ClinVar Miner

Submissions for variant NM_182914.3(SYNE2):c.1129-6_1129-4del

dbSNP: rs34440267
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001652612 SCV001865755 benign not provided 2019-10-07 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001699828 SCV001925334 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001652612 SCV001953338 likely benign not provided no assertion criteria provided clinical testing

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