ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.1315-10A>C

dbSNP: rs1559412159
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000777484 SCV000913346 likely benign Hereditary cancer-predisposing syndrome 2018-02-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003500598 SCV004254300 likely benign Familial cancer of breast 2023-12-05 criteria provided, single submitter clinical testing

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