ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.525G>A (p.Leu175=)

gnomAD frequency: 0.00002  dbSNP: rs975118445
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001488068 SCV001692574 likely benign Acute myeloid leukemia 2023-08-23 criteria provided, single submitter clinical testing

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