ClinVar Miner

Submissions for variant NM_001364905.1(LRBA):c.*9G>T

gnomAD frequency: 0.00194  dbSNP: rs150102345
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
Eurofins Ntd Llc (ga) RCV000402219 SCV000334711 benign not specified 2015-09-11 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000402219 SCV002066182 uncertain significance not specified 2020-02-03 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.