ClinVar Miner

Submissions for variant NM_005591.3(MRE11):c.1783+7A>G (rs774520952)

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
GeneKor MSA RCV000708710 SCV000822030 uncertain significance Hereditary cancer-predisposing syndrome 2018-08-01 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000368990 SCV000374926 uncertain significance Ataxia-telangiectasia-like disorder 1 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000368990 SCV000260306 likely benign Ataxia-telangiectasia-like disorder 1 2017-12-01 criteria provided, single submitter 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.