ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.765G>T (p.Gly255=)

gnomAD frequency: 0.00002  dbSNP: rs1163957359
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001429959 SCV001632681 likely benign Acute myeloid leukemia 2021-11-24 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258011 SCV002537443 uncertain significance Hereditary cancer-predisposing syndrome 2021-11-30 criteria provided, single submitter curation

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