myDNA Pharmacogenomic Test
Fast-track healthcare goals and enable personalization for every patient with pharmacogenomic-guided prescribing.
Clinic Sign-inPay My BillFast-track healthcare goals and enable personalization for every patient with pharmacogenomic-guided prescribing.
Clinic Sign-inWhat is a
Pharmacogenomic Test?
Pharmacogenomics (PGx) is the study of how genetic variations influence the way an individual responds to medications.
PGx is now enabling doctors to test for specific genetic changes to predict whether a patient may have a normal response, a poor response, or a higher risk of side effects before prescribing a specific medication.
Tests We Offer
We offer two PGX Tests:
PGX Testing Benefits
May help reduce the risk of experiencing medication side effects.
By testing certain genetic markers, the risk of possible side effects may be predicted even prior to starting the medication. This can help personalize dosage and choice of medication.
May reduce some of the guesswork around medication selection.
PGx testing may help to reduce some of the "trial and error" that can be involved in prescribing medications. The myDNA test provides you with information that can further assist in prescribing an effective medication sooner, potentially saving you and your patient time and money.
Results last a lifetime.
The test results presented in the report will assist you and your patient, now and in the future, to decide if one of the covered medications is right for your patient.
myDNA Psychotropic PGX Test
The myDNA Psychotropic Test is a PGx test that analyzes how certain genetic variations may affect the response to a range of psychotropic medications used in the treatment of depression, anxiety, ADHD, and other mental health conditions.
Our PGx reports are simple and easy for you to follow and share with your patient. All PGx reports include detailed interpretations and recommendations with references to international PGx guidelines for each gene-drug pair, including suggestions of how to adjust dosages, and where appropriate, to select an alternative medication.
Request Sample ReportMedications Covered
The following is a list of medications with pharmacogenomic associations that are included in the myDNA psychotropic medication PGx report.
Non-italicized medications – Clinical recommendations from evidence-based guidelines (e.g. CPIC, DPWG) and/or regulatory bodies (e.g. FDA) are provided where relevant.
Italicized medications – pharmacogenomic results have limited impact on these medications based on the current evidence-based guidelines.
Genes Covered
The myDNA Psychotropic test covers a broad range of genes which covers up to 14 genes relevant for psychotropic medications.
myDNA Multiple Category Test
The myDNA Multiple Category Test is a PGx test that analyzes how certain genetic variations may affect the response to a range of medications used in various medical specialities such as psychiatry, cardiology, gastroenterology, and pain medicine.
Our PGx reports are simple and easy for you to follow and share with your patient. All PGx reports include detailed interpretations and recommendations with references to international PGx guidelines for each gene-drug pair, including suggestions of how to adjust dosages, and where appropriate, to select an alternative medication.
Request Sample ReportMedication Categories
The main medical categories that are covered are highlighted below; however, insights into other medications are also included with the Multiple Category test.
Medications Covered
The following is a list of medications with pharmacogenomic associations that are included in the myDNA Multiple Category Medication PGx report.
Inquire about Pharmacogenomic Services Online
Are you interested providing the myDNA Psychotropic PGx test to your patients? Submit your information below and we will contact you to help you get started.
Please note: the myDNA PGx test must be ordered by a registered clinician. If you are a patient/caregiver interested in testing, please contact your clinician. Our clinician registration process is simple, quick, and easy.