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
FBXW7	gene	FBXW7	Expert Review Amber;Literature	Cancer Predisposition_Paediatric		Cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Wilms tumour, hereditary, MONDO:0003321, FBXW7-related				PMID: 30885698;PMID: 26482194		False	2	50;50;0	0.131	True		ENSG00000109670	ENSG00000109670	HGNC:16712													
FH	gene	FH	Expert Review Amber;Victorian Clinical Genetics Services	Cancer Predisposition_Paediatric		Cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Leiomyomatosis and renal cell cancer, MIM# 150800						False	2	0;100;0	0.131	True		ENSG00000091483	ENSG00000091483	HGNC:3700													
NYNRIN	gene	NYNRIN	Expert Review Amber;Literature	Cancer Predisposition_Paediatric		Cancer	BIALLELIC, autosomal or pseudoautosomal	Wilms tumour predisposition				PMID: 30885698		False	2	0;100;0	0.131	True		ENSG00000205978	ENSG00000205978	HGNC:20165