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
15 2 148 36 10 2 207

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 15 2 140 32 10 0 199
not specified 0 0 6 4 3 1 14
not provided 0 0 2 0 0 0 2
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 1 2 139 32 7 0 181
Genetic Services Laboratory, University of Chicago 2 0 6 4 1 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 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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