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
FOXO3	gene	FOXO3	Literature	Peutz-Jeghers syndrome	GI tract	Tumour syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hamartomatous polyposis syndromes including Peutz-Jeghers and PTEN hamartoma tumor syndromes				25208626		False	1	0;0;100	0.21	False		ENSG00000118689	ENSG00000118689	HGNC:3821													
SMAD9	gene	SMAD9	Literature	Peutz-Jeghers syndrome	GI tract	Tumour syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hamartomatous Polyposis; Gastrointestinal Ganglioneuromas				26122142		False	1	0;0;100	0.21	False	Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments	ENSG00000120693	ENSG00000120693	HGNC:6774