Variants studied for Fanconi anemia complementation group B

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
19	3	33	5	24	83

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	3	33	5	24	83

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
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	8	8
OMIM	7	0	0	0	0	7
Revvity Omics, Revvity	0	0	6	0	0	6
Baylor Genetics	0	2	3	0	0	5
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	0	1	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	0	1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	0	1	0	0	1
St. Jude Molecular Pathology, St. Jude Children's Research Hospital	0	0	1	0	0	1
Johns Hopkins Genomics, Johns Hopkins University	0	0	1	0	0	1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center	0	0	1	0	0	1
Genome-Nilou Lab	0	0	0	0	1	1
3billion	1	0	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	1	0	0	0	1
Division Of Personalized Genomic Medicine, Columbia University Irving Medical Center	1	0	0	0	0	1

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