ClinVar Miner

Submissions for variant NM_020928.2(ZSWIM6):c.83GCG[7] (p.Gly33dup)

dbSNP: rs528020839
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia RCV000500002 SCV000258164 likely benign not specified 2015-07-30 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000500002 SCV000598099 likely benign not specified 2015-09-04 criteria provided, single submitter clinical testing
GeneDx RCV001707712 SCV001936339 benign not provided 2019-10-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001707712 SCV002460688 benign not provided 2025-02-03 criteria provided, single submitter clinical testing

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