ClinVar Miner

Submissions for variant NM_015021.3(ZNF292):c.5374_5378del (p.Asn1792fs)

dbSNP: rs1775403177
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Center for Mendelian Genomics, University of Washington RCV001261761 SCV001439077 uncertain significance Neurodevelopmental disorder no assertion criteria provided research

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