ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.216-29dup

dbSNP: rs56130510
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001562550 SCV001785331 likely benign not provided 2019-08-19 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002255681 SCV002529581 benign Hereditary cancer-predisposing syndrome 2020-05-27 criteria provided, single submitter curation
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465889 SCV002760258 benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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