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
VWF	gene	VWF	Expert Review Green;NHS GMS	von Willebrand disease		Haematology	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	von Willebrand disease, type 1, OMIM:193400;von Willebrand disease, type 3, OMIM:277480;von Willebrand disease, types 2A, 2B, 2M, and 2N, OMIM:613554;von Willebrand disease 1, MONDO:0008668;von Willebrand disease 2, MONDO:0013304;von Willebrand disease 3, MONDO:0010191						False	3	100;0;0	1.4	False		ENSG00000110799	ENSG00000110799	HGNC:12726