ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.138T>A (p.Pro46=)

dbSNP: rs1387400759
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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 RCV000631439 SCV000752512 likely benign Acute myeloid leukemia 2017-12-27 criteria provided, single submitter clinical testing

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