Carrier Screening

Reasons for Carrier Screening:

• Pregnancy
• Family Planning
• 2 or more family members diagnosed with the same genetic conditions

Our carrier screening service is designed to provide valuable information about the genetic risks that you and your partner may pass on to your future children. Carrier screening is a type of genetic testing that can identify whether a person carries a genetic mutation that could be passed on to their children and potentially cause a serious inherited condition.

The process is simple and straightforward - we provide you with a kit that you can use to collect a sample of your DNA from the comfort of your own home. Once we receive your sample, we use our state-of-the-art laboratory to analyze your DNA and provide you with a detailed report of your carrier status for the conditions included in our panel.

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:
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