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
TSC1	gene	TSC1	Eligibility statement prior genetic testing;Emory Genetics Laboratory;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen;UKGTN	Classical tuberous sclerosis	Neurodevelopmental disorders	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Focal cortical dysplasia, Taylor balloon cell type, 607341Lymphangioleiomyomatosis, 606690Tuberous sclerosis-1, 191100;Tuberous Sclerosis				PMID: 17304050		False	3	100;0;0	1.3	True		ENSG00000165699	ENSG00000165699	HGNC:12362													
TSC2	gene	TSC2	Eligibility statement prior genetic testing;Emory Genetics Laboratory;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen;UKGTN	Classical tuberous sclerosis	Neurodevelopmental disorders	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Tuberous sclerosis-2, 613254;Tuberous Sclerosis				PMID: 17304050		False	3	100;0;0	1.3	True		ENSG00000103197	ENSG00000103197	HGNC:12363