ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.180_183del (p.Ile62fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostics Laboratory, National Institute of Medical Genomics RCV002282598 SCV002104206 pathogenic Acute myeloid leukemia criteria provided, single submitter clinical testing The variant was detected in bone marrow from patients, but it was not confirmed in the matched

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