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Cardiomyopathy and Arrhythmia Panel, Sequencing (85 Genes) and Deletion/Duplication (83 Genes)

CPT Code(s): 81161(DMD); 81280; 81282; 81403 (PLN); 81404 x7 (FKRP, FXN, SCN1B, SCO2, SGCG, SLC25A4, TTR); 81405 x19 (ACTC1, ANKRD1, CASQ2, COX15, DES, EMD, FKTN, GLA, LAMP2, MYL2, MYL3, MYOT, SGCA, SGCB, SGCD, SGCG, TNNC1, TNNI3, TPM1); 81406 x13 (CACNB2, DSC2, DSG2, DSP, GAA, JUP,LDB3, LMNA, PKP2, PRKAG2, TAZ, TMEM43, TNNT2); 81407 x3 (MYBPC3, MYH6, MYH7); 81408 x2 (DMD, RYR2); 81479 x2
Specimen Required: Patient Preparation:
Collect:Lavender (EDTA) or yellow (ACD Solution A or B).
Specimen Preparation:Transport 3 mL whole blood. (Min: 1 mL)
Storage/Transport Temperature:
Stability:Ambient: 72 hours; Refrigerated: 1 week; Frozen: Unacceptable
New York DOH Approval Status: Specimens from New York clients will be sent out to a New York DOH approved laboratory, if possible.
Aliases:
  • 2004543 LMNA-Related Disorders (LMNA) SequencingABCC9, ACTC1, ACTN2, AKAP9, ANK2, ANKRD1, CACNA1C, CACNB2, CASQ2, CAV3, CORIN, COX15, CSRP3, CTF1Arrhythmogenic right ventricular cardiomyopathy (ARVC)Brugada syndrome (BrS)Catecholaminergic polymorphic ventricular tachycardia (CPVT)DES, DMD, DSC2, DSG2, DSP, DTNA, EMD, EYA4, FKRP, FKTN, FXN, GAA, GLA, GPD1L, ILK, JPH2, JUP, KCNE1Dilated cardiomyopathy (DCM)Hypertrophic cardiomyopathy (HCM)KCNE2, KCNE3, KCNH2, KCNJ2, KCNQ1, KLHL3, LAMA4, LAMP2, LDB3, LMNA, MYBPC3, MYH6, MYH7, MYH10, MYL2Left ventricular noncompaction (LVNC)Long QT syndrome (LQTS)MYL3, MYLK2, MYOT, MYOZ2, MYPN, NEXN, OBSCN, PKP2, PLN, PRKAG2, RBM20, RYR2, SCN1B, SCN2B, SCN3BRomano-WardSCN4B, SCN5A, SCO2, SGCA, SGCB, SGCD, SGCG, SLC25A4, SNTA1, SYNE1, TAZ, TCAP, TGFB3, TMEM43, TMPOShort QT syndrome (SQTS)TNNC1, TNNI3, TNNT2, TPM1, TRPM4, TTN, TTR, VCL
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