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
BRCA2	gene	BRCA2	Expert list;Expert Review Green	Familial prostate cancer			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Prostate cancer}, OMIM:176807				26360800;10398279 - no association found with breast/ovarian cance susceptibility variants;26289772;26236408 - literature review indicating there is conflicting reports;26074382;21952622;28031937		False	3	100;0;0	1.4	False		ENSG00000139618	ENSG00000139618	HGNC:1101													
BRCA1	gene	BRCA1	Expert list;Expert Review Amber	Familial prostate cancer			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Prostate cancer, MONDO:0008315				27989354;27899188;27742670;27433846;27317574;27306910 - standardized incidence ratios (SIRs) were used to compare the observed incidence of 20 primary cancer sites to the expected incidence of each cancer based on the calculated risk estimates according to each subject's age, sex, and ethnicity. BRCA1 families had increased SIRs for breast and ovarian cancer (p < .001) and decreased SIRs for kidney, lung, prostate, and thyroid cancer and non-Hodgkin's lymphoma (p < .001);27188668;26926928;26360800 - no increased risk;26236408 - literature review indicating there is conflicting reports;22516946;28031937		False	2	100;0;0	1.4	False		ENSG00000012048	ENSG00000012048	HGNC:1100