23andMe DNA Testing Kit for Health + Ancestry - 23andMe (original) (raw)

FDA AUTHORIZED REPORTS INCLUDED

60% off

Health plus Ancestry Service

Original Price: $199

FDA AUTHORIZED REPORTS INCLUDED

60% off

Health plus Ancestry Service

Original Price: $199

Get personalized genetic insights and tools that can help make it easier for you to take action on your health.

• 150+ personalized reports
• Includes Ancestry Service
• Includes FDA-authorized reports
• FSA/HSA eligibility◆Learn about Important Information for FSA/HSA Reimbursement

Important test info

Discover how your DNA can influence your health.

Using insights backed by the latest science, see how your DNA can affect your chances of developing certain health conditions. Your personalized reports break down your genetic data, the science and potential next steps.

10+ reports, including:

Wellness

Explore how your DNA relates to your lifestyle.

Discover what your DNA has to say about lifestyle factors like diet, exercise, and sleep. Use what you've learned to help you make informed decisions.

5+ reports, including:

See what you may pass on to your future children.

If you’re thinking of starting a family, find out if you’re a carrier for genetic variants linked to certain inherited health conditions.

45+ reports, including:

Check out the reports and insights included in our Health plus Ancestry Service.

• Ancestry Detail Reports (48 reports)

• Family Tree

• Maternal Haplogroup

• Paternal Haplogroup

• Neanderthal Ancestry

• Ability to Match Musical Pitch

• Asparagus Odor Detection

• Back Hair (available for men only)

• Bald Spot (available for men only)

• Bitter Taste

• Bunions

• Cheek Dimples

• Cilantro Taste Aversion

• Cleft Chin

• Dandruff

• Earlobe Type

• Early Hair Loss (available for men only)

• Earwax Type

• Eye Color

• Fear of Heights

• Fear of Public Speaking

• Finger Length Ratio

• Flat Feet

• Freckles

• Hair Photobleaching (hair lightening from the sun)

• Hair Texture

• Hair Thickness

• Ice Cream Flavor Preference

• Light or Dark Hair

• Misophonia (hatred of the sound of chewing)

• Mosquito Bite Frequency

• Motion Sickness

• Newborn Hair

• Photic Sneeze Reflex

• Red Hair

• Skin Pigmentation

• Stretch Marks

• Sweet vs. Salty

• Toe Length Ratio

• Unibrow

• Wake-Up Time

• Widow's Peak

• Type 2 Diabetes (Powered by 23andMe Research)
  Genetic likelihood for a disorder of blood sugar regulation
  1,000+ variants in many genes; variants found in many ethnicities

• Age-Related Macular Degeneration
  Genetic risk for a form of adult-onset vision loss
  2
  variant
  s
  in the
  ARMS2 and CFH
  gene
  s
  ; relevant for European descent

• Alpha-1 Antitrypsin Deficiency
  Genetic risk for lung and liver disease
  2
  variant
  s
  in the
  SERPINA1
  gene
  ; relevant for European descent

• BRCA1/BRCA2 (Selected Variants)
  Genetic risk based on a limited set of variants for breast, ovarian, prostate and pancreatic cancer
  44
  variants in the
  BRCA1 and BRCA2
  genes; most relevant for Ashkenazi Jewish descent; does not include the majority of BRCA1/2 variants found in people of other ethnicities

• Celiac Disease
  Genetic risk for gluten-related autoimmune disorder
  2
  variants near the
  HLA-DQB1 and HLA-DQA1
  genes; relevant for
  European
  decent

• Chronic Kidney Disease (APOL1-Related)
  Genetic risk for a form of chronic kidney disease
  2
  variant
  s
  in the
  APOL1
  gene
  ; relevant for African descent

• Familial Hypercholesterolemia
  Genetic risk for very high cholesterol, which can increase the risk for heart disease
  24
  variant
  s
  in the
  LDLR and APOB
  gene
  s
  ; relevant for European, Lebanese, Old Order Amish descent

• G6PD Deficiency
  Genetic risk for a form of anemia
  2
  variant
  s
  in the
  G6PD
  gene
  ; relevant for African, Southern European, Kurdish Jewish, Middle Eastern, Central Asian, South Asian descent

• Hereditary Amyloidosis (TTR-Related)
  Genetic risk for a form of nerve and heart damage
  3
  variant
  s
  in the
  TTR
  gene
  ; relevant for African American, West African, Portuguese, Brazilian, Northern Swedish, Japanese, Irish, British descent

• Hereditary Hemochromatosis (HFE‑Related)
  Genetic risk for iron overload
  2
  variant
  s
  in the
  HFE
  gene
  ; relevant for European descent

• Hereditary Thrombophilia
  Genetic risk for harmful blood clots
  2
  variant
  s
  in the
  F2 and F5
  gene
  s
  ; relevant for European descent

• Late-Onset Alzheimer's Disease
  Genetic risk for a form of dementia
  1
  variant in the
  APOE
  gene; variant found and studied in many ethnicities

• MUTYH-Associated Polyposis
  Genetic risk for a specific colorectal cancer syndrome
  2
  variant
  s
  in the
  MUTYH
  gene
  ; relevant for Northern European descent

• Parkinson's Disease
  Genetic risk for a form of movement impairment
  2
  variant
  s
  in the
  LRRK2 and GBA
  gene
  s
  ; relevant for European, Ashkenazi Jewish, North African Berber descent

• 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
  variant
  s
  in the
  PKHD1
  gene

• Beta Thalassemia and Related Hemoglobinopathies
  10
  variant
  s
  in the
  HBB
  gene
  ; relevant for Sardinian, Cypriot, Italian/Sicilian, Greek descent

• Bloom Syndrome
  1
  variant
  in the
  BLM
  gene
  ; relevant for Ashkenazi Jewish descent

• Canavan Disease
  3
  variant
  s
  in the
  ASPA
  gene
  ; relevant for Ashkenazi Jewish descent

• Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)
  2
  variant
  s
  in the
  PMM2
  gene
  ; relevant for Ashkenazi Jewish, Danish descent

• Cystic Fibrosis
  29
  variant
  s
  in the
  CFTR
  gene
  ; relevant for Ashkenazi Jewish, European, Hispanic/Latino descent

• D-Bifunctional Protein Deficiency
  2
  variant
  s
  in the
  HSD17B4
  gene

• Dihydrolipoamide Dehydrogenase Deficiency
  1
  variant
  in the
  DLD
  gene
  ; relevant for Ashkenazi Jewish descent

• Familial Dysautonomia
  1
  variant
  in the
  ELP1
  gene
  ; relevant for Ashkenazi Jewish descent

• Familial Hyperinsulinism (ABCC8-Related)
  3
  variant
  s
  in the
  ABCC8
  gene
  ; relevant for Ashkenazi Jewish descent

• Familial Mediterranean Fever
  7
  variant
  s
  in the
  MEFV
  gene
  ; relevant for Arab, Armenian, Sephardic Jewish, Turkish descent

• Fanconi Anemia Group C
  3
  variant
  s
  in the
  FANCC
  gene
  ; relevant for Ashkenazi Jewish descent

• GRACILE Syndrome
  1
  variant
  in the
  BCS1L
  gene
  ; relevant for Finnish descent

• Gaucher Disease Type 1
  3
  variant
  s
  in the
  GBA (also known as GBA1)
  gene
  ; relevant for Ashkenazi Jewish descent

• Glycogen Storage Disease Type Ia
  1
  variant
  in the
  G6PC
  gene
  ; relevant for Ashkenazi Jewish descent

• Glycogen Storage Disease Type Ib
  2
  variant
  s
  in the
  SLC37A4
  gene

• Hereditary Fructose Intolerance
  4
  variant
  s
  in the
  ALDOB
  gene
  ; relevant for European descent

• 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

• Limb-Girdle Muscular Dystrophy Type 2E
  1
  variant
  in the
  SGCB
  gene
  ; relevant for Amish descent

• Limb-Girdle Muscular Dystrophy Type 2I
  1
  variant
  in the
  FKRP
  gene

• MCAD Deficiency
  4
  variant
  s
  in the
  ACADM
  gene
  ; relevant for European descent

• Maple Syrup Urine Disease Type 1B
  2
  variant
  s
  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
  variant
  s
  in the
  PPT1
  gene
  ; relevant for Finnish descent

• Niemann-Pick Disease Type A
  3
  variant
  s
  in the
  SMPD1
  gene
  ; relevant for Ashkenazi Jewish descent

• Nijmegen Breakage Syndrome
  1
  variant
  in the
  NBN
  gene

• Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)
  8
  variant
  s
  in the
  GJB2
  gene
  ; relevant for many ethnicities, including Ashkenazi Jewish, East/Southeast Asian, European, and Ghanaian descent. May also be relevant for Hispanic/Latino, Northern African/Middle Eastern, and South Asian descent

• Pendred Syndrome and DFNB4 Hearing Loss (SLC26A4-Related)
  6
  variant
  s
  in the
  SLC26A4
  gene

• Phenylketonuria and Related Disorders
  23
  variant
  s
  in the
  PAH
  gene
  ; relevant for Irish, Northern European descent

• Pompe Disease
  5
  variant
  s
  in the
  GAA
  gene
  ; relevant for African/African American descent; variants also common in European descent

• Primary Hyperoxaluria Type 2
  1
  variant
  in the
  GRHPR
  gene

• Pyruvate Kinase Deficiency
  1
  variant
  in the
  PKLR
  gene

• Rhizomelic Chondrodysplasia Punctata Type 1
  1
  variant
  in the
  PEX7
  gene

• Salla Disease
  1
  variant
  in the
  SLC17A5
  gene
  ; relevant for Finnish, Swedish descent

• Severe Junctional Epidermolysis Bullosa (LAMB3-Related)
  3
  variant
  s
  in the
  LAMB3
  gene

• Sickle Cell Anemia
  1
  variant
  in the
  HBB
  gene
  ; relevant for African, Middle Eastern, South Asian, Caribbean, Mediterranean, Central and South American descent

• Sjögren-Larsson Syndrome
  1
  variant
  in the
  ALDH3A2
  gene
  ; relevant for Swedish descent

• Tay-Sachs Disease
  4
  variant
  s
  in the
  HEXA
  gene
  ; relevant for Ashkenazi Jewish, Cajun descent

• Tyrosinemia Type I
  4
  variant
  s
  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 Spectrum Disorder (PEX1-Related)
  1
  variant
  in the
  PEX1
  gene

• Alcohol Flush Reaction

• Caffeine Consumption

• Deep Sleep

• Genetic Weight

• Lactose Intolerance

• Muscle Composition

• Saturated Fat and Weight

• Sleep Movement

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Feature	Ancestry Service	Health plus Ancestry Service
Original Price: 119SalePrice:119 Sale Price: 119SalePrice:69Add to cart-ancestry	Original Price: 199SalePrice:199 Sale Price: 199SalePrice:79Add to cart-healthImportant test info
Genotyping reportsGenotyping examines DNA variants at certain pre-identified positions in the genome. The specific variants we look at generally provide coverage of commonly known variations across the entire genome.	80+	150+
Exome Sequencing ReportsΔLearn about Important Information for Total healthExome sequencing is an advanced genetic testing technique that focuses on decoding the exome of an individual's genome. The exome represents the protein-coding regions of genes, which make up only about 2% of the entire genome but contain the majority of genetic variants associated with disease risk.
Ancestry and Trait Reports
DNA Relative Finder and Family Tree (Opt in)
Health Predisposition reports*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health RisksLearn how your genetics can influence your chances of developing certain health conditions.		10+
Carrier Status reports*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health RisksIf you are starting a family, find out if you are a carrier for certain inherited conditions.
Wellness reportsLearn how your genes play a role in your well-being and lifestyle choices.		5+
Family Health History TreeOpt in to easily input, track and download your family health history to share with your healthcare provider.
Pharmacogenetics reports**Learn about Considerations and Limitations for Pharmacogenetics ReportsDiscover how your DNA may impact how your body processes certain medications with three new Pharmacogenetics reports.
Enhanced ancestry featuresGet advanced filtering for DNA Relative Finder and access up to 5000 DNA relatives.
Historical MatchesSMUncover your historical and ancient relatives, linking you to the past.
Just AddedRecords & ArchivesSMLearn more about your family’s history with the help of historical documents.
Breast, Prostate and Colorectal Cancer reportsInsights into your genetic likelihood of developing breast (females only), prostate (males only) and colorectal (certain ethnicities) cancer.all Powered by 23andMe Research
Health TracksSMSee how making healthy choices each day can greatly impact your health over time
Health Action PlanPersonalized and ongoing recommendations based on genetic and non-genetic data.
Ongoing new reports and featuresGet access to new premium reports and features throughout the year.
Blood TestingΔLearn about Important Information for Total healthEligible participants may order in-person blood testing initiated by a clinician and get results in the 23andMe app.		Add-on purchase
Just AddedBiological AgeMonitor how your body is aging physiologically based on key biomarkers and change the trajectory of your health.
Genetics-informed clinical careΔLearn about Important Information for Total healthAccess to clinicians with training in genetics. Includes unlimited direct messaging, plus a dedicated virtual consultation annually.

Customer Stories

Putting insights into action

As more and more people choose DNA testing for health reasons, they’re sharing more and more inspiring stories. These are just a few of the stories of 23andMe Health + Ancestry customers who used what they learned from their DNA to take a more proactive approach to their health.

Customer Reviews

Don’t take our word for it...

Wendy's review

Tennessee, USA

Health plus Ancestry Customer

“Thank you so much for giving me the info that has saved my life. The 23andMe discovery of the two Hereditary Hemochromatosis variants that I have has helped fix my health issues and probably saved me from further damage to my joints and organs. I can’t thank you enough!”

View more reviews

23andMe offers a variety of health reports like Type 2 Diabetes (Powered by 23andMe Research), Celiac Disease Genetic Health Risk Report*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks, BRCA1/BRCA2 (Selected Variants) Genetic Health Risk Report*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks and many more. to see a list of all the reports offered.

Your 23andMe Health reports can tell you how your DNA can impact your chances of developing certain conditions. Wellness reports can help you discover what your DNA has to say about lifestyle factors like diet, exercise, and sleep. And if you're thinking of starting a family, our Carrier Status reports can tell you if you're a carrier for genetic variants linked to certain inherited health conditions.*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks

No, 23andMe reports do not diagnose any health conditions or provide medical advice. While having a particular genetic variant can be linked to a higher risk for a condition, it does not necessarily mean you will develop the condition. It is also important to remember that these reports do not cover all possible genetic variants that could influence risk. Other non-genetic factors, such as environment and lifestyle, can also influence risk for these conditions. We recommend that you consult with a healthcare professional if a condition runs in your family, you think you might have the condition or you have questions about any genetic or non-genetic risk factors you may have.

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*The 23andMe PGS test includes health predisposition and carrier status reports. 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 and reporting carrier status. 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 44 variants in the BRCA1 and BRCA2 genes. The report describes if a person's genetic result is associated with an increased risk of developing breast cancer and ovarian cancer and may be associated with an increased risk for prostate cancer, pancreatic cancer, and potentially other cancers. The variants included in this report do not represent the majority of the BRCA1/BRCA2 variants in people of most ethnicities. 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. This report is for over-the-counter use by adults over the age of 18, and provides genetic information to inform discussions with a healthcare professional. 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. 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. Our SLCO1B1 Pharmacogenetics report provides certain information about variants associated with the processing of some therapeutics and provides interpretive drug information regarding the potential effect of simvastatin therapy. Our DPYD Pharmacogenetics report does not describe the association between detected variants and any specific therapeutic. Results for 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 Pharmacogenetic reports, visit 23andme.com/test-info/pharmacogenetics/

triangleExome Sequencing and blood testing services are available to eligible customers upon completion of the intake questionnaire that must be reviewed, approved and ordered by a third-party clinician. Exome Sequencing is analyzed by a CLIA- and CAP-accredited laboratory. Blood testing is completed by Quest Diagnostics. All telehealth services are provided in accordance with the Telehealth Terms and Consent to Telehealth.

diamondBased on purchase price of $199. Check with your FSA/HSA administrator or your tax professional for confirmation on the specific requirements for individual eligibility and reimbursement, including usage, procedures and qualifications.