ClinVar Miner

Submissions for variant NM_020166.5(MCCC1):c.273+53A>C

dbSNP: rs3732604
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987369 SCV001136648 benign 3-methylcrotonyl-CoA carboxylase 1 deficiency 2019-05-28 criteria provided, single submitter clinical testing
Pars Genome Lab RCV000987369 SCV001738571 benign 3-methylcrotonyl-CoA carboxylase 1 deficiency 2021-06-15 criteria provided, single submitter clinical testing
GeneDx RCV001644870 SCV001858064 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001644870 SCV005302565 benign not provided criteria provided, single submitter not provided

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