ClinVar Miner

Submissions for variant NM_000532.5(PCCB):c.642G>T (p.Thr214=)

dbSNP: rs148056730
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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 RCV001430320 SCV001633052 likely benign Propionic acidemia 2022-01-27 criteria provided, single submitter clinical testing

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