ClinVar Miner

Variants in gene CDH18

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
0 0 77 7 2 86

Condition and significance breakdown #

Total conditions: 5
Download table as spreadsheet
Condition uncertain significance likely benign benign total
not specified 60 1 0 61
not provided 15 4 2 21
CDH18-related disorder 0 2 0 2
Childhood apraxia of speech 1 0 0 1
See cases 1 0 0 1

Submitter and significance breakdown #

Total submitters: 9
Download table as spreadsheet
Submitter uncertain significance likely benign benign total
Ambry Genetics 58 1 0 59
Quest Diagnostics Nichols Institute San Juan Capistrano 10 4 0 14
Bionano Laboratories 5 0 0 5
PreventionGenetics, part of Exact Sciences 0 2 0 2
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories 2 0 0 2
Labcorp Genetics (formerly Invitae), Labcorp 0 0 2 2
Breakthrough Genomics, Breakthrough Genomics 0 0 2 2
University of Washington Center for Mendelian Genomics, University of Washington 1 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 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.