ClinVar Miner

Submissions for variant NM_000016.6(ACADM):c.302G>A (p.Gly101Glu)

dbSNP: rs875989862
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000211456 SCV000268455 uncertain significance Medium-chain acyl-coenzyme A dehydrogenase deficiency 2015-02-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000211456 SCV001375095 uncertain significance Medium-chain acyl-coenzyme A dehydrogenase deficiency 2021-08-31 criteria provided, single submitter clinical testing

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