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

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  • Purple Heart
    MEETS FDA REQUIREMENTS

    Genetic Health Risks*

    3+ REPORTS

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

    Reports include: Hereditary Thrombophilia, Late-Onset Alzheimer's Disease, Parkinson's Disease

    sample report
  • Ancestry Pie

    Ancestry

    3+ REPORTS

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

    Reports include: Ancestry Composition, Haplogroups, Neanderthal Ancestry

    sample report
  • Pie Wellness

    Wellness

    5+ REPORTS

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

    Reports include: Deep Sleep,
    Lactose Intolerance, Genetic Weight

    sample report
  • Carrier Status
    MEETS FDA REQUIREMENTS

    Carrier Status*

    40+ REPORTS

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

    Reports include: Cystic Fibrosis, Sickle Cell Anemia, Hereditary Hearing Loss

    sample report
  • Pie Traits

    Traits

    15+ REPORTS

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

    Reports include: Hair Loss,
    Sweet vs. Salty, Unibrow

    sample report

Discover what your 23 pairs of chromosomes say about you.

Your health, traits, ancestry - and more.

Check out our newest report — Genetic Weight.

learn more

The 23andMe Difference.

Receive an overview of your DNA – your 23 pairs of chromosomes – through detailed reports, tools and more.

Carrier status reports*

40+ reports

If you are starting a family, find out if you are a carrier for an inherited condition.

Example reports*
  • Cystic Fibrosis
  • Sickle Cell Anemia
  • Hereditary Hearing Loss

Ancestry reports

3 reports

Your DNA can tell you about your family history.

All reports

Wellness reports

5+ reports

Your genetics can help you make more informed choices about your diet and exercise.

Example reports
  • Deep Sleep
  • Lactose Intolerance
  • Genetic Weight

Traits reports

15+ reports

Explore what makes you unique, from food preferences to physical features.

Example reports
  • Hair Loss
  • Sweet vs. Salty
  • Unibrow
see all reports

There is a lot to consider with genetic testing. We encourage you to read additional details about the uses and limitations of our health reports on the FDA Information page.

Genetic Trait Report

Genetic Health Risk reports*

4 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.

See sample report

Ancestry reports

4 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.

    Reports include
  • Ancestry Composition
  • Haplogroups
  • Neanderthal Ancestry
  • Your DNA Family
  • and DNA Relative Finder tool
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.

How large is the 23andMe DNA database?

Will I be able to share information with my family?

Whom can I talk to about my health report results?

What services do you provide?

*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 varies 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 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 Alpha-1 Antitrypsin (AAT) Deficiency genetic health risk report (i) is indicated for reporting of the PI*Z and PI*S variants in the SERPINA1 gene, (ii) describes if a person has variants associated with AAT deficiency and a higher risk for lung and liver disease, and (iii) is most relevant for 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 Hereditary Thrombophilia genetic health risk report (i) is indicated for reporting of the Factor V Leiden variant in the F5 gene, and the Prothrombin G20210A variant in the F2 gene, (ii) describes if a person has variants associated with a higher risk of developing harmful blood clots, and (iii) is most relevant for people of European 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.

CHECK OUT OUR NEWEST REPORT

Genetic Weight

kit

Celebrate Mom genes.

SAVE $20. Limit 2 kits.

Offer ends May 14.

Health + Ancestry
Service $199

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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