ClinVar Miner

Submissions for variant NM_001365999.1(SZT2):c.6888C>T (p.Cys2296=) (rs72671125)

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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 RCV000715703 SCV000846534 benign Seizures 2016-05-06 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000713754 SCV000844383 benign not provided 2017-08-14 criteria provided, single submitter clinical testing
Invitae RCV000231248 SCV000290137 benign not specified 2017-01-10 criteria provided, single submitter clinical testing
PreventionGenetics RCV000231248 SCV000312498 benign not specified criteria provided, single submitter clinical testing

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