ClinVar Miner

Submissions for variant NM_000481.3(AMT):c.631G>A (p.Glu211Lys) (rs116192290)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000549987 SCV000636427 benign Non-ketotic hyperglycinemia 2017-07-26 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000549987 SCV000743157 likely benign Non-ketotic hyperglycinemia 2014-10-09 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000549987 SCV000734285 benign Non-ketotic hyperglycinemia no assertion criteria provided clinical testing

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