ClinVar Miner

Variants studied for Pancreatic cancer, susceptibility to, 4

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
2 0 0 0 0 1 3

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic risk factor total
BRCA1 2 1 3

Submitter and significance breakdown #

Total submitters: 3
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Submitter pathogenic risk factor total
OMIM 0 1 1
Human Genetics Bochum, Ruhr University Bochum 1 0 1
Department of Human Genetics, Hannover Medical School 1 0 1

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