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
ANKRD1	gene	ANKRD1	Emory Genetics Laboratory;Expert list;Illumina TruGenome Clinical Sequencing Services;London South GLH;South West GLH	Dilated Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Dilated Cardiomyopathy, Dominant 						False	2	0;67;33	1.97	False		ENSG00000148677	ENSG00000148677	HGNC:15819													
CRYAB	gene	CRYAB	Emory Genetics Laboratory;Expert list;London South GLH;Radboud University Medical Center, Nijmegen;South West GLH	Dilated Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Cardiomyopathy, dilated, 1II, OMIM:615184;Myopathy, myofibrillar, 2, OMIM:608810						False	2	0;67;33	1.97	False		ENSG00000109846	ENSG00000109846	HGNC:2389													
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 Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Cardiomyopathy, dilated, 1X;Dilated Cardiomyopathy, Recessive 						False	2	0;50;50	1.97	False		ENSG00000106692	ENSG00000106692	HGNC:3622													
FLNC	gene	FLNC	Expert Review Amber;Oxford Medical Genetics Laboratory;South West GLH;Wessex and West Midlands GLH	Dilated Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	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				28008423;29551499		False	2	100;0;0	1.97	False		ENSG00000128591	ENSG00000128591	HGNC:3756													
GATAD1	gene	GATAD1	Emory Genetics Laboratory;Expert list;London South GLH;Radboud University Medical Center, Nijmegen;South West GLH	Dilated Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Cardiomyopathy, dilated, 2B 						False	2	33;67;0	1.97	False		ENSG00000157259	ENSG00000157259	HGNC:29941													
LDB3	gene	LDB3	Emory Genetics Laboratory;Expert list;Expert Review Amber;Illumina TruGenome Clinical Sequencing Services;London South GLH;Radboud University Medical Center, Nijmegen;South West GLH	Dilated Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cardiomyopathy, dilated 1C				4662268;14660611;16427346		False	2	0;75;25	1.97	False		ENSG00000122367	ENSG00000122367	HGNC:15710													
MYPN	gene	MYPN	Emory Genetics Laboratory;Expert list;London South GLH;Radboud University Medical Center, Nijmegen;South West GLH	Dilated Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Cardiomyopathy, dilated, 1KK						False	2	0;67;33	1.97	False		ENSG00000138347	ENSG00000138347	HGNC:23246													
PSEN1	gene	PSEN1	Expert list;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen;South West GLH	Dilated Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cardiomyopathy, dilated, 1U						False	2	0;33;67	1.97	False		ENSG00000080815	ENSG00000080815	HGNC:9508													
PSEN2	gene	PSEN2	Expert list;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen;South West GLH	Dilated Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cardiomyopathy, dilated, 1V 						False	2	0;50;50	1.97	False		ENSG00000143801	ENSG00000143801	HGNC:9509													
SCN1B	gene	SCN1B	Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen;South West GLH	Dilated Cardiomyopathy and conduction defects	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Cardiac conduction defect, nonspecific, OMIM:612838;Brugada syndrome 5, OMIM:612838;Atrial fibrillation, familial, 13, OMIM:615377						False	2	0;50;50	1.97	False		ENSG00000105711	ENSG00000105711	HGNC:10586