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
CDC73	gene	CDC73	Eligibility statement prior genetic testing;Expert list;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen;UKGTN	Parathyroid Cancer	Breast and endocrine	Tumour syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hyperparathyroidism, familial primary, 145000; Hyperparathyroidism-jaw tumor syndrome, 145001; Parathyroid adenoma with cystic changes, 145001; Parathyroid carcinoma, 608266;Parathyroid Carcinoma;Pituitary Cancer, Parathyroid and Hypercalcemia;Parathyroid Cancer 						False	3	100;0;0	1.5	True		ENSG00000134371	ENSG00000134371	HGNC:16783													
MEN1	gene	MEN1	Expert Review Green;Radboud University Medical Center, Nijmegen;UKGTN	Parathyroid Cancer	Breast and endocrine	Tumour syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Multiple endocrine neoplasia 1, 131100; Carcinoid tumor of lung; Parathyroid adenoma, somatic; Lipoma, somatic; Angiofibroma, somatic; Adrenal adenoma, somatic;Pituitary Cancer, Parathyroid and Hypercalcemia						False	3	100;0;0	1.5	True		ENSG00000133895	ENSG00000133895	HGNC:7010