ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.*136_*138dup

dbSNP: rs113789798
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987003 SCV001136174 benign Familial cancer of breast 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001561804 SCV001784468 likely benign not provided 2019-08-14 criteria provided, single submitter clinical testing

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