ClinVar Miner

Submissions for variant NM_000532.5(PCCB):c.816G>C (p.Arg272=)

dbSNP: rs762223074
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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 RCV001489495 SCV001694037 likely benign Propionic acidemia 2019-12-23 criteria provided, single submitter clinical testing

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