ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.1314+11T>G

gnomAD frequency: 0.00019  dbSNP: rs192972931
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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 RCV000581493 SCV000688111 likely benign Hereditary cancer-predisposing syndrome 2017-02-27 criteria provided, single submitter clinical testing
GeneDx RCV001597178 SCV001830179 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061733 SCV002433135 likely benign Familial cancer of breast 2024-01-24 criteria provided, single submitter clinical testing

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