ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.567C>T (p.Pro189=)

dbSNP: rs2145261321
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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 RCV001494280 SCV001698932 likely benign Acute myeloid leukemia 2022-03-17 criteria provided, single submitter clinical testing

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