ClinVar Miner

Submissions for variant NM_000016.6(ACADM):c.31-1G>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV004573941 SCV005053061 likely pathogenic Medium-chain acyl-coenzyme A dehydrogenase deficiency 2024-01-23 criteria provided, single submitter clinical testing

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