ClinVar Miner

Submissions for variant NM_001172509.2(SATB2):c.353T>C (p.Ile118Thr)

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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 RCV003990888 SCV004807941 uncertain significance Chromosome 2q32-q33 deletion syndrome 2024-03-29 criteria provided, single submitter clinical testing

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