ClinVar Miner

Variants studied for Fanconi anemia complementation group C

Included ClinVar conditions (1):
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
64 141 233 63 28 9 479

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
AOPEP, FANCC 35 81 181 51 20 3 336
FANCC 26 60 51 12 8 6 139
DCLRE1B 2 0 0 0 0 0 2
FANCC, LOC130002128 1 0 1 0 0 0 2

Submitter and significance breakdown #

Total submitters: 38
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Illumina Laboratory Services, Illumina 1 0 75 19 17 0 112
Fulgent Genetics, Fulgent Genetics 13 10 69 16 0 0 108
Baylor Genetics 31 57 14 0 0 0 102
Natera, Inc. 0 3 70 19 1 0 93
Counsyl 1 55 19 5 0 0 80
Leiden Open Variation Database 33 0 2 0 0 0 35
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 12 17 0 0 0 0 29
Myriad Genetics, Inc. 3 18 0 0 0 0 21
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 5 15 0 20
Revvity Omics, Revvity 8 5 5 0 0 0 18
Mendelics 7 1 5 1 0 0 14
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 1 1 9 1 0 0 12
OMIM 10 0 0 0 0 0 10
Genome-Nilou Lab 0 0 1 3 3 0 7
GeneReviews 0 0 0 0 0 6 6
Department of Pathology and Laboratory Medicine, Sinai Health System 1 0 3 1 0 0 5
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 3 3
Neuberg Centre For Genomic Medicine, NCGM 2 1 0 0 0 0 3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 1 1 0 0 0 0 2
Department of Pediatrics, Memorial Sloan Kettering Cancer Center 2 0 0 0 0 0 2
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 2 0 0 0 2
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 2 0 0 0 0 0 2
New York Genome Center 1 1 0 0 0 0 2
Dept. of Cytogenetics, ICMR- National Institute of Immunohaematology 2 0 0 0 0 0 2
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 1 0 0 0 0 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 0 0 0 0 0 1
Division of Human Genetics, Children's Hospital of Philadelphia 0 1 0 0 0 0 1
Donald Williams Parsons Laboratory, Baylor College of Medicine 1 0 0 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 1 0 0 0 1
Daryl Scott Lab, Baylor College of Medicine 1 0 0 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 1 0 0 0 0 0 1
Laboratory of Medical Genetics Unit, Bambino Gesù Children's Hospital 0 1 0 0 0 0 1
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital 1 0 0 0 0 0 1
Human Genetics Section, Sidra Medicine 0 0 1 0 0 0 1
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ 0 1 0 0 0 0 1
Pars Genome Lab 0 0 1 0 0 0 1
DASA 1 0 0 0 0 0 1
King Fahd Medical Research Center, King Abdulaziz University 0 0 1 0 0 0 1

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