ClinVar Miner

Submissions for variant NM_020166.5(MCCC1):c.867C>A (p.Ala289=)

dbSNP: rs2108505485
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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 RCV002082609 SCV002323177 likely benign 3-methylcrotonyl-CoA carboxylase 1 deficiency 2021-08-14 criteria provided, single submitter clinical testing

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