ClinVar Miner

Submissions for variant NM_001365999.1(SZT2):c.7395T>C (p.Ile2465=) (rs78858677)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000718644 SCV000849508 likely benign Seizures 2016-04-26 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Genetic Services Laboratory, University of Chicago RCV000245444 SCV000597379 likely benign not specified 2017-05-05 criteria provided, single submitter clinical testing
Invitae RCV000245444 SCV000563156 benign not specified 2016-12-20 criteria provided, single submitter clinical testing
PreventionGenetics RCV000245444 SCV000312501 benign not specified criteria provided, single submitter clinical testing

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