ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.3751_3769del (p.Cys1251fs)

dbSNP: rs1567790190
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
German Consortium for Hereditary Breast and Ovarian Cancer, University Hospital Cologne RCV000785594 SCV000924169 pathogenic Ovarian neoplasm 2018-12-01 no assertion criteria provided research

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