Mon-Fri: 8:00 AM – 5:00 PM

5680 Oakbrook Pkwy Ste 100, Norcross, Ga 30093

At-Home Testing

Hereditary Diseases

Who should consider getting tested for genetic health conditions? 

– People who have family members previously diagnosed with genetic conditions.
– Someone who is pregnant or planning a family.
– People who have a personal history of a genetic condition.
– Someone interested in learning about their chance of having or developing hereditary diseases.
 

AT-HOME GENETIC TESTING

How It Works

At Oxy-Gen Laboratory, we offer two payment methods for our Genetic Testing. A self-pay rate and/or payment through insurance is available.

 If you would like to pay through insurance; once you have been approved through one of our genetic counselors for your desired test we will contact you with your coverage to determine how you would like to proceed.

STEPS FOR ORDERING A GENETIC TEST

Instructions

IMPORTANT: Please note the step process is only applicable for those who would like to get a genetic test preformed. If you are ordering any other test that is not genetic you may skip the steps and purchase the kit directly. (No need for a genetic counselor)

STEP ONE

Fill out the simple patient intake form below by entering your information, then click submit.

STEP TWO

After submission, you will be redirected to our partner to request a test online by scheduling an appointment with a genetic counselor.

STEP THREE

Order a test kit from our shop and provide a saliva sample using the kit provided, after simply attach return label and send back.

STEP FOUR

Once your results are available, you may contact your doctor or the genetic counselor for any questions or concerns.

DISCLAIMER: It is important to note that we require every patient to be pre-approved for their desired test, this pre-approval comes from scheduling of your appointment with our genetic counselors

PATIENT INFORMATION

Patient Intake Form

(Genetic Testing Only)

Please note: This section is only for those who would like genetic testing performed, if you are ordering a test that is not genetic you may simply order the test below. Before getting started please enter your information below, once you finish filling out the form Oxy-Gen Laboratory will schedule your appointment with a genetic counselor and we’ll reach out with confirmation.

Click the Patient Intake Form button below to get started.

PURCHASE TESTS

Shop Our Panels

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. If you have any additional questions please see our FAQ or if you’d like a list of genes screened for in each panel please see below.

 

Please note the following pricing is all Self-Pay this means the following rates are all cash payments. You’ll notice that all genetic tests are $199.99 this fee covers the cost of your pre-consultation with a genetic counselor (Required for genetic testing).

 

If you would like to pay through insurance, we will determine your coverage after you have been approved for the desired test through one of our genetic counselors.

Disclaimer: Insurance may or may not cover cost of counseling.

Immunodeficiency Screening

$199.99
Our immunodeficiency screening is a medical examination designed to assess if you have immune system issues.
In stock
1
Product Details

Reasons for Immunodeficiency Screening:

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

Our immunodeficiency screening is a medical examination designed to assess an individual's immune system function and identify any specific deficiencies or abnormalities that may be causing recurrent infections or other immune-related health issues. The screening is usually recommended when an individual experiences persistent or frequent infections that may suggest an underlying immune system disorder.

The screening process for immunodeficiency typically involves a physical exam, medical history review, and laboratory tests that target specific areas of the immune system. The tests may include measuring the levels of certain immune cells, evaluating the function of specific immune cells, and assessing the production of antibodies in response to specific antigens.

The results of the focus screening can help healthcare providers identify any specific immune system deficiencies or abnormalities that may be causing recurrent infections or other immune-related health issues. Based on the results, personalized treatment plans can be developed to manage or prevent complications. Treatment plans may include medication, lifestyle modifications, and immunotherapy.

Do not add to bag and proceed to checkout without approval from an Oxy-Gen Laboratory representative.

Panel Information
______________

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:

Primary Immunodeficiency Focus (108 genes) ADA, AICDA, ATM, B2M, BCL10, BLM, BLNK, BTK, CARD11, CCBE1, CD19, CD27, CD3D, CD3E, CD3G, CD40, CD40LG, CD79A, CD79B, CD81, CD8A, CHD7, CIITA, CR2, CTC1, CTLA4, DCLRE1C, DKC1, DNMT3B, DOCK8, EXTL3, FAT4, FOXN1, GATA2, ICOS, IGLL1, IKBKB, IL21R, IL2RG, IL7R, ITK, JAK3, KDM6A, KMT2D, LCK, LIG1, LRBA, LRRC8A, MAGT1, MALT1, MAP3K14, MCM4, MOGS, MS4A1, NBN, NFKB2, NFKBIA, NHEJ1, NHP2, NOP10, ORAI1, PIK3CD, PIK3R1, PLCG2, PNP, POLE, POLE2, RAG1, RAG2, RFX5, RFXANK, RFXAP, RHOH, RMRP, RNF168, RTEL1, SEMA3E, SH2D1A, SLC46A1, SMARCAL1, SP110, SPINK5, STAT3, STAT5B, STIM1, STK4, STXBP2, TBX1, TCF3, TCN2, TERC, TERT, TFRC, TINF2, TNFRSF13B, TNFRSF13C, TRNT1, TTC37, TTC7A, TYK2, UNG, USB1, WAS, WIPF1, WRAP53, XIAP, ZAP70, ZBTB24


Primary Immunodeficiency EXPANDED (146 genes) ADA, ADA2, ADAR, AICDA, AK2, ATM, B2M, BCL10, BLM, BLNK, BTK, CARD11, CCBE1, CD19, CD247, CD27, CD3D, CD3E, CD3G, CD40, CD40LG, CD79A, CD79B, CD81, CD8A, CHD7, CIITA, CORO1A, CR2, CTC1, CTLA4, CXCR4, DCLRE1C, DKC1, DNASE1L3, DNMT3B, DOCK8, ELANE, EXTL3, FAT4, FOXN1, G6PC, G6PC3, GATA2, HAX1, HPS1, HPS3, HPS4, HPS5, HPS6, ICOS, IFIH1, IGLL1, IKBKB, IL21R, IL2RG, IL7R, ITK, JAK3, KDM6A, KMT2D, LCK, LIG1, LIG4, LPIN2, LRBA, LRRC8A, MAGT1, MALT1, MAP3K14, MCM4, MEFV, MOGS, MS4A1, MTHFD1, MVK, NBN, NFKB2, NFKBIA, NHEJ1, NHP2, NLRC4, NLRP3, NOP10, ORAI1, PGM3, PIK3CD, PIK3R1, PLCG2, PNP, POLE, POLE2, PRKCD, PSTPIP1, PTPRC, RAC2, RAG1, RAG2, RFX5, RFXANK, RFXAP, RHOH, RMRP, RNASEH2A, RNASEH2B, RNASEH2C, RNF168, RTEL1, SAMHD1, SEMA3E, SH2D1A, SLC37A4, SLC46A1, SMARCAL1, SP110, SPINK5, STAT3, STAT5B, STIM1, STK4, STXBP2, TAZ, TBX1, TCF3, TCN2, TERC, TERT, TFRC, TINF2, TNFRSF13B, TNFRSF13C, TNFRSF1A, TREX1, TRNT1, TTC37, TTC7A, TYK2, UNG, USB1, VPS13B, WAS, WIPF1, WRAP53, XIAP, ZAP70, ZBTB24



Primary Immunodeficiency Plus (19 genes) BLM, BRCA2, CFTR, F5, F9, FANCC, G6PC, G6PD, JAK2, MPL, MSH6, MYD88, NRAS, PALB2, PLCG2, PMS2, PTEN, RUNX1, TERT


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PANEL INFORMATION

Gene Lookup

Our gene lookup is designed to provide patients and providers with a comprehensive list with all of the genes screened in our genetic testing panels.

We understand the importance of transparency and empowering patients with knowledge about their genetic health. Our gene lookup table serves as a valuable resource to help you understand which genes are analyzed in each of our panels.

Diabetes & Obesity Genes

This test is a medical examination designed to assess an individual’s risk for developing these two conditions.

Genes:
Monogenic Diabetes Panel (28 genes) ABCC8, APPL1, BLK, EIF2AK3, FOXP3, GATA4, GATA6, GCK, GLIS3, HNF1A, HNF1B, HNF4A, IER3IP1, INS, KCNJ11, KLF11, MNX1, NEUROD1, NEUROG3, NKX2-2, PAX4, PDX1, PPARG, PTF1A, RFX6, SLC19A2, WFS1, ZFP57

Monogenic Obesity Panel (68 genes) ADCY3, AFF4, ALMS1, ARL6, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BDNF, C8ORF37, CEP164, CEP19, CEP290, CPE, CREBBP, CUL4B, DYRK1B, EP300, FBN3, GNAS, GPR101, IFT172, IFT27, IFT74, KDM6A, KIDINS220, KIF7, KMT2D, KSR2, LEP, LEPR, LZTFL1, MAGEL2, MC3R, MC4R, MEGF8, MKKS, MKS1, MRAP2, NLGN2, NPY, NR0B2, NTRK2, PCSK1, PHF6, POMC, PPARG, PRMT7, RAB23, RAI1, RPS6KA3, SCLT1, SDCCAG8, SETD2, SH2B1, SIM1, TRAPPC3, TRAPPC9, TRIM32, TTC8, UCP3, VPS13B, WDPCP

Hereditary Cancer Genes

Our cancer screening gives you a comprehensive genetic analysis on your risk of developing hereditary cancer.

Genes:
Multi-Cancer Panel (84 genes) AIP, ALK, APC, ATM, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CASR, CDC73, CDH1, CDK4, CDKN1B, CDKN1C, CDKN2A, CEBPA, CHEK2, CTNNA1, DICER1, DIS3L2, EGFR, EPCAM, FH, FLCN, GATA2, GPC3, GREM1, HOXB13, HRAS, KIT, MAX, MEN1, MET, MITF, MLH1, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, NTHL1, PALB2, PDGFRA, PHOX2B, PMS2, POLD1, POLE, POT1, PRKAR1A, PTCH1, PTEN, RAD50, RAD51C, RAD51D, RB1, RECQL4, RET, RUNX1, SDHA, SDHAF2, SDHB, SDHC, SDHD, SMAD4, SMARCA4, SMARCB1, SMARCE1, STK11, SUFU, TERC, TERT, TMEM127, TP53, TSC1, TSC2, VHL, WRN, WT1

Common Hereditary Cancers Panel (47 genes) APC, ATM, AXIN2, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, CTNNA1, DICER1, EPCAM, GREM1, HOXB13, KIT, MEN1, MLH1, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NTHL1, PALB2, PDGFRA, PMS2, POLD1, POLE, PTEN, RAD50, RAD51C, RAD51D, SDHA, SDHB, SDHC, SDHD, SMAD4, SMARCA4, STK11, TP53, TSC1, TSC2, VHL

Breast Cancer Guidelines-Based Panel (11 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NF1, PALB2, PTEN, STK11, TP53

Oxy-Gen Breast Cancer Panel (26 genes) Primary Panel (13 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53
Add-on Preliminary-evidence Genes for Breast Cancer (13 genes) ABRAXAS1, AKT1, BRIP1, FANCC, FANCM, MRE11, MUTYH, PIK3CA, RECQL, RINT1, SDHB, SDHD, XRCC2

Breast and Gyn Cancers Guidelines-Based Panel (19 genes) ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, NF1, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53

Breast and Gyn Cancers Panel (36 genes) Primary Panel (21 genes) ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, DICER1, EPCAM, MLH1, MSH2, MSH6, NF1, PALB2, PMS2, PTEN, RAD51C, RAD51D, SMARCA4, STK11, TP53
Add-on Preliminary-evidence Genes for Breast and Gyn Cancer (15 genes) ABRAXAS1, AKT1, CDC73, FANCC, FANCM, MRE11, MUTYH, NBN, PIK3CA, POLD1, RECQL, RINT1, SDHB, SDHD, XRCC2

Colorectal Cancer Guidelines-Based Primary Panel (20 genes) APC, AXIN2, BMPR1A, CDH1, CHEK2, EPCAM, GREM1, MLH1, MSH2, MSH3, MSH6, MUTYH, NTHL1, PMS2, POLD1, POLE, PTEN, SMAD4, STK11, TP53
Add-on Preliminary-evidence Genes for Colorectal Cancer (10 genes) ATM, BLM, BUB1B, CEP57, ENG, FLCN, GALNT12, MLH3, RNF43, RPS20

Prostate Cancer Panel (19 genes) Primary Panel (12 genes) ATM, BRCA1, BRCA2, CHEK2, EPCAM, HOXB13, MLH1, MSH2, MSH6, NBN, PMS2, TP53
Add-on Preliminary-evidence Genes for Prostate Cancer (7 genes) ATR, BRIP1, FANCA, GEN1, PALB2, RAD51C, RAD51D

Nervous System/Brain Cancer Panel (42 genes) Primary Panel (29 genes) AIP, ALK, APC, DICER1, EPCAM, HRAS, LZTR1, MEN1, MLH1, MSH2, MSH6, NBN, NF1, NF2, PHOX2B, PMS2, POT1, PRKAR1A, PTCH1, PTEN, RB1, SMARCA4, SMARCB1, SMARCE1, SUFU, TP53, TSC1, TSC2, VHL
Add-on Preliminary-evidence Genes for Nervous System/Brain Cancer (5 genes) BAP1, EZH2, GPC3, KIF1B, PTCH2
Add-on Hereditary Paraganglioma-Pheochromocytoma Genes (8 genes) MAX, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127

Melanoma Panel (12 genes) Primary Panel (9 genes) BAP1, BRCA2, CDK4, CDKN2A, MITF, POT1, PTEN, RB1, TP53
Add-on Preliminary-evidence Genes for Melanoma (3 genes) BRCA1, MC1R, TERT

Renal/Urinary Tract Cancers Panel (32 genes) Primary Panel (25 genes) BAP1, CDC73, CDKN1C, DICER1, DIS3L2, EPCAM, FH, FLCN, GPC3, MET, MLH1, MSH2, MSH6, PMS2, PTEN, REST, SDHB, SDHC, SMARCA4, SMARCB1, TP53, TSC1, TSC2, VHL, WT1
Add-on Preliminary-evidence Genes for Renal/Urinary Tract Cancers (7 genes) BUB1B, CEP57, CTR9, MITF, PALB2, SDHA, SDHD

Sarcoma Panel (44 genes) Primary Panel (29 genes) APC, BLM, CDKN1C, DICER1, EPCAM, EXT1, EXT2, FH, HRAS, KIT, MLH1, MSH2, MSH6, NBN, NF1, PDGFRA, PMS2, POT1, PRKAR1A, PTCH1, RB1, RECQL4, SDHA, SDHB, SDHC, SDHD, SUFU, TP53, WRN
Add-on Preliminary-evidence Genes for Sarcoma (4 genes) CDKN2A, PTCH2, TSC1, TSC2
Add-on Diamond-Blackfan Anemia Primary Genes (11 genes) GATA1, RPL11, RPL15, RPL26, RPL35A, RPL5, RPS10, RPS19, RPS24, RPS26, RPS7

Thyroid Cancer Panel (11 genes) Primary Panel (7 genes) APC, CHEK2, DICER1, PRKAR1A, PTEN, RET, TP53
Add-on Preliminary-evidence Genes for Thyroid Cancer (4 genes) MEN1, SDHB, SDHD, WRN

Prostate Cancer Panel 19 genes Primary Panel (12 genes) ATM, BRCA1, BRCA2, CHEK2, EPCAM, HOXB13, MLH1, MSH2, MSH6, NBN, PMS2, TP53
Add-on Preliminary-evidence Genes for Prostate Cancer (7 genes) ATR, BRIP1, FANCA, GEN1, PALB2, RAD51C, RAD51D

Parkinson's / Alzheimer's / Dementia Genes

This screening is a medical examination designed to assess an individual’s risk for developing these neurological conditions.

Genes:
Hereditary Parkinson’s Disease and Parkinsonism (29 genes) Primary Panel (26 genes) ATP13A2, ATP7B, CHCHD2, CSF1R, DCTN1, DNAJC6, FBXO7, GBA, GCH1, LRRK2, PARK7, PDE8B, PINK1, PLA2G6, PRKN, PRKRA, RAB39B, SLC6A3, SNCA, SPR, SYNJ1, TH, TMEM230, VPS13C, VPS35, XPR1
Add-on Preliminary-evidence Genes for Hereditary Parkinson’s Disease and Parkinsonism (3 genes) MAPT, PODXL, UCHL1

Hereditary Amyotrophic Lateral Sclerosis, Frontotemporal Dementia, and Alzheimer’s Disease (43 genes) Primary Panel (34 genes) ALS2, ANG, ANXA11, APP, C9ORF72, CHCHD10, CHMP2B, DCTN1, ERBB4, FUS, GRN, HEXA, HNRNPA2B1, ITM2B, KIF5A, MAPT, OPTN, PFN1, PRNP, PSEN1, PSEN2, SETX, SNCA, SOD1, SORL1, SPG11, SQSTM1, TARDBP, TBK1, TFG, TREM2, UBQLN2, VAPB, VCP

Add-on Preliminary-evidence Genes for Hereditary Amyotrophic Lateral Sclerosis, Frontotemporal Dementia and Alzheimer Disease with C9orf72 (9 genes) ATP13A2, DDHD1, ERLIN1, FIG4, LRRK2, MATR3, NEFH, SIGMAR1, TIA1

Carrier Screening Genes

Test over 554 genes to determine if you are a carrier of a genetic disorder that could be passed on to your children.

Genes:
Comprehensive Carrier Screen 569 genes Primary Panel (2 genes) CFTR, SMN1
Add-on Comprehensive Carrier Screen genes (554 genes) AAAS, ABCA12, ABCA3, ABCA4, ABCB11, ABCB4, ABCC2, ABCC8, ABCD1, ACAD9, ACADM, ACADVL, ACAT1, ACOX1, ACSF3, ADA, ADAMTS2, ADAMTSL4, ADGRG1, ADGRV1, AGA, AGL, AGPS, AGXT, AHI1, AIPL1, AIRE, ALDH3A2, ALDH7A1, ALDOB, ALG1, ALG13, ALG6, ALMS1, ALPL, AMN, AMT, ANO10, AP1S1, AQP2, AR, ARG1, ARL6, ARSA, ARSB, ARSE, ARX, ASL, ASNS, ASPA, ASS1, ATM, ATP6V1B1, ATP7A, ATP7B, ATP8B1, ATRX, AVPR2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCKDHA, BCKDHB, BCS1L, BLM, BLOC1S3, BLOC1S6, BMP1, BRIP1, BSND, BTK, CAD, CANT1, CAPN3, CASQ2, CBS, CC2D1A, CC2D2A, CCDC103, CCDC39, CCDC88C, CD3D, CD3E, CD40, CD40LG, CD59, CDH23, CEP152, CEP290, CERKL, CHAT, CHM, CHRNE, CHRNG, CIITA, CLCN1, CLN3, CLN5, CLN6, CLN8, CLRN1, CNGB3, COL11A2, COL17A1, COL27A1, COL4A3, COL4A4, COL4A5, COL7A1, COX15, CPS1, CPT1A, CPT2, CRB1, CRTAP, CTNS, CTSA, CTSC, CTSD, CTSK, CYBA, CYBB, CYP11A1, CYP11B1, CYP11B2, CYP17A1, CYP19A1, CYP1B1, CYP21A2, CYP27A1, CYP27B1, CYP7B1, DBT, DCAF17, DCLRE1C, DDX11, DFNB59, DGAT1, DGUOK, DHCR7, DHDDS, DKC1, DLD, DLL3, DMD, DNAH11, DNAH5, DNAI1, DNAI2, DNMT3B, DOK7, DUOX2, DYNC2H1, DYSF, EDA, EIF2AK3, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, ELP1, EMD, EPG5, ERCC2, ERCC6, ERCC8, ESCO2, ETFA, ETFB, ETFDH, ETHE1, EVC, EVC2, EXOSC3, EYS, F9, FAH, FAM161A, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCG, FANCI, FANCL, FBP1, FBXO7, FH, FHL1, FKBP10, FKRP, FKTN, FMO3, FMR1, FOXN1, FOXRED1, FRAS1, FREM2, FUCA1, G6PC, G6PC3, GAA, GALC, GALE, GALK1, GALNS, GALNT3, GALT, GAMT, GATM, GBA, GBE1, GCDH, GCH1, GDF5, GFM1, GHR, GJB1, GJB2, GLA, GLB1, GLDC, GLE1, GNE, GNPAT, GNPTAB, GNPTG, GNS, GORAB, GRHPR, GRIP1, GSS, GUCY2D, GUSB, HADH, HADHA, HADHB, HAMP, HAX1, HBA1, HBA2, HBB, HCFC1, HEXA, HEXB, HGSNAT, HJV, HLCS, HMGCL, HMOX1, HOGA1, HPD, HPRT1, HPS1, HPS3, HPS4, HPS5, HPS6, HSD17B10, HSD17B3, HSD17B4, HSD3B2, HYAL1, HYLS1, IDS, IDUA, IGHMBP2, IKBKB, IL2RG, IL7R, INVS, ITGA6, ITGB3, ITGB4, IVD, JAK3, KCNJ1, KCNJ11, L1CAM, LAMA2, LAMA3, LAMB3, LAMC2, LARGE1, LCA5, LDLR, LDLRAP1, LHX3, LIFR, LIG4, LIPA, LMBRD1, LOXHD1, LPL, LRAT, LRP2, LRPPRC, LYST, MAK, MAN2B1, MANBA, MCEE, MCOLN1, MCPH1, MECP2, MECR, MED17, MESP2, MFSD8, MID1, MKKS, MKS1, MLC1, MLYCD, MMAA, MMAB, MMACHC, MMADHC, MOCS1, MOCS2, MPI, MPL, MPV17, MRE11, MTHFR, MTM1, MTR, MTRR, MTTP, MUSK, MUT, MVK, MYO15A, MYO7A, NAGA, NAGLU, NAGS, NBN, NCF2, NDRG1, NDUFAF2, NDUFAF5, NDUFS4, NDUFS6, NDUFS7, NDUFV1, NEB, NEU1, NGLY1, NPC1, NPC2, NPHP1, NPHS1, NPHS2, NR0B1, NR2E3, NSMCE3, NTRK1, OAT, OCA2, OCRL, OPA3, OSTM1, OTC, OTOA, OTOF, P3H1, PAH, PANK2, PC, PCBD1, PCCA, PCCB, PCDH15, PCNT, PDHA1, PDHB, PEPD, PET100, PEX1, PEX10, PEX12, PEX13, PEX16, PEX2, PEX26, PEX5, PEX6, PEX7, PFKM, PGM3, PHGDH, PHKB, PHKG2, PHYH, PIGN, PKHD1, PLA2G6, PLEKHG5, PLOD1, PLP1, PMM2, PNPO, POLG, POLH, POMGNT1, POMT1, POMT2, POR, POU1F1, PPT1, PRCD, PRDM5, PRF1, PROP1, PRPS1, PSAP, PTPRC, PTS, PUS1, PYGM, QDPR, RAB23, RAG1, RAG2, RAPSN, RARS2, RDH12, RLBP1, RMRP, RNASEH2A, RNASEH2B, RNASEH2C, RP2, RPE65, RPGRIP1L, RS1, RTEL1, RXYLT1, RYR1, SACS, SAMD9, SAMHD1, SCO2, SEC23B, SEPSECS, SGCA, SGCB, SGCD, SGCG, SGSH, SKIV2L, SLC12A1, SLC12A3, SLC12A6, SLC17A5, SLC19A2, SLC19A3, SLC1A4, SLC22A5, SLC25A13, SLC25A15, SLC25A20, SLC26A2, SLC26A3, SLC26A4, SLC27A4, SLC35A3, SLC37A4, SLC38A8, SLC39A4, SLC45A2, SLC4A11, SLC5A5, SLC6A8, SLC7A7, SMARCAL1, SMPD1, SNAP29, SPG11, SPR, SRD5A2, ST3GAL5, STAR, STX11, STXBP2, SUMF1, SUOX, SURF1, SYNE4, TANGO2, TAT, TAZ, TBCD, TBCE, TCIRG1, TCN2, TECPR2, TERT, TF, TFR2, TG, TGM1, TH, TK2, TMC1, TMEM216, TMEM67, TMPRSS3, TPO, TPP1, TREX1, TRIM32, TRIM37, TRMU, TSEN54, TSFM, TSHB, TSHR, TTC37, TTPA, TULP1, TYMP, TYR, TYRP1, UBR1, UNC13D, USH1C, USH2A, VDR, VLDLR, VPS11, VPS13A, VPS13B, VPS45, VPS53, VRK1, VSX2, WAS, WISP3, WNT10A, WRN, XPA, XPC, ZBTB24, ZFYVE26, ZNF469
Add-on genes with variable presentation (13 genes) BTD, F11, F2, F5, G6PD, GP1BA, GP9, HFE, HGD, MCCC1, MCCC2, MEFV, SERPINA1

Broad Carrier Screen 115 genes Primary Panel (2 genes) CFTR, SMN1
Add-on Broad Carrier Screen genes (113 genes) ABCA3, ABCC8, ABCD1, ACADM, ACADVL, ACAT1, AGA, AGXT, AHI1, AIRE, ALDOB, ALPL, ANO10, ARSA, ARX, ASL, ASPA, ASS1, ATP7B, BBS1, BBS2, BCKDHA, BCKDHB, BLM, CBS, CC2D2A, CCDC88C, CEP290, CHRNE, CLCN1, CLN3, CLRN1, CNGB3, COL7A1, CPT2, CYP11A1, CYP21A2, CYP27A1, CYP27B1, DHCR7, DHDDS, DLD, DMD, DYNC2H1, ELP1, ERCC2, EVC2, F9, FAH, FANCC, FKRP, FKTN, FMO3, FMR1, G6PC, GAA, GALC, GALT, GBA, GBE1, GJB2, GLA, GNPTAB, GRIP1, HBA1, HBA2, HBB, HEXA, HPS1, HPS3, IDUA, IL2RG, L1CAM, LRP2, MCOLN1, MCPH1, MID1, MLC1, MMACHC, MUT, MVK, NAGA, NEB, NPHS1, NPHS2, NR0B1, OCA2, OTC, PAH, PCDH15, PEX1, PEX6, PEX7, PKHD1, PLP1, PMM2, POLG, PRF1, RARS2, RNASEH2B, RS1, SCO2, SLC19A3, SLC26A2, SLC26A4, SLC37A4, SLC6A8, SMPD1, TF, TMEM216, TYR, USH2A, XPC

Core Carrier Screen 3 genes Primary Panel (2 genes) CFTR, SMN1
Add-on Core Carrier Screen genes (1 gene) FMR1

Broad Carrier Screen without X-linked Disorders 101 genes Primary Panel (2 genes) CFTR, SMN1
Add-on Broad Carrier Screen without X-linked Disorders genes (99 genes) ABCA3, ABCC8, ACADM, ACADVL, ACAT1, AGA, AGXT, AHI1, AIRE, ALDOB, ALPL, ANO10, ARSA, ASL, ASPA, ASS1, ATP7B, BBS1, BBS2, BCKDHA, BCKDHB, BLM, CBS, CC2D2A, CCDC88C, CEP290, CHRNE, CLCN1, CLN3, CLRN1, CNGB3, COL7A1, CPT2, CYP11A1, CYP21A2, CYP27A1, CYP27B1, DHCR7, DHDDS, DLD, DYNC2H1, ELP1, ERCC2, EVC2, FAH, FANCC, FKRP, FKTN, FMO3, G6PC, GAA, GALC, GALT, GBA, GBE1, GJB2, GNPTAB, GRIP1, HBA1, HBA2, HBB, HEXA, HPS1, HPS3, IDUA, LRP2, MCOLN1, MCPH1, MLC1, MMACHC, MUT, MVK, NAGA, NEB, NPHS1, NPHS2, OCA2, PAH, PCDH15, PEX1, PEX6, PEX7, PKHD1, PMM2, POLG, PRF1, RARS2, RNASEH2B, SCO2, SLC19A3, SLC26A2, SLC26A4, SLC37A4, SMPD1, TF, TMEM216, TYR, USH2A, XPC

Immunodeficiency Screening Genes

Our immunodeficiency screening is a medical examination designed to assess if you have immune system issues.

Genes:
Primary Immunodeficiency Focus (108 genes) ADA, AICDA, ATM, B2M, BCL10, BLM, BLNK, BTK, CARD11, CCBE1, CD19, CD27, CD3D, CD3E, CD3G, CD40, CD40LG, CD79A, CD79B, CD81, CD8A, CHD7, CIITA, CR2, CTC1, CTLA4, DCLRE1C, DKC1, DNMT3B, DOCK8, EXTL3, FAT4, FOXN1, GATA2, ICOS, IGLL1, IKBKB, IL21R, IL2RG, IL7R, ITK, JAK3, KDM6A, KMT2D, LCK, LIG1, LRBA, LRRC8A, MAGT1, MALT1, MAP3K14, MCM4, MOGS, MS4A1, NBN, NFKB2, NFKBIA, NHEJ1, NHP2, NOP10, ORAI1, PIK3CD, PIK3R1, PLCG2, PNP, POLE, POLE2, RAG1, RAG2, RFX5, RFXANK, RFXAP, RHOH, RMRP, RNF168, RTEL1, SEMA3E, SH2D1A, SLC46A1, SMARCAL1, SP110, SPINK5, STAT3, STAT5B, STIM1, STK4, STXBP2, TBX1, TCF3, TCN2, TERC, TERT, TFRC, TINF2, TNFRSF13B, TNFRSF13C, TRNT1,TTC37, TTC7A, TYK2, UNG, USB1, WAS, WIPF1, WRAP53, XIAP, ZAP70, ZBTB24

Primary Immunodeficiency EXPANDED (146 genes) ADA, ADA2, ADAR, AICDA, AK2, ATM, B2M, BCL10, BLM, BLNK, BTK, CARD11, CCBE1, CD19, CD247, CD27, CD3D, CD3E, CD3G, CD40, CD40LG, CD79A, CD79B, CD81, CD8A, CHD7, CIITA, CORO1A, CR2, CTC1, CTLA4, CXCR4, DCLRE1C, DKC1, DNASE1L3, DNMT3B, DOCK8, ELANE, EXTL3, FAT4, FOXN1, G6PC, G6PC3, GATA2, HAX1, HPS1, HPS3, HPS4, HPS5, HPS6, ICOS, IFIH1, IGLL1, IKBKB, IL21R, IL2RG, IL7R, ITK, JAK3, KDM6A, KMT2D, LCK, LIG1, LIG4, LPIN2, LRBA, LRRC8A, MAGT1, MALT1, MAP3K14, MCM4, MEFV, MOGS, MS4A1, MTHFD1, MVK, NBN, NFKB2, NFKBIA, NHEJ1, NHP2, NLRC4, NLRP3, NOP10, ORAI1, PGM3, PIK3CD, PIK3R1, PLCG2, PNP, POLE, POLE2, PRKCD, PSTPIP1, PTPRC, RAC2, RAG1, RAG2, RFX5, RFXANK, RFXAP, RHOH, RMRP, RNASEH2A, RNASEH2B, RNASEH2C, RNF168, RTEL1, SAMHD1, SEMA3E, SH2D1A, SLC37A4, SLC46A1, SMARCAL1, SP110, SPINK5, STAT3, STAT5B, STIM1, STK4, STXBP2, TAZ, TBX1, TCF3, TCN2, TERC, TERT, TFRC, TINF2, TNFRSF13B, TNFRSF13C, TNFRSF1A, TREX1, TRNT1, TTC37, TTC7A, TYK2, UNG, USB1, VPS13B, WAS, WIPF1, WRAP53, XIAP, ZAP70, ZBTB24

Primary Immunodeficiency Plus (19 genes) BLM, BRCA2, CFTR, F5, F9, FANCC, G6PC, G6PD, JAK2, MPL, MSH6, MYD88, NRAS, PALB2, PLCG2, PMS2, PTEN, RUNX1, TERT

Hereditary Cardiovascular Genes

Test 186 genes to assess your risk of developing an inherited form of cardiovascular (heart) disease.

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

Pharmacogenomics (PGx) Genes

Test specific genes to assess how your genes impact your response to current medications you’re taking.

Genes:
Mental Health Panel: CYP2C19, CYP2D6, CYP3A4, CYP3A5

Psych Panel: CYP2C19, CYP2D6, CYP3A4, CYP3A5, COMPT, MTHFR

Focus Panel: BCHE, CYP2B6, CYP2C19, CYP2C9, CYP2D6, CYP3A5, CYP4F2, DPYD, G6PD, HLA-B, IFNL4, NAT2, NUDT15, RYR1, SLCO1B1, TPMT, UGT1A1, VKORC1

Cardio Panel: APOE, CYP2C9, CYP2C9, CYP2C19, CYP2D6, CYP3A4, CYP3A5, Factor II, Factor V Leiden, MTHFR, SLCO1B1, VKORC1

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At-Home Testing FAQ

Answers for patients and individuals who have questions about how to pay for genetic testing, including insurance options.

Genetic testing should be affordable and accessible to everyone who needs it. We offer multiple billing options and have an exceptional Client Services team ready to work with you.

Insurance (US only)
If you have insurance, that's great! Most insurance plans cover genetic testing. When your provider orders your test, we'll check to make sure your test is covered. When a test is covered, there may still be co-insurance and deductible amounts you would be responsible for. If so, we'll let you know what your estimated out-of-pocket cost might be.

The average out-of-pocket cost after using insurance is between $0 and $100. If your cost is higher than anticipated, we have a few options that just might help-a patient assistance program you may be eligible for, as well as flexible payment plans. Call us when you receive your bill. We will work with you.

Unsure if your insurance company is in network with Oxy-Gen Laboratory? Don't worry, Oxy-Gen Laboratory is in network with most major insurance plans and can also work with your insurance, even if it is out-of-network.

Patient pay
For patients without US insurance, or with insurance that doesn't cover their test, we offer a patient-pay price. For more information about our pricing for a given test, see here. Medicare & Medicaid (US only) Medicare and medicaid frequently cover genetic testing. Please see the "Is Oxy-Gen Laboratory's genetic testing covered by Medicare and Medicaid in the US?" section below for more information about exclusions for the types of tests they may cover.

Most insurance plans cover genetic testing in the US. When your provider orders your test, we'll check to make sure your test is covered. Even when a test is covered, there may still be coinsurance and deductible amounts you are responsible for. We'll let you know what your estimated out-of-pocket cost may be.

Unsure if your insurance company is in network with Oxy-Gen Laboratory? Don't worry, Oxy-Gen Laboratory is in network with most major insurance plans and can also work with your insurance, even if it is out-of-network.

For patients without US insurance, or with insurance that doesn't cover their test, we offer an affordable patient-pay price. For more information about our pricing for a given test.

Tests ordered by a healthcare provider If you decide to pay for your test through our self-pay option (rather than billing your insurance company), once Oxy-Gen Laboratory receives your DNA sample, we will send you an email with instructions on how to pay for your test online via credit card. You can also make a payment here. If you would prefer to pay over the phone or via wire transfer, please contact Client Services.

Tests initiated online

If you initiate a proactive genetic test or carrier screening online, you will be prompted to pay for your test during the check-out process. Payment can be made via credit card in Oxy-Gen Laboratory's secure ordering portal.

Payment plans are available to cover higher than expected out-of-pocket expenses. Please contact our Client Services team for more in depth information regarding a specialized two month plan.