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
HNF1A	gene	HNF1A	Expert Review Red	Newborns additional phenotypes panel 1			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	HNF1A associated MODY						False	1	0;0;0	0.114	False		ENSG00000135100	ENSG00000135100	HGNC:11621													
HNF4A	gene	HNF4A	Expert Review Red	Newborns additional phenotypes panel 1			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	HNF4A associated MODY						False	1	0;0;0	0.114	False		ENSG00000101076	ENSG00000101076	HGNC:5024													
MLH1	gene	MLH1	Expert Review Red	Newborns additional phenotypes panel 1			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Hereditary nonpolyposis colorectal cancer-2						False	1	0;0;0	0.114	False		ENSG00000076242	ENSG00000076242	HGNC:7127													
MSH2	gene	MSH2	Expert Review Red	Newborns additional phenotypes panel 1			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Hereditary nonpolyposis colorectal cancer-1						False	1	0;0;0	0.114	False		ENSG00000095002	ENSG00000095002	HGNC:7325													
MSH6	gene	MSH6	Expert Review Red	Newborns additional phenotypes panel 1			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Hereditary nonpolyposis colorectal cancer-5						False	1	0;0;0	0.114	False		ENSG00000116062	ENSG00000116062	HGNC:7329													
PMS2	gene	PMS2	Expert Review Red	Newborns additional phenotypes panel 1			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Hereditary nonpolyposis colorectal cancer-4						False	1	0;0;0	0.114	False		ENSG00000122512	ENSG00000122512	HGNC:9122													
TNFRSF13B	gene	TNFRSF13B	Expert Review Red	Newborns additional phenotypes panel 1			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Common variable immune deficiency 2, autosomal dominant						False	1	0;0;0	0.114	False		ENSG00000240505	ENSG00000240505	HGNC:18153													
UROD	gene	UROD	Expert Review Red	Newborns additional phenotypes panel 1			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Porphyria cutanea tarda						False	1	0;0;0	0.114	False		ENSG00000126088	ENSG00000126088	HGNC:12591													
WFS1	gene	WFS1	Expert Review Red	Newborns additional phenotypes panel 1			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Wolfram-like Syndrome						False	1	0;0;0	0.114	False	Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments	ENSG00000109501	ENSG00000109501	HGNC:12762