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
APOC3	gene	APOC3	Expert Review Amber;Literature	Periodic fever syndromes	Multi-system inflammatory/autoimmune disorders	Rheumatological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Amyloidosis				PMID: 26790392 		False	2	0;100;0	1.34	False		ENSG00000110245	ENSG00000110245	HGNC:610													
TNFAIP3	gene	TNFAIP3	Expert Review Amber;Literature	Periodic fever syndromes	Multi-system inflammatory/autoimmune disorders	Rheumatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Autoinflammatory syndrome, familial, Behcet-like, OMIM:616744				26642243		False	2	100;0;0	1.34	False		ENSG00000118503	ENSG00000118503	HGNC:11896