ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.378G>A (p.Gly126=)

dbSNP: rs1967186909
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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 RCV002219743 SCV002371594 likely benign Acute myeloid leukemia 2021-08-26 criteria provided, single submitter clinical testing

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