VANTA DIAGNOSTICS™ is a market leader in providing targeted, molecular diagnostics that can improve clinical and economic outcomes.
Personalizing therapy through pharmacogenetic insight.
Pharmacogenetic (PGx) testing helps providers understand how a patient’s genetic makeup may influence their response to medications, enabling more personalized treatment decisions.
Using a simple, one-time buccal swab, our testing analyzes key genetic variants involved in drug metabolism to help guide therapy across a wide range of clinical conditions, including behavioral health, cardiovascular disease, and pain management.
By identifying potential medication risks and opportunities before treatment begins, PGx testing supports more informed prescribing and improved patient outcomes.
Flexible Reporting Options
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 guidance.
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 report designed for patients, offering an easy-to-understand summary of genetic insights and medication recommendations to discuss with their provider.
Best for: Educating patients about their genetic results.
Why Pharmacogenetics?
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.
95%
of clinicians report they can now make safer, more informed treatment decisions with a higher level of confidence.
Pharmacogenomics can play an important role in identifying responders and non-responders to medications, avoiding adverse events, and optimizing drug dose.
U.S. 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 portal after you register.
Order
A test kit is delivered to your office or patient’s home.
Swab
Collect a simple cheek swab sample from patient.
Return
Send sample in prepaid envelope or schedule pickup.
Test
Results available online in 3-5 business days or less.