ClinVar Miner

Submissions for variant NM_012213.3(MLYCD):c.315G>C (p.Gln105His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003132654 SCV003808833 uncertain significance Deficiency of malonyl-CoA decarboxylase 2020-11-30 criteria provided, single submitter clinical testing

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