Welcome to OneOme

OneOme is a Minneapolis-based precision medicine startup offering the RightMed® test, a pharmacogenomic test that may help providers in selecting medications for their patients.

Get started

Recent updates to RightMed: The OneOme RightMed test now provides results in the form of the RightMed gene report. If you have questions, please CONTACT US >

RightMed test

The RightMed test analyzes a patient’s DNA, which may help providers make more informed medication decisions for him or her. Results are presented in the RightMed gene report, which contains the patient’s genotype results and phenotype summaries for the 27 genes covered by the RightMed test.

View Sample Report

Genes covered

The RightMed test covers the following genes:

CYP1A2*1C, *1D, *1E, *1F, *1J, *1K, *1L, *1V, *1WToggle icon

rs12720461NM_000761.4:c.-10+113C>T

rs2069514NG_008431.2:g.28338G>A

rs2069526NM_000761.4:c.-10+103T>G

rs35694136NM_000761.4:c.-1635delT

rs762551NM_000761.4:c.-9-154C>A

CYP2B6*4, *5, *6, *7, *9, *16, *18Toggle icon

rs2279343NM_000767.4:c.785A>G

rs28399499NM_000767.4:c.983T>C

rs3211371NM_000767.4:c.1459C>T

rs3745274NM_000767.4:c.516G>T

CYP2C ClusterG/AToggle icon

rs12777823NC_000010.10:g.96405502G>A

CYP2C9*2, *3, *4, *5, *6, *8, *11Toggle icon

rs1057910NM_000771.3:c.1075A>C

rs1057911NM_000771.3:c.1425A>T

rs1799853NM_000771.3:c.430C>T

rs28371685NM_000771.3:c.1003C>T

rs28371686NM_000771.3:c.1080C>G

rs56165452NM_000771.3:c.1076T>C

rs7900194NM_000771.3:c.449G>A

rs9332131NM_000771.3:c.817delA

CYP2C19*2, *3, *4, *4B, *10, *17Toggle icon

rs12248560NM_000769.2:c.-806C>T

rs28399504NM_000769.2:c.1A>G

rs4244285NM_000769.2:c.681G>A

rs4986893NM_000769.2:c.636G>A

rs6413438NM_000769.2:c.680C>T

CYP2D6*2A, *2, *3, *4, *4N, *4M, *5, *6, *6C, *7, *8, *9, *10, *11, *12, *13, *14A, *14B, *15, *17, *18, *19, *29, *31, *34, *35, *36, *39, *41, *42, *59, *63, *64, *68, *69, *70, *91, *109Toggle icon

hCV32407220 (rs765776661)NM_000106.5:c.1411_1412insTGCCCACTG

rs1065852NM_000106.5:c.100C>T

rs1080985NM_000106.5:c.-1584C>G

rs1135840NM_000106.5:c.1457G>C

rs16947NM_000106.5:c.886C>T

rs201377835NM_000106.5:c.181-1G>C

rs267608319NM_000106.5:c.1319G>A

rs28371706NM_000106.5:c.320C>T

rs28371725NM_000106.5:c.985+39G>A

rs35742686NM_000106.5:c.775delA

rs3892097NM_000106.5:c.506-1G>A

rs5030655NM_000106.5:c.454delT

rs5030656NM_000106.5:c.841_843delAAG

rs5030862NM_000106.5:c.124G>A

rs5030865NM_000106.5:c.505G>A

rs5030867NM_000106.5:c.971A>C

rs59421388NM_000106.5:c.1012G>A

rs72549346NM_000106.5:c.1088_1089insGT

rs72549353NM_000106.5:c.765_768delAACT

rs769258NM_000106.5:c.31G>A

rs774671100NM_000106.5:c.137_138insT

rs79292917NM_000106.5:c.975G>A

CYP3A4*1B, *22Toggle icon

rs2740574NM_017460.5:c.-392G>A

rs35599367NM_017460.5:c.522-191C>T

CYP3A5*3, *6, *7Toggle icon

rs10264272NM_000777.4:c.624G>A

rs41303343NM_000777.4:c.1035_1036insT

rs776746NM_000777.4:c.219-237G>A

CYP4F2*3Toggle icon

rs2108622NM_001082.4:c.1297G>A

COMTVal158MetToggle icon

rs4680NM_000754.3:c.472G>A

DPYD*2A (1905+1G>A, IVS14+1G>A), Asp949Val, *13Toggle icon

rs3918290NM_000110.3:c.1905+1G>A

rs55886062NM_000110.3:c.1679T>G

rs67376798NM_000110.3:c.2846A>T

DRD2Promoter variant -241A>GToggle icon

rs1799978NM_000795.3:c.-585A>G

F220210G>AToggle icon

rs1799963NM_000506.4:c.*97G>A

F5Arg534Gln (Leiden, 1691G>A)Toggle icon

rs6025NM_000130.4:c.1601G>A

GRIK4Non-coding (intronic) T>C variantToggle icon

rs1954787NM_001282470.2:c.83-10039T>C

HLA-AHLA-A*31:01Toggle icon

HLA00097NM_002116 (interrogated at exon 2)

HLA-BHLA-B*15:02, HLA-B*57:01, HLA-B*58:01Toggle icon

HLA00386NM_005514 (interrogated at exon 2 and intron 2)

HLA00381NM_005514 (interrogated at exon 3)

rs144012689NM_005514.7:c.1012+104A>T

HTR2AIntron 2, T>C variantToggle icon

rs7997012NM_000621.4:c.614-2211T>C

HTR2CPromoter variant -759C>TToggle icon

rs3813929NM_000868.3:c.-759C>T

IL28B (IFNL4)Non-coding (intronic) C>T variantToggle icon

rs12979860NM_001276254.2:c.151-152G>A

MTHFR677C>T; 1298A>CToggle icon

rs1801133NM_005957.4:c.665C>T

rs1801131NM_005957.4:c.1286A>C

NUDT15Arg139CysToggle icon

rs116855232NM_018283.3:c.415C>T

OPRM1Asn40Asp; 118A>GToggle icon

rs1799971NM_000914.4:c.118A>G

SLC6A4c.-1810A>G; -1791_-1749del43Toggle icon

rs25531NM_001045.5:c-1936A>G

rs774676466NM_001045.5:c.-1917_-1875del43

SLCO1B1*5, *17, *21Toggle icon

rs4149015NM_006446.4:c.-910G>A

rs4149056NM_006446.4:c.521T>C

rs2306283NM_006446.4:c.388A>G

TPMT*2, *3A, *3B, *3C, *4Toggle icon

rs1142345NM_000367.3:c.719A>G

rs1800460NM_000367.3:c.460G>A

rs1800462NM_000367.3:c.238G>C

rs1800584NM_000367.3:c.626-1G>A

UGT1A1*6, *28 (TA7)Toggle icon

rs1976391NM_001072.3:c.862-9697A>G

rs4148323NM_001072.3:c.862-6536G>A

VKORC1Promoter variant -1639G>AToggle icon

rs9923231NM_001311311.1:c.-1639G>A

rs7200749NM_001311311.1:c.442C>T

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).

View GENE DETAILS to learn more about these genes.

How it works

Step 1

Provider orders the RightMed test for their patient.

Step 2

DNA sample is collected from patient.

Step 3

OneOme processes the sample and returns the RightMed gene report to the provider.

Get started

Providers

Providers can get started now by downloading our TEST REQUISITION FORM and PATIENT CONSENT FORM or by connecting to our PROVIDER PORTAL, which allows you to place orders, download a patient’s test report, and access the RightMed Advisor.

Patients

Patients can get started by talking to their doctor about the RightMed test, or they can BUY THE TEST ONLINE. When buying the test online, an independent provider will review the patient’s information and, if appropriate, order the test for him or her.

  • The RightMed test must be ordered by a physician.
  • The RightMed test, as with all genomic testing, has limitations. Always discuss the test with a healthcare provider knowledgeable about the test and to see if it's right for you.
  • RightMed test results are not a substitute for medical advice and should only be used in consultation with a medical professional.
  • The RightMed test does not determine the best medication for the patient; it is a tool to provide additional information to the patient’s healthcare provider. The healthcare provider should take other factors into consideration regardless of genotype.
  • Independent healthcare providers available through OneOme's service will not have all of your health history, which may cause the test results to be subject to a different interpretation than by your personal physician.
  • DO NOT MAKE ANY CHANGES TO YOUR CURRENT MEDICATIONS OR DOSING WITHOUT CONSULTING YOUR HEALTHCARE PROVIDER.