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
AKAP9	gene	AKAP9	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Long QT syndrome 11, MIM# 611820				31983240		False	1	0;0;100	0.318	True		ENSG00000127914	ENSG00000127914	HGNC:379													
ANK2	gene	ANK2	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Long QT syndrome 4, MIM# 600919				31983240		False	1	0;0;100	0.318	True		ENSG00000145362	ENSG00000145362	HGNC:493													
CACNB2	gene	CACNB2	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Brugada syndrome 4, MIM# 611876				29959160		False	1	0;0;100	0.318	True		ENSG00000165995	ENSG00000165995	HGNC:1402													
CALHM1	gene	CALHM1	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			Unknown							False	1	0;0;100	0.318	True		ENSG00000185933	ENSG00000185933	HGNC:23494													
CLU	gene	CLU	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			Unknown	Alzheimer's Disease (MIM#104300)						False	1	0;0;100	0.318	True		ENSG00000120885	ENSG00000120885	HGNC:2095													
GPD1L	gene	GPD1L	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Brugada syndrome 2, MIM# 611777				17967977;19666841		False	1	0;0;100	0.318	True		ENSG00000152642	ENSG00000152642	HGNC:28956													
NR4A2	gene	NR4A2	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			Unknown							False	1	0;0;100	0.318	True		ENSG00000153234	ENSG00000153234	HGNC:7981													
RABL3	gene	RABL3	Expert Review Red;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	pancreatic carcinoma				31406347;33353859;33724601		False	1	100;0;0	0.318	True		ENSG00000144840	ENSG00000144840	HGNC:18072													
RNASEL	gene	RNASEL	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			Unknown							False	1	0;0;0	0.318	True		ENSG00000135828	ENSG00000135828	HGNC:10050													
SCN3B	gene	SCN3B	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			Unknown							False	1	0;0;0	0.318	False		ENSG00000166257	ENSG00000166257	HGNC:20665													
SCN4B	gene	SCN4B	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Long QT syndrome 10, MIM#	611819"				31983240		False	1	0;0;100	0.318	True		ENSG00000177098	ENSG00000177098	HGNC:10592													
SNCB	gene	SNCB	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Dementia, Lewy body, MIM#127750				15365127;20697047		False	1	0;50;50	0.318	True		ENSG00000074317	ENSG00000074317	HGNC:11140													
SNTA1	gene	SNTA1	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Long QT syndrome 12, MIM# 612955				31983240		False	1	0;0;100	0.318	True		ENSG00000101400	ENSG00000101400	HGNC:11167