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HI, WE'RE 23ANDME. WE'RE ALL ABOUT REAL SCIENCE, REAL DATA AND GENETIC INSIGHTS
THAT CAN HELP MAKE IT EASIER FOR YOU TO TAKE ACTION ON YOUR HEALTH.

Among Health customers surveyed:
76% reported
making healthier
choices
55% reported
eating a healthier
diet

51% reported
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goals
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increasing exercise
Based on 2019 online survey, designed by 23andMe and M/A/R/C Research, of
approximately 1,000 23andMe Health +plus Ancestry customers.
Health Features


KNOW YOUR GENES.
OWN YOUR HEALTH.


 * HEALTH PREDISPOSITIONS*LEARN ABOUT CONSIDERATIONS AND LIMITATIONS FOR HEALTH
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 * WELLNESS
   
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   can influence certain lifestyle choices.

Learn more about Health Service


HEALTH PREDISPOSITIONS*LEARN ABOUT CONSIDERATIONS AND LIMITATIONS FOR HEALTH
PREDISPOSITIONS REPORTS, CARRIER STATUS REPORTS AND GENETIC HEALTH RISKS

Our DNA testing can help you learn how genetics can influence your chances of
developing certain health conditions.

Phone Slide 0: Health Predispositions*Learn about Considerations and Limitations
for Health Predispositions Reports, Carrier Status Reports and Genetic Health
RisksPhone Slide 1: Carrier Status*Learn about Considerations and Limitations
for Health Predispositions Reports, Carrier Status Reports and Genetic Health
RisksPhone Slide 2: Wellness
Learn more
Ancestry Features


KNOW YOUR PERSONAL STORY, IN A WHOLE NEW WAY.


 * ANCESTRY COMPOSITION
   
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   cases down to the county level.


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   It’s just a click away.


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   Relatives. Compare ancestries and traits, then send messages to relatives
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 * ANCESTRY TIMELINE
   
   Learn when your most recent ancestors from each population lived, going back
   over 8 generations.

Learn more about Ancestry Service


ANCESTRY COMPOSITION

Discover where in the world your DNA is from across 2000+ regions — in some
cases down to the county level.

Phone Slide 0: Ancestry CompositionPhone Slide 1: Family TreePhone Slide 2: DNA
Relative FinderPhone Slide 3: Ancestry Timeline
Learn more about Ancestry Service
Traits Features


KNOW WHAT MAKES YOU, YOU. EXPLORE YOUR TRAITS.


 * PHYSICAL FEATURES
   
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   freckles, learn how your DNA can influence your physical features.


 * TASTE AND SMELL
   
   Cilantro: is it delicious, or soapy? See what your DNA might have to say
   about your taste and smell preferences.


 * WEIRD AND WONDERFUL
   
   Endlessly fascinating and occasionally weird. With genetic testing, you can
   discover how DNA might affect your ability to match a musical pitch, or even
   whether you hate the sound of chewing.

Learn more about Health plus Ancestry Service


PHYSICAL FEATURES

Discover what makes you unique. With reports like hair photobleaching and
freckles, learn how your DNA can influence your physical features.

Phone Slide 0: Physical FeaturesPhone Slide 1: Taste and SmellPhone Slide 2:
Weird And Wonderful
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Add to cart-healthImportant test info


23ANDME
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(Original Price: $199 Sale Price: $129 kit
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one year
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Add to cart-subscriptionImportant test info
Total reports80+150+180+
Includes Pharmacogenetics** reports, Heart Health reports, Skin Cancer (Basal
and Squamous Cell Carcinomas) and Skin Cancer (Melanoma) reports (Powered by
23andMe Research), and other exclusive reports.
Ancestry Reports



Family Tree



DNA Relative Finder
Opt in to connect and message with people who share DNA with you.



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



Health Predisposition reports*Learn about Considerations and Limitations for
Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks
Learn how your genetics can influence your chances of developing certain health
conditions.



Carrier Status reports*Learn about Considerations and Limitations for Health
Predispositions Reports, Carrier Status Reports and Genetic Health Risks
If you are starting a family, find out if you are a carrier for certain
inherited conditions.



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



Family Health History Tree
Easily input, track and download your family health history to share with your
healthcare provider.



Pharmacogenetics reports**Learn about Considerations and Limitations for
Pharmacogenetics Reports
Discover how your DNA may impact how your body processes certain medications
with three new Pharmacogenetics reports.



Enhanced ancestry features
Get advanced filtering for DNA Relative Finder and access up to 5000 more DNA
relatives.



Ongoing new reports and features
Get access to new premium reports and features throughout the year.




PRIVACY
KNOW THAT YOU ARE IN CONTROL OF YOUR DNA.

Discovery should never come at the expense of privacy. Your data is encrypted,
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Research


KNOW YOU'RE MAKING A DIFFERENCE.

When you opt in to participate in our research, you join forces with millions of
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discoveries that may one day make an impact on your own health, the health of
your family and ultimately, people around the world. (Look at you go.)

Learn more about research
Learn more about research


FREQUENTLY ASKED QUESTIONS

How accurate is 23andMe?

23andMe has rigorous standards that ensure high-quality results. Our team of
scientists and medical experts use a robust process to develop genetic reports
for our customers. Here are specific examples:

 * With one of the largest reference datasets in the world, 23andMe provides
   customers with one of the most detailed and accurate ancestry breakdowns on
   the market. Our algorithms make ancestry estimates based on probabilities and
   they’re generally very accurate, but your results are not set in stone. We
   are always trying to improve and refine these estimates.
 * Our Genetic Health Risk*Learn about Considerations and Limitations for Health
   Predispositions Reports, Carrier Status Reports and Genetic Health Risks,
   Carrier Status*Learn about Considerations and Limitations for Health
   Predispositions Reports, Carrier Status Reports and Genetic Health Risks,
   Pharmacogenetics**Learn about Considerations and Limitations for
   Pharmacogenetics Reports reports meet FDA requirements. This means that each
   variant in those reports demonstrated >greater than99% accuracy and
   reproducibility when tested under different laboratory conditions. This
   article on the accuracy of 23andMe reports provides additional information.

How does 23andMe DNA testing work?

After you provide a saliva sample, 23andMe uses genotyping to analyze your DNA.
This means we look at specific locations in your genome that are known to differ
between people. We then turn those results into personalized genetic reports on
everything from ancestry composition to traits to genetic health risks. Note
that genotyping is different from DNA sequencing, which looks at every letter in
a particular stretch of DNA.

Who can use 23andMe?

Most adults who are able to provide saliva samples can use the 23andMe kit.
However there are some considerations that can complicate the DNA accuracy.
Check out our Terms of Service for more info on those cases.

How do I get my 23andMe reports and how long does it take?

To begin, visit www.23andme.com/start. Once you have successfully registered
your DNA testing kit, provided a saliva sample and put the kit in the mail, you
can use the return tracking link available on your profile homepage to track
your kit's progress to the lab. Once your sample reaches the lab, it is
typically processed within a few weeks, with results then delivered to your
secure online account.

Do 23andMe DNA test kits expire?

We encourage customers to provide their sample before the "Collect saliva by"
date on the side of the collection tube. If your sample collection kit is lost
or damaged, or if it has expired, please contact customer care to assist you
with getting a replacement kit.

Why should I choose 23andMe?

There are many benefits of DNA testing, including finding relatives, learning
whether you have genetic variants you could pass onto your children, and
receiving personalized insights into your health and ancestry. 23andMe Health +
Ancestry Service offers 150+ DNA reports that do just that. In addition to
taking greater control of your own health and digging deeper into your ancestry,
you can also opt in to participate in research that could help fuel scientific
discoveries that benefit the larger community.

We're also committed to providing you with a safe place where you can learn
about your DNA knowing your privacy is protected. 23andMe has sold 12+ million
kits, and with each and every one of those, privacy has been our number one
priority. You may learn more about our commitment to privacy hereon our privacy
page.


STAY IN THE KNOW.

Keep up-to-date with new discoveries and exclusive promotions on our DNA testing
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*23andMe health predisposition reports include both reports that meet FDA
requirements for genetic health risks and reports which are based on 23andMe
research and have not been reviewed by the FDA. The 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. 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/

**23andMe PGS Pharmacogenetics reports: The 23andMe test uses qualitative
genotyping to detect 3 variants in the CYP2C19 gene, 2 variants in the DPYD gene
and 1 variant in the SLCO1B1 gene in the genomic DNA of adults from saliva for
the purpose of reporting and interpreting information about the processing of
certain therapeutics to inform discussions with a healthcare professional. It
does not describe if a person will or will not respond to a particular
therapeutic and does not describe the association between detected variants and
any specific therapeutic. Our CYP2C19 Pharmacogenetics report provides certain
information about variants associated with metabolism of some therapeutics and
provides interpretive drug information regarding the potential effect of
citalopram and clopidogrel therapy. Results for SLCO1B1 and DPYD and certain
CYP2C19 results should be confirmed by an independent genetic test prescribed by
your own healthcare provider before taking any medical action. Warning: Test
information should not be used to start, stop, or change any course of treatment
and does not test for all possible variants that may affect metabolism or
protein function. The PGS test is not a substitute for visits to a healthcare
professional. Making changes to your current regimen can lead to harmful side
effects or reduced intended benefits of your medication, therefore consult with
your healthcare professional before taking any medical action. For important
information and limitations regarding Pharmacogenetics reports, visit
23andme.com/test-info/pharmacogenetics/


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