ClinVar Miner

Submissions for variant NM_001080414.4(CCDC88C):c.5296G>A (p.Val1766Met) (rs201931182)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000974478 SCV001122301 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000974478 SCV001149298 uncertain significance not provided 2017-06-01 criteria provided, single submitter clinical testing

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