ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.215+9T>G

dbSNP: rs1559441723
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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 RCV000774530 SCV000908233 uncertain significance Hereditary cancer-predisposing syndrome 2019-06-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001218258 SCV001390132 likely benign Familial cancer of breast 2024-04-29 criteria provided, single submitter clinical testing
Baylor Genetics RCV001218258 SCV004217226 uncertain significance Familial cancer of breast 2023-07-18 criteria provided, single submitter clinical testing

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