Discover what your 23 pairs of chromosomes say about you.
Your health, traits, ancestry - and more.
The 23andMe Difference.
Receive an overview of your DNA – your 23 pairs of chromosomes – through detailed reports, tools and more.
Ancestry reports
3 reportsYour DNA can tell you about your family history.
- Ancestry Composition
- Haplogroups
- Neanderthal Ancestry
Wellness reports
5+ reportsYour genetics can help you make more informed choices about your diet and exercise.
- Deep Sleep
- Lactose Intolerance
- Saturated Fat and Weight
Traits reports
19+ reportsExplore what makes you unique, from food preferences to physical features.
- Hair Loss
- Sweet vs. Salty
- Unibrow
See what your DNA can tell you.
Click to explore our service below.
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Carrier
Status* -
Ancestry
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Wellness
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Traits
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Share &
Compare -
DNA Relatives
Carrier Status*
If you are starting a family, find out if you are a carrier for certain inherited conditions.
Learn more
Share & Compare
Explore genetic similarities and differences between you and your relatives.
Learn more
Traits
Learn how your DNA influences your facial features, taste, smell and other traits.
Learn more
Carrier Status* reports
If you are starting a family, find out if you are a carrier for certain inherited conditions.
35+ reports
Example reports* include:
- Cystic Fibrosis
- Sickle Cell Anemia
- Hereditary Hearing Loss
Learn more
Carrier Status*
35+ reports
Example reports* include:
- Cystic Fibrosis
- Sickle Cell Anemia
- Hereditary Hearing Loss
Ancestry reports
Discover where your DNA is from out of 31 populations worldwide - and more.
3 reports
- Ancestry Composition
- Haplogroups
- Neanderthal Ancestry
- Ancestry Composition
- Haplogroups
- Neanderthal Ancestry
Learn more
Wellness reports
Learn how your genes play a role in your well-being and lifestyle choices.
5+ reports
Example reports include:
- Deep Sleep
- Lactose Intolerance
- Saturated Fat and Weight
- Deep Sleep
- Lactose Intolerance
- Saturated Fat and Weight
Learn more
Traits reports
Learn how your DNA influences your facial features, taste, smell and other traits.
19+ traits
Example traits include:
- Male Bald Spot
- Sweet vs. Salty
- Unibrow
- Male Bald Spot
- Sweet vs. Salty
- Unibrow
Learn more
Share & Compare
Explore genetic similarities and differences between you and your relatives.
- See how different traits and ancestries have traveled through generations of your family.*
- Know which relatives share genetic variants and traits with you.
- Share your reports with family and friends (even if they are not customers!)
*Requires relatives to be genotyped.
Learn more
DNA Relatives
Opt-in to connect with people who share DNA with you - and message them.
- Discover DNA relatives from around the world.
- Choose to message and meet relatives - maybe even hear new family stories, share photos and get a better understanding of your family's history.
Learn more
The first and only genetic service available directly to you that includes reports that meet FDA standards for clinical and scientific validity.
Carrier Status reports*
35+ 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. Important information about our Carrier Status Reports.
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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.
Ancestry reports
3 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 database. You will continue to find new relatives as our database of more than one million customers grows over time. Learn more.
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Reports include
- Ancestry Composition
- Haplogroups
- Neanderthal Ancestry
- and DNA Relatives 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.
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
- Saturated Fat and Weight
- See all reports
Take a closer look at a report.
Overview
Find your genetic results and see how it might influence your wellbeing and lifestyle.
How to use this report
Learn what this report can and cannot tell you. Also see which ethnicities are most relevant to the test.
Inheritance
Did you inherit a variant from your mother or your father? See which parent may have contributed to your results.
About the condition
Learn more about the science behind the condition, how the genetics evolved and other contributing factors.
Take action
Take the next step by sharing, comparing or learning more about your results.
Traits reports
19+ 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.
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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.
How large is the 23andMe DNA database?
Our database has more than 1,000,000 genotyped members worldwide.
Will I be able to share information with my family?
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.
Whom can I talk to about my carrier status* results?
If you are considering starting a family, talk to your doctor about appropriate testing or getting your partner tested. Also, your results may be useful to share with family members who may benefit from this information.
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.
What services do you provide?
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 examines your genes to tell you about your ancestry, carrier status,* wellness and traits. We analyze, compile and distill the information extracted from your DNA into 65+ 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 you came from and your family story. We analyze, compile and distill your DNA information into reports on your Ancestry Composition, Haplogroups, Neanderthal Ancestry and provide a DNA Relatives tool to enable you to connect with people who share DNA with you.
*Our tests can be used to determine carrier status in adults from saliva collected using an FDA-cleared collection device (Oragene·DX model OGD-500.001), but cannot determine if you have two copies of the genetic variant. The tests are not intended to diagnose a disease, or tell you anything about your risk for developing a disease in the future. On their own, carrier status tests are not intended to tell you anything about the health of your fetus, or your newborn child's risk of developing a particular disease later in life.
The Cystic Fibrosis carrier status test 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 test 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 tests 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.
Health + Ancestry Service $199
The 23andMe experience helps you understand what your DNA says about your health, traits and ancestry.
Explore your DNA with personalized reports and tools that provide engaging ways to share and compare your results with family and friends.
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.
35+ 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
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ARSACS
1 variant in the SACS gene; relevant for French Canadian descent
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Agenesis of the Corpus Callosum with Peripheral Neuropathy
1 variant in the SLC12A6 gene; relevant for French Canadian descent
-
Autosomal Recessive Polycystic Kidney Disease
3 variants in the PKHD1 gene
-
Beta Thalassemia and Related Hemoglobinopathies
10 variants in the HBB gene; relevant for Cypriot, Greek, Italian, Sardinian descent
-
Bloom Syndrome
1 variant in the BLM gene; relevant for Ashkenazi Jewish descent
-
Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)
2 variants in the PMM2 gene; relevant for Danish descent
-
Cystic Fibrosis
28 variants in the CFTR gene; relevant for European, Hispanic/Latino, Ashkenazi Jewish descent
-
D-Bifunctional Protein Deficiency
2 variants in the HSD17B4 gene
-
Dihydrolipoamide Dehydrogenase Deficiency
1 variant in the DLD gene; relevant for Ashkenazi Jewish descent
-
Familial Dysautonomia
1 variant in the IKBKAP gene; relevant for Ashkenazi Jewish descent
-
Fanconi Anemia Group C
3 variants in the FANCC gene; relevant for Ashkenazi Jewish descent
-
GRACILE Syndrome
1 variant in the BCS1L gene; relevant for Finnish descent
-
Glycogen Storage Disease Type Ia
1 variant in the G6PC gene; relevant for Ashkenazi Jewish descent
-
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
-
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
-
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
-
MCAD Deficiency
3 variants in the ACADM gene; relevant for Northern European descent
-
Maple Syrup Urine Disease Type 1B
2 variants in the BCKDHB 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
-
Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)
2 variants in the GJB2 gene; relevant for Ashkenazi Jewish, European descent
-
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
-
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
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Zellweger Syndrome Spectrum (PEX1-Related)
1 variant in the PEX1 gene
*Our tests can be used to determine carrier status in adults from saliva collected using an FDA-cleared collection device (Oragene·DX model OGD-500.001), but cannot determine if you have two copies of the genetic variant. The tests are not intended to diagnose a disease, or tell you anything about your risk for developing a disease in the future. On their own, carrier status tests are not intended to tell you anything about the health of your fetus, or your newborn child's risk of developing a particular disease later in life.
The Cystic Fibrosis carrier status test 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 test 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 tests 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.
Ancestry
Discover where your DNA is from out of 31 populations worldwide - and more.
3 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 database. You will 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.
DNA Relatives tool
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.
Haplogroups report
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
- Lactose Intolerance
- Saturated Fat and Weight
- Alcohol Flush Reaction
- Caffeine Consumption
- Deep Sleep
- Lactose Intolerance
- Muscle Composition
- Saturated Fat and Weight
- Sleep Movement
Traits reports
Learn how your DNA influences your facial features, taste, smell and other traits.
19+ 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
- 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).
Ancestry reports
Your DNA can tell you about your family history.
See sample report.
See sample report.
3 reports
- Ancestry Composition
- Haplogroups
- Neanderthal Ancestry
Wellness reports
Learn how your genes play a role in your well-being and lifestyle choices.
See sample report.
See sample report.
5+ reports
- Alcohol Flush Reaction
- Caffeine Consumption
- Deep Sleep
- Lactose Intolerance
- Muscle Composition
- Saturated Fat and Weight
- Sleep Movement
Traits reports
Explore what makes you unique, from food preference to physical features.
See sample report.
See sample report.
19+ traits
- 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
Carrier status reports*
If you are starting a family, find out if you are a carrier for
an inherited condition.
See sample report.
See sample report.
35+ reports
| Report | Gene | Variants | Relevant Ethnicities |
|---|---|---|---|
| ARSACS | SACS | 1 Variant | French Canadian |
| Agenesis of the Corpus Callosum with Peripheral Neuropathy | SLC12A6 | 1 Variant | French Canadian |
| Autosomal Recessive Polycystic Kidney Disease | PKHD1 | 3 Variants | N/A |
| Beta Thalassemia and Related Hemoglobinopathies | HBB | 10 Variants | Cypriot, Greek, Italian, Sardinian |
| Bloom Syndrome | BLM | 1 Variant | Ashkenazi Jewish |
| Congenital Disorder of Glycosylation Type 1a (PMM2-CDG) | PMM2 | 2 Variants | Danish |
| Cystic Fibrosis | CFTR | 28 Variants | European, Hispanic/Latino, Ashkenazi Jewish |
| D-Bifunctional Protein Deficiency | HSD17B4 | 2 Variants | N/A |
| Dihydrolipoamide Dehydrogenase Deficiency | DLD | 1 Variant | Ashkenazi Jewish |
| Familial Dysautonomia | IKBKAP | 1 Variant | Ashkenazi Jewish |
| Fanconi Anemia Group C | FANCC | 3 Variants | Ashkenazi Jewish |
| GRACILE Syndrome | BCS1L | 1 Variant | Finnish |
| Glycogen Storage Disease Type Ia | G6PC | 1 Variant | Ashkenazi Jewish |
| Glycogen Storage Disease Type Ib | SLC37A4 | 2 Variants | N/A |
| Hereditary Fructose Intolerance | ALDOB | 3 Variants | European |
| Herlitz Junctional Epidermolysis Bullosa (LAMB3-related) | LAMB3 | 3 Variants | N/A |
| Leigh Syndrome, French Canadian Type | LRPPRC | 1 Variant | French Canadian |
| Limb-Girdle Muscular Dystrophy Type 2D | SGCA | 1 Variant | Finnish |
| Limb-Girdle Muscular Dystrophy Type 2E | SGCB | 1 Variant | Southern Indiana Amish |
| Limb-Girdle Muscular Dystrophy Type 2I | FKRP | 1 Variant | European |
| MCAD Deficiency | ACADM | 3 Variants | Northern European |
| Maple Syrup Urine Disease Type 1B | BCKDHB | 2 Variants | Ashkenazi Jewish |
| Neuronal Ceroid Lipofuscinosis (CLN5-Related) | CLN5 | 1 Variant | Finnish |
| Neuronal Ceroid Lipofuscinosis (PPT1-Related) | PPT1 | 3 Variants | Finnish |
| Niemann-Pick Disease Type A | SMPD1 | 3 Variants | Ashkenazi Jewish |
| Nijmegen Breakage Syndrome | NBN | 1 Variant | Eastern European |
| Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related) | GJB2 | 2 Variants | Ashkenazi Jewish, European |
| Pendred Syndrome and DFNB4 Hearing Loss | SLC26A4 | 6 Variants | N/A |
| Phenylketonuria and Related Disorders | PAH | 23 Variants | Northern European |
| Primary Hyperoxaluria Type 2 | GRHPR | 1 Variant | European |
| Rhizomelic Chondrodysplasia Punctata Type 1 | PEX7 | 1 Variant | N/A |
| Salla Disease | SLC17A5 | 1 Variant | Finnish, Swedish |
| Sickle Cell Anemia | HBB | 1 Variant | African |
| Sjögren-Larsson Syndrome | ALDH3A2 | 1 Variant | Swedish |
| Tay-Sachs Disease | HEXA | 4 Variants | Ashkenazi Jewish, Cajun |
| Tyrosinemia Type I | FAH | 4 Variants | French Canadian, Finnish |
| Usher Syndrome Type 1F | PCDH15 | 1 Variant | Ashkenazi Jewish |
| Usher Syndrome Type 3A | CLRN1 | 1 Variant | Ashkenazi Jewish |
| Zellweger Syndrome Spectrum (PEX1-Related) | PEX1 | 1 Variant | N/A |
-
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
-
Autosomal Recessive Polycystic Kidney Disease
3 variants in the PKHD1 gene
-
Beta Thalassemia and Related Hemoglobinopathies
10 variants in the HBB gene; relevant for Cypriot, Greek, Italian, Sardinian descent
-
Bloom Syndrome
1 variant in the BLM gene; relevant for Ashkenazi Jewish descent
-
Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)
2 variants in the PMM2 gene; relevant for Danish descent
-
Cystic Fibrosis
28 variants in the CFTR gene; relevant for European, Hispanic/Latino, Ashkenazi Jewish descent
-
D-Bifunctional Protein Deficiency
2 variants in the HSD17B4 gene
-
Dihydrolipoamide Dehydrogenase Deficiency
1 variant in the DLD gene; relevant for Ashkenazi Jewish descent
-
Familial Dysautonomia
1 variant in the IKBKAP gene; relevant for Ashkenazi Jewish descent
-
Fanconi Anemia Group C
3 variants in the FANCC gene; relevant for Ashkenazi Jewish descent
-
GRACILE Syndrome
1 variant in the BCS1L gene; relevant for Finnish descent
-
Glycogen Storage Disease Type Ia
1 variant in the G6PC gene; relevant for Ashkenazi Jewish descent
-
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
-
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
-
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
-
MCAD Deficiency
3 variants in the ACADM gene; relevant for Northern European descent
-
Maple Syrup Urine Disease Type 1B
2 variants in the BCKDHB 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
-
Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)
2 variants in the GJB2 gene; relevant for Ashkenazi Jewish, European descent
-
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
-
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
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Usher Syndrome Type 3A
1 variant in the CLRN1 gene; relevant for Ashkenazi Jewish descent
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Zellweger Syndrome Spectrum (PEX1-Related)
1 variant in the PEX1 gene
Carrier status reports*
| Report | Gene | Variants | Relevant Ethnicities |
|---|---|---|---|
| ARSACS | SACS | 1 Variant | French Canadian |
| Agenesis of the Corpus Callosum with Peripheral Neuropathy | SLC12A6 | 1 Variant | French Canadian |
| Autosomal Recessive Polycystic Kidney Disease | PKHD1 | 3 Variants | N/A |
| Beta Thalassemia and Related Hemoglobinopathies | HBB | 10 Variants | Cypriot, Greek, Italian, Sardinian |
| Bloom Syndrome | BLM | 1 Variant | Ashkenazi Jewish |
| Congenital Disorder of Glycosylation Type 1a (PMM2-CDG) | PMM2 | 2 Variants | Danish |
| Cystic Fibrosis | CFTR | 28 Variants | European, Hispanic/Latino, Ashkenazi Jewish |
| D-Bifunctional Protein Deficiency | HSD17B4 | 2 Variants | N/A |
| Dihydrolipoamide Dehydrogenase Deficiency | DLD | 1 Variant | Ashkenazi Jewish |
| Familial Dysautonomia | IKBKAP | 1 Variant | Ashkenazi Jewish |
| Fanconi Anemia Group C | FANCC | 3 Variants | Ashkenazi Jewish |
| GRACILE Syndrome | BCS1L | 1 Variant | Finnish |
| Glycogen Storage Disease Type Ia | G6PC | 1 Variant | Ashkenazi Jewish |
| Glycogen Storage Disease Type Ib | SLC37A4 | 2 Variants | N/A |
| Hereditary Fructose Intolerance | ALDOB | 3 Variants | European |
| Herlitz Junctional Epidermolysis Bullosa (LAMB3-related) | LAMB3 | 3 Variants | N/A |
| Leigh Syndrome, French Canadian Type | LRPPRC | 1 Variant | French Canadian |
| Limb-Girdle Muscular Dystrophy Type 2D | SGCA | 1 Variant | Finnish |
| Limb-Girdle Muscular Dystrophy Type 2E | SGCB | 1 Variant | Southern Indiana Amish |
| Limb-Girdle Muscular Dystrophy Type 2I | FKRP | 1 Variant | European |
| MCAD Deficiency | ACADM | 3 Variants | Northern European |
| Maple Syrup Urine Disease Type 1B | BCKDHB | 2 Variants | Ashkenazi Jewish |
| Neuronal Ceroid Lipofuscinosis (CLN5-Related) | CLN5 | 1 Variant | Finnish |
| Neuronal Ceroid Lipofuscinosis (PPT1-Related) | PPT1 | 3 Variants | Finnish |
| Niemann-Pick Disease Type A | SMPD1 | 3 Variants | Ashkenazi Jewish |
| Nijmegen Breakage Syndrome | NBN | 1 Variant | Eastern European |
| Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related) | GJB2 | 2 Variants | Ashkenazi Jewish, European |
| Pendred Syndrome and DFNB4 Hearing Loss | SLC26A4 | 6 Variants | N/A |
| Phenylketonuria and Related Disorders | PAH | 23 Variants | Northern European |
| Primary Hyperoxaluria Type 2 | GRHPR | 1 Variant | European |
| Rhizomelic Chondrodysplasia Punctata Type 1 | PEX7 | 1 Variant | N/A |
| Salla Disease | SLC17A5 | 1 Variant | Finnish, Swedish |
| Sickle Cell Anemia | HBB | 1 Variant | African |
| Sjögren-Larsson Syndrome | ALDH3A2 | 1 Variant | Swedish |
| Tay-Sachs Disease | HEXA | 4 Variants | Ashkenazi Jewish, Cajun |
| Tyrosinemia Type I | FAH | 4 Variants | French Canadian, Finnish |
| Usher Syndrome Type 1F | PCDH15 | 1 Variant | Ashkenazi Jewish |
| Usher Syndrome Type 3A | CLRN1 | 1 Variant | Ashkenazi Jewish |
| Zellweger Syndrome Spectrum (PEX1-Related) | PEX1 | 1 Variant | N/A |
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ARSACS
1 variant in the SACS gene; relevant for French Canadian descent
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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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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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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
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Hereditary Fructose Intolerance
3 variants in the ALDOB gene; relevant for European descent
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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
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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
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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
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Neuronal Ceroid Lipofuscinosis (CLN5-Related)
1 variant in the CLN5 gene; relevant for Finnish descent
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Neuronal Ceroid Lipofuscinosis (PPT1-Related)
3 variants in the PPT1 gene; relevant for Finnish descent
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Niemann-Pick Disease Type A
3 variants in the SMPD1 gene; relevant for Ashkenazi Jewish descent
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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
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Phenylketonuria and Related Disorders
23 variants in the PAH gene; relevant for Northern European descent
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Primary Hyperoxaluria Type 2
1 variant in the GRHPR gene; relevant for European descent
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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
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Sickle Cell Anemia
1 variant in the HBB gene; relevant for African descent
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Sjögren-Larsson Syndrome
1 variant in the ALDH3A2 gene; relevant for Swedish descent
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Tay-Sachs Disease
4 variants in the HEXA gene; relevant for Ashkenazi Jewish, Cajun descent
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Tyrosinemia Type I
4 variants in the FAH gene; relevant for French Canadian, Finnish descent
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Usher Syndrome Type 1F
1 variant in the PCDH15 gene; relevant for Ashkenazi Jewish descent
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Usher Syndrome Type 3A
1 variant in the CLRN1 gene; relevant for Ashkenazi Jewish descent
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Zellweger Syndrome Spectrum (PEX1-Related)
1 variant in the PEX1 gene
All wellness reports
- Alcohol Flush Reaction
- Caffeine Consumption
- Deep Sleep
- Lactose Intolerance
- Muscle Composition
- Saturated Fat and Weight
- Sleep Movement
All traits reports
- 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
See our 31 populations worldwide
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Northwestern European
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Southern European
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South Asian
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East Asian & Native American
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Native American
- Broadly Native American
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East Asian
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Middle Eastern & North African
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Oceanian
- Broadly Oceanian
Learn the origins of your maternal and paternal ancestors and where they lived thousands of years ago.
Women can only trace their maternal haplogroup. This is because the paternal haplogroup is traced through the Y chromosome, which women do not inherit.
Genetic variants are small changes in your DNA.
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