Pharmacogenomic (PGx) testing analyzes a patient’s DNA and provides insights to help providers make informed prescribing decisions for that patient. The RightMed Test is a PGx test that offers comprehensive coverage backed by rigorous curation of high-level, scientific evidence to give providers and their patients confidence in test results.
The RightMed Test covers 27 genes that may impact how a patient responds to certain medications used to treat varied medical conditions.
The RightMed Test’s gene coverage has been selectively curated by a group of pharmacists and scientists using OneOme’s rigorous standards for pharmacogenomic evidence. Each sample is analyzed at OneOme’s CLIA-certified, CAP-accredited in-house laboratory.
RightMed Test results are presented in the form of PDF reports.
RightMed Comprehensive Report
Available to the ordering provider, this report includes the patient’s genetic results plus 100+ medications classified according to the patient’s genotypes.
RightMed Gene Report
Available to the ordering provider and the patient, this report includes the patient’s genetic results.
The RightMed Test offers valuable insights for providers who care for patients with a variety of health conditions and needs.
These include (but aren't limited to):
Oncology supportive care
Acute or chronic pain
The test analyzes more than 100 alleles in 27 genes
|CYP1A2||*1C, *1D, *1E, *1F, *1J, *1K, *1L, *1V, *1W|
|CYP2B6||*4, *5, *6, *7, *9, *16, *18|
|CYP2C Cluster||G/A (rs12777823)|
|CYP2C9||*2, *3, *4, *5, *6, *8, *11|
|CYP2C19||*2, *3, *4, *4B, *10, *17|
|CYP2D6||*2, *2A, *3, *4, *4J, *4K, *4M, *4N, *5, *6, *6C, *7, *8, *9, *10, *11, *12, *13, *14, *15, *17, *18, *19, *29, *31, *34, *35, *36, *39, *41, *42, *59, *61, *63, *64, *65, *68, *69, *70, *91, *109, *114, copy number variations|
|CYP3A5||*3, *6, *7|
|DPYD||*2A, Asp949Val, *13|
|F5||Arg534Gln (Leiden, 1691G>A)|
|GRIK4||Intronic T>C Variant (rs1954787)|
|HLA-B||HLA-B*15:02, HLA-B*57:01, HLA-B*58:01|
|HTR2A||Intron 2, T>C Variant (rs7997012)|
|IL28B (IFNL4)||Intronic C>T Variant (rs12979860)|
|MTHFR*||677C>T (rs1801133); 1298A>C (rs1801131)|
|SLC6A4||-1936A>G (rs25531); -1917_-1875del43 (rs774676466)|
|SLCO1B1||*1B, *5, *15, *17, *21|
|TPMT||*2, *3A, *3B, *3C, *4|
|UGT1A1||*6, *28 (TA7)|
|VKORC1||-1639G>A (rs9923231); 442C>T (rs7200749)|
NOTE: The test does not detect all known and unknown variations in the gene(s) tested. For drug metabolizing enzyme, the absence of a detectable variant (designated as *1) does not rule out the presence of other variants not tested.
*MTHFR is available for providers to order as an optional, complimentary add-on to the RightMed Test. MTHFR is not available to patients who purchase the test online (ordered through the independent physician network).
Learn more about RightMed
For health systems
Learn more about the value of adding PGx to precision medicine programs, RightMed Solution configurations for institutions, and how to get started. Plus, get access to informative resources to help develop your PGx program.
For payers, PBMS, & employers
Learn more about the value of OneOme’s RightMed for Populations solution, how it works, and how to get started. Plus, access informative resources to help you leverage PGx in your populations.
For providers & pharmacists
Learn more about the benefits of the test, how it works (from ordering to interpretation), and additional tools and services available.
Learn how the test works, the potential benefits of the test, and how to find a provider who can order the test for you.
Have questions about the RightMed Test?
Dedicated experts are available to answer your questions. Speak with a client service representative today.