ClinVar Miner

Submissions for variant NM_000016.6(ACADM):c.-401G>A

gnomAD frequency: 0.04873  dbSNP: rs114005461
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000356437 SCV000358922 likely benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001711893 SCV001944364 benign not provided 2018-06-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711893 SCV005258585 likely benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV000356437 SCV002092787 benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2018-04-06 no assertion criteria provided clinical testing

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