ClinVar Miner

Submissions for variant NM_001282531.3(ADNP):c.2773G>A (p.Glu925Lys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003141220 SCV003820478 uncertain significance ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder 2019-11-15 criteria provided, single submitter clinical testing

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