ClinVar Miner

Submissions for variant NM_000282.4(PCCA):c.914+19A>G (rs4306370)

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000078551 SCV000110407 benign not specified 2014-06-11 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000078551 SCV000303460 benign not specified criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000590009 SCV000696478 benign not provided 2016-02-29 criteria provided, single submitter clinical testing
Invitae RCV000599865 SCV001729951 benign Propionic acidemia 2020-12-08 criteria provided, single submitter clinical testing
Pars Genome Lab RCV000599865 SCV001750048 benign Propionic acidemia 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV000590009 SCV001758137 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000599865 SCV000733194 benign Propionic acidemia no assertion criteria provided clinical testing

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