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
ADGRV1	gene	ADGRV1	Expert Review Red;Radboud University Medical Center, Nijmegen	Genetic Epilepsies with Febrile Seizures Plus (GEFS+)	Inherited Epilepsy Syndromes	Neurology and neurodevelopmental disorders		Febrile seizures, familial, 4, 604352Usher syndrome, type 2C, 605472Usher syndrome, type 2C, GPR98/PDZD7 digenic, 605472						False	1	0;0;0	1.10	True		ENSG00000164199	ENSG00000164199	HGNC:17416													
CPA6	gene	CPA6	Expert Review Red;Radboud University Medical Center, Nijmegen	Genetic Epilepsies with Febrile Seizures Plus (GEFS+)	Inherited Epilepsy Syndromes	Neurology and neurodevelopmental disorders		Febrile seizures, familial, 11; Epilepsy, familial temporal lobe, 5						False	1	0;0;0	1.10	True		ENSG00000165078	ENSG00000165078	HGNC:17245													
SCN9A	gene	SCN9A	Expert Review Red;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Genetic Epilepsies with Febrile Seizures Plus (GEFS+)	Inherited Epilepsy Syndromes	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	 Epilepsy, generalized, with febrile seizures plus, type 7;Febrile seizures, familial, 3B; Familial Febrile Seizures; Generalized Epilepsy with Febrile Seizures Plus						False	1	0;0;0	1.10	True		ENSG00000169432	ENSG00000169432	HGNC:10597