ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.779-9dup (rs567435072)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000596028 SCV000704726 uncertain significance not provided 2017-01-10 criteria provided, single submitter clinical testing
Invitae RCV000596028 SCV001019529 benign not provided 2018-05-01 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000596028 SCV001145992 benign not provided 2019-02-25 criteria provided, single submitter clinical testing

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