ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.1678-6T>C

dbSNP: rs2106021502
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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 RCV001452599 SCV001656268 likely benign Familial cancer of breast 2019-03-25 criteria provided, single submitter clinical testing

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