ClinVar Miner

Submissions for variant NM_002520.7(NPM1):c.847-5T>C

gnomAD frequency: 0.01680  dbSNP: rs191111314
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000956352 SCV001103114 benign not provided 2018-08-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502975 SCV002805826 likely benign Acute myeloid leukemia 2021-12-23 criteria provided, single submitter clinical testing

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