ClinVar Miner

Variants studied for large cell carcinoma

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 not provided total
18 7 33 22 20 1 100

Gene and significance breakdown #

Total genes and gene combinations: 10
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
DICER1 13 7 27 22 20 1 89
TP53 3 0 0 0 0 0 3
KRAS 1 0 0 0 0 0 1
LOC107303340, VHL 0 0 1 0 0 0 1
LOC110806263, TERT 1 0 0 0 0 0 1
MSH6 0 0 1 0 0 0 1
PALB2 0 0 1 0 0 0 1
PDGFRA 0 0 1 0 0 0 1
RAD50 0 0 1 0 0 0 1
ROS1 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 14
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 8 16 0 24
Illumina Laboratory Services, Illumina 0 0 7 6 4 0 17
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 3 0 14 0 0 0 17
Fulgent Genetics, Fulgent Genetics 1 0 4 9 1 0 15
Salgia Laboratory, City of Hope 4 0 6 0 0 0 10
OMIM 7 0 0 0 0 0 7
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 2 2 1 0 0 0 5
MGZ Medical Genetics Center 0 1 2 0 0 0 3
Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research 0 2 0 0 0 0 2
Juno Genomics, Hangzhou Juno Genomics, Inc 1 0 0 0 0 0 1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 1 0 0 0 0 1
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 1 1
Molecular Genetics and NGS Laboratory, Hospital Fundacion Valle Del Lili 1 0 0 0 0 0 1
MVZ Medizinische Genetik Mainz 0 1 0 0 0 0 1

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