ClinVar Miner

Variants studied for Birt-Hogg-Dube syndrome 1

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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
26 3 56 173 296 544

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 26 3 56 173 296 544

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Myriad Genetics, Inc. 15 3 0 171 296 485
Baylor Genetics 5 0 48 0 0 53
Department of Pathology and Laboratory Medicine, Sinai Health System 1 0 2 2 4 9
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 2 0 3 0 0 5
Institute of Human Genetics, University of Leipzig Medical Center 3 0 0 0 0 3
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 0 2 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
Clinical Genetics Laboratory, Region Ostergotland 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
Genetics Department, Catlab 1 0 0 0 0 1

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