ClinVar Miner

Submissions for variant NM_152641.4(ARID2):c.675G>A (p.Trp225Ter)

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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 RCV002291205 SCV002583495 pathogenic Coffin-Siris syndrome 6 2022-06-02 no assertion criteria provided clinical testing

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