ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.1017G>C (p.Arg339=)

dbSNP: rs2145258335
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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 RCV001438956 SCV001641837 likely benign Acute myeloid leukemia 2023-04-12 criteria provided, single submitter clinical testing

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