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
26 11 289 117 11 2 449

Condition and significance breakdown #

Total conditions: 5
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Condition pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Acute myeloid leukemia 17 5 283 106 11 0 420
not provided 11 6 3 20 0 0 40
not specified 0 0 6 1 6 1 14
Autosomal dominant familial acute myeloid leukemia 0 0 0 0 0 1 1
Inborn genetic diseases 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 15
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Invitae 3 5 280 116 8 0 412
Clinical Genetics Karolinska University Hospital,Karolinska University Hospital 11 6 0 0 0 0 17
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
St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital 0 0 1 1 0 0 2
Baylor Genetics 0 0 1 0 0 0 1
Ambry Genetics 0 0 1 0 0 0 1
ITMI 0 0 0 0 0 1 1
Department of Pathology and Laboratory Medicine,Sinai Health System 0 0 1 0 0 0 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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