ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2440-6del

gnomAD frequency: 0.00001  dbSNP: rs745901278
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662600 SCV000785235 likely benign Hereditary diffuse gastric adenocarcinoma 2017-06-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000662600 SCV001656800 likely benign Hereditary diffuse gastric adenocarcinoma 2024-01-24 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000662600 SCV004019535 likely benign Hereditary diffuse gastric adenocarcinoma 2023-03-03 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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.