ClinVar Miner

Variants in gene combination MUTYH, TOE1

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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 57 31 2 89

Condition and significance breakdown #

Total conditions: 5
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Condition pathogenic likely pathogenic uncertain significance likely benign benign total
MYH-associated polyposis 2 0 35 20 2 58
Hereditary cancer-predisposing syndrome 1 1 37 15 1 55
not specified 0 0 5 5 1 11
not provided 0 2 7 1 0 10
Carcinoma of colon 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 15
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 2 0 30 13 1 46
Color Health, Inc 0 0 23 10 1 34
Ambry Genetics 1 1 21 6 0 29
GeneDx 0 1 5 5 1 12
Mendelics 0 0 0 5 0 5
Quest Diagnostics Nichols Institute San Juan Capistrano 0 0 5 0 0 5
Illumina Clinical Services Laboratory,Illumina 0 0 4 1 0 5
Counsyl 0 0 1 1 1 3
PreventionGenetics,PreventionGenetics 0 0 1 0 1 2
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 0 2 0 0 2
CeGaT Praxis fuer Humangenetik Tuebingen 0 1 1 0 0 2
Department of Pathology and Laboratory Medicine,Sinai Health System 0 0 1 1 0 2
Baylor Genetics 0 0 1 0 0 1
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories 0 0 0 0 1 1
Mayo Clinic Laboratories, Mayo Clinic 0 0 1 0 0 1

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