ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8755-14T>C

dbSNP: rs1555288362
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV000501886 SCV000592228 likely benign not specified 2017-10-25 criteria provided, single submitter clinical testing

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