See the list of reports included in each service:
Ancestry Service
now with 3000+ regions
Ancestry Reports
- Ancestry Composition
- Ancestry Detail Reports (48 reports)
Population-specific reports with maps covering 3000+ locations, offering a granular view of your ancestry, plus immersive educational content.
Reports included:
Americas (Caribbean, Mexico & Central America, Indigenous American, South America); East Asia (Chinese, Chinese Dai, Filipino & Austronesian, Indonesian, Thai, Khmer & Myanma, Japanese, Korean, Manchurian & Mongolian, Siberian, Vietnamese); Europe (Ashkenazi Jewish, British & Irish, Eastern European, Finnish, French & German, Greek & Balkan, Italian, Sardinian, Scandinavian, Spanish & Portuguese); Oceania (Melanesian); Central & South Asia (Bengali & Northeast Indian, Central Asian, Gujarati Patidar, Malayali Subgroup, Northern Indian & Pakistani, Southern Indian & Sri Lankan, Southern Indian Subgroup); Sub-Saharan Africa (African Hunter-Gatherer, Angolan & Congolese, Ethiopian & Eritrean, Ghanaian, Liberian & Sierra Leonean, Nigerian, Senegambian & Guinean, Somali, Southern East African, Sudanese); Western Asia & North Africa (Anatolian, Coptic Egyptian, Cypriot, Egyptian, Iranian, Caucasian & Mesopotamian, Levantine, North African, Peninsular Arab) - Family Tree
- Maternal Haplogroup
- Paternal Haplogroup
- Neanderthal Ancestry
Trait Reports
- Ability to Match Musical Pitch
- Asparagus Odour Detection
- Back Hair (available for men only)
- Bald Spot (available for men only)
- Bitter Taste
- Bunions
- Cheek Dimples
- Cilantro (coriander) Taste Aversion
- Cleft Chin
- Dandruff
- Earlobe Type
- Early Hair Loss (available for men only)
- Earwax Type
- Eye Colour
- 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 Flavour 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
Health plus Ancestry Service
Health Predisposition Reports*
- Type 2 Diabetes (Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a disorder of blood sugar regulation1,000+ variants in many genes; variants found in many ethnicities
- Age-Related Macular DegenerationGenetic risk for a form of adult-onset vision loss2 variants in the ARMS2 and CFH genes; relevant for European descent
- Alpha-1 Antitrypsin DeficiencyGenetic risk for lung and liver disease2 variants in the SERPINA1 genes; relevant for European descent
- BRCA1/BRCA2 (Selected Variants)Genetic risk based on a limited set of variants for breast, ovarian, prostate and pancreatic cancer44 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 DiseaseGenetic risk for gluten-related autoimmune disorder2 variants in the HLA-DQB1 and HLA-DQA1 genes; relevant for European descent
- Chronic Kidney Disease (APOL1-Related)Genetic risk for a form of chronic kidney disease2 variants in the APOL1 genes; relevant for African descent
- Familial HypercholesterolemiaGenetic risk for very high cholesterol, which can increase the risk for heart disease24 variants in the LDLR and APOB genes; relevant for European, Lebanese, Old Order Amish descent
- G6PD DeficiencyGenetic risk for a form of anemia2 variants in the G6PD genes; 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 damage3 variants in the TTR genes; relevant for African American, West African, Portuguese, Brazilian, Northern Swedish, Japanese, Irish, British descent
- Hereditary Hemochromatosis (HFE‑Related)Genetic risk for iron overload2 variants in the HFE genes; relevant for European descent
- Hereditary ThrombophiliaGenetic risk for harmful blood clots2 variants in the F2 and F5 genes; relevant for European descent
- Late-Onset Alzheimer's DiseaseGenetic risk for a form of dementia1 variant in the APOE genes; variant found and studied in many ethnicities
- MUTYH-Associated PolyposisGenetic risk for a specific colorectal cancer syndrome2 variants in the MUTYH genes; relevant for Northern European descent
- Parkinson's DiseaseGenetic risk for a form of movement impairment2 variants in the LRRK2 and GBA genes; relevant for European, Ashkenazi Jewish, North African Berber descent
Wellness Reports
- Alcohol Flush Reaction
- Caffeine Consumption
- Deep Sleep
- Genetic Weight
- Lactose Intolerance
- Muscle Composition
- Saturated Fat and Weight
- Sleep Movement
Carrier Status Reports*
- ARSACS1 variant in the SACS genes; relevant for French Canadian descent
- Agenesis of the Corpus Callosum with Peripheral Neuropathy1 variant in the SLC12A6 genes; relevant for French Canadian descent
- Autosomal Recessive Polycystic Kidney Disease3 variants in the PKHD1 genes
- Beta Thalassemia and Related Hemoglobinopathies10 variants in the HBB genes; relevant for Sardinian, Cypriot, Italian/Sicilian, Greek descent
- Bloom Syndrome1 variant in the BLM genes; relevant for Ashkenazi Jewish descent
- Canavan Disease3 variants in the ASPA genes; relevant for Ashkenazi Jewish descent
- Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)2 variants in the PMM2 genes; relevant for Ashkenazi Jewish, Danish descent
- Cystic Fibrosis29 variants in the CFTR genes; relevant for Ashkenazi Jewish, European, Hispanic/Latino descent
- D-Bifunctional Protein Deficiency2 variants in the HSD17B4 genes
- Dihydrolipoamide Dehydrogenase Deficiency1 variant in the DLD genes; relevant for Ashkenazi Jewish descent
- Familial Dysautonomia1 variant in the ELP1 genes; relevant for Ashkenazi Jewish descent
- Familial Hyperinsulinism (ABCC8-Related)3 variants in the ABCC8 genes; relevant for Ashkenazi Jewish descent
- Familial Mediterranean Fever7 variants in the MEFV genes; relevant for Arab, Armenian, Sephardic Jewish, Turkish descent
- Fanconi Anemia Group C3 variants in the FANCC genes; relevant for Ashkenazi Jewish descent
- GRACILE Syndrome1 variant in the BCS1L genes; relevant for Finnish descent
- Gaucher Disease Type 13 variants in the GBA genes; relevant for Ashkenazi Jewish descent
- Glycogen Storage Disease Type Ia1 variant in the G6PC genes; relevant for Ashkenazi Jewish descent
- Glycogen Storage Disease Type Ib2 variants in the SLC37A4 genes
- Hereditary Fructose Intolerance4 variants in the ALDOB genes; relevant for European descent
- Leigh Syndrome, French Canadian Type1 variant in the LRPPRC genes; relevant for French Canadian descent
- Limb-Girdle Muscular Dystrophy Type 2D1 variant in the SGCA genes
- Limb-Girdle Muscular Dystrophy Type 2E1 variant in the SGCB genes; relevant for Amish descent
- Limb-Girdle Muscular Dystrophy Type 2I1 variant in the FKRP genes
- MCAD Deficiency4 variants in the ACADM genes; relevant for European descent
- Maple Syrup Urine Disease Type 1B2 variants in the BCKDHB genes; relevant for Ashkenazi Jewish descent
- Mucolipidosis Type IV1 variant in the MCOLN1 genes; relevant for Ashkenazi Jewish descent
- Neuronal Ceroid Lipofuscinosis (CLN5-Related)1 variant in the CLN5 genes; relevant for Finnish descent
- Neuronal Ceroid Lipofuscinosis (PPT1-Related)3 variants in the PPT1 genes; relevant for Finnish descent
- Niemann-Pick Disease Type A3 variants in the SMPD1 genes; relevant for Ashkenazi Jewish descent
- Nijmegen Breakage Syndrome1 variant in the NBN genes
- Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)8 variants in the GJB2 genes; 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 variants in the SLC26A4 genes
- Phenylketonuria and Related Disorders23 variants in the PAH genes; relevant for Irish, Northern European descent
- Pompe Disease5 variants in the GAA genes; relevant for African/African American descent; variants also common in European descent
- Primary Hyperoxaluria Type 21 variant in the GRHPR genes
- Pyruvate Kinase Deficiency1 variant in the PKLR genes
- Rhizomelic Chondrodysplasia Punctata Type 11 variant in the PEX7 genes
- Salla Disease1 variant in the SLC17A5 genes; relevant for Finnish, Swedish descent
- Severe Junctional Epidermolysis Bullosa (LAMB3-Related)3 variants in the LAMB3 genes
- Sickle Cell Anemia1 variant in the HBB genes; relevant for African, Middle Eastern, South Asian, Caribbean, Mediterranean, Central and South American descent
- Sjögren-Larsson Syndrome1 variant in the ALDH3A2 genes; relevant for Swedish descent
- Tay-Sachs Disease4 variants in the HEXA genes; relevant for Ashkenazi Jewish, Cajun descent
- Tyrosinemia Type I4 variants in the FAH genes; relevant for French Canadian, Finnish descent
- Usher Syndrome Type 1F1 variant in the PCDH15 genes; relevant for Ashkenazi Jewish descent
- Usher Syndrome Type 3A1 variant in the CLRN1 genes; relevant for Ashkenazi Jewish descent
- Zellweger Spectrum Disorder (PEX1-Related)1 variant in the PEX1 genes
*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. The MUTYH-Associated Polyposis Genetic Health Risk Report is indicated for reporting the Y179C and G396D variants in the MUTYH gene and an increased risk for colorectal cancer. The two variants included in this report are most common in people of Northern European descent. These reports do 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. These reports are for over-the-counter use by adults, and provide 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 by an independent genetic test prescribed by your own healthcare provider before taking any medical action. For important information and limitations regarding other genetic health risk reports and carrier status reports, visit 23andme.com/test-info/