ClinVar Miner

Submissions for variant NM_006772.3(SYNGAP1):c.1154C>G (p.Ser385Trp)

dbSNP: rs766006911
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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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 RCV000203123 SCV000258051 benign not specified 2015-02-13 criteria provided, single submitter clinical testing

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