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
FOXN1	gene	FOXN1	Emory Genetics Laboratory;Expert Review Amber	SCID	Primary immunodeficiency disorders	Haematological disorders	BIALLELIC, autosomal or pseudoautosomal	T-B+ SCID;T-B+ SCID, congenital alopecia, nail dystrophy				PMID: 15180707;10206641;21507891		False	2	33;33;33	1.9	True		ENSG00000109101	ENSG00000109101	HGNC:12765													
LAT	gene	LAT	Expert Review Amber;Other	SCID	Primary immunodeficiency disorders	Haematological disorders	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 52, 617514				27522155; 27242165		False	2	0;0;0	1.9	False		ENSG00000213658	ENSG00000213658	HGNC:18874													
TBX1	gene	TBX1	Emory Genetics Laboratory;Expert Review Amber	SCID	Primary immunodeficiency disorders	Haematological disorders		T-B+ SCID						False	2	0;40;60	1.9	True		ENSG00000184058	ENSG00000184058	HGNC:11592