ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.1803+9T>C

gnomAD frequency: 0.00025  dbSNP: rs371726505
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
Genetic Services Laboratory, University of Chicago RCV000503969 SCV000593340 likely benign not specified 2016-01-11 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506219 SCV002810243 likely benign Intellectual disability, autosomal dominant 14 2021-08-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002524154 SCV003261255 likely benign not provided 2023-10-23 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.