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
LMAN1	gene	LMAN1	Expert Review Green;London South GLH;NHS GMS;North West GLH;Wessex and West Midlands GLH;Yorkshire and North EastGLH	Combined factor V and VIII deficiency		Haematology	BIALLELIC, autosomal or pseudoautosomal	Combined factor V and VIII deficiency, OMIM:227300				10090934;10090935;16304051		False	3	80;20;0	1.11	False		ENSG00000074695	ENSG00000074695	HGNC:6631													
MCFD2	gene	MCFD2	Expert Review Green;London South GLH;NHS GMS;North West GLH;Wessex and West Midlands GLH;Yorkshire and North East GLH	Combined factor V and VIII deficiency		Haematology	BIALLELIC, autosomal or pseudoautosomal	Factor V and factor VIII, combined deficiency of, OMIM:613625				20004600;12717434;16304051		False	3	80;20;0	1.11	False		ENSG00000180398	ENSG00000180398	HGNC:18451