ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.1035_1045del (p.Met345fs)

dbSNP: rs1573338559
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NIHR Bioresource Rare Diseases, University of Cambridge RCV001003799 SCV001162243 likely pathogenic Acute myeloid leukemia no assertion criteria provided research

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