ClinVar Miner

Submissions for variant NM_006772.3(SYNGAP1):c.2854G>A (p.Gly952Ser)

dbSNP: rs1038956173
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
New York Genome Center RCV001784160 SCV002025698 uncertain significance Intellectual disability, autosomal dominant 5 2020-04-18 criteria provided, single submitter clinical testing
Invitae RCV001784160 SCV003501838 benign Intellectual disability, autosomal dominant 5 2023-09-03 criteria provided, single submitter clinical testing

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