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
RAD51	gene	RAD51	Expert Review;Expert Review Amber	Radial Ray Abnormalities		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Fanconi anaemia, complementation group R, MIM# 617244			Abnormality of radial ray;HP:0410049	26253028;26681308;30907510		False	2	0;100;0	1.15	True		ENSG00000051180	ENSG00000051180	HGNC:9817													
RFWD3	gene	RFWD3	Expert Review Amber;Literature	Radial Ray Abnormalities		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Fanconi anemia MONDO:0019391			Abnormality of radial ray;HP:0410049	28691929;38058754		False	2	0;100;0	1.15	True		ENSG00000168411	ENSG00000168411	HGNC:25539													
RPS29	gene	RPS29	Expert Review Amber;Victorian Clinical Genetics Services	Radial Ray Abnormalities		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Diamond-Blackfan anemia 13, MIM# 615909			Abnormality of radial ray;HP:0410049	24829207		False	2	0;100;0	1.15	True		ENSG00000213741	ENSG00000213741	HGNC:10419