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
GNB5	gene	GNB5	Expert Review Green;Literature;NHS GMS	Cardiac arrhythmias - additional genes		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Intellectual developmental disorder with cardiac arrhythmia, OMIM:617173;Language delay and ADHD/cognitive impairment with or without cardiac arrhythmia, OMIM:617182				27523599;28697420;29368331;33172956		False	3	100;0;0	3.9	False		ENSG00000069966	ENSG00000069966	HGNC:4401													
TANGO2	gene	TANGO2	Expert Review;Expert Review Amber	Cardiac arrhythmias - additional genes		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration, OMIM:616878;recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome, MONDO:0018820				26805781;26805782;30245509;31339582;32929747;35568137;40156300		False	2	50;50;0	3.9	False		ENSG00000183597	ENSG00000183597	HGNC:25439													
ANK2	gene	ANK2	Expert Review Red;NHS GMS	Cardiac arrhythmias - additional genes		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Long QT syndrome 4, 600919;Cardiac arrhythmia, ankyrin-B-related, 600919				31983240		False	1	33;0;67	3.9	False		ENSG00000145362	ENSG00000145362	HGNC:493													
MLIP	gene	MLIP	Literature	Cardiac arrhythmias - additional genes		Cardiology	BIALLELIC, autosomal or pseudoautosomal	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis, MIM# 620138;Arrhythmia, HP:0011675				26436652;32719146;33802236;34581780;34935254		False	1	0;0;100	3.9	False		ENSG00000146147	ENSG00000146147	HGNC:21355													
