ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.1568+13A>G

gnomAD frequency: 0.00001  dbSNP: rs1559409440
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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 RCV000771288 SCV000903462 likely benign Hereditary cancer-predisposing syndrome 2018-05-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061046 SCV002387462 likely benign Familial cancer of breast 2024-09-30 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV002061046 SCV005912890 likely benign Familial cancer of breast 2021-10-12 criteria provided, single submitter clinical testing

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