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
APOC3	gene	APOC3	Expert Review Red;Royal Melbourne Hospital	Dyslipidaemia		Endocrine disorders; Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Apolipoprotein C-III deficiency MIM#614028			Abnormal circulating lipid concentration;HP:0003119	PMID: 19074352		False	1	0;0;100	0.51	True		ENSG00000110245	ENSG00000110245	HGNC:610													
STAP1	gene	STAP1	Expert Review Red;Literature	Dyslipidaemia		Endocrine disorders; Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Familial hypercholesterolemia MONDO:0005439			Abnormal circulating lipid concentration;HP:0003119	31809983;31996024;32208993		False	1	0;0;100	0.51	True		ENSG00000035720	ENSG00000035720	HGNC:24133