ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4675+53C>A

gnomAD frequency: 0.00004  dbSNP: rs869312522
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Department of Laboratory Medicine, University of Washington RCV000209572 SCV000265010 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV000499454 SCV000591534 likely benign not provided no assertion criteria provided clinical testing

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