ClinVar Miner

Submissions for variant NM_012213.3(MLYCD):c.1368C>T (p.Tyr456=)

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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 RCV003610576 SCV004474879 benign Deficiency of malonyl-CoA decarboxylase 2024-01-08 criteria provided, single submitter clinical testing

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