ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.5075A>C (p.Asp1692Ala) (rs397509222)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Medical Genetics,University Hospital of North Norway RCV000241473 SCV000301435 uncertain significance Breast-ovarian cancer, familial 1 2016-05-01 no assertion criteria provided clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000500821 SCV000591575 uncertain significance not specified 2012-10-12 criteria provided, single submitter clinical testing

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