ClinVar Miner

Submissions for variant NM_000016.6(ACADM):c.1194+11A>G

gnomAD frequency: 0.00084  dbSNP: rs373059851
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000428896 SCV000526102 likely benign not specified 2018-01-25 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 RCV002058968 SCV002450029 benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2024-01-28 criteria provided, single submitter clinical testing

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