ClinVar Miner

Submissions for variant NM_006772.3(SYNGAP1):c.3361A>G (p.Ser1121Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV003234426 SCV003930730 uncertain significance not provided 2022-12-09 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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