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:
- Hereditary Thrombophilia
- 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 moreThere 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.
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*
-
Late-Onset Alzheimer's Disease
-
Parkinson's Disease
- Hereditary Thrombophilia (harmful blood clotting)
- See all reports
Take a closer look at a report.
Overview
This section describes the condition and whether our test detected certain genetic variants in your DNA.
How to use this test
Learn what this report can and cannot tell you. Also see which ethnicities are most relevant to the test.
Report result
Get a short explanation of what your genetic result means.
Other risk factors
Learn about lifestyle and other factors that may influence your risk of developing the condition.
About the condition
Learn more by exploring a list of additional resources.
Take action
Find the suggested next steps based on your results.
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.
-
Reports include
- Ancestry Composition
- Maternal Haplogroup
- Paternal Haplogroup
- Neanderthal Ancestry
- Your DNA Family
- and DNA Relative Finder tool
Take a closer look at a report.
Overview
Get a summary of your Ancestry Composition, and see detailed percentages from regions around the world.
Ancestry timeline
Discover when different ancestries were introduced into your DNA.
The genetics of your ancestry
Learn about your ancestry down to the chromosome level...all 23 of them!
Inheritance
See how each of your biological parents contributed to your Ancestry Composition (feature available when one parent is also a 23andMe customer).
Take action
Find suggested next steps.
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.
-
Reports include
- Deep Sleep
- Lactose Intolerance
- Genetic Weight
- See all reports
Take a closer look at a report.
Overview
Find out if you are genetically predisposed to weigh more or less than average.
About the report
We look at DNA variants associated with weight.
Take action
Discover the habits that make the biggest weight difference in people with similar genetics.
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
Take a closer look at a report.
Overview
This section describes the condition and whether our test detected certain genetic variants in your DNA.
How to use this test
Learn what this report can and cannot tell you. Also see which ethnicities are most relevant to the test.
Report result
Get a short explanation of what your genetic result means.
About the condition
Learn more about the disease or condition. Explore a list of additional resources.
Take action
Find the suggested next steps based on your results.
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
Take a closer look at a report.
Overview
See how likely you are to have the trait and how your prediction compares to other groups.
About the trait
Learn how the trait develops, how it evolved and other contributing factors.
Take action
Take the next step by sharing, comparing or learning more about your results.
Tools
Overview
Use interactive tools to share, compare and discover more with friends and family.
Inheritance Tracing
Trace DNA through your close family, and see how different traits have traveled through generations.
Share and Compare
Share and compare your reports, and explore the genetic similarities and differences between you and family members.
DNA Relatives
Find and connect with new DNA relatives, and see specific DNA segments you share with them to fill in your family tree.
Research
Our research program
An important part of our mission is doing research to help people understand and benefit from the human genome.
You can make a difference
By joining our research program, you can help drive scientific and medical discoveries.
How it works
Contribute to research from home and learn more about genetics along the way.
Learn more.
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.
FAQs
The 23andMe DNA database has more than two million genotyped customers worldwide. You will continue to find new relatives as our database grows over time.
Yes. Our service has tools that enable you to share your reports with friends and family. In fact, the more family members that participate in 23andMe, the more interactive and engaging your results will be. When you share with family members who are 23andMe customers, you can see how genes are passed down in your family – and see the similarities and differences between family members – which can help you understand and connect to one another. Sharing and comparing information can be a great starting point for discussing and learning more about your identities, health conditions, ancestry and more.
Genetic information is hereditary and tells you many things about your close relatives as well as yourself. You should consider whether your family wants to know all of the information available, so be thoughtful about sharing it.
Your results may be useful to share with your doctor.
Genetic counselors can answer your questions about health-related DNA testing. These are health professionals that have special training in genetic conditions. They can help you decide whether genetic testing is right for you, and they can also help you better understand your 23andMe results. We provide a link to resources that can help you locate a genetic counselor in your area and enable you to download a file to share your genetic reports.
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.
*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 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 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
Health + Ancestry
Service $199
MEETS FDA REQUIREMENTS
Genetic Health Risk reports*
Learn how your genetics can influence your risk for certain diseases.
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 included
-
Late-Onset Alzheimer's Disease
-
Parkinson's Disease
- Hereditary Thrombophilia
- sample report
-
Age-Related Macular Degeneration
2 variants in the ARMS2 and CFH genes; relevant for European descent
-
Alpha-1 Antitrypsin Deficiency
2 variants in the SERPINA1 gene; relevant for European descent
-
Hereditary Hemochromatosis (HFE-Related)
2 variants in the HFE gene; relevant for European descent
-
Hereditary Thrombophilia
2 variants in the F2 and F5 genes; relevant for European descent
-
Late-Onset Alzheimer's Disease
1 variant in the APOE gene; variant found and studied in many ethnicities
-
Parkinson's Disease
2 variants in the LRRK2 and GBA genes; relevant for European, Ashkenazi Jewish, North African Berber descent
*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. The relevance of each report may vary based on ethnicity. Our genetic health risk reports describe if a person has variants associated with a higher risk of developing a disease, but do not describe a person's overall risk of developing the disease. The reports are not intended to diagnose any disease, 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. 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 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.
Ancestry
Discover where your DNA is from out of 31 populations worldwide - and more.
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.
Ancestry Composition report
Find out where your DNA comes from around the world. Your DNA can tell you where your ancestors lived more than 500 years ago. See a percentage breakdown by region, including eastern Asia, Sub-Saharan Africa, Europe and more. We look at 31 populations worldwide, and we will continue to refine your results as our database grows.
Discover when different ancestries were introduced into your DNA. Learn how many generations ago you had an ancestor that was descended from a single population or ethnicity.
Your DNA Family report
Receive an overview of the diverse group of people who share your DNA. Get to know your DNA Family with this unique (and anonymous) report and view the places your DNA Relatives call home. You can even learn more about the ancestry and traits of your DNA Relatives.
DNA Relative Finder tool
Find other 23andMe customers who share your DNA and ancestors. Explore matches that range from close family to distant relatives, and make new connections. Shed light on your family story by discovering an unknown relative — nearby or elsewhere around the world. You can always choose to opt in or out of this tool.
Maternal & Paternal Haplogroups
Discover the origins of your maternal (your mother's mother's mother's…) and paternal (your father's father's father's…) ancestors and how they moved around the world over thousands of years.
We report on your maternal and paternal lineage by identifying your haplogroups. A haplogroup can trace part of your ancestry back to a specific group of individuals in the distant past.
Women can only trace their maternal haplogroup. This is because the paternal haplogroup is traced through the Y chromosome, which women do not inherit.
Neanderthal Ancestry report
Neanderthals were ancient humans who interbred with modern humans before becoming extinct 40,000 years ago. Find out how much of your DNA came from Neanderthals. Compare your results with family and friends.
Wellness reports
Learn how your genes play a role in your well-being and lifestyle choices.
5+ reports
When it comes to your wellbeing, your DNA is one part of the story that also includes your environment and lifestyle choices.
Find out how your DNA relates to your caffeine consumption, lactose digestion and muscle type.
Reports included
- Deep Sleep
- Saturated Fat and Weight
- Lactose Intolerance
- sample report
- Alcohol Flush Reaction
- Caffeine Consumption
- Deep Sleep
- Genetic Weight
- Lactose Intolerance
- Muscle Composition
- Saturated Fat and Weight
- Sleep Movement
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.
40+ reports
Being a "carrier" means you "carry" one genetic variant for a condition. Genetic variants are changes in your DNA. 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. You may also choose to share your carrier status with other family members who may benefit from this information.
Reports included*
- Cystic Fibrosis
- Sickle Cell Anemia
- Hereditary Hearing Loss
- sample report
-
ARSACS
1 variant in the SACS gene; relevant for French Canadian descent
-
Agenesis of the Corpus Callosum with Peripheral Neuropathy
1 variant in the SLC12A6 gene; relevant for French Canadian descent
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Autosomal Recessive Polycystic Kidney Disease
3 variants in the PKHD1 gene
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Beta Thalassemia and Related Hemoglobinopathies
10 variants in the HBB gene; relevant for Cypriot, Greek, Italian, Sardinian descent
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Bloom Syndrome
1 variant in the BLM gene; relevant for Ashkenazi Jewish descent
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Canavan Disease
3 variants in the ASPA gene; relevant for Ashkenazi Jewish descent
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Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)
2 variants in the PMM2 gene; relevant for Danish descent
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Cystic Fibrosis
28 variants in the CFTR gene; relevant for European, Hispanic/Latino, Ashkenazi Jewish descent
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D-Bifunctional Protein Deficiency
2 variants in the HSD17B4 gene
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Dihydrolipoamide Dehydrogenase Deficiency
1 variant in the DLD gene; relevant for Ashkenazi Jewish descent
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Familial Dysautonomia
1 variant in the IKBKAP gene; relevant for Ashkenazi Jewish descent
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Fanconi Anemia Group C
3 variants in the FANCC gene; relevant for Ashkenazi Jewish descent
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GRACILE Syndrome
1 variant in the BCS1L gene; relevant for Finnish descent
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Gaucher Disease Type 1
3 variants in the GBA gene; relevant for Ashkenazi Jewish descent
-
Glycogen Storage Disease Type Ia
1 variant in the G6PC gene; relevant for Ashkenazi Jewish descent
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Glycogen Storage Disease Type Ib
2 variants in the SLC37A4 gene
-
Hereditary Fructose Intolerance
3 variants in the ALDOB gene; relevant for European descent
-
Herlitz Junctional Epidermolysis Bullosa (LAMB3-related)
3 variants in the LAMB3 gene
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Leigh Syndrome, French Canadian Type
1 variant in the LRPPRC gene; relevant for French Canadian descent
-
Limb-Girdle Muscular Dystrophy Type 2D
1 variant in the SGCA gene; relevant for Finnish descent
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Limb-Girdle Muscular Dystrophy Type 2E
1 variant in the SGCB gene; relevant for Southern Indiana Amish descent
-
Limb-Girdle Muscular Dystrophy Type 2I
1 variant in the FKRP gene; relevant for European descent
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MCAD Deficiency
3 variants in the ACADM gene; relevant for Northern European descent
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Maple Syrup Urine Disease Type 1B
2 variants in the BCKDHB gene; relevant for Ashkenazi Jewish descent
-
Mucolipidosis Type IV
1 variant in the MCOLN1 gene; relevant for Ashkenazi Jewish descent
-
Neuronal Ceroid Lipofuscinosis (CLN5-Related)
1 variant in the CLN5 gene; relevant for Finnish descent
-
Neuronal Ceroid Lipofuscinosis (PPT1-Related)
3 variants in the PPT1 gene; relevant for Finnish descent
-
Niemann-Pick Disease Type A
3 variants in the SMPD1 gene; relevant for Ashkenazi Jewish descent
-
Nijmegen Breakage Syndrome
1 variant in the NBN gene; relevant for Eastern European descent
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Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)
2 variants in the GJB2 gene; relevant for Ashkenazi Jewish, European descent
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Pendred Syndrome and DFNB4 Hearing Loss
6 variants in the SLC26A4 gene
-
Phenylketonuria and Related Disorders
23 variants in the PAH gene; relevant for Northern European descent
-
Primary Hyperoxaluria Type 2
1 variant in the GRHPR gene; relevant for European descent
-
Rhizomelic Chondrodysplasia Punctata Type 1
1 variant in the PEX7 gene
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Salla Disease
1 variant in the SLC17A5 gene; relevant for Finnish, Swedish descent
-
Sickle Cell Anemia
1 variant in the HBB gene; relevant for African descent
-
Sjögren-Larsson Syndrome
1 variant in the ALDH3A2 gene; relevant for Swedish descent
-
Tay-Sachs Disease
4 variants in the HEXA gene; relevant for Ashkenazi Jewish, Cajun descent
-
Tyrosinemia Type I
4 variants in the FAH gene; relevant for French Canadian, Finnish descent
-
Usher Syndrome Type 1F
1 variant in the PCDH15 gene; relevant for Ashkenazi Jewish descent
-
Usher Syndrome Type 3A
1 variant in the CLRN1 gene; relevant for Ashkenazi Jewish descent
-
Zellweger Syndrome Spectrum (PEX1-Related)
1 variant in the PEX1 gene
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 carrier status and reporting and interpreting genetic health risks. The relevance of each report may vary based on ethnicity. 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 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.
Traits reports
Learn how your DNA influences your facial features, taste, smell and other traits.
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 with other 23andMe customers.
Reports included
- Hair: Color, Curliness, Male Bald Spot
- Taste & Smell: Sweet vs. Salty, Bitter
- Facial Features: Cheek Dimples, Unibrow
- sample report
- Asparagus Odor Detection
- Back Hair (available for men only)
- Bald Spot (available for men only)
- Bitter Taste Perception
- Cheek Dimples
- Cleft Chin
- Earlobe Type
- Earwax Type
- Eye Color
- Finger Length Ratio
- Freckles
- Hair Curliness
- Light or Dark Hair
- Male Hair Loss (available for men only)
- Newborn Hair Amount
- Photic Sneeze Reflex
- Red Hair
- Skin Pigmentation
- Sweet Taste Preference
- Toe Length Ratio
- Unibrow
- Widow's Peak
What you can do
Use interactive tools to share, compare and discover more with friends and family.
Share and Compare
Share and compare your health, traits and ancestry reports with friends and family. You can even explore the genetic similarities and differences between you and a family member in a side-by-side comparison. Requires relatives to be genotyped.
Inheritance Tracing
See how different traits and ancestries have traveled through generations of your family. Requires relatives to be genotyped.
DNA Relatives
Find people who share your DNA and ancestors. Explore matches that range from close family to distant relatives, and make new connections. Shed light on your family story by discovering an unknown relative — nearby or elsewhere around the world. You can always choose to opt in or out of this tool.
Research
You can make a difference by participating in a new kind of research — online, from anywhere. Genetics are a foundation for understanding human health and have been a key to medical breakthroughs.
Start by answering questions and allowing researchers to link your genetic data with millions of other data points. By aggregating these data points, researchers can link genetic markers to diseases and drive medical discoveries. We protect your privacy by removing personal information like your name, email and address from your genetic data. You can always choose to opt in or out of this feature.
Our research activities are reviewed by an independent ethics committee, also known as an Institutional Review Board (IRB).
Raw data included 
Raw data is for information purposes only; must not be used for medical or diagnostic purposes.
Carrier Status
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