ClinVar Miner

Variants studied for Hereditary nonpolyposis colorectal cancer type 5

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 total
40 25 259 117 27 442

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
MSH6 40 25 256 117 27 439
FBXO11, MSH6 0 0 3 0 0 3

Submitter and significance breakdown #

Total submitters: 18
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Counsyl 17 18 174 72 2 283
Mendelics 4 6 42 43 9 104
Illumina Clinical Services Laboratory,Illumina 0 1 61 8 10 80
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center 5 0 3 1 13 22
Center for Human Genetics, Inc,Center for Human Genetics, Inc 2 1 11 5 0 19
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen 4 0 1 5 9 19
OMIM 10 0 1 0 0 11
Genome Diagnostics Laboratory,VU University Medical Center Amsterdam 0 0 1 5 4 10
Genome Diagnostics Laboratory,University Medical Center Utrecht 3 0 1 0 1 5
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 4 1 0 0 0 5
Institute of Human Genetics, University of Leipzig Medical Center 2 0 2 0 0 4
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 2 1 0 0 0 3
Genetic Services Laboratory,University of Chicago 2 0 0 0 0 2
Division of Medical Genetics, University of Washington 2 0 0 0 0 2
Biesecker Lab/Clinical Genomics Section,National Institutes of Health 1 0 0 0 0 1
Institute of Human Genetics,University of Goettingen 1 0 0 0 0 1
MVZ Praenatalmedizin und Genetik Nuernberg 1 0 0 0 0 1
Johns Hopkins Genomics,Johns Hopkins University 1 0 0 0 0 1

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