ClinVar Miner

Submissions for variant NM_014717.3(ZNF536):c.1015G>T (p.Glu339Ter)

dbSNP: rs774965623
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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 Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes RCV002277660 SCV002564472 uncertain significance Neurodevelopmental disorder 2022-01-31 criteria provided, single submitter clinical testing

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