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
86 41 607 294 47 1 1007

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 85 41 605 294 47 1 1004
CDH1, LOC112486201 1 0 2 0 0 0 3

Submitter and significance breakdown #

Total submitters: 17
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Invitae 61 25 552 235 36 0 909
Counsyl 4 8 91 41 2 0 146
Illumina Clinical Services Laboratory,Illumina 0 0 28 44 11 0 83
ClinGen CDH1 Variant Curation Expert Panel 15 5 14 1 15 0 50
Mendelics 2 1 25 4 0 0 32
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 Medical Center 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
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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