ClinVar Miner

List of variants reported as pathogenic for breast-ovarian cancer, familial, susceptibility to, 3 by Institute of Human Genetics, University of Leipzig Medical Center

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.224dup (p.Tyr75Ter) rs730881939 0.00002
NM_058216.3(RAD51C):c.706-2A>G rs587780259 0.00002
NC_000017.11:g.58709788_58734292del
NM_058216.2:c.(235+1_236-1)_(*120_?)del
NM_058216.3(RAD51C):c.525dup (p.Cys176fs) rs768793789

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