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.

Discover if you have hereditary disorders with at-home testing.

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?

Are you a provider for Oxy-Gen Laboratory?

Click here to request a specimen pick-up or a supplies drop off.

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We are driven to give healthcare providers the most advanced testing information available so you can determine the best treatment options for your patients.

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.

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Genetic Testing

Priority Turnaround Results

Take A Look At Everything Oxy-Gen Has To Offer!

Oxy-Gen offers a vast array of services, to get started; click the learn more button for additional information.

Infectious Disease Testing

Our infectious diseases testing provides information about viral, fungal and bacterial pathogens in the patient’s system from either urine, stool or swab.

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Next Generation Sequencing

Carrier screening provides you and your doctor with information about your risks of having a child with a serious genetic disease prior to or during pregnancy.

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Genotyping Pharma Testing

Pharmacogenomics is the relationship between a patient’s unique genetic makeup and their response to certain medications.

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Oxy-Gen's Services

Infectious Disease Testing

Covid-19 Testing

Flu Testing

Genetic Testing

Pharmacogenomics (PGx)

Cancer Screening (CGX)

Diabetes and Obesity

Cardiovascular Diseases

Immunodeficiency Screening

Parkinson’s- Alzheimer’s-Dementia

Carrier Screening

Drug Screening

Toxicology

Take A Look At What We Offer.

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.

Genetic Solutions:

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.

Infectious Diseases Testing:

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.

Toxicology:

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.

PURCHASE TESTS

At-Home Testing

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

Hereditary Cardiovascular Screening

$199.99

Test genes to assess your risk of developing an inherited form of cardiovascular (heart) disease.

In stock

Quantity:

Product Details

Reasons for Hereditary Cardiovascular Screening:

2 or more family members diagnosed with the same genetic conditions
Previous personal history of a genetic condition

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