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
EXO1	gene	EXO1	ClinGen	Colorectal Cancer and Polyposis		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Lynch syndrome, MONDO:0005835			Hereditary nonpolyposis colorectal carcinoma;HP:0006716; Colorectal polyposis;HP:0200063			False	1	0;0;100	1.4	False		ENSG00000174371	ENSG00000174371	HGNC:3511													
PMS1	gene	PMS1	ClinGen;Expert Review Red	Colorectal Cancer and Polyposis		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Lynch syndrome, MONDO:0005835			Hereditary nonpolyposis colorectal carcinoma;HP:0006716; Colorectal polyposis;HP:0200063			False	1	0;0;100	1.4	True		ENSG00000064933	ENSG00000064933	HGNC:9121													
SEMA4A	gene	SEMA4A	ClinGen;Expert Review Red	Colorectal Cancer and Polyposis		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Lynch syndrome, MONDO:0005835			Hereditary nonpolyposis colorectal carcinoma;HP:0006716; Colorectal polyposis;HP:0200063			False	1	0;0;100	1.4	True		ENSG00000196189	ENSG00000196189	HGNC:10729