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
DPYD	gene	DPYD	Expert Review Amber;Other	Pharmacogenomics_Paediatric		Screening	Other	Fluoropyrimidine				29152729		False	2	0;100;0	0.50	True	Other	ENSG00000188641	ENSG00000188641	HGNC:3012													
POLG	gene	POLG	Expert Review Amber;Other	Pharmacogenomics_Paediatric		Screening	BIALLELIC, autosomal or pseudoautosomal	Alpers syndrome				20138553		False	2	0;100;0	0.50	True		ENSG00000140521	ENSG00000140521	HGNC:9179