ClinVar Miner

Submissions for variant NM_000282.4(PCCA):c.756T>C (p.Ser252=)

dbSNP: rs2152564931
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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 RCV002187474 SCV002349058 likely benign Propionic acidemia 2021-04-23 criteria provided, single submitter clinical testing

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