ClinVar Miner

Submissions for variant NM_020166.5(MCCC1):c.89+17T>C

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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 RCV003599968 SCV004461219 likely benign 3-methylcrotonyl-CoA carboxylase 1 deficiency 2023-08-25 criteria provided, single submitter clinical testing

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