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
CLDN2	gene	CLDN2	Expert Review Red;Victorian Clinical Genetics Services	Pancreatitis		Gastroenterological disorders	Other	Susceptibility to pancreatitis			Pancreatitis;HP:0001733	29884332;31163246		False	1	0;0;100	1.6	True		ENSG00000165376	ENSG00000165376	HGNC:2041