ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.741G>C (p.Pro247=)

dbSNP: rs1600021917
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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 RCV001475112 SCV001679299 likely benign Acute myeloid leukemia 2018-04-27 criteria provided, single submitter clinical testing

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