ClinVar Miner

Variants from Hereditary Cancer Group, L’Institut d'Investigació Biomèdica de Bellvitge

Location: Spain  Primary collection method: clinical testing
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
30 20 86 44 1 181

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
DICER1 3 2 63 39 1 108
RAD51C 11 9 17 3 0 40
RAD51D, RAD51L3-RFFL 6 7 5 2 0 20
LOC129390903, RAD51C 5 1 1 0 0 7
RAD51D 5 1 0 0 0 6

Condition and significance breakdown #

Total conditions: 5
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Condition pathogenic likely pathogenic uncertain significance likely benign benign total
Hereditary cancer-predisposing syndrome 1 1 63 39 1 105
Breast-ovarian cancer, familial, susceptibility to, 3 16 10 18 4 0 48
Breast-ovarian cancer, familial, susceptibility to, 4 10 6 5 1 0 22
DICER1-related tumor predisposition 2 1 0 0 0 3
Deleterious RAD51D Gene Mutation 1 2 0 0 0 3

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