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
LCP2	gene	LCP2	Expert Review Amber;Literature	Severe Combined Immunodeficiency (absent T absent B cells)		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency 81, MIM# 619374;Severe combined immunodeficiency			Severe combined immunodeficiency;HP:0004430	33231617		False	2	0;100;0	1.13	True		ENSG00000043462	ENSG00000043462	HGNC:6529