See the list of reports included in each service:

Ancestry Service
Now with 2000+ regions Ancestry Reports
- Ancestry Composition
-
Ancestry Detail Reports (48 reports)
Population-specific reports with maps covering 2000+ regions, 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 Odor 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 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

Health + Ancestry Service
Health Predisposition Reports*
-
Type 2 Diabetes ( Powered by 23andMe Research )Learn moreGenetic 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 gene; relevant for European descent
-
BRCA1/BRCA2 (Selected Variants)Learn moreGenetic risk based on a limited set of variants for breast, ovarian and other cancers3 variants in the BRCA1 and BRCA2 genes; relevant for Ashkenazi Jewish descent
-
Celiac DiseaseGenetic risk for gluten-related
autoimmune disorder2 variants near 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 gene; 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 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 damage3 variants in the TTR gene; relevant for African American, West African, Portuguese, Northern Swedish, Japanese, Irish, British descent
-
Hereditary Hemochromatosis (HFE‑Related)Genetic risk for iron overload2 variants in the HFE gene; 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 gene; variant found and studied in many ethnicities
-
MUTYH-Associated PolyposisGenetic risk for a specific colorectal cancer syndrome2 variants in the MUTYH gene; 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 gene; relevant for French Canadian descent
-
Agenesis of the Corpus Callosum with Peripheral Neuropathy1 variant in the SLC12A6 gene; relevant for French Canadian descent
-
Autosomal Recessive Polycystic Kidney Disease3 variants in the PKHD1 gene
-
Beta Thalassemia and Related Hemoglobinopathies10 variants in the HBB gene; relevant for Sardinian, Cypriot, Italian/Sicilian, Greek descent
-
Bloom Syndrome1 variant in the BLM gene; relevant for Ashkenazi Jewish descent
-
Canavan Disease3 variants in the ASPA gene; relevant for Ashkenazi Jewish descent
-
Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)2 variants in the PMM2 gene; relevant for Ashkenazi Jewish, Danish descent
-
Cystic Fibrosis29 variants in the CFTR gene; relevant for Ashkenazi Jewish, European, Hispanic/Latino descent
-
D-Bifunctional Protein Deficiency2 variants in the HSD17B4 gene
-
Dihydrolipoamide Dehydrogenase Deficiency1 variant in the DLD gene; relevant for Ashkenazi Jewish descent
-
Familial Dysautonomia1 variant in the ELP1 gene; relevant for Ashkenazi Jewish descent
-
Familial Hyperinsulinism (ABCC8-Related)3 variants in the ABCC8 gene; relevant for Ashkenazi Jewish descent
-
Familial Mediterranean Fever7 variants in the MEFV gene; relevant for Arab, Armenian, Sephardic Jewish, Turkish descent
-
Fanconi Anemia Group C3 variants in the FANCC gene; relevant for Ashkenazi Jewish descent
-
GRACILE Syndrome1 variant in the BCS1L gene; relevant for Finnish descent
-
Gaucher Disease Type 13 variants in the GBA gene; relevant for Ashkenazi Jewish descent
-
Glycogen Storage Disease Type Ia1 variant in the G6PC gene; relevant for Ashkenazi Jewish descent
-
Glycogen Storage Disease Type Ib2 variants in the SLC37A4 gene
-
Hereditary Fructose Intolerance4 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 Type1 variant in the LRPPRC gene; relevant for French Canadian descent
-
Limb-Girdle Muscular Dystrophy Type 2D1 variant in the SGCA gene
-
Limb-Girdle Muscular Dystrophy Type 2E1 variant in the SGCB gene; relevant for Amish descent
-
Limb-Girdle Muscular Dystrophy Type 2I1 variant in the FKRP gene
-
MCAD Deficiency4 variants in the ACADM gene; relevant for European descent
-
Maple Syrup Urine Disease Type 1B2 variants in the BCKDHB gene; relevant for Ashkenazi Jewish descent
-
Mucolipidosis Type IV1 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 A3 variants in the SMPD1 gene; relevant for Ashkenazi Jewish descent
-
Nijmegen Breakage Syndrome1 variant in the NBN gene
-
Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)8 variants 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 variants in the SLC26A4 gene
-
Phenylketonuria and Related Disorders23 variants in the PAH gene; relevant for Irish, Northern European descent
-
Primary Hyperoxaluria Type 21 variant in the GRHPR gene
-
Pyruvate Kinase Deficiency1 variant in the PKLR gene
-
Rhizomelic Chondrodysplasia Punctata Type 11 variant in the PEX7 gene
-
Salla Disease1 variant in the SLC17A5 gene; relevant for Finnish, Swedish descent
-
Sickle Cell Anemia1 variant in the HBB gene; relevant for African, Middle Eastern, South Asian, Caribbean, Mediterranean, Central and South American descent
-
Sjögren-Larsson Syndrome1 variant in the ALDH3A2 gene; relevant for Swedish descent
-
Tay-Sachs Disease4 variants in the HEXA gene; relevant for Ashkenazi Jewish, Cajun descent
-
Tyrosinemia Type I4 variants in the FAH gene; relevant for French Canadian, Finnish descent
-
Usher Syndrome Type 1F1 variant in the PCDH15 gene; relevant for Ashkenazi Jewish descent
-
Usher Syndrome Type 3A1 variant in the CLRN1 gene; relevant for Ashkenazi Jewish descent
-
Zellweger Spectrum Disorder (PEX1-Related)1 variant in the PEX1 gene