ClinVar Miner

Submissions for variant NM_000018.4(ACADVL):c.62+10del

dbSNP: rs1251002707
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000671242 SCV000796199 likely benign Very long chain acyl-CoA dehydrogenase deficiency 2017-12-08 criteria provided, single submitter clinical testing
Invitae RCV000671242 SCV001655853 likely benign Very long chain acyl-CoA dehydrogenase deficiency 2023-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000671242 SCV002049485 likely benign Very long chain acyl-CoA dehydrogenase deficiency 2021-06-04 criteria provided, single submitter clinical testing

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