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
CASR	gene	CASR	Expert Review Amber;Victorian Clinical Genetics Services	Pancreatitis		Gastroenterological disorders	Other	Susceptibility to pancreatitis			Pancreatitis;HP:0001733	16497624;26166472		False	2	0;100;0	1.6	True		ENSG00000036828	ENSG00000036828	HGNC:1514													
CELA3B	gene	CELA3B	Expert Review Amber;Literature	Pancreatitis		Gastroenterological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Chronic pancreatitis			Pancreatitis;HP:0001733	31369399;33565216		False	2	0;100;0	1.6	True	Other	ENSG00000219073	ENSG00000219073	HGNC:15945													
CTRC	gene	CTRC	Expert Review Amber;Victorian Clinical Genetics Services	Pancreatitis		Gastroenterological disorders	Other	{Pancreatitis, chronic, susceptibility to}, MIM#167800			Pancreatitis;HP:0001733	18059268;18172691;28502372		False	2	0;100;0	1.6	True		ENSG00000162438	ENSG00000162438	HGNC:2523