ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.282C>T (p.Asp94=)

dbSNP: rs1695561998
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001489643 SCV001694190 likely benign Familial cancer of breast 2024-07-19 criteria provided, single submitter clinical testing

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