ClinVar Miner

Variants studied for Familial cancer of breast; Breast-ovarian cancer, familial 2; Fanconi anemia, complementation group D1; Medulloblastoma; Wilms tumor 1; Malignant tumor of prostate; Pancreatic cancer 2; Glioma susceptibility 3

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 total
16 0 32 0 1 49

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance benign total
BRCA2 16 32 1 49

Submitter and significance breakdown #

Total submitters: 2
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Submitter pathogenic uncertain significance benign total
Fulgent Genetics,Fulgent Genetics 16 31 1 48
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 1 0 1

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