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	Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Left Ventricular Noncompaction Cardiomyopathy	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Left ventricular noncompaction 4 ;Left Ventricular Noncompaction Cardiomyopathy 						False	3	100;0;0	1.5	True		ENSG00000159251	ENSG00000159251	HGNC:143													
MYBPC3	gene	MYBPC3	Eligibility statement prior genetic testing;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Left Ventricular Noncompaction Cardiomyopathy	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Left ventricular noncompaction 10, ;Hypertrophic cardiomyopathy 						False	3	100;0;0	1.5	True		ENSG00000134571	ENSG00000134571	HGNC:7551													
MYH7	gene	MYH7	Eligibility statement prior genetic testing;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Left Ventricular Noncompaction Cardiomyopathy	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Left ventricular noncompaction 5, OMIM:613426;Dilated cardiomyopathy 1S, MONDO:0013262						False	3	100;0;0	1.5	True		ENSG00000092054	ENSG00000092054	HGNC:7577													
TAZ	gene	TAZ	Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services	Left Ventricular Noncompaction 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)	Left Ventricular Noncompaction Cardiomyopathy 						False	3	100;0;0	1.5	True		ENSG00000102125	ENSG00000102125	HGNC:11577													
TNNT2	gene	TNNT2	Eligibility statement prior genetic testing;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Left Ventricular Noncompaction Cardiomyopathy	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Left ventricular noncompaction 6, ;Hypertrophic cardiomyopathy 						False	3	100;0;0	1.5	True		ENSG00000118194	ENSG00000118194	HGNC:11949													
TPM1	gene	TPM1	Expert list;Expert Review Green;Radboud University Medical Center, Nijmegen	Left Ventricular Noncompaction Cardiomyopathy	Cardiomyopathy	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Left ventricular noncompaction 9, 						False	3	100;0;0	1.5	True		ENSG00000140416	ENSG00000140416	HGNC:12010													
