ClinVar Miner

Submissions for variant NM_000018.4(ACADVL):c.1435-27T>A

dbSNP: rs1281849589
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001287099 SCV001473745 likely benign Very long chain acyl-CoA dehydrogenase deficiency 2019-11-14 criteria provided, single submitter clinical testing

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