ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.1396-22del

gnomAD frequency: 0.00001  dbSNP: rs750290706
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002226338 SCV002505118 likely benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV005232915 SCV005873107 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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