ClinVar Miner

Submissions for variant NM_000170.2(GLDC):c.1156-7C>G (rs150095531)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000268617 SCV000734701 likely benign Non-ketotic hyperglycinemia no assertion criteria provided clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000268617 SCV000480518 uncertain significance Non-ketotic hyperglycinemia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000268617 SCV000636348 benign Non-ketotic hyperglycinemia 2017-07-17 criteria provided, single submitter clinical testing

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