ClinVar Miner

Variants studied for Breast-ovarian cancer, familial, susceptibility to, 4

Coded as:
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 risk factor not provided total
155 113 754 527 28 6 6 1496

Gene and significance breakdown #

Total genes and gene combinations: 6
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
RAD51D, RAD51L3-RFFL 133 109 746 525 27 6 6 1459
RAD51D 21 4 6 0 0 0 0 31
FMN1 1 0 0 1 0 0 0 2
LOC130060715, RAD51D, RAD51L3-RFFL 0 0 0 1 1 0 0 2
FNDC8 0 0 1 0 0 0 0 1
FNDC8, LOC130060715, RAD51D, RAD51L3-RFFL 0 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 31
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
Labcorp Genetics (formerly Invitae), Labcorp 109 56 695 491 23 0 0 1374
Baylor Genetics 20 21 142 1 0 0 0 184
Myriad Genetics, Inc. 75 48 14 23 12 0 0 172
Counsyl 6 13 23 27 4 0 0 73
Fulgent Genetics, Fulgent Genetics 6 4 32 1 0 0 0 43
Mendelics 1 4 13 12 0 0 0 30
Department of Pathology and Laboratory Medicine, Sinai Health System 5 1 12 6 0 0 0 24
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 2 1 7 9 4 0 0 23
Hereditary Cancer Group, L’Institut d'Investigació Biomèdica de Bellvitge 10 6 5 1 0 0 0 22
MGZ Medical Genetics Center 2 2 10 0 0 0 0 14
Institute of Human Genetics, University of Leipzig Medical Center 2 2 5 0 1 0 0 10
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 2 7 0 0 0 0 9
Neuberg Centre For Genomic Medicine, NCGM 3 0 5 0 0 0 0 8
OMIM 0 0 0 0 0 6 0 6
Genetics and Molecular Pathology, SA Pathology 0 0 4 0 0 0 0 4
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 0 1 3 0 0 0 0 4
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 0 4 4
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 1 0 3 0 0 0 0 4
Juno Genomics, Hangzhou Juno Genomics, Inc 3 0 0 0 0 0 0 3
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 0 2 0 0 0 0 0 2
GenomeConnect, ClinGen 0 0 0 0 0 0 2 2
Department of Human Genetics, Hannover Medical School 0 0 2 0 0 0 0 2
BRCAlab, Lund University 1 1 0 0 0 0 0 2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 1 0 0 0 0 0 0 1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 0 1 0 0 0 0 1
Department of Molecular Diagnostics, Institute of Oncology Ljubljana 0 1 0 0 0 0 0 1
Genetics and Genomic Medicine Centre, NeuroGen Healthcare, NeuroGen Healthcare 1 0 0 0 0 0 0 1
University of Washington Department of Laboratory Medicine, University of Washington 0 0 0 1 0 0 0 1
Division of Medical Genetics, University of Washington 0 0 1 0 0 0 0 1
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ 0 0 1 0 0 0 0 1
Human Genetics Bochum, Ruhr University Bochum 0 1 0 0 0 0 0 1

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