ClinVar Miner

Submissions for variant NM_006772.3(SYNGAP1):c.1677-129_1677-128del

gnomAD frequency: 0.00699  dbSNP: rs567989593
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001575432 SCV001802425 likely benign not provided 2018-08-10 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001575432 SCV003917051 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing SYNGAP1: BS1

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