ClinVar Miner

Submissions for variant NM_000282.4(PCCA):c.24A>T (p.Thr8=)

dbSNP: rs117397004
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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 RCV000941849 SCV001087751 likely benign Propionic acidemia 2023-12-27 criteria provided, single submitter clinical testing

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