Explore 23andMe genetic reports

23andMe currently offers more than 75 direct access genetic reports in five categories: Genetic Health Risk*, Carrier Status*, Ancestry, Wellness and Traits.

Each report provides accurate, high-quality data in a format that is easy to understand and interpret. Take some time to download the report examples that interest you to better understand the types of information your patients receive and may share with you.

Genetic Health Risk reports*

Each genetic health risk report describes if a person has variants associated with a higher risk of developing a disease, but does not describe a person’s overall risk of developing the disease. These reports are not intended to tell a person anything about his or her current state of health, or to be used to make medical decisions, including whether or not he or she should take a medication or how much of a medication should be taken.

Genetic health risk reports package insert

Report Gene Variants Relevant Ethnicities
Alpha-1 Antitrypsin Deficiency SERPINA1 2 European
Hereditary Thrombophilia F2, F5 2 European
Late-Onset Alzheimer’s Disease APOE 1 European
Parkinson’s Disease LRRK2, GBA 2 European , Ashkenazi Jewish , North African Berber

Carrier Status reports*

Click any condition below to view a sample report with the “0 variants detected” result. See Bloom Syndrome, Cystic Fibrosis, or Sickle Cell Anemia to view sample reports for the following results-“1 variant detected”, “2 variants detected”, and “variant not determined”.

Note: Sample reports do not cover all possible result variations and for many reports, residual risk estimates vary by ethnicity.

View the carrier status reports package insert

White paper: carrier status report methodology

 

Report Gene Variants Relevant Ethnicities
Agenesis of the Corpus Callosum with Peripheral Neuropathy SLC12A6 1 French Canadian
ARSACS SACS 1 French Canadian
Autosomal Recessive Polycystic Kidney Disease PKHD1 3 Not applicable
Beta Thalassemia and Related Hemoglobinopathies HBB 10 Cypriot , Greek , Italian , Sicilian , Sardinian
Bloom Syndrome BLM 1 Ashkenazi Jewish
Canavan Disease ASPA 1 Ashkenazi Jewish
Congenital Disorder of Glycosylation Type 1a (PMM2-CDG) PMM2 2 Danish
Cystic Fibrosis CFTR 28 European , Hispanic/Latino , Ashkenazi Jewish
D-Bifunctional Protein Deficiency HSD17B4 2 Not applicable
Dihydrolipoamide Dehydrogenase Deficiency DLD 1 Ashkenazi Jewish
Familial Dysautonomia IKBKAP 1 Ashkenazi Jewish
Fanconi Anemia Group C FANCC 3 Ashkenazi Jewish
Gaucher Disease Type 1 GBA 3 Ashkenazi Jewish
Glycogen Storage Disease Type Ia G6PC 1 Ashkenazi Jewish
Glycogen Storage Disease Type Ib SLC37A4 2 Not applicable
GRACILE Syndrome BCS1L 1 Finnish
Hereditary Fructose Intolerance ALDOB 3 European
Herlitz Junctional Epidermolysis Bullosa (LAMB3-related) LAMB3 3 Not applicable
Leigh Syndrome, French Canadian Type LRPPRC 1 French Canadian
Limb-Girdle Muscular Dystrophy Type 2D SGCA 1 Finnish
Limb-Girdle Muscular Dystrophy Type 2E SGCB 1 Southern Indiana Amish
Limb-Girdle Muscular Dystrophy Type 2I FKRP 1 European
Maple Syrup Urine Disease Type 1B BCKDHB 2 Ashkenazi Jewish
MCAD Deficiency ACADM 3 Northern European
Mucolipidosis Type IV MCOLN1 1 Ashkenazi Jewish
Neuronal Ceroid Lipofuscinosis (CLN5-Related) CLN5 1 Finnish
Neuronal Ceroid Lipofuscinosis (PPT1-Related) PPT1 3 Finnish
Niemann-Pick Disease Type A SMPD1 3 Ashkenazi Jewish
Nijmegen Breakage Syndrome NBN 1 Eastern European
Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related) GJB2 2 Ashkenazi Jewish , European
Pendred Syndrome and DFNB4 Hearing Loss SLC26A4 6 Not applicable
Phenylketonuria and Related Disorders PAH 23 Northern European
Primary Hyperoxaluria Type 2 GRHPR 1 European
Rhizomelic Chondrodysplasia Punctata Type 1 PEX7 1 Not applicable
Salla Disease SLC17A5 1 Finnish , Swedish
Sickle Cell Anemia HBB 1 African
Sjögren-Larsson Syndrome ALDH3A2 1 Swedish
Tay-Sachs Disease HEXA 4 Ashkenazi Jewish , Cajun
Tyrosinemia Type I FAH 4 French Canadian , Finnish
Usher Syndrome Type 1F PCDH15 1 Ashkenazi Jewish
Usher Syndrome Type 3A CLRN1 1 Ashkenazi Jewish
Zellweger Syndrome Spectrum (PEX1-related) PEX1 1 Not applicable
* Our tests can be used to determine carrier status in adults, but cannot determine if you have two copies of the genetic variant. Each test is most relevant for people of certain ethnicities. The tests are not intended to diagnose a disease, or tell you anything about your risk for developing a disease in the future. On their own, carrier status tests are not intended to tell you anything about the health of your fetus, or your newborn child’s risk of developing a particular disease later in life.

Wellness reports

Report Gene Variants Relevant Ethnicities
Alcohol Flush Not applicable Not applicable Not applicable
Caffeine Metabolism Not applicable Not applicable Not applicable
Deep Sleep Not applicable Not applicable Not applicable
Genetic Weight Not applicable Not applicable Not applicable
Lactose Intolerance Not applicable Not applicable Not applicable
Muscle Performance Not applicable Not applicable Not applicable
Saturated Fat and Weight Not applicable Not applicable Not applicable
Sleep Movement Not applicable Not applicable Not applicable

Ancestry reports

Report Gene Variants Relevant Ethnicities
Ancestry Composition Not applicable Not applicable Not applicable
Maternal and Paternal Lineage (Haplogroups) Not applicable Not applicable Not applicable
Neanderthal Ancestry Not applicable Not applicable Not applicable

Traits reports

Report Gene Variants Relevant Ethnicities
Asparagus Odor Detection Not applicable Not applicable Not applicable
Back Hair (available for men only) Not applicable Not applicable Not applicable
Bald Spot (available for men only) Not applicable Not applicable Not applicable
Digit Ratio^ Not applicable Not applicable Not applicable
Earlobe Type Not applicable Not applicable Not applicable
Earwax Type Not applicable Not applicable Not applicable
Eye Color Not applicable Not applicable Not applicable
Facial Features^ Not applicable Not applicable Not applicable
Hair Color^ Not applicable Not applicable Not applicable
Hair Curliness Not applicable Not applicable Not applicable
Male Hair Loss (available for men only) Not applicable Not applicable Not applicable
Newborn Hair Amount Not applicable Not applicable Not applicable
Photic Sneeze Reflex Not applicable Not applicable Not applicable
Skin Pigmentation^ Not applicable Not applicable Not applicable
Taste Preference and Perception Not applicable Not applicable Not applicable
^multiple trait reports included

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