ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.364+16A>G

dbSNP: rs201219625
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000412228 SCV000489583 likely benign Familial cancer of breast 2016-10-24 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000582238 SCV000688195 likely benign Hereditary cancer-predisposing syndrome 2015-06-15 criteria provided, single submitter clinical testing
GeneDx RCV001672747 SCV001888887 benign not provided 2015-06-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000412228 SCV002407058 likely benign Familial cancer of breast 2024-01-31 criteria provided, single submitter clinical testing

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