ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.10800G>A (p.Leu3600=) (rs114858512)

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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 RCV000332328 SCV000342481 uncertain significance not provided 2016-05-31 criteria provided, single submitter clinical testing
Invitae RCV000332328 SCV000649007 likely benign not provided 2019-01-08 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000332328 SCV001145848 benign not provided 2019-02-13 criteria provided, single submitter clinical testing

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