ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.1032G>A (p.Gln344=)

dbSNP: rs1967157574
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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 RCV002132530 SCV002432537 likely benign Acute myeloid leukemia 2021-08-10 criteria provided, single submitter clinical testing

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