ClinVar Miner

Variants studied for Fanconi anemia complementation group B

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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
19 4 96 18 28 159

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
FANCB 19 4 96 18 28 159

Submitter and significance breakdown #

Total submitters: 21
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Fulgent Genetics, Fulgent Genetics 0 1 61 12 0 74
Illumina Laboratory Services, Illumina 0 0 18 4 20 42
Leiden Open Variation Database 18 0 3 0 0 21
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 0 9 9
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 0 1 6 7
OMIM 7 0 0 0 0 7
Revvity Omics, Revvity 0 0 6 0 0 6
Baylor Genetics 0 2 3 0 0 5
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 0 0 2 0 0 2
3billion 1 0 0 0 0 1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 0 0 1
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 1 0 0 1
Division Of Personalized Genomic Medicine, Columbia University Irving Medical Center 1 0 0 0 0 1
GeNE CliniK, Regional Hospital Limbe 0 0 1 0 0 1
Genome-Nilou Lab 0 0 0 0 1 1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 0 0 0 1 1
Institute of Human Genetics, University of Leipzig Medical Center 0 0 1 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 0 1 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 1 0 0 0 1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center 0 0 1 0 0 1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 0 1 0 1

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