ClinVar Miner

Submissions for variant NM_000282.4(PCCA):c.783A>G (p.Glu261=)

dbSNP: rs917366865
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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 RCV002118814 SCV002448379 likely benign Propionic acidemia 2023-07-17 criteria provided, single submitter clinical testing

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