23andMe Research Institute
Genomic engine designed for scale, patient understanding, and clinical action
Platform · Cloud SaaSCompany source
Company profile
About 23andMe
23andMe uses AI to analyze genetic data and provide personalized health summaries, risk assessments, and wellness recommendations based on genomic insights.
Company description 23andMe official website
Primary marketPrecision Medicine & Genomics
Commercial modelCommercial information available on request
Company presenceOfficial website
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01 · Operating footprint
Where the Company operates
Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.
Clinical focus
- 55+ common chronic diseases and high-impact conditions
- Alzheimer's disease
- asthma
- cancer
- diabetes
- heart health
- lupus
- mental health
- Parkinson's disease
Who it serves
- clinical practices
- consumers
- health systems
- healthcare professionals
- research institutions
Deployment & integration
Cloud Saas · Hybrid deployment with recorded integration context.
Geographic context
MarketsUnited States · worldwide
Company sourceOfficial website
Company milestones
Platform expansion
Launch of 23andMe Total Health platform with exome sequencing and biannual blood testing, 23andMe Research Institute for healthcare partnerships, TIME Best Inventions 2025 recognition
Partnerships
Recorded partners
- Alnylam Pharmaceuticals
- Biogen
- Broad Institute of MIT and Harvard
- Genentech
- GlaxoSmithKline (GSK)
- Lupus Research Institute
- MRC Epidemiology Unit at Cambridge University
- National Parkinson Foundation
- P&G Beauty
- Parkinson's Institute and Clinical Center
- Pfizer
- Stanford University
- The Michael J. Fox Foundation
- University of Chicago
02 · Flagship portfolio
Products, workflows, and platform capabilities
Selected source-backed Company products and the available commercial context.
23andMe+ Premium
Membership fueled by discovery, sharpened by time with 100+ genetic insights and action tools
Platform · Cloud SaaSCompany source
23andMe+ Total Health
Next gen longevity platform with exome sequencing, biannual blood testing and genetics-informed clinical care
Platform · HybridCompany source
Ancestry Service
The most comprehensive ancestry breakdown on the market
Service · Cloud SaaSCompany source
03 · Research intelligence
Research Intelligence evidence
Publications, preprints, clinical validation, and regulatory records in Evidence Position order.
Evidence position
Publications, clinical validation, and regulatory records connected to this Company appear here.
Research
Publications & preprints
Preparing primary care professionals for genomics-informed healthcare.Trends in genetics : TIG · Sep 28, 2026
Germline EGFR T790M mutation and lung cancer risk.Science (New York, N.Y.) · Sep 17, 2026
A Phenotype Risk Score-Triggered E-Visit Pathway to Capture TTR V142I in a Heart Failure Population.JACC. Case reports · Sep 16, 2026
Large-scale analysis demonstrates the influence of CYP2C19 genotype on specific SSRI side effects.The pharmacogenomics journal · Aug 5, 2026
Factors Facilitating Adoption of Pharmacogenetic Testing by Prescribers of Antidepressants in Four US Health Systems: A Multi-Site Cross-Sectional PGx Implementation Science Study.Journal of personalized medicine · Jul 30, 2026
Prediction of alcohol consumption: The role of genetics, impulsivity, and sensation seeking from adolescence to adulthood.Drug and alcohol dependence · Jul 29, 2026
Clinical validation
Clinical-trial records
No linked records are currently available.
Regulatory
Regulatory records
23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary ThrombophiliaDEN160026 · De Novo · Apr 6, 2017
04 · Company-reported outcomes
Outcomes and case studies
Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.
1 in 11 patients received medically actionable hereditary disease sequencing result
directly changing care plan
82% of patients with highly actionable risks had no prior awareness
before testing
88% adherence to medical recommendations
given to address genetic results
Clinical Practice (unnamed)
Comprehensive genomic risk assessment and patient screening
1 in 11 patients received medically actionable hereditary disease sequencing result directly changing care plan; 82% of patients with highly actionable risks had no prior awareness; 88% adherence to medical recommendations
05 · Leadership
Leadership team
Leadership profiles and professional links from the current Company record.
No active leadership profiles are currently listed.
06 · Company updates
Updates from 23andMe
Recent articles published on 23andMe's official website.
1,000 Historical Matches and Counting: Celebrating International Archaeology Day
Read on 23andMe23andMe Research Institute Attending ASHG 2026
Read on 23andMeIs Your Doctor Ready for Your Genetic Test Results?
Read on 23andMeUnderstanding Genetic Breast Cancer Risk: BRCA and Beyond
Read on 23andMe23andMe Reaches 5,000 Ancestry Regions With 163 New Genetic Groups Across North Africa, Egypt and the Arabian Peninsula
Read on 23andMe07 · HAIC coverage
Coverage and analysis
Health AI Central reporting that mentions this Company.
Why Security Experts Are Sounding the Alarm on OpenAI's New Medical Records Feature
ChatGPT Health bypasses federal privacy protections that safeguard patient data at hospitals and clinics, creating what cybersecurity researchers call a dangerous new target for hackers.
Policy & Regulation · Oct 4, 2026
AI Decoded a Human Genome in 30 Minutes for $5—But Who's Checking the Answers?
A researcher's experiment with Claude AI replicated a year-long genomic analysis in half an hour, exposing the urgent need for quality standards as consumer genome interpretation goes mainstream.
Clinical AI · Oct 3, 2026
When Wall Street Meets the Cancer Ward: Prediction Markets Now Let Traders Bet on Whether Your Clinical Trial Will Succeed
Kalshi and Polymarket face mounting criticism from patients and bioethicists as platforms open betting markets on experimental drug trials and FDA approvals, raising fears of manipulation and exploitation.
Policy & Regulation · Aug 8, 2026
The Privacy Gamble Millions Are Taking With Their Medical Records and AI Chatbots
As one in three Americans consult AI for health advice and upload personal medical data, experts warn of accuracy failures in emergencies and inadequate legal protections against breaches.
Policy & Regulation · Jul 31, 2026
South Carolina's 50,000-Person Genetic Screening Initiative Reveals How Population Genomics Can Achieve Health Equity at Scale
The \"In Our DNA SC\" program has enrolled participants across all 46 counties with equal reach in rural and urban areas, identifying treatable inherited disease risks in approximately 1 in 60 adults.
Health Equity & Access · Jul 18, 2026
08 · Official presence
Company sources and channels
Curated official destinations from the active Company record.
09 · Market pathway
Additional Companies in this Market
Other active Companies in the same market, selected alphabetically from the HAIC directory.
Market context
Precision Medicine & Genomics
Companies using AI to analyze genomic, proteomic, metabolomic, or multi-omics data to provide personalized treatment recommendations, identify genetic risks, or develop targeted therapies. Includes genomic sequencing platforms with AI analysis, preventive medicine based on genetic risk assessment, and longevity care based on molecular and genetic data.
Explore the full market directory or compare this Company with additional active profiles.
View all Companies in this market
10 · Pro research
Coming soon
Expanded Company research is in development.
Health AI Central Pro · Coming Soon
Deeper Company research is coming soon.
Pro Research will introduce expanded technical context, linked evidence analysis, and comparative Company research.
Linked research, clinical, and regulatory source pathways.
Expanded product, deployment, integration, and partnership research.
Record-level provenance and review context.