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23andMe

Full company profile

uuid000064s

Namestring
23andMe
Legal namestring
23andMe Research Institute
Websiteurl
23andme.com
Company typeenum
Private
Founded yearint
2006
Descriptiontext

23andMe is a consumer genetics and preventative health company that sells DNA testing kits and tiered subscription memberships directly to health-conscious individuals. Founded in 2006 by Anne Wojcicki, the company has built a consented genetic database of 15M+ users and operates three service tiers: Ancestry Service ($99 one-time), 23andMe+ Premium membership ($199 first year, $69/year renewal), and 23andMe+ Total Health ($499 first year, $199/year renewal), with Total Health adding clinical-grade exome sequencing and biannual blood testing through Quest Diagnostics plus genetics-trained clinician consultations.

The platform combines DNA genotyping via microarray chips (and next-generation exome sequencing on Total Health) processed in CLIA-certified and CAP-accredited labs, with proprietary technology including the GRAMPA algorithm powering Reconstructed Ancestors, Polygenic Risk Score models, and a beta AI Health Summary feature that integrates genetic, biomarker, and lifestyle data. 23andMe holds the only FDA-authorized direct-to-consumer pharmacogenetics reports (CYP2C19, DPYD, SLCO1B1) and an FDA-cleared BRCA1/BRCA2 (Selected Variants) report. The platform spans 4,500+ ancestry regions, Historical Matches linking members to ancient figures, and an expanding library of health predisposition, carrier status, and wellness reports.

The business model combines one-time kit sales with auto-renewing annual subscriptions and a B2B data-monetization stream via pharmaceutical research partnerships, most notably with GSK where over 70% of research targets now have genetic validation. The company filed for Chapter 11 bankruptcy in March 2025 following a 2023 credential-stuffing data breach that exposed 6.9M users, leading to a $50M U.S. class-action settlement, a £2.31M UK ICO fine, a California AG lawsuit, and opposition from 28 state AGs to the bankruptcy sale. Assets were acquired in July 2025 by Anne Wojcicki's nonprofit TTAM Research Institute for $305M, outbidding Regeneron's $256M offer, and the company now operates as the 23andMe Research Institute — a nonprofit medical research organization operating from a 19,000 sq ft Palo Alto office (down from 155,000 sq ft in Sunnyvale) after approximately a 40% post-IPO workforce reduction and the divestiture of the Lemonaid Health telehealth subsidiary for $10M.

Short descriptiontext

23andMe is a consumer genetics company that sells DTC DNA testing kits and tiered subscription memberships for ancestry, health predisposition, and preventative care; following 2025 bankruptcy it now operates as the nonprofit 23andMe Research Institute.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersPalo Alto, United States
HQ citystring
Palo Alto
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
consumer genetic testing, direct-to-consumer DNA testing, personal genomics services, ancestry DNA analysis, clinical-grade exome sequencing
Industry4 codes
1Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics)
CodeHLAAALADPrimaryYes
2Genetic, Cytogenetic & Prenatal Screening IVD
CodeHLAHAAAIPrimaryNo
3Clinical Biomarker Testing Services (central labs, trial enrollment/monitoring assays)
CodeHLAAAMACPrimaryNo
4Genomics & Molecular Diagnostics (Trial Support)
CodeHLAGAEADPrimaryNo
NAICS code2 codes
  • Medical Laboratories621511
  • Medical and Diagnostic Laboratories6215
SIC code2 codes
  • Services-Medical Laboratories8071
  • In Vitro & In Vivo Diagnostic Substances2835
Product category
Consumer Genetic Testing & Personal Genomics
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model4 records
1One-time Kit Sales
TypeOne Time License
Description

Upfront purchase of DNA testing kits: Ancestry Service at $99 and Total Health kit at $499. Includes initial genotyping and exome sequencing.

23andme.com
2Annual Membership Subscriptions
TypeSubscription Recurring
Description

Recurring annual subscriptions: 23andMe+ Premium renews at $69/year and Total Health renews at $199/year, providing ongoing access to new reports and features added throughout the year.

23andme.com
3Data Monetization / Research Partnerships
TypeData Monetisation
Description

Revenue from licensed use of large consented genetic database for pharmaceutical drug discovery (e.g., GSK data alliance, Regeneron acquisition). Data contributed by research participants used to advance drug targets.

klover.ai
4Healthcare Services & Telehealth
TypeProfessional Services
Description

Biannual blood testing via Quest Diagnostics plus clinician consultations and unlimited messaging for Total Health members, providing genetics-informed preventive care services.

23andme.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels5 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Technology or R&D, Marketing or Sales, Operations, Infrastructure, Supply Chain
Pricing details3 tiers
1Ancestry Service - Basic ancestry breakdown with 4,500+ regions
ModelOne time/ perpetual licenseBilling cadenceAnnual
Notes

$99 one-time. Includes 4,500+ geographic regions, automatic Family Tree Builder, 30+ Trait reports, DNA Relative Finder.

23andme.com
223andMe+ Premium - Advanced Ancestry + Health membership
ModelSubscriptionBilling cadenceAnnual
Notes

$199 first year, renews at $69/year. Includes 100+ genetic insights, health predisposition reports for 45+ conditions, wellness, carrier status, pharmacogenetics reports, Health Action Plan, new reports added throughout the year.

23andme.com
323andMe+ Total Health - Ultimate Health + Advanced Ancestry
ModelSubscriptionBilling cadenceAnnual
Notes

$499 first year, renews at $199/year. Includes everything in Premium plus clinical-grade exome sequencing of 100+ genes (55+ conditions), biannual blood testing (55+ biomarkers), Biological Age tracking, dedicated virtual consultation with clinicians, unlimited messaging. Detects 200x more disease-causing variants.

23andme.com
GTM typeB2C
B2C
Offering typeServices
Services
Brand1 of 3 records shown
123andMe+ Premium™
Description

Annual membership service providing 100+ genetic health and ancestry insights, with reports powered by 23andMe Research and new features added regularly.

23andme.com
+2 more records
Core offering1 text field

23andMe sells direct-to-consumer saliva-based DNA test kits and recurring membership services that translate raw genotyping and whole-exome sequencing into consumer-facing reports covering ancestry composition, genetic health risks, carrier status, wellness, traits, and pharmacogenetics. Its higher-tier 23andMe+ Total Health membership extends the service with biannual blood testing through Quest Diagnostics, clinician telehealth consultations, and exome-sequencing reports, while a parallel business line licenses de-identified genetic and phenotypic data from consenting customers to pharmaceutical and biotech research partners.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

23andMe operates a single integrated consumer genomics platform sold through three tiered service offerings that build upon one another. The entry-level Ancestry Service ($99, one-time) provides genotyping-based ancestry breakdowns across 4,500+ regions, DNA Relatives, Family Tree, and 30+ trait reports. The mid-tier 23andMe+ Premium ($199 first year / $69 annual membership) layers in 100+ health predisposition, carrier status, FDA-authorized pharmacogenetics, and wellness reports, plus ongoing features like Historical Matches, Reconstructed Ancestors, the Health Action Plan, and the new AI Health Summary (Beta). The flagship 23andMe+ Total Health ($499 first year / $199 annual) extends the platform with clinical-grade exome sequencing covering 100+ genes across 55+ hereditary conditions, biannual blood biomarker testing (processed via Quest Diagnostics), Biological Age tracking, dedicated genetics-trained clinician consultations, and a GLP-1 Medication Response report. Supporting modules include the Pharmacogenetics Reports suite, Carrier Status Reports, Wellness Reports, and the Lung Cancer Genetics Study data platform, all backed by the 23andMe Research Institute which conducts large-scale GWAS and partners with organizations such as HealthEx, Lifebit, the Smithsonian, Harvard, and Mayo Clinic.

Product and service3 records
123andMe Ancestry Service
CategoryAncestry DNA test
Description

One-time saliva-based DNA test kit sold for approximately $99 that delivers an autosomal-DNA analysis with reports on ancestry composition (geographic breakdown), DNA Relative matching against other 23andMe customers, and basic trait reports. Targeted at individual consumers seeking family heritage and ethnicity insights.

223andMe+ Premium Membership
CategoryConsumer genomics subscription
Description

Annual membership (first-year price approximately $199, renewing at approximately $69 per year) that adds ongoing access to genetic health risk reports, carrier status reports, wellness and trait reports, and updates as new reports and features are released. Targeted at individual consumers who want continuous access to new genetic health insights.

323andMe+ Total Health Membership
CategoryIntegrated consumer genomics and preventive health membership
Description

Annual membership (first-year price approximately $499, renewing at approximately $199 per year) that extends Premium with whole-exome sequencing and exome-level reports, biannual blood-based lab testing delivered through Quest Diagnostics, clinician-led telehealth consultations, AI-powered personalized health action plans, and ongoing updates. Targeted at consumers seeking clinical-grade, longitudinal preventive-health services integrated with their genetic data.

Scale indicator10 records

Each record includes

Type, Value, Description, Source

Partnership13 partners
Strategic tierCoreTypeTechnology or IntegrationAnnounced on2026-05-20
Description

Partnership to allow users to securely link their electronic medical records to their genetic profiles. Utilizes federally recognized TEFCA framework and FHIR data standards. The integration enables 23andMe to combine real-world clinical data such as lab results, diagnoses, and prescription histories with genomic profiles to build personalized disease risk models, serving as the engine for 23andMe's AI-driven Health Summary tool.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-14
Description

Collaboration on DNA analysis of 49 colonists buried in St. Mary's City, Maryland between 1634-1730, identifying over 1.3 million living genetic relatives of the founding population. Study published in Current Biology used novel approach combining 23andMe genetic data with genealogical records to trace colonial migration patterns.

3Educators and Scientists (school genetics education initiative)
Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2026-04-03
Description

Collaborative effort between educators and scientists to develop engaging classroom activities for teaching complex genetics concepts, utilizing real-world research data from 23andMe to illustrate the influence of multiple genetic variants on traits such as height.

blog.23andme.com
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-02-17
Description

Since 2014, collaboration between UCSD researchers and 23andMe has been exploring the genetic basis of human behaviors related to substance use, resulting in numerous publications and insights. The partnership involves large-scale genetic and survey data analysis to understand addiction and behavioral health risks.

5Kael Reicin (CFO appointment)
Strategic tierCoreTypeOthersAnnounced on2025-11-05
Description

Appointed as Chief Financial Officer of 23andMe Research Institute as it transitions to a nonprofit organization. Brings extensive experience from American Cancer Society, Bloomberg LP, and Thomson Reuters.

globenewswire.com
6Privacy Advisory Board
Strategic tierCoreTypeOthersAnnounced on2025-10-30
Description

23andMe Research Institute announced formation of Privacy Advisory Board composed of experts in health data privacy, data ethics, and consumer advocacy, providing guidance on data protection, privacy regulations, and ethical technology use.

globenewswire.com
7Brad Margus and Stephen Quake
Strategic tierCoreTypeOthersAnnounced on2025-10-24
Description

Two new members appointed to 23andMe Research Institute Board of Directors. Margus brings experience in genetic research and drug development, while Quake is known for pioneering genomics technologies. Both aim to enhance the Institute's impact on human genetics and health.

globenewswire.com
Strategic tierMinorTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-09-19
Description

Acquired Lemonaid Health (23andMe's telehealth subsidiary) for $10 million in cash through stock purchase agreement completed September 10 following competitive bidding. Represents 97.5% markdown from the $400 million 23andMe paid for Lemonaid in 2021. Plans to expand Lemonaid's on-demand telehealth services and online pharmacy.

Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2025-06-14
Description

Acquisition by nonprofit TTAM Research Institute for $305 million after bankruptcy auction. Plans to continue existing privacy policies and establish a consumer privacy advisory board. Company is transitioning to a nonprofit medical research organization.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-01-01
Description

Launched the Lung Cancer Genetics Study in 2024, with the open-source data platform hosted on Lifebit's Trusted Research Environment. Study has enrolled over 1,200 participants aiming to reach 10,000 individuals diagnosed with lung cancer by 2027.

Strategic tierMajorTypeStrategic or Co-development Partner
Description

Research partnership noted among multiple genetic testing company collaborations for research and consumer wellness genomics.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Data alliance with GSK for genetics-first drug discovery, central to GSK's AI strategy. Over 70% of GSK's research targets now have genetic validation, supported by £6.4 billion R&D investment in 2024.

Strategic tierCoreTypeImplementation/ SI/ Consulting Partner
Description

Blood testing fulfillment partner for 23andMe+ Total Health tier. Quest Diagnostics completes biannual blood testing analyzing 55+ biomarkers including comprehensive metabolic panel, complete blood count, advanced lipid panel, and endocrine blood tests.

Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Ancestry's consumer DNA testing service is 23andMe's largest direct competitor in the DTC genetic genealogy space, offering autosomal DNA testing with the largest family tree database globally. It competes head-to-head on ancestry reporting and increasingly on health traits, and is the natural share donor/leader in the category.

TypeDirect peer
Description

MyHeritage offers DTC DNA testing kits with strong international reach (particularly Europe) and integrated family tree tools, competing directly with 23andMe on ancestry reporting and DNA Relative matching. It has expanded into health-related genetic reports, positioning it as a growing peer in the same niche.

TypeDirect peer
Description

FamilyTreeDNA is a pioneer in DTC genetic genealogy, offering autosomal, Y-DNA, and mtDNA testing with deep genealogist appeal. It competes with 23andMe on ancestry granularity and relative matching, particularly for serious genealogy hobbyists.

TypeDirect peer
Description

Color provides clinical-grade genetic testing accessible to consumers and employers, including hereditary cancer, cardiovascular, and pharmacogenomics panels. It competes most directly with 23andMe's Total Health tier by offering medically actionable results integrated with clinician support.

TypeEmerging player
Description

Helix operates a DNA app-store marketplace model where consumers sequence once and access multiple health and ancestry applications through partner developers. Its platform approach is an alternative consumer genomics model that overlaps with 23andMe's expanding report catalog.

TypeEmerging player
Description

Nebula Genomics offers whole-genome sequencing to consumers with a privacy-first positioning and blockchain-based data controls. It targets a similar health-conscious consumer segment as 23andMe's Premium and Total Health tiers but differentiates on depth of sequencing and data ownership.

TypeBroad incumbent
Description

Natera is a clinical genetic testing company specializing in cell-free DNA testing for reproductive health, oncology, and organ transplant monitoring. While primarily B2B, its expanding consumer-facing offerings (e.g., Empower hereditary cancer screening) overlap with 23andMe's clinical health positioning.

TypeBroad incumbent
Description

Myriad Genetics is an established clinical molecular diagnostics company known for BRACAnalysis and broader hereditary cancer testing. It competes with 23andMe's Total Health exome and pharmacogenomics reports through clinician-ordered testing channels.

TypeOthers
Description

Quest Diagnostics is both a partner (completing biannual blood biomarker testing for Total Health members) and a broader clinical laboratory incumbent. Its scale and physician relationships position it as a potential channel competitor as genetic testing moves further into mainstream clinical care.

TypeBroad incumbent
Description

Labcorp is one of the largest clinical laboratory networks in the US and acquired Invitae (a major genetic testing company) out of bankruptcy in 2024. It overlaps with 23andMe in clinical genetic and pharmacogenomic testing and represents a major scaled incumbent that could absorb DTC genetics demand.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers6 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

Integration3 records

Each record includes

Title, Type, Description, Source

AI capability11 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles14 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries2 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance4 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds14 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors30 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A2 records

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment2 records

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

23andMe

Consumer Genetic Testing & Personal Genomics23andme.com

23andMe is a consumer genetics company that sells DTC DNA testing kits and tiered subscription memberships for ancestry, health predisposition, and preventative care; following 2025 bankruptcy it now operates as the nonprofit 23andMe Research Institute.

What 23andMe does

23andMe is a consumer genetics and preventative health company that sells DNA testing kits and tiered subscription memberships directly to health-conscious individuals. Founded in 2006 by Anne Wojcicki, the company has built a consented genetic database of 15M+ users and operates three service tiers: Ancestry Service ($99 one-time), 23andMe+ Premium membership ($199 first year, $69/year renewal), and 23andMe+ Total Health ($499 first year, $199/year renewal), with Total Health adding clinical-grade exome sequencing and biannual blood testing through Quest Diagnostics plus genetics-trained clinician consultations.

The platform combines DNA genotyping via microarray chips (and next-generation exome sequencing on Total Health) processed in CLIA-certified and CAP-accredited labs, with proprietary technology including the GRAMPA algorithm powering Reconstructed Ancestors, Polygenic Risk Score models, and a beta AI Health Summary feature that integrates genetic, biomarker, and lifestyle data. 23andMe holds the only FDA-authorized direct-to-consumer pharmacogenetics reports (CYP2C19, DPYD, SLCO1B1) and an FDA-cleared BRCA1/BRCA2 (Selected Variants) report. The platform spans 4,500+ ancestry regions, Historical Matches linking members to ancient figures, and an expanding library of health predisposition, carrier status, and wellness reports.

The business model combines one-time kit sales with auto-renewing annual subscriptions and a B2B data-monetization stream via pharmaceutical research partnerships, most notably with GSK where over 70% of research targets now have genetic validation. The company filed for Chapter 11 bankruptcy in March 2025 following a 2023 credential-stuffing data breach that exposed 6.9M users, leading to a $50M U.S. class-action settlement, a £2.31M UK ICO fine, a California AG lawsuit, and opposition from 28 state AGs to the bankruptcy sale. Assets were acquired in July 2025 by Anne Wojcicki's nonprofit TTAM Research Institute for $305M, outbidding Regeneron's $256M offer, and the company now operates as the 23andMe Research Institute — a nonprofit medical research organization operating from a 19,000 sq ft Palo Alto office (down from 155,000 sq ft in Sunnyvale) after approximately a 40% post-IPO workforce reduction and the divestiture of the Lemonaid Health telehealth subsidiary for $10M.

23andMe firmographics

Firmographics
Name
23andMe
Legal name
23andMe Research Institute
Website
https://23andme.com
Company type
Private
Founded year
2006
Operating status
Acquired
Headcount range
251–500 employees
Short description
23andMe is a consumer genetics company that sells DTC DNA testing kits and tiered subscription memberships for ancestry, health predisposition, and preventative care; following 2025 bankruptcy it now operates as the nonprofit 23andMe Research Institute.
Ownership category
akta.pro rank

23andMe industry classification

Industry
Product category
Consumer Genetic Testing & Personal Genomics
NAICS
Medical Laboratories (621511), Medical and Diagnostic Laboratories (6215)
SIC
Services-Medical Laboratories (8071), In Vitro & In Vivo Diagnostic Substances (2835)
akta.pro primary industry
Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics) (HLAAALAD)
akta.pro secondary industries
Genetic, Cytogenetic & Prenatal Screening IVD (HLAHAAAI), Clinical Biomarker Testing Services (central labs, trial enrollment/monitoring assays) (HLAAAMAC), Genomics & Molecular Diagnostics (Trial Support) (HLAGAEAD)

Keywords

  • Consumer genetic testing
  • Direct-to-consumer DNA testing
  • Personal genomics services
  • Ancestry DNA analysis
  • Clinical-grade exome sequencing

Where 23andMe is headquartered

Location

Headquarters

HQ city
Palo Alto
HQ country
United States
HQ region
North America

Offices2 records

Markets served

23andMe business model

Business model
GTM type
B2C
Offering type
Services
Cost components
Personnel, Technology or R&D, Marketing or Sales, Operations, Infrastructure, Supply Chain

Revenue model

  1. One-time Kit Sales: Upfront purchase of DNA testing kits: Ancestry Service at $99 and Total Health kit at $499. Includes initial genotyping and exome sequencing.
  2. Annual Membership Subscriptions: Recurring annual subscriptions: 23andMe+ Premium renews at $69/year and Total Health renews at $199/year, providing ongoing access to new reports and features added throughout the year.
  3. Data Monetization / Research Partnerships: Revenue from licensed use of large consented genetic database for pharmaceutical drug discovery (e.g., GSK data alliance, Regeneron acquisition). Data contributed by research participants used to advance drug targets.
  4. Healthcare Services & Telehealth: Biannual blood testing via Quest Diagnostics plus clinician consultations and unlimited messaging for Total Health members, providing genetics-informed preventive care services.

Pricing tiers

ModelBillingPrice
One time/ perpetual licenseAnnualAncestry Service - Basic ancestry breakdown with 4,500+ regions
SubscriptionAnnual23andMe+ Premium - Advanced Ancestry + Health membership
SubscriptionAnnual23andMe+ Total Health - Ultimate Health + Advanced Ancestry

Go-to-market motion3 records

Distribution channels5 records

Marketing channels7 records

23andMe product offering

Product offering

Core offering

23andMe sells direct-to-consumer saliva-based DNA test kits and recurring membership services that translate raw genotyping and whole-exome sequencing into consumer-facing reports covering ancestry composition, genetic health risks, carrier status, wellness, traits, and pharmacogenetics. Its higher-tier 23andMe+ Total Health membership extends the service with biannual blood testing through Quest Diagnostics, clinician telehealth consultations, and exome-sequencing reports, while a parallel business line licenses de-identified genetic and phenotypic data from consenting customers to pharmaceutical and biotech research partners.

Product overview

23andMe operates a single integrated consumer genomics platform sold through three tiered service offerings that build upon one another. The entry-level Ancestry Service ($99, one-time) provides genotyping-based ancestry breakdowns across 4,500+ regions, DNA Relatives, Family Tree, and 30+ trait reports. The mid-tier 23andMe+ Premium ($199 first year / $69 annual membership) layers in 100+ health predisposition, carrier status, FDA-authorized pharmacogenetics, and wellness reports, plus ongoing features like Historical Matches, Reconstructed Ancestors, the Health Action Plan, and the new AI Health Summary (Beta). The flagship 23andMe+ Total Health ($499 first year / $199 annual) extends the platform with clinical-grade exome sequencing covering 100+ genes across 55+ hereditary conditions, biannual blood biomarker testing (processed via Quest Diagnostics), Biological Age tracking, dedicated genetics-trained clinician consultations, and a GLP-1 Medication Response report. Supporting modules include the Pharmacogenetics Reports suite, Carrier Status Reports, Wellness Reports, and the Lung Cancer Genetics Study data platform, all backed by the 23andMe Research Institute which conducts large-scale GWAS and partners with organizations such as HealthEx, Lifebit, the Smithsonian, Harvard, and Mayo Clinic.

Differentiator

Problem solved

Functional benefit

Brands

  • 23andMe+ Premium™: Annual membership service providing 100+ genetic health and ancestry insights, with reports powered by 23andMe Research and new features added regularly.
  • 23andMe+ Total Health™
  • Ancestry Service

Products and services

  • 23andMe Ancestry Service One-time saliva-based DNA test kit sold for approximately $99 that delivers an autosomal-DNA analysis with reports on ancestry composition (geographic breakdown), DNA Relative matching against other 23andMe customers, and basic trait reports. Targeted at individual consumers seeking family heritage and ethnicity insights.
  • 23andMe+ Premium Membership Annual membership (first-year price approximately $199, renewing at approximately $69 per year) that adds ongoing access to genetic health risk reports, carrier status reports, wellness and trait reports, and updates as new reports and features are released. Targeted at individual consumers who want continuous access to new genetic health insights.
  • 23andMe+ Total Health Membership Annual membership (first-year price approximately $499, renewing at approximately $199 per year) that extends Premium with whole-exome sequencing and exome-level reports, biannual blood-based lab testing delivered through Quest Diagnostics, clinician-led telehealth consultations, AI-powered personalized health action plans, and ongoing updates. Targeted at consumers seeking clinical-grade, longitudinal preventive-health services integrated with their genetic data.

Companies that use 23andMe

Customer profile

Named customers6 records

Segments3 records

Ideal customer profiles2 records

23andMe technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration3 records

AI capability11 records

Feature6 records

23andMe partnerships and signals

Strategic signal

Partnerships

13 partnerships are on record, tiered core, minor, flagship and major.

  • HealthExcoreTechnology or Integration · 20 May 2026Partnership to allow users to securely link their electronic medical records to their genetic profiles. Utilizes federally recognized TEFCA framework and FHIR data standards. The integration enables 23andMe to combine real-world clinical data such as lab results, diagnoses, and prescription histories with genomic profiles to build personalized disease risk models, serving as the engine for 23andMe's AI-driven Health Summary tool.
  • Harvard University and Smithsonian InstitutioncoreStrategic or Co-development Partner · 14 May 2026Collaboration on DNA analysis of 49 colonists buried in St. Mary's City, Maryland between 1634-1730, identifying over 1.3 million living genetic relatives of the founding population. Study published in Current Biology used novel approach combining 23andMe genetic data with genealogical records to trace colonial migration patterns.
  • Educators and Scientists (school genetics education initiative)minorStrategic or Co-development Partner · 3 April 2026Collaborative effort between educators and scientists to develop engaging classroom activities for teaching complex genetics concepts, utilizing real-world research data from 23andMe to illustrate the influence of multiple genetic variants on traits such as height.
  • UCSD (University of California San Diego)coreStrategic or Co-development Partner · 17 February 2026Since 2014, collaboration between UCSD researchers and 23andMe has been exploring the genetic basis of human behaviors related to substance use, resulting in numerous publications and insights. The partnership involves large-scale genetic and survey data analysis to understand addiction and behavioral health risks.
  • Kael Reicin (CFO appointment)coreOthers · 5 November 2025Appointed as Chief Financial Officer of 23andMe Research Institute as it transitions to a nonprofit organization. Brings extensive experience from American Cancer Society, Bloomberg LP, and Thomson Reuters.
  • Privacy Advisory BoardcoreOthers · 30 October 202523andMe Research Institute announced formation of Privacy Advisory Board composed of experts in health data privacy, data ethics, and consumer advocacy, providing guidance on data protection, privacy regulations, and ethical technology use.
  • Brad Margus and Stephen QuakecoreOthers · 24 October 2025Two new members appointed to 23andMe Research Institute Board of Directors. Margus brings experience in genetic research and drug development, while Quake is known for pioneering genomics technologies. Both aim to enhance the Institute's impact on human genetics and health.
  • Bambu Ventures and Innova Capital PartnersminorChannel Partner/ Reseller/ Distributor · 19 September 2025Acquired Lemonaid Health (23andMe's telehealth subsidiary) for $10 million in cash through stock purchase agreement completed September 10 following competitive bidding. Represents 97.5% markdown from the $400 million 23andMe paid for Lemonaid in 2021. Plans to expand Lemonaid's on-demand telehealth services and online pharmacy.
  • TTAM Research Institute (Anne Wojcicki's nonprofit)flagshipStrategic or Co-development Partner · 14 June 2025Acquisition by nonprofit TTAM Research Institute for $305 million after bankruptcy auction. Plans to continue existing privacy policies and establish a consumer privacy advisory board. Company is transitioning to a nonprofit medical research organization.
  • Lifebit and Troper Wojcicki PhilanthropiescoreStrategic or Co-development Partner · 1 January 2024Launched the Lung Cancer Genetics Study in 2024, with the open-source data platform hosted on Lifebit's Trusted Research Environment. Study has enrolled over 1,200 participants aiming to reach 10,000 individuals diagnosed with lung cancer by 2027.
  • Mayo ClinicmajorStrategic or Co-development PartnerResearch partnership noted among multiple genetic testing company collaborations for research and consumer wellness genomics.
  • GlaxoSmithKline (GSK)coreStrategic or Co-development PartnerData alliance with GSK for genetics-first drug discovery, central to GSK's AI strategy. Over 70% of GSK's research targets now have genetic validation, supported by £6.4 billion R&D investment in 2024.
  • Quest DiagnosticscoreImplementation/ SI/ Consulting PartnerBlood testing fulfillment partner for 23andMe+ Total Health tier. Quest Diagnostics completes biannual blood testing analyzing 55+ biomarkers including comprehensive metabolic panel, complete blood count, advanced lipid panel, and endocrine blood tests.

Scale indicators10 records

Recent moves9 records

Expansion highlights6 records

23andMe competitors and assessment

Company assessment

Direct peers

  • Ancestry (AncestryDNA): Ancestry's consumer DNA testing service is 23andMe's largest direct competitor in the DTC genetic genealogy space, offering autosomal DNA testing with the largest family tree database globally. It competes head-to-head on ancestry reporting and increasingly on health traits, and is the natural share donor/leader in the category.
  • MyHeritage DNA: MyHeritage offers DTC DNA testing kits with strong international reach (particularly Europe) and integrated family tree tools, competing directly with 23andMe on ancestry reporting and DNA Relative matching. It has expanded into health-related genetic reports, positioning it as a growing peer in the same niche.
  • FamilyTreeDNA (Gene by Gene): FamilyTreeDNA is a pioneer in DTC genetic genealogy, offering autosomal, Y-DNA, and mtDNA testing with deep genealogist appeal. It competes with 23andMe on ancestry granularity and relative matching, particularly for serious genealogy hobbyists.
  • Color: Color provides clinical-grade genetic testing accessible to consumers and employers, including hereditary cancer, cardiovascular, and pharmacogenomics panels. It competes most directly with 23andMe's Total Health tier by offering medically actionable results integrated with clinician support.

Emerging players

  • Helix: Helix operates a DNA app-store marketplace model where consumers sequence once and access multiple health and ancestry applications through partner developers. Its platform approach is an alternative consumer genomics model that overlaps with 23andMe's expanding report catalog.
  • Nebula Genomics: Nebula Genomics offers whole-genome sequencing to consumers with a privacy-first positioning and blockchain-based data controls. It targets a similar health-conscious consumer segment as 23andMe's Premium and Total Health tiers but differentiates on depth of sequencing and data ownership.

Broad incumbents

  • Natera: Natera is a clinical genetic testing company specializing in cell-free DNA testing for reproductive health, oncology, and organ transplant monitoring. While primarily B2B, its expanding consumer-facing offerings (e.g., Empower hereditary cancer screening) overlap with 23andMe's clinical health positioning.
  • Myriad Genetics: Myriad Genetics is an established clinical molecular diagnostics company known for BRACAnalysis and broader hereditary cancer testing. It competes with 23andMe's Total Health exome and pharmacogenomics reports through clinician-ordered testing channels.
  • Laboratory Corporation of America (Labcorp): Labcorp is one of the largest clinical laboratory networks in the US and acquired Invitae (a major genetic testing company) out of bankruptcy in 2024. It overlaps with 23andMe in clinical genetic and pharmacogenomic testing and represents a major scaled incumbent that could absorb DTC genetics demand.

Others

  • Quest Diagnostics: Quest Diagnostics is both a partner (completing biannual blood biomarker testing for Total Health members) and a broader clinical laboratory incumbent. Its scale and physician relationships position it as a potential channel competitor as genetic testing moves further into mainstream clinical care.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks7 records

Key highlights7 records

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23andMe social profiles

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23andMe compliance and trust

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Compliance4 records

23andMe financial estimates

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23andMe leadership team

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Profiles14 records

23andMe subsidiaries and ownership

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Subsidiaries2 records

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Investors30 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

23andMe M&A and investment

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M&A2 records

Investments2 records

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Frequently asked questions about 23andMe

What does 23andMe do?

23andMe sells direct-to-consumer saliva-based DNA test kits and recurring membership services that translate raw genotyping and whole-exome sequencing into consumer-facing reports covering ancestry composition, genetic health risks, carrier status, wellness, traits, and pharmacogenetics. Its higher-tier 23andMe+ Total Health membership extends the service with biannual blood testing through Quest Diagnostics, clinician telehealth consultations, and exome-sequencing reports, while a parallel business line licenses de-identified genetic and phenotypic data from consenting customers to pharmaceutical and biotech research partners.

Is 23andMe a public or private company?

23andMe is a private company. It is classified as nonprofit foundation owned and is currently acquired.

When was 23andMe founded?

23andMe was founded in 2006. It employs 251 to 500 people.

Where is 23andMe based?

23andMe is headquartered in Palo Alto, United States, in the North America region.

How does 23andMe make money?

Four revenue lines are on record. One-time Kit Sales are the primary driver. The others are annual Membership Subscriptions, data Monetization / Research Partnerships and healthcare Services & Telehealth.

Who are 23andMe's main competitors?

Direct peers on record are Ancestry (AncestryDNA), MyHeritage DNA, FamilyTreeDNA (Gene by Gene) and Color. Emerging players are Helix and Nebula Genomics. Broad incumbents are Natera, Myriad Genetics and Laboratory Corporation of America (Labcorp). Quest Diagnostics is listed as an others.

Does 23andMe have an API?

No public API is recorded for 23andMe.

What industry is 23andMe in?

23andMe's product category is Consumer Genetic Testing & Personal Genomics. Its primary akta.pro industry code is HLAAALAD, Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics), with a secondary code of HLAHAAAI, Genetic, Cytogenetic & Prenatal Screening IVD. Its NAICS code is 621511 and its SIC code is 8071.

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Live signals
The Times of IndiaSt. Louis man Michael Goessling was adopted nearly 60 years ago; after an unknown half-brother took a 23andMe test, he learned five-time Grammy winner Michael McDonald was his biological fatherMichael Goessling, adopted nearly 60 years ago, learned via a half-brother's 23andMe test that Michael McDonald is his biological father. He met his birth mother on his 58th birthday and later spoke with McDonald, who confirmed his identity. The reunion also revealed McDonald had grandchildren.WikipediaWikipedia23andMe filed for Chapter 11 bankruptcy in March 2025, and CEO Anne Wojcicki resigned. TTAM Research Institute acquired the company's assets for $305 million, completing the purchase on July 14, 2025. The company had genotyped over 14 million individuals as of February 2024.StartupiSua startup está construindo marca ou só gerando conteúdo com IA?The article examines whether startups use AI to build brand or merely generate content, citing Pangram's $9M raise and DoubleVerify's detection of over 500 million AI-slop impressions. It uses 23andMe's 2023 data breach and subsequent Chapter 11 filing as a case study, and advises startups to align AI tools with their brand promise.STATWhy do ‘never smokers’ get lung cancer? In some cases, rare genetic variant may be a factorResearchers identified a rare genetic variant associated with 25-fold higher odds of lung cancer in never-smokers, reported in Science. The variant is more common in Southern Appalachia, and experts say it likely plays a role in only a small portion of never-smoker lung cancer cases. The study highlights the value of large genetic datasets like 23andMe.Sequoia Capital23andMe: How the DNA Pioneer Took On the FDA and Redefined Health Tech23andMe's founder Anne Wojcicki led the company through an FDA order to stop selling health tests, complying over two years to become the only FDA-approved direct-to-consumer genetic testing company. The company later pivoted into drug discovery and adapted to flatlining sales by introducing a subscription model and telehealth.Psychiatric TimesWeighing the Benefits of Genetic Information in Clinical PsychiatryThe article examines the growing adoption of pharmacogenomic testing by psychiatrists to guide medication selection for treatment-resistant patients, highlighting services from Genomind and GeneSight. It presents a debate between clinicians who find the data useful for understanding drug metabolism and geneticists who caution that clinical evidence for many tested genes remains underwhelming or unproven. The piece also addresses the rise of direct-to-consumer genetic testing platforms like 23andMe and their regulatory history.MedicalEconomicsWho profits from our medical records?The article details how hospitals and health networks currently strip identifiers from medical records to sell them to aggregators like Truven Health Analytics, which then license the data to pharmaceutical and insurance companies. It contrasts this with genetic databases such as 23andMe and Ancestry.com, while highlighting emerging regulatory pressures from Europe and California that may shift ownership models toward patients.Villanova University23andMe’s Bankruptcy Exposes Fragility of How Genetic Data is Utilized Beyond Fee-For-Service, Says Villanova Law Professor23andMe's 2025 bankruptcy is an inflection point for how genetic data is used beyond fee-for-service, according to a Villanova law professor. The professor argues that data-use policies depend on individual companies, and bankruptcy could allow new ownership to change those policies. The case highlights the need for public awareness of secondary data uses.GlobeNewswireNew 23andMe Research Institute Study First to Identify Association Between Specific Side Effects from Common Antidepressants and GeneticsA 23andMe Research Institute study of over 114,000 participants linked CYP2C19 genetic variants to specific side effects from SSRIs like escitalopram, citalopram, and sertraline. Slower metabolizers had higher risks of sleep, sexual, and tremor issues, and were more likely to discontinue medication. The findings suggest genetics can inform SSRI treatment choices.FinancialContent Business PageNew 23andMe Research Institute Study First to Identify Association Between Specific Side Effects from Common Antidepressants and Genetics23andMe Research Institute published a study in The Pharmacogenomics Journal demonstrating that genetic variation in the CYP2C19 gene is associated with specific side effects from common SSRI antidepressants including escitalopram, citalopram, and sertraline. The research examined more than 114,000 individuals and found that slower CYP2C19 metabolizers face significantly increased risks of side effects such as tremors, sleep issues, and sexual dysfunction, and are more likely to discontinue medication due to these effects. The findings highlight how genetic ancestry impacts drug metabolism, with approximately 17.8% of East Asian-ancestry participants being poor metabolizers compared to about 2.3% of European-ancestry participants.