ClinVar Miner

Submissions for variant NM_001346813.1(ARID1B):c.5653C>T (p.Arg1885Cys)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Kariminejad - Najmabadi Pathology & Genetics Center	RCV000850084	SCV000992249	uncertain significance	Neurodevelopmental delay	2018-08-04	criteria provided, single submitter	clinical testing

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