ClinVar Miner

Variants in gene combination BRCA2, LOC112163653

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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
4 0 1 0 1 6

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic uncertain significance benign total
Hereditary breast and ovarian cancer syndrome 3 1 0 4
Breast-ovarian cancer, familial 2 1 0 1 2

Submitter and significance breakdown #

Total submitters: 3
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Submitter pathogenic uncertain significance benign total
Invitae 3 1 0 4
Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) 0 0 1 1
Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), c/o University of Cambridge 1 0 0 1

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