Entity Name Entity type Gene Symbol Sources(; separated) Level4 Level3 Level2 Model_Of_Inheritance Phenotypes Omim Orphanet HPO Publications Description Flagged GEL_Status UserRatings_Green_amber_red version ready Mode of pathogenicity EnsemblId(GRch37) EnsemblId(GRch38) HGNC Position Chromosome Position GRCh37 Start Position GRCh37 End Position GRCh38 Start Position GRCh38 End STR Repeated Sequence STR Normal Repeats STR Pathogenic Repeats Region Haploinsufficiency Score Region Triplosensitivity Score Region Required Overlap Percentage Region Variant Type Region Verbose Name ACTC1 gene ACTC1 Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, hypertrophic, 11 (612098);Left ventricular noncompaction 4 (613424);Cardiomyopathy, dilated, 1R (613424);Cardiomyopathy, dilated, 1R;Atrial septal defect 5 (612794) 26061005;27532257 False 3 50;17;33 2.20 False ENSG00000159251 ENSG00000159251 HGNC:143 ACTN2 gene ACTN2 Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, hypertrophic, 23, with or without LVNC (612158);Cardiomyopathy, dilated, 1AA, with or without LVNC (612158);Dilated Cardiomyopathy, Dominant 25224718;27532257;26312134 False 3 43;43;14 2.20 False ENSG00000077522 ENSG00000077522 HGNC:164 BAG3 gene BAG3 Expert Review Green;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Cardiomyopathy, dilated, 1HH, 613881;Myopathy, myofibrillar, 6, 612954 30442290;28737513;28211974 False 3 100;0;0 2.20 False ENSG00000151929 ENSG00000151929 HGNC:939 CDH2 gene CDH2 Expert Review Green;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown False 3 50;50;0 2.20 False ENSG00000170558 ENSG00000170558 HGNC:1759 DES gene DES Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BOTH monoallelic and biallelic, autosomal or pseudoautosomal Scapuloperoneal syndrome, neurogenic, Kaeser type (181400);Myopathy, myofibrillar, 1 (601419);Cardiomyopathy, dilated, 1I, (604765);Cardiomyopathy, dilated, 1I, 20186049;27532257 False 3 57;14;29 2.20 False ENSG00000175084 ENSG00000175084 HGNC:2770 DMD gene DMD Expert Review Green;Literature;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) Becker muscular dystrophy, 300376;Cardiomyopathy, dilated, 3B, 302045;Duchenne muscular dystrophy, 310200 GeneReviews: Dystrophinopathies False 3 100;0;0 2.20 False ENSG00000198947 ENSG00000198947 HGNC:2928 DOLK gene DOLK Expert Review Green;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal False 3 50;50;0 2.20 False ENSG00000175283 ENSG00000175283 HGNC:23406 DSC2 gene DSC2 Expert List;Expert Review Green;London South GLH;North West GLH;South West GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BOTH monoallelic and biallelic, autosomal or pseudoautosomal Arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair;Arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair (610476);Arrhythmogenic right ventricular dysplasia 11;Arrhythmogenic right ventricular dysplasia 11 (610476) 23500315;27532257 False 3 86;14;0 2.20 False ENSG00000134755 ENSG00000134755 HGNC:3036 DSG2 gene DSG2 Expert List;Expert Review Green;London South GLH;North West GLH;South West GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Arrhythmogenic right ventricular dysplasia 10;Arrhythmogenic right ventricular dysplasia 10 (610193);Cardiomyopathy, dilated, 1BB (612877) 23500315;27532257 False 3 86;14;0 2.20 False ENSG00000046604 ENSG00000046604 HGNC:3049 DSP gene DSP Expert List;Expert Review Green;London South GLH;North West GLH;South West GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BOTH monoallelic and biallelic, autosomal or pseudoautosomal Cardiomyopathy, dilated, with woolly hair and keratoderma, OMIM:605676 (AR);Dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis, OMIM:615821 (AD);Arrhythmogenic right ventricular dysplasia 8, OMIM:607450 (AD) 23500315;27532257;35348702 False 3 86;14;0 2.20 False ENSG00000096696 ENSG00000096696 HGNC:3052 EMD gene EMD Expert Review Green;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders X-LINKED: hemizygous mutation in males, biallelic mutations in females False 3 50;50;0 2.20 False ENSG00000102119 ENSG00000102119 HGNC:3331 FLNC gene FLNC Expert Review Green;Literature;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Cardiomyopathy, familial hypertrophic, 26, OMIM:617047;Cardiomyopathy, familial restrictive 5, OMIM:617047;Hypertrophic cardiomyopathy 26, MONDO:0014883;Myopathy, myofibrillar, 5, OMIM:609524;Myopathy, myofibrillar, 5, MONDO:0012289 30067491;28008423 False 3 100;0;0 2.20 False ENSG00000128591 ENSG00000128591 HGNC:3756 JUP gene JUP Expert List;Expert Review Green;London South GLH;North West GLH;South West GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BOTH monoallelic and biallelic, autosomal or pseudoautosomal Naxos disease, OMIM:601214;Arrhythmogenic right ventricular dysplasia 12, OMIM:611528 23500315;27532257 False 3 86;14;0 2.20 False ENSG00000173801 ENSG00000173801 HGNC:6207 LAMP2 gene LAMP2 Expert Review Green;Literature;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) Danon disease (300257) 21415759;12084876 False 3 100;0;0 2.20 False ENSG00000005893 ENSG00000005893 HGNC:6501 LMNA gene LMNA Eligibility statement prior genetic testing;Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Muscular dystrophy, congenital (613205);Malouf syndrome (212112);Emery-Dreifuss muscular dystrophy 2, autosomal dominant (181350);Heart-hand syndrome, Slovenian type (610140);Hutchinson-Gilford progeria (176670);Cardiomyopathy, dilated, 1A (115200);Restrictive dermopathy, lethal (275210);Lipodystrophy, familial partial, type 2 (151660);Emery-Dreifuss muscular dystrophy 3, autosomal recessive (616516);Charcot-Marie-Tooth disease, type 2B1 (605588);Mandibuloacral dysplasia (248370);Cardiomyopathy, dilated, 1A 20186049;27532257;35348702 False 3 71;14;14 2.20 False ENSG00000160789 ENSG00000160789 HGNC:6636 MYBPC3 gene MYBPC3 Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, dilated, 1MM;Cardiomyopathy, hypertrophic, 4 (115197);Left ventricular noncompaction 10 (615396);Cardiomyopathy, dilated, 1MM (615396) 20186049;27532257 False 3 33;33;33 2.20 False ENSG00000134571 ENSG00000134571 HGNC:7551 MYH7 gene MYH7 Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Cardiomyopathy, dilated, 1S, OMIM:613426;Dilated cardiomyopathy 1S, MONDO:0013262;Laing distal myopathy, OMIM:160500;Laing early-onset distal myopathy, MONDO:0008050 20186049;27532257 False 3 83;17;0 2.20 False ENSG00000092054 ENSG00000092054 HGNC:7577 NEXN gene NEXN Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, dilated, 1CC, OMIM:613122 19881492;27532257 False 3 29;57;14 2.20 False ENSG00000162614 ENSG00000162614 HGNC:29557 NKX2-5 gene NKX2-5 Expert Review Green;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown False 3 100;0;0 2.20 False ENSG00000183072 ENSG00000183072 HGNC:2488 PKP2 gene PKP2 Expert List;Expert Review Green;London South GLH;North West GLH;South West GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Arrhythmogenic right ventricular cardiomyopathy;Arrhythmogenic right ventricular dysplasia 9;Arrhythmogenic right ventricular dysplasia 9 (609040) 23500315;27532257 False 3 86;14;0 2.20 False ENSG00000057294 ENSG00000057294 HGNC:9024 PLN gene PLN Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, dilated, 1P (609909);Cardiomyopathy, dilated, 1P;Cardiomyopathy, hypertrophic, 18 (613874) 20186049;27532257 False 3 71;14;14 2.20 False ENSG00000198523 ENSG00000198523 HGNC:9080 RBM20 gene RBM20 Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, dilated, 1DD;Cardiomyopathy, dilated, 1DD (613172) 20186049;27532257 False 3 83;17;0 2.20 False ENSG00000203867 ENSG00000203867 HGNC:27424 RYR2 gene RYR2 Expert List;Expert Review Green;London South GLH;South West GLH;Wessex and West Midlands GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Arrhythmogenic right ventricular dysplasia 2;Arrhythmogenic right ventricular dysplasia 2 (600996);Ventricular tachycardia, catecholaminergic polymorphic, 1 (604772) 20301310;19926015;17875969;25163546;32748945 False 3 44;44;11 2.20 False ENSG00000198626 ENSG00000198626 HGNC:10484 SCN5A gene SCN5A Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Cardiomyopathy, dilated, 1E 20186049;27532257;35701104 False 3 83;17;0 2.20 False ENSG00000183873 ENSG00000183873 HGNC:10593 TMEM43 gene TMEM43 Expert List;Expert Review Green;London South GLH;North West GLH;South West GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Arrhythmogenic right ventricular dysplasia 5;Arrhythmogenic right ventricular dysplasia 5 (604400);Emery-Dreifuss muscular dystrophy 7, AD (614302) 23812740;27532257 False 3 86;14;0 2.20 False ENSG00000170876 ENSG00000170876 HGNC:28472 TNNC1 gene TNNC1 Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, hypertrophic, 13 (613243);Cardiomyopathy, dilated, 1Z;Cardiomyopathy, dilated, 1Z (611879) 20186049;27532257 False 3 50;33;17 2.20 False ENSG00000114854 ENSG00000114854 HGNC:11943 TNNI3 gene TNNI3 Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BOTH monoallelic and biallelic, autosomal or pseudoautosomal Cardiomyopathy, dilated, 1FF (613286);Cardiomyopathy, dilated, 2A,;?Cardiomyopathy, dilated, 2A (611880);Cardiomyopathy, familial restrictive, 1 (115210);Cardiomyopathy, dilated, 1FF;Cardiomyopathy, hypertrophic, 7 (613690) 20186049;27532257;21533915 False 3 83;17;0 2.20 False ENSG00000129991 ENSG00000129991 HGNC:11947 TNNI3K gene TNNI3K Expert Review Green;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown False 3 50;50;0 2.20 False ENSG00000116783 ENSG00000116783 HGNC:19661 TNNT2 gene TNNT2 Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, dilated, 1D;Cardiomyopathy, familial restrictive, 3 (612422);Cardiomyopathy, hypertrophic, 2 (115195);Cardiomyopathy, dilated, 1D (601494);Left ventricular noncompaction 6 (601494) 20186049;27532257;20031601 False 3 83;17;0 2.20 False ENSG00000118194 ENSG00000118194 HGNC:11949 TPM1 gene TPM1 Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, dilated, 1Y;Cardiomyopathy, dilated, 1Y (611878);Cardiomyopathy, hypertrophic, 3 (115196);Left ventricular noncompaction 9 ( 611878) 20186049;27532257 False 3 83;17;0 2.20 False ENSG00000140416 ENSG00000140416 HGNC:12010 TTN gene TTN Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Myopathy, proximal, with early respiratory muscle involvement (603689);Cardiomyopathy, familial hypertrophic, 9 (613765);Tibial muscular dystrophy, tardive (600334);Muscular dystrophy, limb-girdle, autosomal recessive 10 (608807);Cardiomyopathy, dilated, 1G (604145);Salih myopathy (611705);Cardiomyopathy, dilated, 1G 20186049;27532257;22335739;25589632;29238064;26777568;27869827 False 3 71;14;14 2.20 False ENSG00000155657 ENSG00000155657 HGNC:12403 VCL gene VCL Emory Genetics Laboratory;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, dilated, 1W;Cardiomyopathy, dilated, 1W (611407);Cardiomyopathy, hypertrophic, 15 (613255) 20186049;27532257 False 3 83;17;0 2.20 False ENSG00000035403 ENSG00000035403 HGNC:12665 ANK2 gene ANK2 Expert Review Amber;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown False 2 0;100;0 2.20 False ENSG00000145362 ENSG00000145362 HGNC:493 ANKRD1 gene ANKRD1 Expert Review Amber;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown False 2 0;100;0 2.20 False ENSG00000148677 ENSG00000148677 HGNC:15819 CRYAB gene CRYAB Expert Review Amber;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Cardiomyopathy, dilated, 1II, OMIM:615184;Myopathy, myofibrillar, 2, OMIM:608810 False 2 0;100;0 2.20 False ENSG00000109846 ENSG00000109846 HGNC:2389 CSRP3 gene CSRP3 Emory Genetics Laboratory;Expert list;Expert Review Amber;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted ?Cardiomyopathy, dilated, 1M (607482);Cardiomyopathy, dilated, 1M;Cardiomyopathy, hypertrophic, 12 (612124) 18505755;27532257 False 2 0;67;33 2.20 False ENSG00000129170 ENSG00000129170 HGNC:2472 FKRP gene FKRP Expert Review Amber;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5, OMIM:607155 15833432;18060779;19705481;32914449 False 2 67;33;0 2.20 False ENSG00000181027 ENSG00000181027 HGNC:17997 FKTN gene FKTN Emory Genetics Laboratory;Expert list;Expert Review Amber;Illumina TruGenome Clinical Sequencing Services;London South GLH;Radboud University Medical Center, Nijmegen;South West GLH;Wessex and West Midlands GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal Dilated Cardiomyopathy, Recessive;Cardiomyopathy, dilated, 1X 17878207, 18177472, 18752264 , 19266496, 27065010 False 2 0;67;33 2.20 False ENSG00000106692 ENSG00000106692 HGNC:3622 FLII gene FLII Expert Review Amber;Literature Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal Dilated cardiomyopathy, MONDO:0005021 32870709 False 2 50;50;0 2.20 False ENSG00000177731 ENSG00000177731 HGNC:3750 GATA6 gene GATA6 Expert Review Amber;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown False 2 0;100;0 2.20 False ENSG00000141448 ENSG00000141448 HGNC:4174 LDB3 gene LDB3 Expert Review Amber;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown False 2 0;100;0 2.20 False ENSG00000122367 ENSG00000122367 HGNC:15710 MYH6 gene MYH6 Emory Genetics Laboratory;Expert list;Expert Review Amber;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Cardiomyopathy, hypertrophic, 14 (613251);Cardiomyopathy, dilated, 1EE (613252);{Sick sinus syndrome 3} (614090);Atrial septal defect 3 (614089);Cardiomyopathy, dilated, 1EE 15998695;27532257 False 2 20;20;60 2.20 False ENSG00000197616 ENSG00000197616 HGNC:7576 MYLK3 gene MYLK3 Expert Review Amber;Literature Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BOTH monoallelic and biallelic, autosomal or pseudoautosomal Dilated cardiomyopathy, MONDO:0005021 29235529;31244672;32213617;32870709;30690923 False 2 50;50;0 2.20 False ENSG00000140795 ENSG00000140795 HGNC:29826 MYPN gene MYPN Expert Review Amber;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BOTH monoallelic and biallelic, autosomal or pseudoautosomal False 2 0;100;0 2.20 False ENSG00000138347 ENSG00000138347 HGNC:23246 NRAP gene NRAP Expert Review Amber;Literature Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal Dilated cardiomyopathy, MONDO:0005021 30384889;33534821;28611399;https://doi.org/10.1101/2020.10.12.20211474;32870709 False 2 67;33;0 2.20 False ENSG00000197893 ENSG00000197893 HGNC:7988 PPA2 gene PPA2 Expert Review;Expert Review Amber Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal Sudden cardiac failure, infantile, OMIM:617222;?Sudden cardiac failure, alcohol-induced, OMIM:617223 34400813 False 2 100;0;0 2.20 False ENSG00000138777 ENSG00000138777 HGNC:28883 PRDM16 gene PRDM16 Expert Review Amber;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown False 2 0;100;0 2.20 False ENSG00000142611 ENSG00000142611 HGNC:14000 RHBDF1 gene RHBDF1 Expert Review Amber;Literature Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal 32870709 False 2 0;100;0 2.20 False ENSG00000007384 ENSG00000007384 HGNC:20561 RPL3L gene RPL3L Expert Review Amber;Literature Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal Neonatal dilated cardiomyopathy;dilated cardiomyopathy, MONDO:0005021 32514796;32870709 False 2 50;50;0 2.20 False ENSG00000140986 ENSG00000140986 HGNC:10351 RRAGC gene RRAGC Expert Review Amber;Literature;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Dilated cardiomyopathy, hepatopathy and brain abnormalities 27234373;37057673 False 2 100;0;0 2.20 False ENSG00000116954 ENSG00000116954 HGNC:19902 RRAGD gene RRAGD Expert Review Amber;Literature;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted hypomagnesaemia;cardiomyopathy;tubular renal disease-cardiomyopathy syndrome, MONDO:0019130 34607910 False 2 50;50;0 2.20 False Other ENSG00000025039 ENSG00000025039 HGNC:19903 SGCD gene SGCD Emory Genetics Laboratory;Expert list;Expert Review Amber;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN;Wessex and West Midlands GLH Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BOTH monoallelic and biallelic, autosomal or pseudoautosomal Muscular dystrophy, limb-girdle, autosomal recessive 6 (601287);Cardiomyopathy, dilated, 1L;Cardiomyopathy, dilated, 1L (606685) 19259135;20186049;27532257 False 2 20;60;20 2.20 False ENSG00000170624 ENSG00000170624 HGNC:10807 SLC6A6 gene SLC6A6 Expert Review Amber;Literature Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal Early retinal degeneration;cardiomyopathy 31345061;31903486;29886034;17875433;20804595 False 2 0;100;0 2.20 False ENSG00000131389 ENSG00000131389 HGNC:11052 SPEG gene SPEG Expert Review Amber;Literature Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BIALLELIC, autosomal or pseudoautosomal Dilated cardiomyopathy, MONDO:0005021;Centronuclear myopathy 5, OMIM:615959 32925938;33794647;33926407 False 2 50;50;0 2.20 False ENSG00000072195 ENSG00000072195 HGNC:16901 TAB2 gene TAB2 Expert Review Amber;London South GLH;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Congenital heart defects, nonsyndromic, 2, OMIM:614980 28464518;29700987;32183715;34456334;34990405;34741306;36000780;37153890 False 2 33;33;33 2.20 False ENSG00000055208 ENSG00000055208 HGNC:17075 TBX20 gene TBX20 Expert Review Amber;NHS GMS Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown False 2 0;100;0 2.20 False ENSG00000164532 ENSG00000164532 HGNC:11598 TBX5 gene TBX5 Expert Review Amber;Literature Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Holt-Oram syndrome, OMIM:142900;Dilated cardiomyopathy 32449309;32236096;25963046;25725155 False 2 50;50;0 2.20 False ENSG00000089225 ENSG00000089225 HGNC:11604 TCAP gene TCAP Emory Genetics Laboratory;Expert list;Expert Review Amber;Illumina TruGenome Clinical Sequencing Services;London South GLH;North West GLH;Radboud University Medical Center, Nijmegen;South West GLH;UKGTN Dilated and arrhythmogenic cardiomyopathy Cardiomyopathy Cardiovascular disorders BOTH monoallelic and biallelic, autosomal or pseudoautosomal Cardiomyopathy, hypertrophic, 25 (607487);Cardiomyopathy, dilated, 1N;Muscular dystrophy, limb-girdle, autosomal recessive 7 (601954) 15582318;20186049;27532257 False 2 20;40;40 2.20 False ENSG00000173991 ENSG00000173991 HGNC:11610