ABCB1, ABCG2, ADRA2A, ADRB2, ANKK1, APOE, C11orf65, COMT, CYP1A2, CYP2B6, CYP2C, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4, CYP3A5, CYP4F2, DPYD, DRD2, EPHX1, F2, F5, GRIK4, HTR1A, HTR2A, HTR2C, ITGB3, MTHFR, NUDT15, OPRM1, SLC6A2, SLCO1B1, TPMT, UGT2B15, VKORC1
Molecular PGx’s Oncology Pharmacogenetics Gene Variation Panel offers critical genetic information for patients undergoing cancer treatment with medications including: Avatrombopag, belinostat, capecitabine, eltrombopag, erdafitinib, fluorouracil, fluorouracil topical, gefitinib, irinotecan, mercaptopurine, nilotinib, pazopanib, Sacituzumab govitecan-hziy, tamoxifen, thioguanine
CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4, CYP3A5, DPYD, MTHFR, NUDT15, TPMT
The Cardio Pharmacogenetics Gene Variation Panel by MolecularPGx furnishes genetic findings to enhance treatment for cardiovascular conditions by identifying the most suitable medication for your needs. Common medications covered include: atorvastatin, carvedilol, clopidogrel, Fluvastatin, hydralazine, lovastatin, pitavastatin, pravastatin, propafenone, rosuvastatin, simvastatin, warfarin
ABCB1, ABCG2, APOE, CYP2C, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4, CYP3A5, CYP4F2, F2, F5, ITGB3, MTHFR, SLCO1B1, VKORC1
The Molecular PGx Pain Management Pharmacogenetics Gene Variation panel examines individual patient reactions to the most frequently prescribed pain management medications, encompassing: Carisoprodol, celecoxib, codeine, flurbiprofen, hydrocodone, ibuprofen, meloxicam, methadone, oliceridine, piroxicam, tramadol
Learn MoreCOMT, CYP1A2, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP3A4, CYP3A5, OPRM1
The Psychotropic test assesses the impact of your genetic composition on the effectiveness of medications typically prescribed for depression, anxiety, ADHD, and related mental health issues. It furnishes your clinician with insights into whether certain medications may necessitate dosage modifications, exhibit reduced efficacy, or pose a heightened risk of side effects due to your genetic profile.
The results from Molecular PGx’s Psychotropic Pharmacogenetics Gene Variation Panel provide genetic insights and treatment recommendations for a diverse range of psychotropic medications, comprising: Amitriptyline, amoxapine, aripiprazole, aripiprazole lauroxil, atomoxetine, brexpiprazole, citalopram, clomipramine, clozapine, desipramine, diazepam, doxepin, duloxetine, escitalopram, fluvoxamine, iloperidone, imipramine, lofexidine, nortriptyline, paroxetine, perphenazine, protriptyline, risperidone, sertraline, thioridazine, trimipramine, venlafaxine, vortioxetine
Learn MoreADRA2, ANKK1, COMT, CYP1A2, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP3A4, CYP3A5, DRD2, EPHX1, GRIK4, HTR2A, HTR2C, MTHFR, OPRM1, UGT2B15
Our Weight loss PGx panel test for variations of most common drug metabolizers, transporters, and receptors that actively participate in drug metabolism and transportation, processing broad spectrum of diabetic and weight loss drugs used for diabetes and weight loss treatment.
Glucagon-like peptide 1 receptor agonists (GLP-1-RAs) lower blood glucose through different mechanisms. They represent the antidiabetic class with the most pronounced weight reduction and have the below profound effects on visceral and ectopic fat and other organs.
HDL PGx weight loss gene variation panel can help physicians and other clinicians identify the most effective drug for each individual patient. This will not only help find which drug may be most effective before treatment starts, but also minimize the risk of adverse reactions and hospitalizations.
Weight Loss PGx results offer genetic information for patients taking some common diabetic and weight loss medications including: Ozempic, Munjaro, Wegovy, Trulicity, Byetta, Victoza, Saxenda
Learn MoreGLP-1R, DDP4, TCF7L2, CNR1, SLC5A2, CYP2C9, SLCO1B1, UGT1A9.
Genetic testing looks for changes, sometimes called mutations or variants, in your DNA. Genetic testing is useful in many areas of medicine and can change the medical care you or your family member receives. For example, genetic testing can provide a diagnosis for a genetic condition such as Fragile X or information about your risk to develop cancer.
There are many different kinds of genetic tests. Genetic tests are done using a blood or spit sample and results are usually ready in a few weeks. Because we share DNA with our family members, if you are found to have a genetic change, your family members may have the same change. Genetic counseling before and after genetic testing can help make sure that you are the right person in your family to get a genetic test, you’re getting the right genetic test, and that you understand your results.
After learning more about genetic testing, you might decide it’s not right for you. Some reasons might be that it’s not relevant to you or won’t change your medical care, it’s too expensive, and the results may make you worried or anxious.
Clinical genetic tests are different from direct-to-consumer (DTC) genetic tests, which can give some information about medical and non-medical traits. Clinical genetic tests are ordered by your doctor for a specific medical reason. DTC tests are usually purchased by healthy individuals who are interested in learning more about traits like ancestry, responses to medications, or risk for developing certain complex conditions. DTC test results can be used to make decisions about lifestyle choices or provide issues to discuss with your doctor. However, DTC tests cannot definitely determine whether or not you will get a disease and should not be used alone for decisions about your treatment or medical care.
There are many different kinds of genetic tests. There is no single genetic test that can detect all genetic conditions. The approach to genetic testing is individualized based on your medical and family history and what condition you’re being tested for.
Single gene testing. Single gene tests look for changes in only one gene. Single gene testing is done when your doctor believes you or your child have symptoms of a specific condition or syndrome. Some examples of this are Duchene muscular dystrophy or sickle cell disease. Single gene testing is also used when there is a known genetic mutation in a family.
Panel testing. A panel genetic test looks for changes in many genes in one test. Genetic testing panels are usually grouped in categories based on different kinds of medical concerns. Some examples of genetic panel tests are low muscle tone, short stature, or epilepsy. Panel genetic tests can also be grouped into genes that are all associated with higher risk of developing certain kinds of cancer, like breast or colorectal (colon) cancer.
Large-scale genetic or genomic testing. There are two different kinds of large-scale genetic tests.
A good way to think about genetic testing is as if you’re asking the DNA a question. Sometimes we don’t find an answer because we weren’t asking the right question or science just didn’t have the answer yet.