ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.693C>G (p.Pro231=)

gnomAD frequency: 0.00808  dbSNP: rs550308123
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000468430 SCV000559472 benign Acute myeloid leukemia 2024-01-29 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000502793 SCV000593989 benign not specified 2018-11-15 criteria provided, single submitter clinical testing
GeneDx RCV001559352 SCV001781566 likely benign not provided 2020-12-14 criteria provided, single submitter clinical testing

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