ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.17203-6dup

dbSNP: rs55633181
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000292960 SCV000331641 benign not specified 2016-08-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000870523 SCV001012026 benign not provided 2018-01-02 criteria provided, single submitter clinical testing
GeneDx RCV000870523 SCV001947168 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000870523 SCV001797888 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000292960 SCV001918755 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000292960 SCV001929847 benign not specified no assertion criteria provided clinical testing

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