ClinVar Miner

Submissions for variant NM_000016.6(ACADM):c.708+8A>C

dbSNP: rs372454296
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000604114 SCV000725040 likely benign not specified 2017-12-11 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV002065411 SCV002446123 likely benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2022-12-07 criteria provided, single submitter clinical testing

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