ClinVar Miner

Submissions for variant NM_001346813.1(ARID1B):c.5653C>T (p.Arg1885Cys) (rs766931727)

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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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