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
IL21	gene	IL21	Expert Review Red;Literature	Common Variable Immunodeficiency		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency, common variable, 11 MIM#615767			Recurrent bacterial infections;HP:0002718; Abnormal immunoglobulin level;HP:0010701	24746753;19738033		False	1	0;0;100	1.12	True		ENSG00000138684	ENSG00000138684	HGNC:6005													
NFKBID	gene	NFKBID	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Common Variable Immunodeficiency		Immunological disorders	Unknown				Recurrent bacterial infections;HP:0002718; Abnormal immunoglobulin level;HP:0010701	26973645;25347393;22761313		False	1	0;0;100	1.12	True		ENSG00000167604	ENSG00000167604	HGNC:15671													
TNFSF12	gene	TNFSF12	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Common Variable Immunodeficiency		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Recurrent infections, poor antibody responses, decreased immunoglobulins			Recurrent bacterial infections;HP:0002718; Abnormal immunoglobulin level;HP:0010701	23493554		False	1	0;50;50	1.12	True		ENSG00000239697	ENSG00000239697	HGNC:11927													
VAV1	gene	VAV1	Expert Review Red;Literature	Common Variable Immunodeficiency		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Common variable immnodeficiency			Recurrent bacterial infections;HP:0002718; Abnormal immunoglobulin level;HP:0010701	20638113;23058036		False	1	0;0;100	1.12	True		ENSG00000141968	ENSG00000141968	HGNC:12657