ClinVar Miner

Variants studied for Pancreatic cancer, susceptibility to, 2

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 risk factor total
3 2 3 0 0 1 9

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance risk factor total
BRCA2 3 2 3 1 9

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance risk factor total
Human Genetics Bochum, Ruhr University Bochum 1 1 0 0 2
Department of Human Genetics, Hannover Medical School 1 0 1 0 2
OMIM 0 0 0 1 1
Baylor Genetics 0 0 1 0 1
Institute of Human Genetics, University of Leipzig Medical Center 1 0 0 0 1
HUSP Clinical Genetics Laboratory, Hospital Universitario San Pedro De Logroño (HUSP) 0 1 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 1 0 1

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