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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 a previous personal history of a genetic condition?
– Are you interested in learning about your chance of having a genetic condition?

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

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Oxy-Gen offers a vast array of services ranging from infectious disease panels, to different genetic solutions. To get started, click the learn more button for more in-depth information.

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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.

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Hereditary Cardiovascular Screening

$199.99

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

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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