Genetic Testing
What is Genetic Testing?
Genetic testing is a powerful tool that enables us to delve into the intricate details of your genetic makeup. At Amerilab, we understand the significance of genetic testing in unraveling the mysteries of inherited traits and disease risk. As a trusted molecular diagnostic laboratory, we are dedicated to providing accurate and reliable genetic testing services to individuals, healthcare providers, and researchers.
Benefits of Genetic Testing
Genetic testing can unlock a wealth of information about your genetic makeup and offer several benefits:
Identification of Genetic Predispositions
Discovering potential inherited conditions or diseases can enable proactive management and preventive measures.
Personalized Healthcare and Treatment
Genetic insights empower healthcare providers to tailor treatments and medications specifically to your genetic profile.
Enhanced Family Planning
Knowing your carrier status for certain genetic disorders can help you make informed decisions about starting or expanding your family.
Understanding Disease Risk
Genetic testing can provide valuable information about your susceptibility to certain diseases, empowering you to make lifestyle changes for disease prevention.
Contribution to Scientific Research
By participating in genetic testing, you can contribute to ongoing research, leading to advancements in the field of genetics and improved healthcare outcomes.
Our Genetic Testing Services
Amerilab offers a comprehensive range of genetic testing services, utilizing state-of-the-art technology and adhering to the highest quality standards.
Prenatal Testing
Pharmacogenomic Testing
Predictive and Presymptomatic Testing
Carrier Testing
Diagnostic Testing
Oncology Panels
Genetic Disease Panels
Understanding the Process
To ensure a seamless experience, let us guide you through the genetic testing process:
Step 1
Sample
Collection
Step 2
Laboratory
Analysis
Step 3
Data
Interpretation
Step 4
Report
Delivery
Panel Details
Comprehensive Neurology NGS
ADNP, AFF2, ALDH7A1, ANG, APTX, ARX, ASPA, ASXL1, ATN1, ATP1A2, ATP7B, ATXN1, ATXN10, ATXN2, ATXN3, ATXN7, ATXN8OS, BCL11A, BSCL2, C12orf4, CACNA1A, CACNA1C, CC2D1A, CDKL5, CHD2, CNOT3, CNTN6, COL4A1, COL4A3BP, CSNK2A1, CSTB, CTNND2, DHCR7, DPYD, EGR2, EHMT1, EN2, EZH2, FBXO11, FMR1, FOXG1, FOXP1, FTSJ1, FXN, GABRG2, GAMT, GARS, GATM, GBA, GCH1, GRIN2A, GRN, HEXA, HFE, HSPB1, HTT, IKBKAP, KCNQ2, KDM5C, L1CAM, LRRK2, MAPT, MBOAT7, MECP2, MED12, MTHFR, MTM1, NCX3, NDP, NDUFA1, NLGN3, NLGN4X, NOTCH3, NSD1, NTRK1, NTRK2, PABPN1, PCDH19, PDGFB, PDHA1, PIK3CA, PINK1, PMP22, PNKD, POLG, PPP2R2B, PRRT2, PSEN1, PTEN, REEP1, SCN1A, SCN1B, SCN2A, SCN8A, SCN9A, SCO2, SGCE, SLC16A2, SLC2A1, SLC6A8, SLC9A6, SMN1, SMN2, SOD1, GALT, GBE1, GJB1, HBB, MCOLN1, MFN2, MPV17, MPZ, NPC1, OPA1, OPTN, PAH, PDSS2, PLCG2, POLG2, PRNP, PSEN2, SPG11, STXBP1, SYNGAP1, TARDBP, TBP, TCF4, TH, THAP1, TOR1A, TPP1, TSC1, TSC2, TTR, UBA1, ZEB2, ZNF41, ACADM, APOE, APP, ARSA, ATM, BCKDHA, BCKDHB, BCS1L, BLM, C10orf2, COQ2, COX10, DGUOK, ERBB4, FANCC, FUS, G6PC, GAA, RRM2B, SCO1, SETX, SLC25A4, SPAST, SPTLC1, SUCLA2, SUCLG1, TAZ, TK2, TYMP
Comprehensive Primary Immunodeficiency NGS
BLM, BRCA2, CFTR, F9, F5, FANCC, G6PD, G6PC, JAK2, MSH6, MYD88, PALB2, NRAS, PMS2, PLCG2, PTEN, RUNX1, MPL, TERT, F13B, F7, FGB, STAT1, STAT3, MEFV, CYBB, JAGN1, STK4, CYBA, NFKB2, CDX1, PIK3CD, MSH2, VPS13B, BRCA1, ATM, RFXANK, PTPRC, NCF1, TNFRSF13B, ITGB2, IFNGR1, IFNGR2, RAG1, RAG2, SPINK5, BTK, HLA, IRF5, NCF2, PTPN22, STAT4, TREX1
Comprehensive Cancergenomics NGS
MUTYH, PTEN, BMPR1A, ATM, POLE, CDK4, GJB2, GJB6, BRCA2, BLM, FBN1, GREM1, PALB2, CDH1, RAD51D, COL1A1, BRIP1, TP53, NF1, RAD51C, MITF, BAP1, KIT, TERT, APC, MSH2, BARD1, MSH6, CHEK2, MLH1, BRCA1, SMAD4, STK11, POLD1, EPCAM, PMS2, NBN, CDKN2A, CDK4, GJB2, GJB6, BRCA2, BLM, FBN1, GREM1, PALB2, CDH1, RAD51D, COL1A1, BRIP1, TP53, NF1, RAD51C, MITF, BAP1, KIT, TERT, APC, MSH2, BARD1, MSH6, CHEK2, MLH1, BRCA1, SMAD4, STK11, POLD1, EPCAM
Pharmacogenomics NGS
CYP2C9, VKORC1, CYP2C19, CYP2D6, CYP3A4, CYP3A5, FACTOR II, FACTOR V, MTHFR, ABCB1, ABCG2, ADRA2A, DRD2/TA1A, Apolipoprotein E, COMT, SLC6A4, CYP1A2, CYP2B6, CYP2C8, DHB, DPYD, GRIK4, HTR2A, HTR2C, IL28B, ITGB3, OPRK1, OPRM1, SLCO1B1, UGT1A1, UGT2B15
Comprehensive Thyroid Panel NGS
PIK3CA, TRH, THRB, CTNNB1, KRAS, DUOX1, SLC5A5, CACNA1A, PRKCG, HAMP, SLC40A1, TPO, PAX8, GLIS3, FOXE1, SECISBP2, GNAQ, PLCG2, TGFBI, TG, THRA, TP53, TSHB, NRAS, ATP1A2, HRAS, TTR, IYD, HFE, ESR1, PLN, TFR2, SLC26A4, TSHR, NKX2, 1, MECP2, IRAK1, G6PD, SLC16A2, IGSF1, TBL1X, IRS4, CST3, CST1, CSTB, DUOX2
Comprehensive Eye Disorders NGS
ATXN7, CACNA1A, CDH23, CDKL5, CFH, CHD2, CLRN1, CNGA1, CTSD, EYS, FTL, GABRG2, GJB2, GJB6, GPR98, GRIN2A, KCNQ2, MECP2, MTRNR1, ALDH7A1, MYO15A, MYO7A, OTOF, PAX2, PCDH15, PCDH19, PDE6A, PDE6B, POLG, PRPF31, PRRT2, RDH12, RP2, RPGR, SCN1A, SCN1B, SCN2A, SCN8A, SLC26A4, SLC2A1, SLC9A6, STXBP1, SYNGAP1, TCF4, TGFBI, TMC1, TMPRSS3, TPP1, TSC1, TSC2, USH1C, USH1G, USH2A, WFS1, ZEB2, HSF4, BFSP2, GALK1, BFSP1, CRYAA, CRYAB, CRYGC, FOXE3, BEST1, NR2E3, NRL, RHO, RP1, RPE65, CAV1, CAV2, SIX1, SIX6, CDKN2B, AS, TMCO1, CYP1B1, LTBP2, PITX2, PAX6, FOXC1, OPN1LW, MYOC
Comprehensive Cardiovascular NGS
ABCC9, ACTA2, ACTC1, ACTN2, ACVRL1, ADAMTS2, AKAP9, ALDH18A1, ALMS1, ALPK3, ANK2, ANKRD1, APOB, ATP6V0A2, ATP6V1E1, ATP7A, B3GAT3, B4GALT7, BAG3, BGN, BMPR2, BRAF, CACNA1C, CACNA2D1, B3GALT6, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV1, CAV3, CBS, CHRM2, CHST14, COL11A1, COL11A2, COL12A1, COL1A1, COL1A2, COL2A1, COL3A1, COL5A1, COL5A2, COL9A1, COL9A2, COL9A3, CRYAB, CSRP3, CTNNA3, DES, DMD, DOLK, DSC2, DSE, DSG2, DSP, DTNA, EFEMP2, EIF2AK4, ELN, EMD, ENG, EYA4, FBLN5, FBN1, FBN2, FHL1, FKBP14, FKRP, FKTN, FLNA, F9, FLNC, GAA, GATA4, GATA5, GATA6, GATAD1, GDF2, GJA5, KCNJ8, KCNK3, KCNQ1, KRAS, LAMA4, LAMP2, LDB3, LDLR, LDLRAP1, LMNA, LOX, LRRC10, LTBP4, MAP2K1, MAP2K2, MAT2A, MED12, MFAP5, MIB1, MURC, MYBPC3, MYH11, MYH6, MYH7, MYL2, MYL3, MYL4, MYLK, MYLK2, MYOZ2, MYPN, NEBL, NEXN, NKX2, 5, NOTCH1, NRAS, PCSK9, PDLIM3, PKP2, PLN, PLOD1, PPA2, PRDM16, PRDM5, PRKAG2, PRKG1, PTPN11, PYCR1, RAF1, RANGRF, RASA1, RBM20, RIN2, RIT1, RYR2, SCN10A, SCN1B, SCN2B, SCN3B, VCL, ZNF469, SCN4B, SCN5A, SGCD, SHOC2, SKI, SLC2A10, SLC39A13, SMAD2, SMAD3, SMAD4, SMAD9, SNTA1, SOS1, TAZ, TBX20, TCAP, TECRL, TGFB3, TGFB2, TGFBR1, TGFBR2, TMEM11, TMPO, VTNNC1, TNNT2, TNXB, TOR1AIP1, TPM1, TRD, TRPM4, TTN, TXNRD2
Comprehensive Pulmonary NGS
CCDC39, CCDC40, CFTR, CHAT, CHRNA1, CHRNB1, CHRNE, COLQ, CSF2RA, CSF2RB, DKC1, CHRND, DNAAF1, DNAAF2, DNAH1, DNAH1I, DNAH5, DNAI1, DNAI2, DNAL1, EDN3, ELMOD2, FLCN, FOXF1, GAS8, GLRA1, HPS1, HPS4, ITGA3, MECP2, NAF1, NF1, NKX2, 1, NME8, PARN, PHOX2B, PIH1D3, RAPSN, RET, RSPH3, RSPH4A, RSPH9, RTEL1, SCNA4, SCNN1A, SCNN1B, SERPINA1, SFTPA1, SFTPA2, SFTPB, SFTPC, SLC34A2, SLC6A5, SLC7A7, SMPD1, STAT3, TERC, TERT, TINF2, TSC1, TSC2, ZEB2, EFEMP2, FBLN5, ELN, LTBP4
Comprehensive Metabolic Disorder NGS
ABCA1, ABCB4, ABCC2, ABCD1, ABCD3, ABCD4, ABCG5, ABCG8, ACACA, ACADM, ACADS, ACADVL, APOE, ARSA, ASPA, ASS1, ATP7B, BCKDHA, BCKDHB, BLM, BSCL2, BTD, CACNA1A, CBS, CFTR, CLCNKB, COX10, COX15, CPOX, CPT1A, CSTB, DGUOK, DHCR7, DLD, DPYD, F9, FAH, FANCC, FH, G6PC, G6PD, GAA, GALNS, GALT, GALC, GAMT, GATM, GBA, GBE1, GLUD1, GCDH, GCK, GLA, GNE, GYS1, GYS2, HADH, HADHA, HADHB, HBB, HEXA, HFE, HMGCL, HPRT1, HSD17B10, HYAL1, IDH2, IDS, LCT, LIPA, LPL, MAN2B1, IKBKAP, ISCU, MCCC1, MCCC2, MCOLN1, MMAB, MMACHC, MMAA, MMADHC, MTHFR, MUT, NAGA, NAGLU, OTC, PAH, NHEG1, PCCA, PC, PCCB, PCK1, PCK2, PDHA1, PDHX, PEPD, PEX1, PEX10, PEX12, PEX13, PEX14, PEX14, PEX16, PEX19, PEX2, PEX5, PEX6, PEX7, PHKA1, PHKA2, PHKB, PHKG1, PHKG2, PHYH, POLG, PPARG, PRKAG2, PRPS1, PTS, PYGL, PYGM, QDPR, RBCK1, RFT1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, SEC23B, SERPINA1, SGSH, SLC12A3, SLC16A1, SLC17A5, SLC22A5, SLC25A13, SLC25A15, SLC25A20, SLC25A26, SLC25A4, SLC2A1, SLC2A2, SLC30A10, SLC35A1, SLC35A2, SLC35C1, SLC39A4, SLC3A1, SLC40A1, SLC41A3, SLC46A1, SLC5A1, SLC6A19, SLC6A8, SLC6A9, SLC7A7, SUCLA2, SUCLG1, SUOX, SURF1, TALDO1, TAT, TBC1D4, TCN2, TFR2, TFAM, TIMM8A, TMEM126A, TMEM165, TNPO3, TMEM70, TFAP2A, TRPM7, TSFM, TTC19, TUFM, TUSC3, TYMP, UGT1A1, UMPS, UCP2, UPB1, UQCRB, UQCRQ, UROD, WFS1, XDH, YARS2, ZMPSTE24
How to Get Started
Unlock the power of your genetic information with Amerilab’s comprehensive genetic testing services. Contact your healthcare provider to discuss your specific testing needs.
Frequently Asked Questions
How long does genetic testing take?
The turnaround time for genetic testing varies depending on the type of test. Diagnostic testing can take several weeks, while other tests may have shorter processing times.
Will my genetic information be kept confidential?
Yes, Amerilab takes your privacy seriously. We follow strict data security protocols to ensure the confidentiality and privacy of your genetic information.
Can genetic testing determine my entire genetic makeup?
Genetic testing focuses on specific genes or gene variations related to particular conditions or traits. While it provides valuable insights, it does not provide a comprehensive analysis of your entire genetic makeup.
Is genetic testing covered by insurance?
Coverage for genetic testing varies among insurance providers and depends on the specific test and individual circumstances. We recommend checking with your insurance provider to determine your coverage.