ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.364+11T>C

dbSNP: rs1695552018
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001189814 SCV001357180 likely benign Hereditary cancer-predisposing syndrome 2019-06-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002560066 SCV003002063 likely benign Familial cancer of breast 2024-06-12 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003493814 SCV004243124 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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