Pharmacogenetic (PGx) Testing
Flexible Reporting Options for Tailored Treatment Planning
Choose the report that best fits your clinical needs. Each report offers a unique view of patient genetic data to support informed decision-making.Express Report
A concise summary of medications to avoid, along with suggested alternatives, based on the patient’s unique gene-drug interaction profile and published PGx guidelines.
Best for: Quick reference and treatment adjustments.
NeuroPsych Report
A comprehensive report with five sections analyzing 26 genes, offering insights into 130+ neuropsychiatric medications.
Best for: Detailed psychiatric treatment planning.
Diagnosis Report
Visual representations of genetic results organized by clinical diagnosis, designed for fast interpretation when time is limited.
Best for: Fast, diagnosis-specific genetic insights.
Patient Report
A simplified report designed for patients, offering an easy-to-understand summary of genetic insights and medication recommendations to discuss with their healthcare provider.
Best for: Educating patients about their genetic results.
Genetic information should be essential when prescribing
Gain a better understanding of the patient’s unique genetic profile to reduce the painful process of trial and error and interaction risk.
270+
medications contain FDA warnings, dosage recommendations or drug-drug interaction guidance based on specific gene variants.9
95%
- Food and Drug Administration
Personalize medication plans with ease
We make it easy for you and your patient to assess these critical
treatment insights without compromising accuracy or depth of information.
Access comprehensive genetic insights
with 15 PD genes, 11 PK genes to
assess over 700 medications
Enjoy fast, easy, and accurate processing. Painless cheek swab collection, results in 3-5 days or less with a 99.9% laboratory accuracy
Seamlessly incorporate into your
care model with collection options
for your office or directly to your
patient’s home
Offer payment options that work for
your patients. HSA/FSA eligible,
flexible payment plans, and financial
assistance available
How it works
Ordering, tracking, and status updates related to your testing results can be easily accessed by logging on to our Precision Health Platform after you register with Genomind.
Built on the most up-to-date clinical evidence
As science evolves, so do we. Learn about the evidence the report
was built on and our commitment to staying current.
PGx is the future of medicine. I use it to bring precision to my prescribing. Now, I can more accurately predict adverse drug events, even outside of my specialty. This process builds better relationships with patients and other providers.
Jennifer Reed, FNP-BC, PMHNP-BC
Private Practice Owner, Board Certified in Family Practice and Psychiatric Mental Health
