ClinVar Miner

Submissions for variant NM_000532.5(PCCB):c.1090+8G>A

dbSNP: rs2108226738
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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 RCV002175426 SCV002345985 likely benign Propionic acidemia 2021-04-12 criteria provided, single submitter clinical testing

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