ClinVar Miner

Submissions for variant NM_001123383.1(BCOR):c.711C>T (p.Val237=) (rs727503827)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000152860 SCV000202256 uncertain significance not provided 2014-03-17 criteria provided, single submitter clinical testing
Invitae RCV000640958 SCV000762563 benign Oculofaciocardiodental syndrome 2017-11-17 criteria provided, single submitter clinical testing

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