ClinVar Miner

Submissions for variant NM_000282.4(PCCA):c.897G>C (p.Val299=)

dbSNP: rs770113371
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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 RCV001489853 SCV001694406 likely benign Propionic acidemia 2021-04-05 criteria provided, single submitter clinical testing

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