ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.5513T>G (p.Val1838Gly) (rs80357107)

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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,Oslo University Hospital RCV000241502 SCV000564325 likely pathogenic Breast-ovarian cancer, familial 1 2015-07-01 criteria provided, single submitter clinical testing
Department of Medical Genetics,University Hospital of North Norway RCV000241502 SCV000301441 uncertain significance Breast-ovarian cancer, familial 1 2016-05-01 no assertion criteria provided clinical testing

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