Health testing has never been faster, easier, and more personalized with Oxy-Gen Laboratory, click here to view our genetic testing menu.
Using precision medicine and innovative techniques to help healthcare professionals improve the treatment and outcomes of their patients.
Do any of these apply to you?
– Do you have any family members who have been diagnosed with a genetic condition?
– Are you pregnant or planning a family?
– Do you have previous personal history of a genetic condition?
– Are you interested in learning about your chance of having a genetic condition?
Our suite of diagnostic services includes toxicology, infectious diseases testing, hereditary cancer screening, hereditary cardiovascular, hereditary parkinson’s-alzheimer’s-dementia, hereditary diabetes and obesity, primary immunodeficiency response, pharmacogenomics, and carrier screening. Oxy-Gen Laboratory is a pioneer in scientific innovations and client partnerships.
Oxy-Gen offers a vast array of services, to get started; click the learn more button for additional information.
Covid-19 Testing
Flu Testing
Pharmacogenomics (PGx)
Cancer Screening (CGX)
Diabetes and Obesity
Cardiovascular Diseases
Immunodeficiency Screening
Parkinson’s- Alzheimer’s-Dementia
Carrier Screening
Toxicology
Oxy-Gen offers a vast array of services ranging from infectious disease panels, different genetic solutions, and even toxicology . To get started, click the learn more button for more in depth information.
Our genetic solutions range anywhere from hereditary cancer screening, hereditary cardiovascular, hereditary parkinson's-alzheimer's-dementia, hereditary diabetes and obesity, primary immunodeficiency response, pharmacogenomics, and carrier screening.
Our genetic solutions analyze a patient’s DNA for mutations/variants associated with carrier screening, oncology, and pharmacogenomics. We provide a comprehensive report indicating a patient’s potential susceptibility to various pathogenic variants associated with these conditions.
Our infectious diseases testing provides information about viral and bacterial pathogens in the system.
Our infectious diseases testing provides information about viral and bacterial pathogens in the patient’s system. This information helps guide a clinician’s treatment of a patient. In addition, this testing ensures the safe use of prescriptions and is designed to help doctors provide the highest level of care.
Our toxicology screening provides critical information and knowledge regarding use of various drugs. These results can be used by physicians, regulatory agencies, and even healthcare providers.
With an ongoing epidemic of drug misuse and abuse in America, it’s more important than ever for healthcare providers to monitor their patients as they treat them for pain, addiction, or chronic conditions. Oxy-Gen Laboratory's toxicology testing can help verify adherence, prevent diversion, and reduce the risks of addiction and adverse drug events. Oxy-Gen can also help the provider perform more thorough medication reconciliations.
Health testing has never been easier, faster, and more personalized. Browse the growing selection of tests available from Oxy-Gen Laboratory. You can view your cart or check the status of an order when you select my account below.
We accept self -pay and insurance. If you would like to pay with either one, please schedule a pre-counseling session with our professionals
Reasons for Hereditary Cardiovascular Screening:
Our hereditary cardiovascular screen is a medical test designed to identify genetic mutations or abnormalities that may increase the risk of developing cardiovascular diseases. This screening test involves analyzing a patient's DNA sample to identify specific gene mutations associated with inherited heart conditions such as hypertrophic cardiomyopathy, familial hypercholesterolemia, and long QT syndrome.
The hereditary cardiovascular screen may be recommended for individuals with a family history of cardiovascular diseases or sudden cardiac death at a young age. The test can also be beneficial for individuals with unexplained cardiac symptoms, such as chest pain, palpitations, or shortness of breath.
The screening process involves a saliva sample collection, which is sent to a laboratory for genetic analysis. Once the results are available, a genetic counselor or healthcare provider can help interpret the findings and provide recommendations for further testing, treatment, or lifestyle modifications.
Do not add to bag and proceed to checkout without approval from an Oxy-Gen Laboratory representative.
Panel Information
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Turnaround time: 2-4 weeks for results
Collection Method: Buccal Swab or Saliva
DISCLAIMER: The service and fee selected above covers your pre-consult or post-consult telehealth visit with one of our genetic counselors. Prior to ordering this test, you must have a medical necessity that will be determined by our Genetic Counselors.
Additionally, if you do not meet your insurance's medical necessity you may still be eligible for the test. Oxy-Gen Laboratory will follow up with you in this case to discuss our self-pay cost of the test.
Genes:
Hereditary Cardio Screen (117 genes) ABCC9, ACTA2, ACTC1, ACTN2, ACVRL1, AGL, AKAP9, ALMS1, ANK2, APOB, BAG3, BMPR2, CACNA1C, CACNA1S, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV1, CAV3, COL3A1,CRYAB, CSRP3,DES,DMD,DOLK,DSC2,DSG2,DSP,EMD,ENG,EYA4,F9,FBN1,FHL1,FKRP,FKTN,FLNC,GAA,GATAD1,GDF2,GLA,GPD1L,HCN4,JPH2,JUP, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNQ1, LAMA4, LAMP2, LDB3, LDLR, LDLRAP1, LMNA, MYBPC3, MYH11, MYH6, MYH7, MYL2, MYL3, MYLK, MYOZ2, MYPN, NEXN, NKX2-5, PCSK9, PKP2, PLN, PRKAG2, PRKG1, PROC, PROS1, PTPN11, RAF1, RBM20, RIT1, RYR1, RYR2, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SERPINC1, SGCD, SLC22A5, SMAD3, SMAD4, SNTA1, SOS1, TAZ, TBX20, TBX5, TCAP, TGFB2, TGFB3, TGFBR1, TGFBR2, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TRPM4, TTN, TTR, VCL
Hereditary Cardio Screen Focus (44 genes) ACTA2, ACTC1, APOB, BAG3, CACNA1S, COL3A1, DES, DSC2, DSG2, DSP, F9, FBN1, FLNC, GLA, JUP, KCNH2, KCNQ1, LDLR, LMNA, MYBPC3, MYH11, MYH7, MYL2, MYL3, MYLK, PCSK9, PKP2, PRKAG2, PRKG1, RBM20, RYR1, RYR2, SCN5A, SMAD3, TGFB2, TGFBR1, TGFBR2, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR
Actionable Cardiovascular (32 genes) ACTA2,ACTC1,APOB,CACNA1S,COL3A1,DSC2,DSG2,DSP, FBN1,GLA,KCNH2,KCNQ1,LDLR,LMNA,MYBPC3,MYH11,MYH7,MYL2,MYL3,PCSK9,PKP2,PRKAG2,RYR1, RYR2, SCN5A, SMAD3, TGFBR1, TGFBR2, TMEM43, TNNI3, TNNT2, TPM1
Long QT Syndrome Panel 17 genes Primary Panel (10 genes) CACNA1C, CALM1, CALM2, CALM3, KCNE1, KCNH2, KCNJ2, KCNQ1, SCN5A, TRDN
Add-on Preliminary-evidence Genes for Long QT Syndrome (7 genes) AKAP9, ANK2, CAV3, KCNE2, KCNJ5, SCN4B, SNTA1
Familial Hypercholesterolemia (4 genes) APOB, LDLR, LDLRAP1, PCSK9
Arrhythmia and Cardiomyopathy Comprehensive Panel 186 genes Primary Panel (100 genes) ABCC9, ACADVL, ACTC1, ACTN2, AGL, ALMS1, ALPK3, BAG3, BRAF, CACNA1C, CACNA1D, CALM1, CALM2, CALM3, CASQ2, CBL, CDH2, CPT2, CRYAB, CSRP3, DES, DMD, DNAJC19, DOLK, DSC2, DSG2, DSP, ELAC2, EMD, EYA4, FHL1, FKRP, FKTN, FLNC, GAA, GATA4, GATA5, GJA5, GLA, HCN4, HRAS, JUP, KCNE1, KCNH2, KCNJ2, KCNQ1, KRAS, LAMP2, LMNA, LZTR1, MAP2K1, MAP2K2, MRAS, MTO1, MYBPC3, MYH7, MYL2, MYL3, MYL4, MYLK3, NF1, NKX2-5, NRAS, PCCA, PCCB, PKP2, PLN, PPA2, PPCS, PPP1CB, PRKAG2, PTPN11, RAF1, RASA1, RBM20, RIT1, RYR2, SCN5A, SDHA, SGCD, SHOC2, SLC22A5, SOS1, SOS2, SPRED1, TAZ, TBX20, TCAP, TMEM43, TMEM70, TNNC1, TNNI3, TNNI3K, TNNT2, TPM1, TRDN, TRPM4, TTN, TTR, VCL
Add-on Preliminary-evidence Genes for Arrhythmia and Cardiomyopathy (57 genes) A2ML1, AKAP9, ANK2, ANKRD1, CACNA2D1, CACNB2, CALR3, CAV3, CHRM2, CTF1, CTNNA3, DTNA, FHL2, GATA6, GATAD1, GPD1L, HAND1, ILK, JPH2, KCNA5, KCND3, KCNE2, KCNE3, KCNE5, KCNJ5, KCNJ8, KCNK3, KIF20A, KLF10, LAMA4, LDB3, LRRC10, MAP3K8, MED12, MYH6, MYLK2, MYOM1, MYOZ2, MYPN, NEBL, NEXN, NPPA, PDLIM3, PLEKHM2, PRDM16, RANGRF, RASA2, RRAS, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SLMAP, SNTA1, TMPO, TXNRD2
Add-on Sudden Unexpected Death in Epilepsy (SUDEP) Genes (11 genes) DEPDC5, KCNA1, KCNQ2, KCNQ3, KCNT1, PCDH19, PRRT2, SCN1A, SCN8A, SCN9A, SLC2A1
We’re located in Peachtree Corners, Georgia. Our laboratory is in suite 300, take a look at the map to route directions.
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