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
GGCX	gene	GGCX	Expert Review Green;NHS GMS	Combined vitamin K-dependent clotting factor deficiency		Haematology	BIALLELIC, autosomal or pseudoautosomal	Vitamin K-dependent clotting factors, combined deficiency of, 1, OMIM:277450;vitamin K-dependent clotting factors, combined deficiency of, type 1,  MONDO:0010187						False	3	100;0;0	1.4	False		ENSG00000115486	ENSG00000115486	HGNC:4247													
VKORC1	gene	VKORC1	Expert Review Green;NHS GMS	Combined vitamin K-dependent clotting factor deficiency		Haematology	BIALLELIC, autosomal or pseudoautosomal	Vitamin K-dependent clotting factors, combined deficiency of, type 2, OMIM:607473;vitamin K-dependent clotting factors, combined deficiency of, type 2, MONDO:0011837						False	3	100;0;0	1.4	False		ENSG00000167397	ENSG00000167397	HGNC:23663													
