ClinVar Miner

Submissions for variant NM_002878.3(RAD51D):c.346-4C>G (rs767328693)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000584502 SCV000691331 likely benign Hereditary cancer-predisposing syndrome 2017-04-24 criteria provided, single submitter clinical testing
Invitae RCV000649725 SCV000771557 likely benign Breast-ovarian cancer, familial 4 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000584502 SCV001181835 uncertain significance Hereditary cancer-predisposing syndrome 2019-04-16 criteria provided, single submitter clinical testing Insufficient evidence

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