Northwest Clinical Genomics Laboratory

Test NamePanelDisease NameGeneLaboratoryCPT Code
Cardiac Arrhythmia PanelYesCardiac Arrhythmia
ABCC9, ANK2, CACNA1C, CACNA1D, CACNB2, CALM1, CALM2, CASQ2, CAV3, DES, DPP6, DSC2, DSG2, DSP, EMD, GJA5, GLA, GNAI2, GPD1L, HCN4, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LDB3, LMNA, MYH6, NKX2-5, NPPA, PKP2, PLN, PRKAG2, RBM20, RYR2, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SNTA1, TMEM43, TNNT2, TRDN, TRPM4, TTN
Northwest Clinical Genomics Lab 81413
Cardiomyopathy PanelYesCardiomyopathy
ABCC9, ACTC1, ACTN2, ANKRD1, BAG3, BRAF, CASQ2, CAV3, CBL, CHRM2, CRYAB, CSRP3, DES, DMD, DOLK, DSC2, DSG2, DSP, DTNA, EMD, FHL2, FKTN, GAA, GATAD1, GLA, HRAS, ILK, JPH2, JUP, KRAS, LAMA4, LAMP2, LDB3, LMNA, MAP2K1, MAP2K2, MURC, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEBL, NEXN, NRAS, PDLIM3, PKP2, PLN, PRDM16, PRKAG2, PSEN1, PSEN2, PTPN11, RAF1, RBM20, RIT1, RYR2, SCN5A, SGCD, SHOC2, SOS1, TAZ, TCAP, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TTN, TTR, VCL
Northwest Clinical Genomics Lab 81439
Comprehensive Cardiac Arrhythmia/Cardiomyopathy PanelYesCardiac Arrhythmia and/or Cardiomyopathy
ABCC9, ACTC1, ACTN2, ANK2, ANKRD1, BAG3, BRAF, CACNA1C, CACNA1D, CACNB2, CALM1, CALM2, CASQ2, CAV3, CBL, CHRM2, CRYAB, CSRP3, DES, DMD, DOLK, DPP6, DSC2, DSG2, DSP, DTNA, EMD, FHL2, FKTN, GAA, GATAD1, GJA5, GLA, GNAI2, GPD1L, HCN4, HRAS, ILK, JPH2, JUP, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, KRAS, LAMA4, LAMP2, LDB3, LMNA, MAP2K1, MAP2K2, MURC, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEBL, NEXN, NKX2-5, NPPA, NRAS, PDLIM3, PKP2, PLN, PRDM16, PRKAG2, PSEN1, PSEN2, PTPN11, RAF1, RBM20, RIT1, RYR2, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SGCD, SHOC2, SNTA1, SOS1, TAZ, TCAP, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TRDN, TRPM4, TTN, TTR, VCL
Northwest Clinical Genomics Lab 81479
Exome SequencingPossible Genetic Disorder
Coding sequence of the genome
Northwest Clinical Genomics Lab 81415 Proband 81416 Comparator
Exome Sequencing Re-analysisPossible Genetic Disorder
Coding sequence of the genome
Northwest Clinical Genomics Lab 81417
Genome SequencingPossible Genetic Disorder
Whole Genome Sequence
Northwest Clinical Genomics Lab 81425 Proband 81426 Comparator
Genome Sequencing Re-analysisPossible Genetic Disorder
Whole Genome Sequence
Northwest Clinical Genomics Lab 81427
Mini Exome Panel on DemandYesPossible Genetic Disorder
Selected genes
Northwest Clinical Genomics Lab 81479
Movement Disorder PanelYesHeritable Movement Disorders
ABCB7, ABCD1, ABHD12, ACAT1, ACOX1, ACTB, ACVR1, ADAR, ADCK3, ADCY5, ADD3, ADGRG1, AFG3L2, AHI1, ALAS2, ALDH5A1, ALG6, ALS2, AMACR, AMPD2, ANG, ANO10, ANO3, ANO5, AP1S2, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, APTX, ARHGEF28, ARL13B, ARL6, ARL6IP1, ARSA, ARSI, ARX, ASAH1, ATCAY, ATL1, ATM, ATP13A2, ATP1A2, ATP1A3, ATP6AP2, ATP7A, ATP7B, ATP8A2, AUH, B4GALNT1, BAG3, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCAP31, BEAN1, BICD2, BIN1, BSCL2, BTD, C10orf2, C12orf65, C19orf12, C5orf42, CA8, CACNA1A, CACNB4, CAMTA1, CASQ1, CAV3, CC2D2A, CCDC28B, CCDC78, CCDC88C, CCT5, CEP290, CEP41, CFL2, CHCHD10, CHMP2B, CIZ1, CLCN2, CLN3, CLN5, CLPP, CNTN1, COL12A1, COL6A1, COL6A2, COL6A3, COMT, COX20, CP, CRAT, CRYAB, CSF1R, CSTB, CTC1, CTSD, CWF19L1, CYP27A1, CYP2U1, CYP7B1, DARS2, DCAF17, DCTN1, DDB2, DDC, DDHD1, DDHD2, DES, DLAT, DNA2, DNAJC13, DNAJC19, DNAJC3, DNAJC5, DNAJC6, DNM2, DNMT1, DRD2, DRD5, DYSF, DYT1, EARS2, EEF2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF4G1, ELOVL4, ELOVL5, ENTPD1, EPM2A, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERLIN2, FA2H, FASTKD2, FBXL4, FBXO7, FGF14, FHL1, FKBP14, FLNC, FLRT1, FLVCR1, FOXG1, FOXRED1, FTL, FUS, GAD1, GALC, GAMT, GAN, GARS, GBA, GBA2, GBE1, GCDH, GCH1, GCLC, GFAP, GIGYF2, GJA1, GJB1, GJC2, GLB1, GNAL, GNE, GOSR2, GRID2, GRM1, HACD1, HARS, HEPACAM, HEXA, HEXB, HNRNPA1, HNRNPA2B1, HPRT1, HSPB1, HSPB3, HSPB8, HSPD1, HTRA2, IGHMBP2, ISCU, ITM2B, ITPR1, KANK1, KBTBD13, KCNA1, KCNC3, KCND3, KCNJ10, KCNMA1, KCNQ2, KDM5C, KIAA0196, KIF1A, KIF1C, KIF5C, KIF7, KLHL40, KLHL41, KLHL9, L2HGDH, LAMP2, LARS2, LDB3, LMNB1, LMOD3, LRRK2, LYST, MAG, MAPT, MARS, MARS2, MAT1A, MATR3, MCOLN1, MECP2, MEGF10, MKKS, MKS1, MLC1, MMADHC, MPV17, MR1, MRE11A, MSTN, MTHFR, MTM1, MTMR14, MTPAP, MYF6, MYH14, MYH2, MYH7, MYOT, NDUFV1, NEB, NEDD4, NEFH, NEU1, NHLRC1, NIPA1, NKX2-1, NOL3, NOP56, NPC1, NPC2, NPHP1, NT5C2, OFD1, OPA1, OPA3, OPTN, PABPN1, PANK2, PARK2, PARK7, PAX6, PDGFB, PDGFRB, PDHX, PDSS1, PDSS2, PEX10, PEX2, PEX7, PFN1, PGAP1, PHYH, PIK3R5, PINK1, PLA2G6, PLEC, PLEKHG4, PLEKHG5, PLP1, PMM2, PMPCA, PNKD, PNKP, PNPLA6, PNPT1, POLG, POLG2, POLH, PPP2R2B, PQBP1, PRICKLE1, PRKCG, PRKRA, PRNP, PRPH, PRRT2, PSEN1, PTEN, PTS, QDPR, RAB29, RAB39B, RAB3GAP1, RAB3GAP2, RARS2, REEP1, REEP2, RELN, RNASEH2A, RNASEH2B, RNASEH2C, RNF170, RNF216, RPGRIP1L, RRM2B, RTN2, RUBCN, RYR1, SACS, SAMD9L, SAMHD1, SCN8A, SCO2, SCP2, SDHAF1, SERAC1, SETX, SGCE, SIGMAR1, SIL1, SLC16A2, SLC17A5, SLC19A3, SLC1A3, SLC20A2, SLC25A15, SLC2A1, SLC30A10, SLC33A1, SLC46A1, SLC52A2, SLC52A3, SLC5A2, SLC6A3, SMPD1, SNCA, SNX14, SOD1, SPAST, SPEG, SPG11, SPG20, SPG21, SPG7, SPR, SPTBN2, STAC3, STIM1, STUB1, STXBP1, SUCLA2, SUOX, SYNE1, SYNJ1, SYT14, TAF1, TARDBP, TBP, TCTN1, TCTN2, TCTN3, TDP1, TECPR2, TFG, TGM6, TH, THAP1, TIA1, TIMM8A, TK2, TMEM138, TMEM216, TMEM230, TMEM231, TMEM237, TMEM240, TMEM67, TNNT1, TOR1A, TPK1, TPM2, TPM3, TPP1, TREM2, TREX1, TRIM32, TRPV4, TSEN2, TSEN34, TSEN54, TTBK2, TTC8, TTN, TTPA, TTR, TUBB4A, UBA1, UBQLN2, UCHL1, USP8, VAMP1, VAPB, VCP, VEGFA, VLDLR, VMA21, VPS13A, VPS13C, VPS35, VPS37A, VPS54, VRK1, WDPCP, WDR45, WDR48, WDR81, WFS1, WWOX, XPA, XPC, YARS2, ZFR, ZFYVE26, ZFYVE27, ZNF423, ZNF592
Northwest Clinical Genomics Lab 81479
Neurodegenerative Disorder PanelYesNeurodegenerative Disease Panel
AARS2, ABAT, ABCD1, ACAT1, ACOX1, ACTB, ACVR1, ADAR, ADCK3, ADCY5, ADK, AFG3L2, AIMP1, AIRE, ALDH3A2, ALS2, ANG, ANO3, ANO5, AP1S2, APOE, APOPT1, APP, APTX, ARHGEF28, ARSA, ARX, ASAH1, ASPA, ATM, ATP13A2, ATP1A2, ATP1A3, ATP6AP2, ATP7A, ATP7B, ATPAF2, ATXN2, AUH, B3GALNT2, BAG3, BCAP31, BCS1L, BEST1, BIN1, BRAF, C10orf2, C19orf12, CA2, CACNA1A, CASQ1, CAV3, CCDC78, CFL2, CHCHD10, CHMP2B, CIZ1, CLCN2, CLN3, CLN5, CLN6, CLN8, CNTN1, COASY, COL12A1, COL4A1, COL6A1, COL6A2, COL6A3, COMT, COQ2, COQ9, COX10, COX15, COX20, CP, CRYAB, CSF1R, CSTB, CTC1, CTSD, CTSF, CYP27A1, CYP2U1, CYP7B1, D2HGDH, DARS, DARS2, DCAF17, DCTN1, DDC, DES, DGUOK, DLAT, DNA2, DNAJC13, DNAJC5, DNAJC6, DNM2, DNMT1, DRD2, DRD5, DYSF, DYT1, EARS2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF4G1, EPM2A, ERBB4, ERCC3, ERCC6, ERCC8, ETFDH, FA2H, FAM126A, FASTKD2, FBXL4, FBXO7, FHL1, FIG4, FKBP14, FKRP, FLNC, FOLR1, FOXG1, FOXRED1, FTL, FUCA1, FUS, GALC, GAMT, GAN, GATA3, GBA, GBE1, GCDH, GCH1, GFAP, GFM1, GIGYF2, GJA1, GJC2, GLA, GLB1, GNAL, GNAQ, GNE, GOSR2, GRN, GTF2H5, HACD1, HEPACAM, HEXA, HNRNPA1, HNRNPA2B1, HPRT1, HSD17B4, HSPD1, HTRA1, HTRA2, HTT, ISCU, ITM2B, KBTBD13, KCNMA1, KCNQ2, KCNT1, KCTD7, KIF1C, KLHL40, KLHL41, KLHL9, L2HGDH, LAMP2, LDB3, LMNB1, LMOD3, LRRK2, MAPT, MARS2, MAT1A, MATR3, MCOLN1, MECP2, MEGF10, MFSD8, MLC1, MLYCD, MMADHC, MPLKIP, MPV17, MR1, MRPS16, MRPS22, MSTN, MTFMT, MTM1, MTMR14, MYF6, MYH14, MYH2, MYH7, MYOT, NDUFA1, NDUFA10, NDUFA11, NDUFA12, NDUFA2, NDUFA9, NDUFAF1, NDUFAF2, NDUFAF3, NDUFAF4, NDUFAF5, NDUFAF6, NDUFB3, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS5, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NDUFV3, NEB, NEFH, NEK1, NHLRC1, NKX2-1, NOTCH3, NPC1, NPC2, NUBPL, OCLN, OCRL, OPA1, OPTN, PABPN1, PAH, PANK2, PARK2, PARK7, PC, PDGFB, PDGFRB, PDHX, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PFN1, PHGDH, PHYH, PINK1, PLA2G6, PLEC, PLP1, PNKD, PNPT1, POLG, POLG2, POLR3A, POLR3B, PPT1, PPT2, PRF1, PRICKLE1, PRICKLE2, PRKRA, PRNP, PRPH, PRPS1, PRRT2, PSAP, PSAT1, PSEN1, PSEN2, PSMB8, PTEN, PTPN11, PTS, QDPR, RAB29, RAB39B, RAF1, RARS2, REPS1, RNASEH2A, RNASEH2B, RNASEH2C, RNASET2, ROGDI, RRM2B, RYR1, SAMHD1, SCARB2, SCO1, SCO2, SCP2, SDHA, SDHAF1, SDHB, SERAC1, SETX, SGCE, SIGMAR1, SIL1, SLC16A2, SLC17A5, SLC19A3, SLC20A2, SLC25A1, SLC25A12, SLC25A15, SLC25A4, SLC2A1, SLC30A10, SLC46A1, SLC6A3, SMPD1, SNCA, SOD1, SOX10, SPAST, SPEG, SPG11, SPG20, SPG21, SPG7, SPR, SQSTM1, SRRT, STAC3, STIM1, STX11, STXBP1, SUCLA2, SUMF1, SUOX, SURF1, SYNJ1, TACO1, TAF1, TARDBP, TARS2, TBK1, TBP, TH, THAP1, TIA1, TIMM8A, TK2, TMEM230, TNNT1, TOR1A, TPK1, TPM2, TPM3, TPP1, TREM2, TREX1, TRIM32, TTC3, TTN, TUBB4A, TUFM, TYMP, TYROBP, UBQLN2, UCHL1, UNC13D, VAPB, VARS, VCP, VEGFA, VMA21, VPS13A, VPS13C, VPS35, VPS37A, VPS54, WDR45, YARS2, ZFYVE26, ZNF592
Northwest Clinical Genomics Lab 81479
Neuromuscular Disorder PanelYesHeritable Neuromuscular Disorders
AARS, ABHD12, ABHD5, ACAD9, ACADL, ACADM, ACADS, ACADVL, ACTA1, ACVR1, ADCY6, AGL, AGRN, AIFM1, ALG13, ALG14, ALG2, AMPD1, ANO5, ARHGEF10, ASAH1, ATL1, ATL3, ATP2A1, ATP7A, B3GALNT2, B4GAT1, BAG3, BICD2, BIN1, BSCL2, C10orf2, C12orf65, CAPN3, CASQ1, CAV3, CCDC78, CCT5, CFL2, CHAT, CHCHD10, CHKB, CHRNA1, CHRNB1, CHRND, CHRNE, CHRNG, CHST14, CLCN1, CNTN1, CNTNAP1, COL12A1, COL4A1, COL6A1, COL6A2, COL6A3, COLQ, COX6A1, CPT2, CRYAB, CTDP1, DAG1, DCAF8, DCTN1, DES, DHTKD1, DMD, DNA2, DNAJB2, DNAJB6, DNM2, DNMT1, DOK7, DPAGT1, DPM2, DPM3, DST, DYNC1H1, DYSF, ECEL1, EGR2, EMD, ENO3, ERBB3, ETFA, ETFB, ETFDH, FAM134B, FBLN5, FBN2, FBXO38, FGD4, FHL1, FIG4, FKBP10, FKBP14, FKRP, FKTN, FLNC, FUS, GAA, GAN, GARS, GBE1, GDAP1, GFPT1, GJB1, GLE1, GMPPB, GNB4, GNE, GYG1, GYS1, HACD1, HADH, HADHA, HADHB, HARS, HINT1, HK1, HNRNPA1, HNRNPA2B1, HNRNPDL, HOXD10, HSPB1, HSPB3, HSPB8, IGHMBP2, IKBKAP, INF2, ISCU, ISPD, ITGA7, KARS, KBTBD13, KIF1A, KIF1B, KIF5A, KLHL40, KLHL41, KLHL9, LAMA2, LAMC1, LAMP2, LARGE, LAS1L, LDB3, LDHA, LITAF, LMNA, LMOD3, LPIN1, LRP4, LRSAM1, MARS, MATR3, MED25, MEGF10, MFN2, MPZ, MSTN, MTM1, MTMR14, MTMR2, MUSK, MYBPC1, MYF6, MYH14, MYH2, MYH3, MYH8, MYOT, NALCN, NDRG1, NEB, NEFL, NGF, NTRK1, OPA1, ORAI1, PABPN1, PDHA1, PDK3, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKB, PIEZO2, PIP5K1C, PLEC, PLEKHG5, PLOD2, PMP22, PNPLA2, POLG, POLG2, POMGNT1, POMGNT2, POMK, POMT1, POMT2, PREPL, PRPS1, PRX, PTRF, PUS1, PYGM, RAB7A, RAPSN, RBCK1, REEP1, RRM2B, RYR1, SBF1, SBF2, SCN10A, SCN11A, SCN4A, SCN9A, SCO2, SEPN1, SEPT9, SGCA, SGCB, SGCD, SGCG, SH3TC2, SIL1, SLC12A6, SLC16A1, SLC22A5, SLC25A20, SLC5A7, SMCHD1, SNAP25, SOX10, SPEG, SPTLC1, SPTLC2, STAC3, STIM1, SUCLA2, SURF1, SYNE1, SYNE2, SYT2, TAZ, TCAP, TFG, TIA1, TK2, TMEM43, TMEM5, TNNI2, TNNT1, TNNT3, TNPO3, TPM2, TPM3, TRAPPC11, TRIM2, TRIM32, TRPV4, TTN, TTR, TUBB3, TYMP, UBA1, VAPB, VCP, VMA21, VRK1, WNK1, YARS, YARS2, ZC4H2
Northwest Clinical Genomics Lab 81479
Panel on DemandYesPossible Genetic Disorder
Selected genes
Northwest Clinical Genomics Lab 81479
REFLEX to Exome SequencingPossible genetic disorder
Coding sequence of the genome
Northwest Clinical Genomics Lab 81417
Testing for Known Pathogenic VariantAll diseases
All genes
Northwest Clinical Genomics Lab 81479

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