ClinVar Miner

Variants studied for MYH-associated polyposis

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
72 50 383 146 12 629

Gene and significance breakdown #

Total genes and gene combinations: 2
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
MUTYH 72 50 365 136 11 600
MUTYH, TOE1 0 0 18 10 1 29

Submitter and significance breakdown #

Total submitters: 18
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 59 26 346 132 11 574
Counsyl 13 19 68 30 1 131
Mendelics 11 3 30 1 0 45
Illumina Clinical Services Laboratory,Illumina 6 3 23 1 1 34
Department of Pathology and Laboratory Medicine,Sinai Health System 20 3 0 0 0 23
GeneReviews 11 0 0 0 0 11
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 7 0 0 0 0 7
OMIM 6 0 0 0 0 6
Center for Human Genetics, Inc 2 1 2 0 0 5
Biesecker Lab/Human Development Section,National Institutes of Health 2 2 0 0 0 4
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia 1 0 1 1 1 4
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 1 1 2 0 0 4
Molecular Oncology Laboratory,Hospital Clínico San Carlos 1 1 1 0 0 3
Knight Diagnostic Laboratories,Oregon Health and Sciences University 1 1 0 0 0 2
University of Washington Department of Laboratory Medicine,University of Washington 0 1 0 1 0 2
Genomic Research Center,Shahid Beheshti University of Medical Sciences 1 0 0 0 0 1
CSER_CC_NCGL; University of Washington Medical Center 0 0 1 0 0 1
Donald Williams Parsons Laboratory,Baylor College of Medicine 1 0 0 0 0 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.