ClinVar Miner

Variants studied for Fanconi anemia complementation group F

Included ClinVar conditions (1):
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
18 28 137 11 21 205

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
FANCF 18 25 118 11 19 182
FANCF, LOC130005443 0 2 16 0 2 19
FANCF, LOC130005444 0 1 3 0 0 4

Submitter and significance breakdown #

Total submitters: 17
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Fulgent Genetics, Fulgent Genetics 6 6 89 3 0 104
Illumina Laboratory Services, Illumina 1 0 49 5 16 71
Baylor Genetics 9 20 8 0 0 37
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 1 0 1 3 7 12
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 1 8 9
Leiden Open Variation Database 8 0 0 0 0 8
OMIM 8 0 0 0 0 8
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 1 1 1 3
Revvity Omics, Revvity 1 0 2 0 0 3
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 2 0 0 2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 1 1 0 0 2
CENTOGENE GmbH and LLC - Guiding Precision Medicine 0 1 0 0 0 1
Genome-Nilou Lab 0 0 0 0 1 1
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 1 0 0 0 0 1
Human Genetics Section, Sidra Medicine 1 0 0 0 0 1
Istanbul Faculty of Medicine, Istanbul University 1 0 0 0 0 1
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 0 1 0 0 0 1

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