ClinVar Miner

Variants studied for colorectal cancer, hereditary nonpolyposis, type 7

Included ClinVar conditions (3):
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
3 2 780 307 54 1098

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
MLH3 2 2 780 304 51 1093
EIF2B2, MLH3 0 0 0 1 2 3
AREL1, MLH3 1 0 0 2 1 2

Submitter and significance breakdown #

Total submitters: 12
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 0 0 706 270 47 1023
Illumina Laboratory Services, Illumina 0 0 86 36 15 137
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 4 4 17 25
OMIM 3 0 4 0 0 7
Fulgent Genetics, Fulgent Genetics 0 0 5 2 0 7
Baylor Genetics 0 0 1 0 0 1
Center for Individualized Medicine, Mayo Clinic 0 1 0 0 0 1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 0 1 0 0 1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 0 1 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 0 0 1 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 1 0 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 1 0 0 1

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