ClinVar Miner

Submissions for variant NM_015100.4(POGZ):c.757C>T (p.Pro253Ser) (rs926772662)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000717135 SCV000847981 uncertain significance History of neurodevelopmental disorder 2016-10-10 criteria provided, single submitter clinical testing Insufficient evidence
Center of Medical Genetics,Central South University RCV000754542 SCV000803254 association Autism spectrum disorder no assertion criteria provided clinical testing

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