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
CETP	gene	CETP	Expert Review Amber;Literature	Dyslipidaemia		Endocrine disorders; Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Hyperalphalipoproteinemia MIM#143470;Disorders of high density lipoprotein metabolism			Abnormal circulating lipid concentration;HP:0003119	12070157;2586614;27604308;2215607;2390095		False	2	100;0;0	0.51	True		ENSG00000087237	ENSG00000087237	HGNC:1869													
SCARB1	gene	SCARB1	Expert Review Amber;Literature	Dyslipidaemia		Endocrine disorders; Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	High density lipoprotein cholesterol level QTL6 MIM#610762;Scavenger receptor class B type I deficiency;Inherited hypolipidaemias			Abnormal circulating lipid concentration;HP:0003119	21226579;30720493;21480869;26965621;27604308		False	2	100;0;0	0.51	True		ENSG00000073060	ENSG00000073060	HGNC:1664