ClinVar Miner

Submissions for variant NM_000532.5(PCCB):c.763+3GA[4]

dbSNP: rs1553778916
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000665988 SCV000790216 uncertain significance Propionic acidemia 2017-03-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000665988 SCV003476856 likely benign Propionic acidemia 2024-02-02 criteria provided, single submitter clinical testing

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