ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.1041G>A (p.Glu347=)

gnomAD frequency: 0.00752  dbSNP: rs141430731
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000470798 SCV000559475 benign Acute myeloid leukemia 2024-01-29 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000504052 SCV000593987 benign not specified 2016-10-05 criteria provided, single submitter clinical testing
GeneDx RCV001548002 SCV001767844 likely benign not provided 2020-12-14 criteria provided, single submitter clinical testing

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