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
39 25 213 112 25 399

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 39 25 210 112 25 396
FBXO11, MSH6 0 0 3 0 0 3

Submitter and significance breakdown #

Total submitters: 15
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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
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center 5 0 3 1 13 22
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
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
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
Illumina Clinical Services Laboratory,Illumina 0 1 0 0 0 1
MVZ Praenatalmedizin und Genetik Nuernberg 1 0 0 0 0 1

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