ActX Genomic Service
Overview
ActX offers real-time genomic decision support integrated into Electronic Health Records (EHRs), fulfilling the promise of widespread personalized medical care based on genetics. It removes the “last mile” barrier that has prevented effective medical use of an individual’s genetics by making genetics an integral part of medical care.
The service automatically checks all prescriptions for efficacy, adverse reactions, and dosing based on the patient’s genetics. It provides a customizable, EHR-integrated, real-time genomic decision solution that can be live in a matter of weeks for health systems.
For providers, ActX offers a practical way to add precision medicine to their practice, including real-time pharmacogenomics, without impacting workflow. Individuals can also learn how their DNA makes them unique and use that information to help their doctor make better decisions about their care. ActX can also provide a professional medical analysis of 23andMe data, adding genetics into the medical chart for comprehensive coverage on medications, risks, and carrier conditions.
Reviewed by Pouyan Golshani, MD — Interventional Radiologist
Key Features
- EHR Integrated Genomic Decision Support
- Real-time Pharmacogenomics (medication-genome interactions)
- Automated prescription checking for efficacy, adverse reactions, and dosing
- Customizable solution for health systems
- Integration and professional medical analysis of 23andMe data
- Identification of actionable hereditary risks (e.g., cancer, cardiovascular, metabolic)
- Carrier status reporting
- Continuously updated, evidence-based knowledge base
- Patient mobile app for accessing and sharing genomic profile
- Saliva-based DNA testing via CLIA-certified lab
Use Cases
- Personalized prescription management and optimization
- Proactive identification and management of hereditary disease risks
- Integration of genetic data into routine clinical workflow for providers
- Enhancing precision medicine initiatives for health systems
- Professional interpretation of direct-to-consumer genetic data (e.g., 23andMe)
- Patient engagement and education on genetic health
What Physicians Need to Know
ActX empowers you to seamlessly integrate actionable genomic insights into your daily practice. Leverage the real-time alerts within your EHR for medication prescribing to optimize drug efficacy and avoid adverse reactions. Proactively identify and manage serious hereditary risks and carrier statuses to enable earlier interventions and personalized prevention strategies. Remember that ActX focuses on evidence-based, actionable risks, providing management suggestions and references to support your clinical decisions without requiring you to be a genetics expert. For serious non-medication risks, confirmatory testing by a genetics specialist is recommended.
ActX's strength lies in its deep and real-time integration with a wide array of leading EHR systems, including Epic, Oracle Health (Cerner), athenahealth, and Greenway Health. This allows for automated checking of prescriptions against a patient's genetic profile and direct alerts for actionable genomic risks within your existing clinical workflow. The platform is designed for rapid implementation and can utilize existing patient genomic data or facilitate new saliva-based testing.
Details
| Category | Pharmacology & Dosing AI |
| Pricing |
Contact for pricing
|
| Deployment | EHR integrated (e.g., Epic, Oracle Health, eClinicalWorks), accessible via secure website and mobile app. |
| Compliance | |
| BAA Available | Unknown AI-estimated |
| HIPAA Compliant | Unknown AI-estimated |
| FDA Status |
Not applicable AI-estimated ActX is a CAP (College of American Pathologists) accredited Laboratory. Because a physician authorizes the service, FDA approval is not required for its broader interpretation in the U.S. |
| Integrations | |
| EHR | Not specified |
| Specialties | Cardiology, Internal Medicine, Oncology |
What the Web Says
ActX Genomic Service integrates actionable genomic insights directly into a clinician's workflow, providing real-time decision support for personalized medicine. It helps physicians tailor treatments, predict medication reactions, and identify hereditary risks based on a patient's genetic profile. The service is designed for busy clinicians and aims to make genomics a practical part of everyday medical care.
Overall: PositiveStrengths
- Seamless integration with various Electronic Health Records (EHRs) like Epic, athenahealth, Oracle Health (Cerner EHR), Greenway PrimeSUITE, and Veradigm.
- Provides real-time genomic decision support for medication efficacy, dosing, and potential adverse effects.
- Identifies actionable genetic risks for conditions like hereditary cancers and cardiovascular diseases, allowing for early intervention.
- Continuously updates its knowledge base with the latest medical research and reanalyzes patient data, alerting physicians and patients to new findings.
- Offers affordable saliva-based genetic testing and can also analyze raw data from 23andMe.
- Results are accessible to both physicians (through EHR) and patients (via a secure website or mobile app).
Limitations
- Public information on the cost of the service is not readily available, as it's typically billed through insurance.
- Some users have reported negative experiences with customer service and long waiting times for results.
- Patients must be affiliated with a doctor to utilize the service.
- The service is a screening tool and not intended for the diagnosis of high-risk patients, focusing only on selected genetic variants.
Based on reviews from: Nebula Genomics, ActX (works within Epic), athenahealth | athenaConnect, CompuGroup Medical (CGM), ActX (Personalize medical care using genetics), ActX (works within Oracle Health), Greenway Health, DNA Testing Choice, App Store (My ActX Genomic Profile), ActX (Patient Stories), ActX (Personalize medical care using genetics), Altera App Expo, ActX (23andme), DNA Testing Choice (ActX Health Testing Reviews)
Last updated: 2026-08-08
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Press & Coverage
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Product demos, reviews, and walkthroughs for ActX Genomic Service.
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ACT Genomics
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