ClinVar Miner

Variants in gene CEBPA

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign not provided total
17 4 224 81 11 2 335

Condition and significance breakdown #

Total conditions: 8
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Condition pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Acute myeloid leukemia 17 4 217 60 11 0 308
not provided 0 0 2 20 0 0 22
not specified 0 0 6 1 6 1 14
Autosomal dominant familial acute myeloid leukemia 0 0 0 0 0 1 1
B Lymphoblastic Leukemia/Lymphoma with Hypodiploidy 0 0 1 0 0 0 1
B Lymphoblastic Leukemia/Lymphoma with t(v;11q23.3); KMT2A Rearranged 0 0 1 0 0 0 1
Inborn genetic diseases 0 0 1 0 0 0 1
Retinoblastoma 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 12
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Invitae 3 4 215 80 8 0 310
Genetic Services Laboratory, University of Chicago 2 0 6 1 4 0 13
GeneReviews 6 0 0 0 3 0 9
OMIM 7 0 0 0 0 0 7
Fulgent Genetics,Fulgent Genetics 0 0 5 0 0 0 5
GeneDx 0 0 2 0 0 0 2
PreventionGenetics,PreventionGenetics 0 0 0 0 2 0 2
Clinical Genomics Lab,St. Jude Children's Research Hospital 0 0 2 0 0 0 2
Ambry Genetics 0 0 1 0 0 0 1
ITMI 0 0 0 0 0 1 1
GenomeConnect, ClinGen 0 0 0 0 0 1 1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 0 0 0 1

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