ClinVar Miner

Submissions for variant NM_000282.4(PCCA):c.2040+9TG[5]

dbSNP: rs751014655
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000674050 SCV000799323 likely benign Propionic acidemia 2018-04-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000674050 SCV002372772 likely benign Propionic acidemia 2024-11-30 criteria provided, single submitter clinical testing

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