ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.7007+7C>G

dbSNP: rs2072615724
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001182907 SCV001348507 likely benign Hereditary cancer-predisposing syndrome 2019-10-07 criteria provided, single submitter clinical testing

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