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
SMARCA4	gene	SMARCA4	Expert Review;Expert Review Green;NHS GMS	Familial rhabdoid tumours		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	{Rhabdoid tumor predisposition syndrome 2}, OMIM:613325;Rhabdoid tumor predisposition syndrome 2, MONDO:0013224						False	3	100;0;0	1.11	False		ENSG00000127616	ENSG00000127616	HGNC:11100													
SMARCB1	gene	SMARCB1	Expert Review;Expert Review Green;NHS GMS	Familial rhabdoid tumours		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	{Rhabdoid tumor predisposition syndrome 1}, OMIM:609322;Rhabdoid tumor predisposition syndrome 1, MONDO:0012252						False	3	100;0;0	1.11	False		ENSG00000099956	ENSG00000099956	HGNC:11103