ClinVar Miner

Submissions for variant NM_000016.6(ACADM):c.-257G>A

dbSNP: rs17848068
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000322244 SCV000358927 likely benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2016-06-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000322244 SCV001750245 benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001612933 SCV001833914 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001612933 SCV005258587 likely benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV000322244 SCV002092789 benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2018-04-06 no assertion criteria provided clinical testing

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