ClinVar Miner

Submissions for variant NM_000282.4(PCCA):c.996T>C (p.Ala332=)

dbSNP: rs2152588809
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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 RCV002137123 SCV002415971 likely benign Propionic acidemia 2021-10-18 criteria provided, single submitter clinical testing

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