ClinVar Miner

Submissions for variant NM_000016.6(ACADM):c.945+99T>C

gnomAD frequency: 0.23825  dbSNP: rs11161521
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001533629 SCV001750350 benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001673141 SCV001886723 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001673141 SCV005280886 benign not provided criteria provided, single submitter not provided

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