ClinVar Miner

Submissions for variant NM_014575.4(SCHIP1):c.1354C>T (p.Arg452Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003988764 SCV004805041 likely pathogenic Familial meningioma 2024-03-17 criteria provided, single submitter research

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