ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.67+40G>A (rs371493518)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Genome Diagnostics Laboratory,University Medical Center Utrecht	RCV000624976	SCV000743235	likely benign	Breast-ovarian cancer, familial 2	2015-02-02	criteria provided, single submitter	clinical testing

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