ClinVar Miner

Submissions for variant NM_015021.3(ZNF292):c.4839_4840del (p.Asn1614fs)

dbSNP: rs2127867376
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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 RCV001374995 SCV001572283 pathogenic Neurodevelopmental disorder 2020-12-01 criteria provided, single submitter clinical testing

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