ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.332_339del (p.Ala111fs)

dbSNP: rs1555742213
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502416 SCV000594000 pathogenic Acute myeloid leukemia 2017-04-19 criteria provided, single submitter clinical testing
Clinical Genetics and Genomics, Karolinska University Hospital RCV001269596 SCV001449691 pathogenic not provided 2017-07-14 criteria provided, single submitter clinical testing

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