• Ancestry Composition
• Maternal Haplogroup
• Paternal Haplogroup
• Neanderthal Ancestry
• Your DNA Family

• Age-Related Macular Degeneration
  2 variants in the ARMS2 and CFH genes; relevant for European descent
• Alpha-1 Antitrypsin Deficiency
  2 variants in the SERPINA1 gene; relevant for European descent
• Celiac Disease
  2 variants near the HLA-DQA1 and HLA-DQB1 genes; relevant for European descent
• Hereditary Hemochromatosis (HFE‑Related)
  2 variants in the HFE gene; relevant for European descent
• Hereditary Thrombophilia
  2 variants in the F2 and F5 genes; relevant for European descent
• Late-Onset Alzheimer’s Disease
  1 variant in the APOE gene; variant found and studied in many ethnicities
• Parkinson’s Disease
  2 variants in the LRRK2 and GBA genes; relevant for European, Ashkenazi Jewish, North African Berber descent

• Alcohol Flush Reaction
• Caffeine Consumption
• Deep Sleep
• Genetic Weight
• Lactose Intolerance
• Muscle Composition
• Saturated Fat and Weight
• Sleep Movement

• Asparagus Odor Detection
• Back Hair (available for men only)
• Bald Spot (available for men only)
• Bitter Taste Perception
• Cheek Dimples
• Cleft Chin
• Earlobe Type
• Earwax Type
• Eye Color
• Finger Length Ratio
• Freckles
• Hair Curliness
• Light or Dark Hair
• Male Hair Loss (available for men only)
• Newborn Hair Amount
• Photic Sneeze Reflex
• Red Hair
• Skin Pigmentation
• Sweet Taste Preference
• Toe Length Ratio
• Unibrow
• Widow’s Peak

• 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 Cypriot, Greek, Italian, Sardinian 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
  28 variants in the CFTR gene; relevant for European, Hispanic/Latino, Ashkenazi Jewish 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
• 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
  3 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; relevant for Finnish descent
• Limb-Girdle Muscular Dystrophy Type 2E
  1 variant in the SGCB gene; relevant for Southern Indiana Amish descent
• Limb-Girdle Muscular Dystrophy Type 2I
  1 variant in the FKRP gene; relevant for European descent
• MCAD Deficiency
  3 variants in the ACADM gene; relevant for Northern 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; relevant for Eastern European descent
• 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
  6 variants in the SLC26A4 gene
• Phenylketonuria and Related Disorders
  23 variants in the PAH gene; relevant for Northern European descent
• Primary Hyperoxaluria Type 2
  1 variant in the GRHPR gene; relevant for European descent
• 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 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