ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.158+15T>C

dbSNP: rs1232574568
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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 RCV002074691 SCV002424808 likely benign Familial cancer of breast 2021-11-06 criteria provided, single submitter clinical testing

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