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
STK11	gene	STK11	Expert Review Green;NHS GMS	Peutz Jeghers Syndrome		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Peutz-Jeghers syndrome, OMIM:175200;Peutz-Jeghers syndrome, MONDO:0008280						False	3	100;0;0	1.3	False		ENSG00000118046	ENSG00000118046	HGNC:11389