ClinVar Miner

Submissions for variant NM_001348323.3(TRIP12):c.1090C>T (p.Arg364Trp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein RCV002291116 SCV002583360 uncertain significance Clark-Baraitser syndrome 2021-12-01 no assertion criteria provided clinical testing

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