Ancestry Service
€109
Add to cart-Ancestry Service
Health plus Ancestry Service
€219
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23andMe DNA Ancestry test kit - add to cart

Ancestry Service

€109
Add to cartAncestry Service

now with 2750+ regions
Ancestry Reports

50+ reports
  • Ancestry Composition
  • Ancestry Detail Reports (48 reports)
  • Family Tree
  • Maternal Haplogroup
  • Paternal Haplogroup
  • Neanderthal Ancestry
See sample report - AncestrySee sample report - Ancestry

Trait Reports

30+ traits
  • 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
See sample report - TraitsSee sample report - Traits
23andMe DNA Ancestry test kit - add to cart

Health plus Ancestry Service

€219
Add to cartHealth plus Ancestry Service

Health Predisposition Reports*

10+ reports
  • 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 variants in the ARMS2 and CFH genes; relevant for European descent
  • Alpha-1 Antitrypsin Deficiency
    Genetic risk for lung and liver disease
    2 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 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 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 disease
    2 variants in the APOL1 genes; relevant for African descent
  • Familial Hypercholesterolemia
    Genetic risk for very high cholesterol, which can increase the risk for heart disease
    24 variants in the LDLR and APOB genes; relevant for European, Lebanese, Old Order Amish descent
  • G6PD Deficiency
    Genetic risk for a form of anemia
    2 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 damage
    3 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 overload
    2 variants in the HFE genes; relevant for European descent
  • Hereditary Thrombophilia
    Genetic risk for harmful blood clots
    2 variants in the F2 and F5 genes; relevant for European descent
  • Late-Onset Alzheimer's Disease
    Genetic risk for a form of dementia
    1 variant in the APOE genes; variant found and studied in many ethnicities
  • MUTYH-Associated Polyposis
    Genetic risk for a specific colorectal cancer syndrome
    2 variants in the MUTYH genes; relevant for Northern European descent
  • Parkinson's Disease
    Genetic risk for a form of movement impairment
    2 variants in the LRRK2 and GBA genes; relevant for European, Ashkenazi Jewish, North African Berber descent
See sample report - Health PredispositionSee sample report - Health Predisposition

Wellness Reports

5+ reports
  • Alcohol Flush Reaction
  • Caffeine Consumption
  • Deep Sleep
  • Genetic Weight
  • Lactose Intolerance
  • Muscle Composition
  • Saturated Fat and Weight
  • Sleep Movement
See sample report - WellnessSee sample report - Wellness

Carrier Status Reports*

45+ reports
  • ARSACS
    1 variant in the SACS genes; relevant for French Canadian descent
  • Agenesis of the Corpus Callosum with Peripheral Neuropathy
    1 variant in the SLC12A6 genes; relevant for French Canadian descent
  • Autosomal Recessive Polycystic Kidney Disease
    3 variants in the PKHD1 genes
  • Beta Thalassemia and Related Hemoglobinopathies
    10 variants in the HBB genes; relevant for Sardinian, Cypriot, Italian/Sicilian, Greek descent
  • Bloom Syndrome
    1 variant in the BLM genes; relevant for Ashkenazi Jewish descent
  • Canavan Disease
    3 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 Fibrosis
    29 variants in the CFTR genes; relevant for Ashkenazi Jewish, European, Hispanic/Latino descent
  • D-Bifunctional Protein Deficiency
    2 variants in the HSD17B4 genes
  • Dihydrolipoamide Dehydrogenase Deficiency
    1 variant in the DLD genes; relevant for Ashkenazi Jewish descent
  • Familial Dysautonomia
    1 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 Fever
    7 variants in the MEFV genes; relevant for Arab, Armenian, Sephardic Jewish, Turkish descent
  • Fanconi Anemia Group C
    3 variants in the FANCC genes; relevant for Ashkenazi Jewish descent
  • GRACILE Syndrome
    1 variant in the BCS1L genes; relevant for Finnish descent
  • Gaucher Disease Type 1
    3 variants in the GBA genes; relevant for Ashkenazi Jewish descent
  • Glycogen Storage Disease Type Ia
    1 variant in the G6PC genes; relevant for Ashkenazi Jewish descent
  • Glycogen Storage Disease Type Ib
    2 variants in the SLC37A4 genes
  • Hereditary Fructose Intolerance
    4 variants in the ALDOB genes; relevant for European descent
  • Leigh Syndrome, French Canadian Type
    1 variant in the LRPPRC genes; relevant for French Canadian descent
  • Limb-Girdle Muscular Dystrophy Type 2D
    1 variant in the SGCA genes
  • Limb-Girdle Muscular Dystrophy Type 2E
    1 variant in the SGCB genes; relevant for Amish descent
  • Limb-Girdle Muscular Dystrophy Type 2I
    1 variant in the FKRP genes
  • MCAD Deficiency
    4 variants in the ACADM genes; relevant for European descent
  • Maple Syrup Urine Disease Type 1B
    2 variants in the BCKDHB genes; relevant for Ashkenazi Jewish descent
  • Mucolipidosis Type IV
    1 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 A
    3 variants in the SMPD1 genes; relevant for Ashkenazi Jewish descent
  • Nijmegen Breakage Syndrome
    1 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 Disorders
    23 variants in the PAH genes; relevant for Irish, Northern European descent
  • Pompe Disease
    5 variants in the GAA genes; relevant for African/African American descent; variants also common in European descent
  • Primary Hyperoxaluria Type 2
    1 variant in the GRHPR genes
  • Pyruvate Kinase Deficiency
    1 variant in the PKLR genes
  • Rhizomelic Chondrodysplasia Punctata Type 1
    1 variant in the PEX7 genes
  • Salla Disease
    1 variant in the SLC17A5 genes; relevant for Finnish, Swedish descent
  • Severe Junctional Epidermolysis Bullosa (LAMB3-Related)
    3 variants in the LAMB3 genes
  • Sickle Cell Anemia
    1 variant in the HBB genes; relevant for African, Middle Eastern, South Asian, Caribbean, Mediterranean, Central and South American descent
  • Sjögren-Larsson Syndrome
    1 variant in the ALDH3A2 genes; relevant for Swedish descent
  • Tay-Sachs Disease
    4 variants in the HEXA genes; relevant for Ashkenazi Jewish, Cajun descent
  • Tyrosinemia Type I
    4 variants in the FAH genes; relevant for French Canadian, Finnish descent
  • Usher Syndrome Type 1F
    1 variant in the PCDH15 genes; relevant for Ashkenazi Jewish descent
  • Usher Syndrome Type 3A
    1 variant in the CLRN1 genes; relevant for Ashkenazi Jewish descent
  • Zellweger Spectrum Disorder (PEX1-Related)
    1 variant in the PEX1 genes
See sample report - Carrier StatusSee sample report - Carrier Status