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
APOB	gene	APOB	Expert Review Red;NHS GMS;South West GLH	Familial chylomicronaemia syndrome (FCS)		Lipids	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Hypercholesterolemia, familial, 2 OMIM:144010;hypercholesterolemia, autosomal dominant, type B MONDO:0007751;Hypobetalipoproteinemia OMIM:615558;familial hypobetalipoproteinemia 1 MONDO:0014252						False	1	50;0;50	3.4	False		ENSG00000084674	ENSG00000084674	HGNC:603													
LIPI	gene	LIPI	Expert Review Red;NHS GMS;South West GLH	Familial chylomicronaemia syndrome (FCS)		Lipids	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	hypertriglyceridemia (disease) MONDO:0005347						False	1	0;0;100	3.4	False		ENSG00000188992	ENSG00000188992	HGNC:18821