Because you’re never done being healthy, here’s an annual membership with access to new premium reports and features delivered to you throughout the year to keep fueling your health journey.
- Get everything from our Health plus Ancestry kit including our updated BRCA1/BRCA2 (Selected Variants) Genetic Health Risk report*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks
- PLUS access to reports that help you learn about your heart health, how you process certain medications**Learn about Considerations and Limitations for Pharmacogenetics Reports, anxiety, and more.
- Our latest Breast, Prostate and Colorectal Cancer reports Powered by 23andMe Research offer new, innovative insights for personalized next steps.‡ More info
- Trace your family’s journey through time with the power of Historical Matches and our new Records & Archives feature.
- Our Health Tracks feature helps you understand how genetics and lifestyle can impact your likelihood of developing certain conditions.
- Valid payment method required at kit registration.
- FSA/HSA eligibility◆Learn about Important Information for FSA/HSA Reimbursement
There is a lot to consider with genetic testing. We encourage you to review relevant information about Pharmacogenetics**Learn about Considerations and Limitations for Pharmacogenetics Reports, Carrier Status*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks and Genetic Health Risk*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks reports.
Important test info23andMe+ members get even more insights into their health.
Get our base Health + Ancestry Service with 150+ personalized DNA reports
Learn more about Health + Ancestrykit
Exclusive Accessto new premium reports and features throughout the year
Take a look at what you’ll get from the start
Personalized Health Features.Personalized insights for prevention and better health over time.
Our Health Tracks feature is another step forward in preventive health, helping you easily visualize and understand how genetics and lifestyle together can impact your likelihood of developing type 2 diabetes, high blood pressure and coronary artery disease over time.
Image Description: A sample of Health Tracks showing how your lifestyle and genetics can impact the likelihood of Type 2 Diabetes over time.
Health TracksSM
Our Health Tracks feature is another step forward in preventive health, helping you easily visualize and understand how genetics and lifestyle together can impact your likelihood of developing type 2 diabetes, high blood pressure and coronary artery disease over time.
PremiumYear
Heart Health.Exclusive DNA insights to stay proactive with your heart health.
Get a better picture of what may be in store for your heart’s health and learn about lifestyle factors and steps that can help you stay healthy.
Cancer Reports Powered by 23andMe Research.Innovative cancer insights for personalized next steps.
- (females only)
Image Description: A sample result for Breast Cancer report; "Your genetics are associated with a typical likelihood." Other factors can include age, family history, and reproductive history.
- (males only)
Image Description: A sample result for Prostate Cancer report; "Your genetics are associated with an increased likelihood." Other factors can include age, ethnicity, and family history.
- (certain ethnicities)
Image Description: A sample result for Colorectal Cancer report; "Your genetics are associated with a typical likelihood." Other factors can include age, ethnicity, and family history.
Breast Cancer
.Get smarter about the prescriptions you’re taking.
Medications don’t always “work” the same way in different bodies. Discover how your DNA may impact the way your body processes certain medications with three Pharmacogenetics reports plus Medication Insights on citalopram and clopidogrel, and simvastatin. Share these reports with your doctor to make smarter decisions together.
Plus more exclusive DNA insights to better understand your health.
Advanced Ancestry Features.Research your ancestry faster and more efficiently.
Historical MatchesSM
Uncover your historical and ancient relatives linking you to individuals, groups and events from hundreds or even thousands of years ago.
Check out the 190+ personalized reports included in our premium membership.
Plus more reports and features added throughout the year.
- Ancestry Detail Reports (48 reports)
Population-specific reports with maps covering 3500+ regions, offering a granular view of your ancestry, plus immersive educational content.
Reports included:
Americas (Caribbean, Mexico & Central America, Indigenous American, South America);
East Asia (Chinese, Chinese Dai, Filipino & Austronesian, Indonesian, Thai, Khmer & Myanma, Japanese, Korean, Manchurian & Mongolian, Siberian, Vietnamese);
Europe (Ashkenazi Jewish, British & Irish, Eastern European, Finnish, French & German, Greek & Balkan, Italian, Sardinian, Scandinavian, Spanish & Portuguese);
Oceania (Melanesian);
Central & South Asia (Bengali & Northeast Indian, Central Asian, Gujarati Patidar, Malayali Subgroup, Northern Indian & Pakistani, Southern Indian & Sri Lankan, Southern Indian Subgroup);
Sub-Saharan Africa (African Hunter-Gatherer, Angolan & Congolese, Ethiopian & Eritrean, Ghanaian, Liberian & Sierra Leonean, Nigerian, Senegambian & Guinean, Somali, Southern East African, Sudanese);
Western Asia & North Africa (Anatolian, Coptic Egyptian, Cypriot, Egyptian, Iranian, Caucasian & Mesopotamian, Levantine, North African, Peninsular Arab) - Family Tree
- Maternal Haplogroup
- Paternal Haplogroup
- Neanderthal Ancestry
- 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 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
- Hereditary Prostate Cancer (HOXB13-Related)A DNA variant that increases risk for prostate cancer1 variant in the HOXB13 gene; relevant for European (especially Northern European) descent
- Anxiety
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing anxiety that interferes with daily lifeBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Asthma
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing a chronic lung condition characterized by shortness of breath, wheezing, and coughingBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Atrial Fibrillation
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a type of irregular heartbeatBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Attention-Deficit/Hyperactivity Disorder (ADHD)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of having ADHD, which can be associated with differences in attention, memory, and managing thoughts or behaviorsBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Bipolar Disorder
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of experiencing unusual shifts in mood, energy, activity, behavior, and sleep, beyond the normal ups and downs of lifeBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Breast Cancer (available for females only)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing breast cancerBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Colorectal Cancer
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing cancer of the colon or rectumBased on a genetic model that includes customers' results for more than a thousand genetic markers; genetic result available for people with predominantly European and Hispanic/Latino ancestryThere is not enough data to create a genetic prediction that meets our scientific standards for people with other ancestries at this time. - Coronary Artery Disease
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a type of heart diseaseBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Depression
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing persistent low mood, loss of interest, and other symptoms that interfere with daily lifeBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Diverticulitis
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a condition that occurs when small pouches in the digestive tract become inflamedBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Eczema (Atopic Dermatitis)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a skin condition characterized by dry, discolored, and itchy skinBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Fibromyalgia
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing a condition characterized by chronic pain and tenderness throughout the bodyBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Gallstones
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing solid, pebble-like masses that form in the gallbladderBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Gestational Diabetes (available for females only)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing a type of diabetes that occurs during pregnancyBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Glaucoma
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing an eye condition that can cause partial vision loss and blindnessBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Gout
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a condition where one or more joints suddenly becomes painful and swollenBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Hashimoto’s Disease
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing an autoimmune condition in which the immune system causes damage to the thyroid glandBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - HDL Cholesterol
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing low levels of HDL (“good”) cholesterolBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - High Blood Pressure
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing high blood pressureBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Insomnia
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing a sleep disorder that causes chronic trouble with falling or staying asleepBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Irritable Bowel Syndrome
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing a chronic condition that impacts the large intestineBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Kidney Stones
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for solid, pebble-like masses that form in the kidneysBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - LDL Cholesterol
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing high levels of LDL ("bad") cholesterolBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Lupus
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing a chronic autoimmune condition that can affect many parts of the body, such as the joints, skin, lungs, kidneys, and heartBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Migraine
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of experiencing migraine headachesBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Nonalcoholic Fatty Liver Disease
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a condition where fat builds up in the liverBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Obstructive Sleep Apnea
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a condition where breathing stops and starts repeatedly during sleepBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Panic Attacks
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of experiencing episodes of intense fear that last a few minutes to an hourBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Polycystic Ovary Syndrome (PCOS) (available for females only)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a hormone disorder that affects femalesBased on a genetic model that includes customers' results for more than a thousand genetic markers; variants found in many ethnicities - Preeclampsia (available for females only)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing persistent high blood pressure during pregnancyBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Prostate Cancer (available for males only)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing cancer of the prostate, a male reproductive organBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Psoriasis
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing an autoimmune condition that can cause itchy, discolored patches to form on the skinBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Restless Legs Syndrome
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a condition characterized by an uncontrollable urge to move one's legsBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Rosacea
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a chronic skin condition that often causes redness or visible blood vessels in the faceBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Severe Acne
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a skin condition characterized by many deep and painful types of pimples along with many whiteheads and blackheadsBased on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities - Skin Cancer (Basal and Squamous Cell Carcinomas)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing the two most common types of skin cancerBased on a genetic model that includes customers’ results for thousands of genetic markers; genetic result available for people of European, Hispanic/Latino, Northern African/Central & Western Asian, and Sub-Saharan African/African American descentOnly about 3 in 1000 23andMe research participants of East/Southeast Asian or South Asian descent report having been diagnosed with basal or squamous cell skin cancers. This means there is not enough data to create a genetic prediction that meets our scientific standards for people of these ethnicities at this time. - Skin Cancer (Melanoma)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing a common type of skin cancerBased on a genetic model that includes customers’ results for more than a thousand genetic markers; genetic result available for people of European, Hispanic/Latino, and Northern African/Central & Western Asian descentOnly about 1 in 1000 23andMe research participants of East/Southeast Asian, South Asian, or Sub-Saharan African/African American descent report having been diagnosed with melanoma. This means there is not enough data to create a genetic prediction that meets our scientific standards for people of these ethnicities at this time. - Triglycerides
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood of developing high levels of triglycerides (a type of lipid)Based on a genetic model that includes customers' results for more than a thousand genetic markers; variants found in many ethnicities - Uterine Fibroids (available for females only)
(Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a common type of non-cancerous growth in the uterusBased on a genetic model that includes customers' results for more than a thousand genetic markers; variants found in many ethnicities - Type 2 Diabetes (Powered by 23andMe Research)Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research.Genetic likelihood for a disorder of blood sugar regulation1,000+ variants in many genes; variants found in many ethnicities
- Age-Related Macular DegenerationGenetic risk for a form of adult-onset vision loss2 variants in the ARMS2 and CFH genes; relevant for European descent
- Alpha-1 Antitrypsin DeficiencyGenetic risk for lung and liver disease2 variants in the SERPINA1 gene; relevant for European descent
- BRCA1/BRCA2 (Selected Variants)Genetic risk based on a limited set of variants for breast, ovarian, prostate and pancreatic cancer44 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 DiseaseGenetic risk for gluten-related autoimmune disorder2 variants near the HLA-DQB1 and HLA-DQA1 genes; relevant for European decent
- Chronic Kidney Disease (APOL1-Related)Genetic risk for a form of chronic kidney disease2 variants in the APOL1 gene; relevant for African descent
- Familial HypercholesterolemiaGenetic risk for very high cholesterol, which can increase the risk for heart disease24 variants in the LDLR and APOB genes; relevant for European, Lebanese, Old Order Amish descent
- G6PD DeficiencyGenetic risk for a form of anemia2 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 damage3 variants in the TTR gene; relevant for African American, West African, Portuguese, Brazilian, Northern Swedish, Japanese, Irish, British descent
- Hereditary Hemochromatosis (HFE‑Related)Genetic risk for iron overload2 variants in the HFE gene; relevant for European descent
- Hereditary ThrombophiliaGenetic risk for harmful blood clots2 variants in the F2 and F5 genes; relevant for European descent
- Late-Onset Alzheimer's DiseaseGenetic risk for a form of dementia1 variant in the APOE gene; variant found and studied in many ethnicities
- MUTYH-Associated PolyposisGenetic risk for a specific colorectal cancer syndrome2 variants in the MUTYH gene; relevant for Northern European descent
- Parkinson's DiseaseGenetic risk for a form of movement impairment2 variants in the LRRK2 and GBA genes; relevant for European, Ashkenazi Jewish, North African Berber descent
- ARSACS1 variant in the SACS gene; relevant for French Canadian descent
- Agenesis of the Corpus Callosum with Peripheral Neuropathy1 variant in the SLC12A6 gene; relevant for French Canadian descent
- Autosomal Recessive Polycystic Kidney Disease3 variants in the PKHD1 gene
- Beta Thalassemia and Related Hemoglobinopathies10 variants in the HBB gene; relevant for Sardinian, Cypriot, Italian/Sicilian, Greek descent
- Bloom Syndrome1 variant in the BLM gene; relevant for Ashkenazi Jewish descent
- Canavan Disease3 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 Fibrosis29 variants in the CFTR gene; relevant for Ashkenazi Jewish, European, Hispanic/Latino descent
- D-Bifunctional Protein Deficiency2 variants in the HSD17B4 gene
- Dihydrolipoamide Dehydrogenase Deficiency1 variant in the DLD gene; relevant for Ashkenazi Jewish descent
- Familial Dysautonomia1 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 Fever7 variants in the MEFV gene; relevant for Arab, Armenian, Sephardic Jewish, Turkish descent
- Fanconi Anemia Group C3 variants in the FANCC gene; relevant for Ashkenazi Jewish descent
- GRACILE Syndrome1 variant in the BCS1L gene; relevant for Finnish descent
- Gaucher Disease Type 13 variants in the GBA (also known as GBA1) gene; relevant for Ashkenazi Jewish descent
- Glycogen Storage Disease Type Ia1 variant in the G6PC gene; relevant for Ashkenazi Jewish descent
- Glycogen Storage Disease Type Ib2 variants in the SLC37A4 gene
- Hereditary Fructose Intolerance4 variants in the ALDOB gene; relevant for European descent
- Leigh Syndrome, French Canadian Type1 variant in the LRPPRC gene; relevant for French Canadian descent
- Limb-Girdle Muscular Dystrophy Type 2D1 variant in the SGCA gene
- Limb-Girdle Muscular Dystrophy Type 2E1 variant in the SGCB gene; relevant for Amish descent
- Limb-Girdle Muscular Dystrophy Type 2I1 variant in the FKRP gene
- MCAD Deficiency4 variants in the ACADM gene; relevant for European descent
- Maple Syrup Urine Disease Type 1B2 variants in the BCKDHB gene; relevant for Ashkenazi Jewish descent
- Mucolipidosis Type IV1 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 A3 variants in the SMPD1 gene; relevant for Ashkenazi Jewish descent
- Nijmegen Breakage Syndrome1 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 Disorders23 variants in the PAH gene; relevant for Irish, Northern European descent
- Pompe Disease5 variants in the GAA gene; relevant for African/African American descent; variants also common in European descent
- Primary Hyperoxaluria Type 21 variant in the GRHPR gene
- Pyruvate Kinase Deficiency1 variant in the PKLR gene
- Rhizomelic Chondrodysplasia Punctata Type 11 variant in the PEX7 gene
- Salla Disease1 variant in the SLC17A5 gene; relevant for Finnish, Swedish descent
- Severe Junctional Epidermolysis Bullosa (LAMB3-Related)3 variants in the LAMB3 gene
- Sickle Cell Anemia1 variant in the HBB gene; relevant for African, Middle Eastern, South Asian, Caribbean, Mediterranean, Central and South American descent
- Sjögren-Larsson Syndrome1 variant in the ALDH3A2 gene; relevant for Swedish descent
- Tay-Sachs Disease4 variants in the HEXA gene; relevant for Ashkenazi Jewish, Cajun descent
- Tyrosinemia Type I4 variants in the FAH gene; relevant for French Canadian, Finnish descent
- Usher Syndrome Type 1F1 variant in the PCDH15 gene; relevant for Ashkenazi Jewish descent
- Usher Syndrome Type 3A1 variant in the CLRN1 gene; relevant for Ashkenazi Jewish descent
- Zellweger Spectrum Disorder (PEX1-Related)1 variant in the PEX1 gene
- Cat Allergy
- Dog Allergy
- Emotional Eating
- Nearsightedness
- Seasonal Allergies
- Alcohol Flush Reaction
- Caffeine Consumption
- Deep Sleep
- Genetic Weight
- Lactose Intolerance
- Muscle Composition
- Saturated Fat and Weight
- Sleep Movement
- CYP2C19 Drug Metabolism*DNA variants that influence how the body processes certain medications for depression, acid reflux, heart disease and other conditions3 variants in the CYP2C19 gene; variant found and studied in many ethnicities. Example medications: citalopram, omeprazole, clopidogrel
- Citalopram Medication InsightMedication Insight about how DNA variants may affect citalopram, a medication used to treat depression
- Clopidogrel Medication InsightMedication Insight about how DNA variants may affect clopidogrel, a medication used to reduce the risk for heart attack and stroke
- Citalopram Medication Insight
- DPYD Drug Metabolism*DNA variants that influence how the body processes certain cancer medications2 variants in the DPYD gene; variant found and studied in many ethnicities. Example medications: fluorouracil (5-FU), capecitabine
- SLCO1B1 Drug Transport*A DNA variant that influences how the body processes certain cholesterol-lowering medications1 variant in the SLCO1B1 gene; variant found and studied in many ethnicities
- Simvastatin Medication InsightMedication Insight about how DNA variants may affect simvastatin, a medication used to lower cholesterol levels and reduce the risk for heart attack, stroke, and other heart problems
- Simvastatin Medication Insight
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| Feature | Ancestry Service | Health plus Ancestry Service |
|---|---|---|
Health plus Ancestry | ||
| Total reports | 80+ | 150+ |
| Ancestry and Trait Reports |  | |
| DNA Relative Finder and Family Tree (Opt in) | | |
| Health Predisposition reports*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks Learn how your genetics can influence your chances of developing certain health conditions. |  | 10+ |
| Carrier Status reports*Learn about Considerations and Limitations for Health Predispositions Reports, Carrier Status Reports and Genetic Health Risks If you are starting a family, find out if you are a carrier for certain inherited conditions. | | |
| Wellness reports Learn how your genes play a role in your well-being and lifestyle choices. | | 5+ |
| Family Health History Tree Opt in to easily input, track and download your family health history to share with your healthcare provider. | | |
| Pharmacogenetics reports**Learn about Considerations and Limitations for Pharmacogenetics Reports Discover how your DNA may impact how your body processes certain medications with three new Pharmacogenetics reports. | | |
| Enhanced ancestry features Get advanced filtering for DNA Relative Finder and access up to 5000 DNA relatives. | | |
| Historical Matches Uncover your historical and ancient relatives, linking you to the past. | | |
Just Added Records & Archives Learn more about your family’s history with the help of historical documents. | | |
| Breast, Prostate and Colorectal Cancer reports Insights into your genetic likelihood of developing breast (females only), prostate (males only) and colorectal (certain ethnicities) cancer. all Powered by 23andMe Research | | |
| Health Tracks See how making healthy choices each day can greatly impact your health over time | | |
| Ongoing new reports and features Get access to new premium reports and features throughout the year. | | |
Frequently asked questions
We offer two base DNA kits, Ancestry Service and Health plus Ancestry, which are a one-time fee. We also have an optional add-on to the Health plus Ancestry kit, 23andMeplus, which is our annual membership service that offers exclusive access to new premium reports and features throughout the year.
23andMeplus costs $99 for a one year membership.
You can cancel your annual 23andMeplus Premium at any time from within your 23andMe Account Settings. Read more about canceling your membership here: https://www.23andme.com/about/tos/subscription/
The 23andMeplus Premium is an annual membership and includes everything from our Health plus Ancestry Service plus access to exclusive reports and features that can help you learn more about your heart health, how you process certain medications**Learn about Considerations and Limitations for Pharmacogenetics Reports, likelihood for having migraine, and more. You’ll also receive enhanced ancestry features. Together, these 23andMe reports and features provide a more in-depth dive into your health and ancestry.
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*The 23andMe PGS test includes health predisposition and carrier status reports. Health predisposition reports include both reports that meet FDA requirements for genetic health risks and reports which are based on 23andMe research and have not been reviewed by the FDA. The test uses qualitative genotyping to detect select clinically relevant variants in the genomic DNA of adults from saliva for the purpose of reporting and interpreting genetic health risks and reporting carrier status. It is not intended to diagnose any disease. Your ethnicity may affect the relevance of each report and how your genetic health risk results are interpreted. 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. The test is not intended to tell you anything about your current state of health, or to be used to make medical decisions, including whether or not you should take a medication, how much of a medication you should take, or determine any treatment. Our carrier status reports can be used to determine carrier status, but cannot determine if you have two copies of any genetic variant. These carrier reports are not intended to tell you anything about your risk for developing a disease in the future, the health of your fetus, or your newborn child's risk of developing a particular disease later in life. For certain conditions, we provide a single report that includes information on both carrier status and genetic health risk. Warnings & Limitations: The 23andMe PGS Genetic Health Risk Report for BRCA1/BRCA2 (Selected Variants) is indicated for reporting of 44 variants in the BRCA1 and BRCA2 genes. The report describes if a person's genetic result is associated with an increased risk of developing breast cancer and ovarian cancer and may be associated with an increased risk for prostate cancer, pancreatic cancer, and potentially other cancers. The variants included in this report do not represent the majority of the BRCA1/BRCA2 variants in people of most ethnicities. This report does not include variants in other genes linked to hereditary cancers and the absence of variants included in this report does not rule out the presence of other genetic variants that may impact cancer risk. This report is for over-the-counter use by adults over the age of 18, and provides genetic information to inform discussions with a healthcare professional. The PGS test is not a substitute for visits to a healthcare professional for recommended screenings or appropriate follow-up. Results should be confirmed in a clinical setting before taking any medical action. For important information and limitations regarding each genetic health risk and carrier status report, visit 23andme.com/test-info/
**23andMe PGS Pharmacogenetics reports: The 23andMe test uses qualitative genotyping to detect 3 variants in the CYP2C19 gene, 2 variants in the DPYD gene and 1 variant in the SLCO1B1 gene in the genomic DNA of adults from saliva for the purpose of reporting and interpreting information about the processing of certain therapeutics to inform discussions with a healthcare professional. It does not describe if a person will or will not respond to a particular therapeutic. Our CYP2C19 Pharmacogenetics report provides certain information about variants associated with metabolism of some therapeutics and provides interpretive drug information regarding the potential effect of citalopram and clopidogrel therapy. Our SLCO1B1 Pharmacogenetics report provides certain information about variants associated with the processing of some therapeutics and provides interpretive drug information regarding the potential effect of simvastatin therapy. Our DPYD Pharmacogenetics report does not describe the association between detected variants and any specific therapeutic. Results for DPYD and certain CYP2C19 results should be confirmed by an independent genetic test prescribed by your own healthcare provider before taking any medical action. Warning: Test information should not be used to start, stop, or change any course of treatment and does not test for all possible variants that may affect metabolism or protein function. The PGS test is not a substitute for visits to a healthcare professional. Making changes to your current regimen can lead to harmful side effects or reduced intended benefits of your medication, therefore consult with your healthcare professional before taking any medical action. For important information and limitations regarding Pharmacogenetic reports, visit 23andme.com/test-info/pharmacogenetics/