ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.421G>C (p.Gly141Arg)

dbSNP: rs1408671093
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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 RCV001938151 SCV002185068 likely benign Acute myeloid leukemia 2023-07-26 criteria provided, single submitter clinical testing

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