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
CFTR	gene	CFTR	Eligibility statement prior genetic testing;Emory Genetics Laboratory;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Non-CF bronchiectasis	Respiratory ciliopathies	Ciliopathies	BIALLELIC, autosomal or pseudoautosomal	Cystic fibrosis, 219700;Congenital bilateral absence of vas deferens, 277180;Sweat chloride elevation without CF;{Pancreatitis, idiopathic}, 167800;{Hypertrypsinemia, neonatal};{Bronchiectasis with or without elevated sweat chloride 1, modifier of}, 211400;Cystic Fibrosis;Bronchiectasis						False	3	0;0;100	1.32	True		ENSG00000001626	ENSG00000001626	HGNC:1884													
DAW1	gene	DAW1	Expert Review Green;Literature	Non-CF bronchiectasis	Respiratory ciliopathies	Ciliopathies	BIALLELIC, autosomal or pseudoautosomal	Ciliary dyskinesia, primary, 52, OMIM:620570				36074124;28991257		False	3	100;0;0	1.32	False		ENSG00000123977	ENSG00000123977	HGNC:26383													
DNAH5	gene	DNAH5	Emory Genetics Laboratory;Expert Review Green	Non-CF bronchiectasis	Respiratory ciliopathies	Ciliopathies	BIALLELIC, autosomal or pseudoautosomal	Bronchiectasis;Primary Ciliary Dyskinesia;Ciliary dyskinesia, primary, 3, with or without situs inversus, 608644;situs inversus				18037990;11788826		False	3	50;0;50	1.32	False		ENSG00000039139	ENSG00000039139	HGNC:2950													
PIK3CD	gene	PIK3CD	Expert list;Expert Review Green	Non-CF bronchiectasis	Respiratory ciliopathies	Ciliopathies	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Immunodeficiency 14A, autosomal dominant, OMIM:615513						False	3	100;0;0	1.32	True	Other - please provide details in the comments	ENSG00000171608	ENSG00000171608	HGNC:8977													
SCNN1A	gene	SCNN1A	Emory Genetics Laboratory;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Non-CF bronchiectasis	Respiratory ciliopathies	Ciliopathies	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Pseudohypoaldosteronism, type I, 264350;Bronchiectasis with or without elevated sweat chloride 2, 613021;Bronchiectasis						False	3	0;0;0	1.32	True		ENSG00000111319	ENSG00000111319	HGNC:10599													
SCNN1B	gene	SCNN1B	Emory Genetics Laboratory;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Non-CF bronchiectasis	Respiratory ciliopathies	Ciliopathies	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Non-Classic Cystic Fibrosis-Like Syndrome;Liddle syndrome, 177200Pseudohypoaldosteronism, type I, 264350;Bronchiectasis with or without elevated sweat chloride 1, 211400;Bronchiectasis				PMID: 23837941		False	3	100;0;0	1.32	True		ENSG00000168447	ENSG00000168447	HGNC:10600													
SCNN1G	gene	SCNN1G	Emory Genetics Laboratory;Expert Review Green;Radboud University Medical Center, Nijmegen	Non-CF bronchiectasis	Respiratory ciliopathies	Ciliopathies	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Liddle syndrome, 177200;Pseudohypoaldosteronism, type I, 264350;Bronchiectasis with or without elevated sweat chloride 3, 613071;Bronchiectasis						False	3	100;0;0	1.32	True		ENSG00000166828	ENSG00000166828	HGNC:10602