ClinVar Miner

Submissions for variant PCDH15, 3-BP DEL, 5601AAC

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000005219 SCV000025397 pathogenic Usher syndrome, type 1F 2005-03-01 no assertion criteria provided literature only
OMIM RCV000005220 SCV000025398 pathogenic USHER SYNDROME, TYPE ID/F, DIGENIC 2005-03-01 no assertion criteria provided literature only

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.