Go beyond routine care1 More info with
a personalized path for cancer
prevention2 More info.

Genetic testing can help you identify potential risks of developing certain cancers.

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Original Price: $298 Sale Price: $229First
Year
Membership renews at $69peryr.
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Knowledge is power.


  • Early action can lead to a healthier you.
    ~40%
    of cancer deaths are linked to modifiable risk factors and may be preventable.3 More info

  • Cancer can affect people of all ages.
    4/10
    people will develop cancer during their lifetime.4 More info

  • Make more informed decisions about your care.
    #2
    Cancer is the second most common cause of death in the US.5 More info

Why genetic testing matters. We're here to help.

Your genetics are associated with a typical likelihood
  • Unlike routine cancer screening that may signal you already have a condition, genetic insights offer you information you can use for early intervention.
  • Survival rates improve dramatically when cancer is diagnosed early.6 More info Depending on your genetics, standard screening and preventive steps may not be enough.
  • Genetic insights can provide you with information on ways to take action and help you make more informed decisions.

We have three types of genetic reports to give you innovative insights for personalized next steps.

A sample Heart Health report. Your genetics are associated with an increased likelihood.

Genetic information for cancer and drug response.

Also included in your 23andMe+ Premium membership.


  • BRCA1/BRCA2 (Selected Variants)
  • Hereditary Prostate Cancer (HOXB13-Related)
  • MUTYH-Associated Polyposis
  • Breast Cancer PRS report (females only)
  • Prostate Cancer PRS report (males only)
  • Colorectal Cancer PRS report (certain ethnicities)
  • Skin Cancer (Melanoma)
  • Skin Cancer (Basal and Squamous Cell Carcinomas)
  • DPYD Drug Metabolism

Tools for preventive action and better health over time.

Also included in your 23andMe+ Premium membership.

Health Action Plan

Your Health Action Plan allows you to opt in and receive personalized recommendations based on genetic and non-genetic data.

Family Health History Tree

Opt in to easily input, track and download your family health history to share with your healthcare provider.

Find out what else you can learn from your DNA.

You’ll also receive 190+ reports with new insights and features added throughout the year.

  • Type 2 Diabetes (Powered by 23andMe Research)
  • Gestational Diabetes (Powered by 23andMe Research) (available for females only)
  • High Blood Pressure (Powered by 23andMe Research)
  • HDL Cholesterol (Powered by 23andMe Research)
  • Triglycerides (Powered by 23andMe Research)
Wellness Reports
Genetic Weight
Saturated Fat and Weight
  • Late-Onset Alzheimer’s Disease Genetic Health Risk Report
  • Related Condition: Parkinson’s Disease Genetic Health Risk Report
  • Depression (Powered by 23andMe Research)
  • Anxiety (Powered by 23andMe Research)
  • Panic Attacks (Powered by 23andMe Research)
  • ADHD (Powered by 23andMe Research)
Sleep Health Matters to Mental Health
Insomnia (Powered by 23andMe Research)
Obstructive Sleep Apnea (Powered by 23andMe Research)
Restless Legs Syndrome (Powered by 23andMe Research)
Wellness and Trait Reports
Deep Sleep
Sleep Movement
Wake-Up Time
  • Familial Hypercholesterolemia Genetic Health Risk Report
  • Hereditary Amyloidosis (TTR-Related) Genetic Health Risk Report
  • Atrial Fibrillation (Powered by 23andMe Research)
  • Coronary Artery Disease (Powered by 23andMe Research)
  • High Blood Pressure (Powered by 23andMe Research)
  • Type 2 Diabetes (Powered by 23andMe Research)
  • LDL Cholesterol (Powered by 23andMe Research)
  • HDL Cholesterol (Powered by 23andMe Research)
  • Triglycerides (Powered by 23andMe Research)
Wellness Reports
Genetic Weight
Saturated Fat and Weight
Pharmacogenetics Reports
SLCO1B1 Drug Transport
CYP2C19 Drug Metabolism
  • Historical MatchesSM feature
  • Advanced DNA Relative filters
  • Access to up to 5000 DNA relatives
Ancestry Reports
50+ reports
  • Ancestry Detail Reports (48 reports)

    Population-specific reports with maps covering 3000+ 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
Trait Reports
30+ reports
  • 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*
40+ reports
  • Hereditary Prostate Cancer (HOXB13-Related)
    A DNA variant that increases risk for prostate cancer
    1 variant in the HOXB13 gene; relevant for European (especially Northern European) descent
  • Anxiety
    (Powered by 23andMe Research)
    Genetic likelihood of developing anxiety that interferes with daily life
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Asthma
    (Powered by 23andMe Research)
    Genetic likelihood of developing a chronic lung condition characterized by shortness of breath, wheezing, and coughing
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Atrial Fibrillation
    (Powered by 23andMe Research)
    Genetic likelihood for a type of irregular heartbeat
    Based 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)
    Genetic likelihood of having ADHD, which can be associated with differences in attention, memory, and managing thoughts or behaviors
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Bipolar Disorder
    (Powered by 23andMe Research)
    Genetic likelihood of experiencing unusual shifts in mood, energy, activity, behavior, and sleep, beyond the normal ups and downs of life
    Based 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)
    Genetic likelihood of developing breast cancer
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Colorectal Cancer
    (Powered by 23andMe Research)
    Genetic likelihood of developing cancer of the colon or rectum
    Based 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 ancestry
  • Coronary Artery Disease
    (Powered by 23andMe Research)
    Genetic likelihood for a type of heart disease
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Depression
    (Powered by 23andMe Research)
    Genetic likelihood of developing persistent low mood, loss of interest, and other symptoms that interfere with daily life
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Diverticulitis
    (Powered by 23andMe Research)
    Genetic likelihood for a condition that occurs when small pouches in the digestive tract become inflamed
    Based 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)
    Genetic likelihood for a skin condition characterized by dry, discolored, and itchy skin
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Fibromyalgia
    (Powered by 23andMe Research)
    Genetic likelihood of developing a condition characterized by chronic pain and tenderness throughout the body
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Gallstones
    (Powered by 23andMe Research)
    Genetic likelihood of developing solid, pebble-like masses that form in the gallbladder
    Based 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)
    Genetic likelihood of developing a type of diabetes that occurs during pregnancy
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Glaucoma
    (Powered by 23andMe Research)
    Genetic likelihood of developing an eye condition that can cause partial vision loss and blindness
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Gout
    (Powered by 23andMe Research)
    Genetic likelihood for a condition where one or more joints suddenly becomes painful and swollen
    Based 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)
    Genetic likelihood of developing an autoimmune condition in which the immune system causes damage to the thyroid gland
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • HDL Cholesterol
    (Powered by 23andMe Research)
    Genetic likelihood of developing low levels of HDL (“good”) cholesterol
    Based 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)
    Genetic likelihood of developing high blood pressure
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Insomnia
    (Powered by 23andMe Research)
    Genetic likelihood of developing a sleep disorder that causes chronic trouble with falling or staying asleep
    Based 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)
    Genetic likelihood of developing a chronic condition that impacts the large intestine
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Kidney Stones
    (Powered by 23andMe Research)
    Genetic likelihood for solid, pebble-like masses that form in the kidneys
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • LDL Cholesterol
    (Powered by 23andMe Research)
    Genetic likelihood of developing high levels of LDL ("bad") cholesterol
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Lupus
    (Powered by 23andMe 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 heart
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Migraine
    (Powered by 23andMe Research)
    Genetic likelihood of experiencing migraine headaches
    Based 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)
    Genetic likelihood for a condition where fat builds up in the liver
    Based 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)
    Genetic likelihood for a condition where breathing stops and starts repeatedly during sleep
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Panic Attacks
    (Powered by 23andMe Research)
    Genetic likelihood of experiencing episodes of intense fear that last a few minutes to an hour
    Based 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)
    Genetic likelihood for a hormone disorder that affects females
    Based 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)
    Genetic likelihood of developing persistent high blood pressure during pregnancy
    Based 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)
    Genetic likelihood of developing cancer of the prostate, a male reproductive organ
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Psoriasis
    (Powered by 23andMe Research)
    Genetic likelihood of developing an autoimmune condition that can cause itchy, discolored patches to form on the skin
    Based 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)
    Genetic likelihood for a condition characterized by an uncontrollable urge to move one's legs
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Rosacea
    (Powered by 23andMe Research)
    Genetic likelihood for a chronic skin condition that often causes redness or visible blood vessels in the face
    Based on a genetic model that includes customers' results for thousands of genetic markers; variants found in many ethnicities
  • Severe Acne
    (Powered by 23andMe Research)
    Genetic likelihood for a skin condition characterized by many deep and painful types of pimples along with many whiteheads and blackheads
    Based 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)
    Genetic likelihood of developing the two most common types of skin cancer
    Based 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 descent
  • Skin Cancer (Melanoma)
    (Powered by 23andMe Research)
    Genetic likelihood of developing a common type of skin cancer
    Based 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 descent
  • Triglycerides
    (Powered by 23andMe 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)
    Genetic likelihood for a common type of non-cancerous growth in the uterus
    Based 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)
    Genetic 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 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
  • BRCA1/BRCA2 (Selected Variants)
    Genetic risk based on a limited set of variants for breast, ovarian, prostate and pancreatic cancer
    44 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 Disease
    Genetic risk for gluten-related autoimmune disorder
    2 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 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, Brazilian, 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 impairment
    2 variants in the LRRK2 and GBA genes; relevant for European, Ashkenazi Jewish, North African Berber descent
Carrier Status Reports*
45+ 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
  • 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
  • Severe Junctional Epidermolysis Bullosa (LAMB3-Related)
    3 variants in the LAMB3 gene
  • 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

Wellness Reports
10+ reports
  • Cat Allergy
  • Dog Allergy
  • Nearsightedness
  • Seasonal Allergies
  • Alcohol Flush Reaction
  • Caffeine Consumption
  • Deep Sleep
  • Genetic Weight
  • Lactose Intolerance
  • Muscle Composition
  • Saturated Fat and Weight
  • Sleep Movement
Pharmacogenetic Reports**
3 reports
  • CYP2C19 Drug Metabolism*
    DNA variants that influence how the body processes certain medications for depression, acid reflux, heart disease and other conditions
    3 variants in the CYP2C19 gene; variant found and studied in many ethnicities. Example medications: citalopram, omeprazole, clopidogrel
    • Citalopram Medication Insight
      Medication Insight about how DNA variants may affect citalopram, a medication used to treat depression
    • Clopidogrel Medication Insight
      Medication Insight about how DNA variants may affect clopidogrel, a medication used to reduce the risk for heart attack and stroke
  • DPYD Drug Metabolism*
    DNA variants that influence how the body processes certain cancer medications
    2 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 medications
    1 variant in the SLCO1B1 gene; variant found and studied in many ethnicities
    • Simvastatin Medication Insight
      Medication 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

Let’s learn more together.

Add to cartImportant test info

Frequently Asked Questions

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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.
How much does it cost to join 23andMe+ Premium?
A 23andMeplus Premium membership costs original price: $298 sale price: $229 for new customers (original price: $229 sale price: $160 for kit plus $69 for membership). Existing Ancestry Service customers can upgrade here. Existing Health + Ancestry customers can upgrade here. Membership for new and existing customers renews automatically at $69peryr.
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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 Premium, which is our annual membership service that offers exclusive access to new premium reports and features throughout the year.