ClinVar Miner

Submissions for variant NM_015100.4(POGZ):c.600dup (p.Gly201fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of genome editing, Research Centre for Medical Genetics RCV003460396 SCV004190228 pathogenic Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome criteria provided, single submitter clinical testing

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