ClinVar Miner

Submissions for variant NM_000082.4(ERCC8):c.1042-1G>A

gnomAD frequency: 0.00001  dbSNP: rs897535441
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
Counsyl RCV000674160 SCV000799447 likely pathogenic Cockayne syndrome type 1 2018-04-18 criteria provided, single submitter clinical testing
Children's Hospital of Soochow University, Soochow University RCV000674160 SCV000808973 pathogenic Cockayne syndrome type 1 2018-09-01 no assertion criteria provided clinical testing

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.