ClinVar Miner

Submissions for variant NM_006772.3(SYNGAP1):c.67+15del

dbSNP: rs753367470
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000645754 SCV000767509 likely benign Intellectual disability, autosomal dominant 5 2024-10-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000645754 SCV002795785 likely benign Intellectual disability, autosomal dominant 5 2022-01-17 criteria provided, single submitter clinical testing

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