ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.132C>T (p.Ala44=)

dbSNP: rs1060504474
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000472313 SCV000559467 likely benign Acute myeloid leukemia 2022-10-06 criteria provided, single submitter clinical testing

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