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
CDKN1A	gene	CDKN1A	Expert Review Amber;UKGTN	Familial hyperparathyroidism or hypocalciuric hypercalcaemia		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	No OMIM number;Multiple endocrine neoplasia 1				19141585;23715670;30536424		False	2	0;0;100	3.7	False		ENSG00000124762	ENSG00000124762	HGNC:1784													
CDKN2B	gene	CDKN2B	Expert Review Amber;UKGTN	Familial hyperparathyroidism or hypocalciuric hypercalcaemia		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	No OMIM number;Multiple endocrine neoplasia 1				19141585;23715670;30536424		False	2	0;0;100	3.7	False		ENSG00000147883	ENSG00000147883	HGNC:1788													
CDKN2C	gene	CDKN2C	Expert Review Amber;UKGTN	Familial hyperparathyroidism or hypocalciuric hypercalcaemia		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	No OMIM number;Multiple endocrine neoplasia 1				19141585;23715670;30536424		False	2	0;0;100	3.7	False		ENSG00000123080	ENSG00000123080	HGNC:1789