ClinVar Miner

Variants studied for Hereditary diffuse gastric cancer

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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
115 61 727 154 35 1 1028

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 not provided total
CDH1 113 61 725 154 35 1 1024
CDH1, LOC112486201 2 0 2 0 0 0 4

Submitter and significance breakdown #

Total submitters: 18
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Invitae 83 26 667 53 3 0 832
Counsyl 4 8 91 41 2 0 146
ClinGen CDH1 Variant Curation Expert Panel 37 26 16 16 20 0 115
Illumina Clinical Services Laboratory,Illumina 0 0 28 44 11 0 83
Mendelics 3 2 40 19 3 0 67
OMIM 15 0 0 0 0 0 15
Pathway Genomics 4 0 2 1 1 0 8
Integrated Genetics/Laboratory Corporation of America 3 4 0 0 0 0 7
CSER _CC_NCGL, University of Washington 1 0 2 0 0 0 3
Knight Diagnostic Laboratories,Oregon Health and Sciences University 0 0 3 0 0 0 3
Laboratório de Genética Humana e Médica, Universidade Federal do Pará 1 0 0 0 0 1 2
University of Washington Department of Laboratory Medicine, University of Washington 0 0 0 2 0 0 2
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 0 1 0 0 0 1
Fundacion Rioja Salud,Center for Biomedical Research (CIBIR) 1 0 0 0 0 0 1
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 0 1 0 0 0 0 1
Immunopatologia e Biomarcatori Oncologici/Bio-proteomics facility,Centro di Riferimento Oncologico 1 0 0 0 0 0 1
Familial Cancer Clinical Unit,Spanish National Cancer Research Centre (CNIO) 1 0 0 0 0 0 1
GeneID Lab - Advanced Molecular Diagnostics 0 1 0 0 0 0 1

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