ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.466C>G (p.Leu156Val)

dbSNP: rs587778115
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001180529 SCV001345469 uncertain significance Hereditary cancer-predisposing syndrome 2019-04-09 criteria provided, single submitter clinical testing
ITMI RCV000120268 SCV000084420 not provided not specified 2013-09-19 no assertion provided reference population

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