See the list of reports included in each service:

Ancestry Service
£79
buy
Health + Ancestry Service
£149
buy
23andMe DNA Test Kit
Ancestry Service
£79
Now with 150+ regions Ancestry reports
5 reports
  • Ancestry Composition
  • Maternal Haplogroup
  • Paternal Haplogroup
  • Neanderthal Ancestry
  • Your DNA Family
See sample report See sample report
23andMe DNA Test Kit
Health + Ancestry Service
£149
Now with 150+ regions Ancestry reports
5 reports
  • Ancestry Composition
  • Maternal Haplogroup
  • Paternal Haplogroup
  • Neanderthal Ancestry
  • Your DNA Family
See sample report See sample report
Genetic Health Risk reports*
5+ reports
  • BRCA1/BRCA2 (Selected Variants)
    Genetic risk based on a limited
    set of variants for breast, ovarian
    and other cancers
    3 variants in the BRCA1 and BRCA2 genes; relevant for Ashkenazi Jewish descent
  • 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 gene; relevant for European descent
  • Celiac Disease
    Genetic risk for gluten-related
    autoimmune disorder
    2 variants near the HLA-DQB1 and HLA-DQA1 genes; relevant for European descent
  • Hereditary Hemochromatosis (HFE‑Related)
    Genetic risk for iron overload
    2 variants in the HFE gene; 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 gene; variant found and studied in many ethnicities
  • 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 See sample report
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 See sample report
Traits reports
15+ traits
  • Asparagus Odor Detection
  • Back Hair (available for men only)
  • Bald Spot (available for men only)
  • Bitter Taste
  • Cheek Dimples
  • Cleft Chin
  • Earlobe Type
  • Earwax Type
  • Eye Color
  • Finger Length Ratio
  • Freckles
  • Hair Texture
  • Light or Dark Hair
  • Early Hair Loss (available for men only)
  • Newborn Hair
  • Photic Sneeze Reflex
  • Red Hair
  • Skin Pigmentation
  • Sweet vs. Salty
  • Toe Length Ratio
  • Unibrow
  • Widow's Peak
See sample report See sample report
Carrier Status reports*
40+ reports
  • 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 Sardinian, Cypriot, Italian/Sicilian, Greek descent
  • Bloom Syndrome
    1 variant in the BLM gene; relevant for Ashkenazi Jewish descent
  • Canavan Disease
    3 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 Danish descent
  • Cystic Fibrosis
    29 variants in the CFTR gene; relevant for Ashkenazi Jewish, European, Hispanic/Latino 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
  • Familial Hyperinsulinism (ABCC8-Related)
    3 variants in the ABCC8 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
  • Gaucher Disease Type 1
    3 variants in the GBA 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 variants in the SLC37A4 gene
  • Hereditary Fructose Intolerance
    4 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
  • 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 variants in the ACADM gene; relevant for European descent
  • Maple Syrup Urine Disease Type 1B
    2 variants 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 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
  • 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 (SLC26A4-Related)
    6 variants in the SLC26A4 gene
  • Phenylketonuria and Related Disorders
    23 variants in the PAH gene; relevant for Irish, Northern European descent
  • Primary Hyperoxaluria Type 2
    1 variant in the GRHPR 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
  • Sickle Cell Anemia
    1 variant in the HBB gene; relevant for African American, 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
  • Zellweger Syndrome Spectrum (PEX1-Related)
    1 variant in the PEX1 gene
See sample report See sample report