Variants studied for Birt-Hogg-Dube syndrome 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
22	2	54	171	295	537

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
FLCN	22	2	54	171	295	537

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Myriad Genetics, Inc.	13	2	0	171	295	481
Baylor Genetics	5	0	48	0	0	53
St. Jude Molecular Pathology, St. Jude Children's Research Hospital	2	0	3	0	0	5
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	0	2	0	0	2
Institute of Human Genetics, University of Leipzig Medical Center	2	0	0	0	0	2
KCCC/NGS Laboratory, Kuwait Cancer Control Center	0	0	0	0	2	2
Institute of Human Genetics, Cologne University	0	0	1	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	0	0	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	1	0	0	0	0	1
Institute of Immunology and Genetics Kaiserslautern	1	0	0	0	0	1

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