ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.111G>C (p.Ala37=)

gnomAD frequency: 0.00001  dbSNP: rs1323312485
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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 RCV000631445 SCV000752518 likely benign Acute myeloid leukemia 2024-03-06 criteria provided, single submitter clinical testing

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