ClinVar Miner

Variants studied for Hereditary nonpolyposis colorectal cancer type 7

Coded as:
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 1 326 84 48 426

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 1 326 82 45 422
EIF2B2, MLH3 0 0 0 1 2 3
AREL1, MLH3 1 0 0 1 1 1

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 0 0 248 48 38 334
Illumina Clinical Services Laboratory,Illumina 0 0 86 36 15 137
OMIM 3 0 4 0 0 7
Center for Individualized Medicine,Mayo Clinic 0 1 0 0 0 1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 0 1 0 0 1

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