Ancestry + Traits
$119
Ancestry Reports
50+ reports
Trait Reports
30+ traits
- 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 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
$229
Ancestry Reports
50+ reports
Trait Reports
30+ traits
- 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 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 Predisposition Reports*
10+ reports
-
Type 2 Diabetes ( Powered by 23andMe Research )
Learn moreGenetic 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 loss2 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
-
BRCA1/BRCA2 (Selected Variants)
Learn moreGenetic 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
-
Celiac Disease
Genetic 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 disease
2 variants in the APOL1 gene; 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 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 damage
3 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 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
-
MUTYH-Associated Polyposis
Genetic risk for a specific colorectal cancer syndrome
2 variants in the MUTYH gene; relevant for Northern European descent
-
Parkinson's Disease
Genetic 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
5+ reports
- Alcohol Flush Reaction
- Caffeine Consumption
- Deep Sleep
- Genetic Weight
- Lactose Intolerance
- Muscle Composition
- Saturated Fat and Weight
- Sleep Movement
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 Ashkenazi Jewish, 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 ELP1 gene; relevant for Ashkenazi Jewish descent
-
Familial Hyperinsulinism (ABCC8-Related)
3 variants in the ABCC8 gene; relevant for Ashkenazi Jewish descent
-
Familial Mediterranean Fever
7 variants in the MEFV gene; relevant for Arab, Armenian, Sephardic Jewish, Turkish 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)
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 Disorders
23 variants in the PAH gene; relevant for Irish, Northern European descent
-
Pompe Disease
5 variants in the GAA gene; relevant for African/African American descent; variants also common in European descent
-
Primary Hyperoxaluria Type 2
1 variant in the GRHPR gene
-
Pyruvate Kinase Deficiency
1 variant in the PKLR 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, Middle Eastern, South Asian, Caribbean, Mediterranean, Central and South American 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 Spectrum Disorder (PEX1-Related)
1 variant in the PEX1 gene