ClinVar Miner

Submissions for variant NM_001039876.3(SYNE4):c.129-17C>T

dbSNP: rs13344146
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001540424 SCV001758309 likely benign not provided 2018-07-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001540424 SCV002425653 benign not provided 2024-01-30 criteria provided, single submitter clinical testing

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