ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4356dup (p.Ala1453fs)

dbSNP: rs1567782959
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001706912 SCV001934496 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 1 2021-03-24 criteria provided, single submitter clinical testing

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