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
RASA2	gene	RASA2	Expert Review Amber;Victorian Clinical Genetics Services	Rasopathy		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Rasopathy			Rasopathy;MONDO:0021060	25049390;30311384		False	2	0;100;0	0.105	True		ENSG00000155903	ENSG00000155903	HGNC:9872													
RRAS	gene	RRAS	Expert Review Amber;Victorian Clinical Genetics Services	Rasopathy		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Noonan syndrome			Rasopathy;MONDO:0021060	24705357		False	2	0;100;0	0.105	True		ENSG00000126458	ENSG00000126458	HGNC:10447													
RREB1	gene	RREB1	Expert Review Amber;Literature	Rasopathy		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Rasopathy, MONDO:0021060, RREB1-related			Rasopathy;MONDO:0021060	32938917;38332451		False	2	0;100;0	0.105	True		ENSG00000124782	ENSG00000124782	HGNC:10449