ClinVar Miner

Submissions for variant NM_000018.4(ACADVL):c.1678+29T>C

dbSNP: rs1023643662
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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 RCV001001135 SCV001158278 likely benign Very long chain acyl-CoA dehydrogenase deficiency 2019-03-11 criteria provided, single submitter clinical testing

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