ClinVar Miner

Submissions for variant NM_001379659.1(ZNF142):c.2585A>T (p.Glu862Val)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV003989881 SCV004805919 likely benign Neurodevelopmental disorder with impaired speech and hyperkinetic movements 2024-03-25 criteria provided, single submitter clinical testing

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