ClinVar Miner

Variants studied for chronic myelomonocytic leukemia

Included ClinVar conditions (6):
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 total
59 4 27 1 0 90

Gene and significance breakdown #

Total genes and gene combinations: 8
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign total
NF1 19 1 22 0 42
PTPN11 27 1 3 1 32
CBL 3 1 1 0 4
KRAS 4 0 0 0 4
ARHGAP26 3 0 0 0 3
NRAS 3 0 0 0 3
ASXL1 0 0 1 0 1
ETV6, FLT3 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance likely benign total
Fulgent Genetics,Fulgent Genetics 32 1 26 1 60
OMIM 16 0 0 0 16
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 14 1 0 0 15
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 3 0 0 0 3
Baylor Genetics 0 1 0 0 1
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 1 0 0 0 1
Genomic Research Center,Shahid Beheshti University of Medical Sciences 0 0 1 0 1
Knight Cancer Institute, Oregon Health and Science University 0 1 0 0 1

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