ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.6421_6424dup (p.Ser2142fs)

dbSNP: rs1566234560
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Molecular Diagnostics, Institute of Oncology Ljubljana RCV000755021 SCV000882841 likely pathogenic Hereditary cancer-predisposing syndrome 2018-10-24 criteria provided, single submitter clinical testing

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