ClinVar Miner

Variants studied for colorectal cancer, susceptibility to, 12

Included ClinVar conditions (3):
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
19 14 476 251 62 1 6 801

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 risk factor not provided total
POLE 18 14 457 246 61 1 6 775
LOC130009266, POLE 0 0 18 5 1 0 0 24
ANKLE2, CHFR, GOLGA3, PGAM5, POLE, PXMP2, ZNF140, ZNF26, ZNF605, ZNF84 1 0 0 0 0 0 0 1
DDX51, EP400, FBRSL1, LRCOL1, MUC8, NOC4L, P2RX2, POLE, PUS1 0 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 26
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
Invitae 17 10 178 118 1 0 0 324
Counsyl 0 1 67 71 12 0 0 151
Fulgent Genetics, Fulgent Genetics 1 0 88 22 3 0 0 114
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 1 5 25 56 0 0 87
Baylor Genetics 0 0 67 0 0 0 0 67
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 0 0 54 0 0 0 0 54
Mendelics 0 0 21 27 1 0 0 49
MGZ Medical Genetics Center 0 0 17 0 0 0 0 17
Myriad Genetics, Inc. 0 0 15 1 1 0 0 17
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 8 0 0 0 0 8
University of Washington Department of Laboratory Medicine, University of Washington 0 0 0 6 1 0 0 7
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 6 0 0 0 0 6
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 0 5 5
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 5 0 0 0 0 5
Molecular Oncology Laboratory, Hospital Clínico San Carlos 0 1 2 1 0 0 0 4
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine 0 0 4 0 0 0 0 4
Genetics and Molecular Pathology, SA Pathology 0 0 1 2 0 0 0 3
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas 0 1 2 0 0 0 0 3
Division of Medical Genetics, University of Washington 0 0 3 0 0 0 0 3
Institute of Human Genetics, University of Goettingen 0 0 2 0 0 0 0 2
OMIM 0 0 0 0 0 1 0 1
Genetic Predisposition to Colorectal Cancer Group, Institut d’Investigacions Biomediques August Pi i Sunyer 1 0 0 0 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 0 1 0 0 0 0 1
GenomeConnect, ClinGen 0 0 0 0 0 0 1 1
New York Genome Center 0 0 1 0 0 0 0 1
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ 0 0 1 0 0 0 0 1

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