ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.1824T>G (p.Val608=)

gnomAD frequency: 0.00001  dbSNP: rs1268678327
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001457445 SCV001661248 likely benign Familial cancer of breast 2024-03-07 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001457445 SCV005407037 benign Familial cancer of breast 2024-07-26 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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