ClinVar Miner

Variants in gene combination FANCG, VCP

See also:
Minimum submission review status: Collection method:
Minimum conflict level:
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 not provided total
2 0 3 5 6 4 7

Condition and significance breakdown #

Total conditions: 6
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Condition pathogenic uncertain significance likely benign benign not provided total
Fanconi anemia 0 2 4 6 0 7
Amyotrophic Lateral Sclerosis, Dominant 0 0 5 1 0 6
Fanconi anemia complementation group G 1 1 3 5 0 6
Inclusion Body Myopathy, Dominant 0 0 5 1 0 6
not specified 0 0 3 5 4 6
not provided 1 0 3 4 0 5

Submitter and significance breakdown #

Total submitters: 18
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Submitter pathogenic uncertain significance likely benign benign not provided total
Invitae 0 1 0 6 0 7
Illumina Laboratory Services, Illumina 0 2 5 3 0 6
GeneDx 0 0 2 3 0 5
Preventiongenetics, part of Exact Sciences 0 0 2 3 0 5
Natera, Inc. 0 0 1 4 0 5
ITMI 0 0 0 0 4 4
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 4 0 4
Genetic Services Laboratory, University of Chicago 0 0 1 2 0 3
Sema4, Sema4 0 0 2 1 0 3
Genome Diagnostics Laboratory, Amsterdam University Medical Center 0 0 0 3 0 3
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 0 2 0 2
Genome Diagnostics Laboratory, University Medical Center Utrecht 0 0 0 2 0 2
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 0 1 1 0 2
CeGaT Center for Human Genetics Tuebingen 0 0 1 1 0 2
Leiden Open Variation Database 2 0 0 0 0 2
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) 0 0 2 0 0 2
Genome-Nilou Lab 0 0 1 1 0 2
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics 0 0 0 1 0 1

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