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
A2M	gene	A2M	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Alzheimer disease, MONDO:0004975						False	1	0;0;100	0.433	True		ENSG00000175899	ENSG00000175899	HGNC:7													
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	0.433	True		ENSG00000127914	ENSG00000127914	HGNC:379													
ALG10B	gene	ALG10B	ClinGen	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	long QT syndrome MONDO:0002442				37071726		False	1	0;0;100	0.433	False		ENSG00000175548	ENSG00000175548	HGNC:31088													
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	0.433	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	0.433	True		ENSG00000165995	ENSG00000165995	HGNC:1402													
CALHM1	gene	CALHM1	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			Unknown							False	1	0;0;100	0.433	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	0.433	True		ENSG00000120885	ENSG00000120885	HGNC:2095													
DLST	gene	DLST	Expert list;Expert Review;Expert Review Red;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Paragangliomas 7, MONDO:0032771;Pheochromocytoma, MONDO:0008233;Hereditary pheochromocytoma-paraganglioma, MONDO:0017366;Pheochromocytoma/paraganglioma syndrome 7, MIM#618475				PMID: 30929736, 33180916		False	1	0;0;100	0.433	False		ENSG00000119689	ENSG00000119689	HGNC:2911													
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	0.433	True		ENSG00000152642	ENSG00000152642	HGNC:28956													
KCNE2	gene	KCNE2	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Long QT syndrome 6, MIM# 613693				31983240;28794082;31983240		False	1	0;67;33	0.433	True		ENSG00000159197	ENSG00000159197	HGNC:6242													
NR4A2	gene	NR4A2	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			Unknown							False	1	0;0;100	0.433	True		ENSG00000153234	ENSG00000153234	HGNC:7981													
PBRM1	gene	PBRM1	Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	renal cell carcinoma MONDO:0005086				25911086		False	1	0;0;100	0.433	False		ENSG00000163939	ENSG00000163939	HGNC:30064													
PCP4	gene	PCP4	Expert Review Red;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Familial amyotrophic lateral sclerosis, MONDO:0005144, PCP4-related				39852553		False	1	0;0;100	0.433	True		ENSG00000183036	ENSG00000183036	HGNC:8742													
PLA2G2A	gene	PLA2G2A	Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	colorectal cancer MONDO:0005575				9272153;8912789		False	1	0;0;100	0.433	False		ENSG00000188257	ENSG00000188257	HGNC:9031													
RABL3	gene	RABL3	Expert Review Red;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	pancreatic carcinoma				31406347;33353859;33724601		False	1	100;0;0	0.433	True		ENSG00000144840	ENSG00000144840	HGNC:18072													
RNASEL	gene	RNASEL	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			Unknown							False	1	0;0;0	0.433	True		ENSG00000135828	ENSG00000135828	HGNC:10050													
SCN3B	gene	SCN3B	Expert Review Red;Victorian Clinical Genetics Services	Incidentalome			Unknown							False	1	0;0;0	0.433	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	0.433	True		ENSG00000177098	ENSG00000177098	HGNC:10592													
SLC25A11	gene	SLC25A11	Expert list;Expert Review;Expert Review Red;Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Paragangliomas 6, MONDO:0032767;Pheochromocytoma, MONDO:0008233;Hereditary pheochromocytoma-paraganglioma, MONDO:0017366;Pheochromocytoma/paraganglioma syndrome 6, MIM#618464				PMID: 29431636		False	1	0;0;100	0.433	False		ENSG00000108528	ENSG00000108528	HGNC:10981													
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	0.433	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	0.433	True		ENSG00000101400	ENSG00000101400	HGNC:11167													
TMEM168	gene	TMEM168	ClinGen	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Brugada syndrome MONDO:0015263				https://search.clinicalgenome.org/CCID:009114		False	1	0;0;100	0.433	False		ENSG00000146802	ENSG00000146802	HGNC:25826													
TMEM230	gene	TMEM230	Expert Review;Expert Review Red	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Parkinson disease 21, MONDO:0005180				30804554;27270108;28115417;28017548;30804555;30804556;31323517		False	1	0;0;100	0.433	True		ENSG00000089063	ENSG00000089063	HGNC:15876													
VEZF1	gene	VEZF1	Literature	Incidentalome			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	dilated cardiomyopathy MONDO:0005021				36657711		False	1	0;0;100	0.433	False		ENSG00000136451	ENSG00000136451	HGNC:12949