carrier Status reports*

40+ reports

Being a "carrier" means you "carry" one genetic variant for a condition. Carriers do not typically have the genetic condition, but they can pass a genetic variant down to their children. If both parents are carriers, there is a 25% chance their child will have the condition.

Understanding your carrier status helps you work with your doctor to prepare for the health of your future family.

    Reports include*
  • Cystic Fibrosis
  • Sickle Cell Anemia
  • Hereditary Hearing Loss
  • See all reports
See sample report
Genetic Trait Report

Traits reports

15+ reports

Find out your likelihood of having certain characteristics. See how your DNA affects your hair color, taste preferences and more. You can also compare your results to other 23andMe customers.

    Reports include
  • Hair: Color, Curliness, Male Bald Spot
  • Taste & Smell: Sweet vs. Salty, Bitter
  • Facial Features: Cheek Dimples, Unibrow, Freckles
  • See all traits
See sample report

Hi. Still have questions about service?

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 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.

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Genetic Weight

Health + Ancestry
Service $199

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5% of every (PRODUCT)REDTM Health + Ancestry Service kit purchase goes to fight AIDS.

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MEETS FDA REQUIREMENTS

Genetic Health Risk reports*

Learn how your genetics can influence your risk for certain diseases.

Ancestry

Discover where your DNA is from out of 31 populations worldwide - and more.

Wellness reports

Learn how your genes play a role in your well-being and lifestyle choices.

MEETS FDA REQUIREMENTS

Carrier Status reports*

If you are starting a family, find out if you are a carrier for an inherited condition that could affect your children.

Traits reports

Learn how your DNA influences your facial features, taste, smell and other traits.

What you can do

Use interactive tools to share, compare and discover more with friends and family.

Raw data included  

Raw data is for information purposes only; must not be used for medical or diagnostic purposes.

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