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
CELA3B	gene	CELA3B	Expert Review Green;Literature	Pancreatitis		Gastrohepatology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Chronic Pancreatitis, MONDO:0005003;diabetes mellitus (disease), MONDO:0005015;Pancreatic cancer				31369399;33565216		False	3	100;0;0	3.5	False	Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments	ENSG00000219073	ENSG00000219073	HGNC:15945													
CFTR	gene	CFTR	EUROPAC;Expert Review Green;NHS GMS	Pancreatitis		Gastrohepatology	BIALLELIC, autosomal or pseudoautosomal	"{Pancreatitis, hereditary} 167800;Cystic fibrosis 	219700"				9725921;15987793;16134171;16193325;11729110;23951356;22427236;25033378;22658665;26856995;27555793;1345141;15749233;25033378;20977904;22427236		False	3	100;0;0	3.5	True		ENSG00000001626	ENSG00000001626	HGNC:1884													
PRSS1	gene	PRSS1	EUROPAC;Expert Review Green;NHS GMS	Pancreatitis		Gastrohepatology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Pancreatitis, hereditary 167800				8841182;10204851;10529393;11097832;11702203;15776435;16791840;18461367;17072318		False	3	100;0;0	3.5	True	Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments	ENSG00000204983	ENSG00000204983	HGNC:9475													
SPINK1	gene	SPINK1	EUROPAC;Expert Review Green;NHS GMS	Pancreatitis		Gastrohepatology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Pancreatitis, hereditary 167800				10835640;11355022;11938439;16823394;17274009;27535533		False	3	100;0;0	3.5	True		ENSG00000164266	ENSG00000164266	HGNC:11244