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
GLRA1	gene	GLRA1	Emory Genetics Laboratory;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen;UKGTN	Sudden death in young people	Cardiac arrhythmia	Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Hyperekplexia, hereditary 1, 149400						False	3	0;0;0	1.16	False		ENSG00000145888	ENSG00000145888	HGNC:4326													
PHOX2B	gene	PHOX2B	Emory Genetics Laboratory;Expert Review Green;Literature;Other;Radboud University Medical Center, Nijmegen	Sudden death in young people	Cardiac arrhythmia	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	sudden infant death syndrome; unclassified sudden infant death; USID;Congenital Central Hypoventilation Syndrome; CCHS;Central hypoventilation syndrome, congenital, with or without Hirschsprung disease, 209880						False	3	0;0;0	1.16	False	Other - please provide details in the comments	ENSG00000109132	ENSG00000109132	HGNC:9143													
PPA2	gene	PPA2	Expert Review;Expert Review Green;Literature	Sudden death in young people	Cardiac arrhythmia	Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Unexpected cardiac arrest in infancy				27523598		False	3	100;0;0	1.16	False		ENSG00000138777	ENSG00000138777	HGNC:28883													
TSPYL1	gene	TSPYL1	Expert Review Green;Other;Radboud University Medical Center, Nijmegen	Sudden death in young people	Cardiac arrhythmia	Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Sudden infant death with dysgenesis of the testes syndrome OMIM:608800;sudden infant death-dysgenesis of the testes syndrome MONDO:0012124				32885560;33075815;15273283;25449952;16418600;19463995;22137496		False	3	100;0;0	1.16	False		ENSG00000189241	ENSG00000189241	HGNC:12382													
KCNJ8	gene	KCNJ8	Emory Genetics Laboratory;Expert Review Amber;Radboud University Medical Center, Nijmegen	Sudden death in young people	Cardiac arrhythmia	Cardiovascular disorders	Unknown	arrhythmia;Sudden infant death syndrome; ?Ventricular fibrillation				PMID: 21836131		False	2	0;0;0	1.16	False		ENSG00000121361	ENSG00000121361	HGNC:6269