ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7806-6del (rs764374133)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000554027 SCV000635607 likely benign Hereditary breast and ovarian cancer syndrome 2017-01-31 criteria provided, single submitter clinical testing
Color RCV000776223 SCV000911416 likely benign Hereditary cancer-predisposing syndrome 2016-12-12 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000239242 SCV000297451 uncertain significance Breast-ovarian cancer, familial 2 2010-06-08 no assertion criteria provided clinical testing

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