ClinVar Miner

Submissions for variant NM_015100.4(POGZ):c.3206_3207del (p.Ser1068_Tyr1069insTer)

dbSNP: rs1553212374
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne RCV000677634 SCV000803764 likely pathogenic Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome 2017-12-19 criteria provided, single submitter clinical testing

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