ClinVar Miner

Submissions for variant NM_000016.6(ACADM):c.602A>G (p.Tyr201Cys)

dbSNP: rs875989871
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000211497 SCV000268493 uncertain significance Medium-chain acyl-coenzyme A dehydrogenase deficiency 2015-02-20 criteria provided, single submitter clinical testing

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