ClinVar Miner

Submissions for variant NM_001365999.1(SZT2):c.8626-3T>C (rs2255632)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000715369 SCV000846198 benign Seizures 2016-01-08 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000713761 SCV000844390 benign not provided 2017-04-20 criteria provided, single submitter clinical testing
PreventionGenetics RCV000242391 SCV000312503 benign not specified criteria provided, single submitter clinical testing

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