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
FGFR2	gene	FGFR2	Expert Review Amber;Literature	Familial hidradenitis suppurativa	Skin adnexa disorders	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Nevus comedonicus, multifocal hidradenitis suppurativa and acne				28293556		False	2	0;100;0	1.5	False		ENSG00000066468	ENSG00000066468	HGNC:3689													
GJB2	gene	GJB2	Expert Review Amber;Literature	Familial hidradenitis suppurativa	Skin adnexa disorders	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Keratitis-ichthyosis-deafness syndrome, 148210 with follicular occlusion triad (includes hidradenitis suppurativa)				16172043; 15337980		False	2	0;100;0	1.5	False		ENSG00000165474	ENSG00000165474	HGNC:4284													
PSTPIP1	gene	PSTPIP1	Expert Review Amber;Literature	Familial hidradenitis suppurativa	Skin adnexa disorders	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne, OMIM:604416				21745697; 23571383; 25501066		False	2	0;100;0	1.5	False		ENSG00000140368	ENSG00000140368	HGNC:9580