ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.1675G>A (p.Asp559Asn) (rs1555282012)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000605045 SCV000744413 likely benign Breast-ovarian cancer, familial 2 2015-09-21 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000605045 SCV000733232 likely benign Breast-ovarian cancer, familial 2 no assertion criteria provided clinical testing

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