ClinVar Miner

Submissions for variant NM_000016.5(ACADM):c.119-20T>C (rs74090724)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000077880 SCV000109709 benign not specified 2013-01-24 criteria provided, single submitter clinical testing
GeneDx RCV000077880 SCV000166809 benign not specified 2013-05-29 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
PreventionGenetics,PreventionGenetics RCV000077880 SCV000301494 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001381 SCV001158581 benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2018-11-15 criteria provided, single submitter clinical testing

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