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
CASR	gene	CASR	Expert Review Amber	Newborns additional phenotypes panel 3			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Autosomal dominant hypocalcemia 1						False	2	0;0;0	0.13	False	Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments	ENSG00000036828	ENSG00000036828	HGNC:1514													
CFH	gene	CFH	Expert Review Amber	Newborns additional phenotypes panel 3			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Hemolytic uremic syndrome, atypical, susceptibility to, 1, autosomal dominant						False	2	0;0;0	0.13	False		ENSG00000000971	ENSG00000000971	HGNC:4883													
SCN4A	gene	SCN4A	Expert Review Amber	Newborns additional phenotypes panel 3			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Paramyotonia congenita and Sodium channel myotonia						False	2	0;0;0	0.13	False	Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments	ENSG00000007314	ENSG00000007314	HGNC:10591