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
ABCC8	gene	ABCC8	Eligibility statement prior genetic testing;Expert Review Amber;Illumina TruGenome Clinical Sequencing Services;NHS GMS;Radboud University Medical Center, Nijmegen;UKGTN	DEMO Diabetes neonatal onset	Disorders of unusual phenotypes	Endocrine disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Transient Neonatal Diabetes, Dominant;Isolated permanent neonatal diabetes;Diabetes mellitus, noninsulin-dependent, 125853;Diabetes mellitus, transient neonatal 2,  610374;Permanent Neonatal Diabetes Mellitus;Hyperinsulinemic hypoglycemia, familial, 1, 256450;transient neonatal diabetes (Dominant);Diabetes mellitus, permanent neonatal, 606176;isolated transient neonatal diabetes, neonatal diabetes and developmental delay;Permanent neonatal diabetes mellitus;Hypoglycemia of infancy, leucine-sensitive, 240800						False	2	100;0;0	1.4	False		ENSG00000006071	ENSG00000006071	HGNC:59