ClinVar Miner

Submissions for variant NM_000016.6(ACADM):c.31-5T>C

gnomAD frequency: 0.00001  dbSNP: rs756654520
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002088233 SCV002377177 likely benign Medium-chain acyl-coenzyme A dehydrogenase deficiency 2022-12-17 criteria provided, single submitter clinical testing

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