ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.2001+9C>G

dbSNP: rs2105990348
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001496415 SCV001701114 likely benign Familial cancer of breast 2024-10-26 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV004596465 SCV005090524 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001496415 SCV005404459 likely benign Familial cancer of breast 2024-07-29 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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