ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.939G>A (p.Lys313=)

dbSNP: rs1600021081
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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 RCV000922837 SCV001068283 likely benign Acute myeloid leukemia 2024-05-22 criteria provided, single submitter clinical testing

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