ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.222C>T (p.Asn74=)

dbSNP: rs1324116336
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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 RCV001490350 SCV001694911 likely benign Acute myeloid leukemia 2019-11-01 criteria provided, single submitter clinical testing

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