ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5578del (p.His1860fs)

dbSNP: rs397507254
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics and Genomics, Karolinska University Hospital RCV001269983 SCV001450386 likely pathogenic not provided 2018-01-05 criteria provided, single submitter clinical testing
BRCAlab, Lund University RCV003155972 SCV002588841 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 1 2022-08-26 no assertion criteria provided clinical testing

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