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 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.
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)
Fill out the simple patient intake form below by entering your information, then click submit.
After submission, you will be redirected to our partner to request a test online by scheduling an appointment with a genetic counselor.
Order a test kit from our shop and provide a saliva sample using the kit provided, after simply attach return label and send back.
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
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.
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.
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
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
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
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
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
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
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
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.
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.
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