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
BDNF	gene	BDNF	Other	Refuted genes			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Central hypoventilation syndrome, congenital, 209880						False	1	0;0;0	0.14	False		ENSG00000176697	ENSG00000176697	HGNC:1033													
FANCM	gene	FANCM	Literature	Refuted genes			BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group M, 614087; Fanconi Anemia; Fanconi Anaemia				28837157		False	1	0;0;100	0.14	False		ENSG00000187790	ENSG00000187790	HGNC:23168													
LIPI	gene	LIPI	Expert list	Refuted genes			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	hypertriglyceridemia						False	1	0;0;100	0.14	False		ENSG00000188992	ENSG00000188992	HGNC:18821													
RAD51C	gene	RAD51C	Other	Refuted genes			BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia, complementation group O, 613390						False	1	0;0;0	0.14	False		ENSG00000108384	ENSG00000108384	HGNC:9820													
TMPO	gene	TMPO	Expert Review	Refuted genes			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Dilated Cardiomyopathy, 115200						False	1	0;0;100	0.14	False		ENSG00000120802	ENSG00000120802	HGNC:11875