ClinVar Miner

Submissions for variant NM_017519.2(ARID1B):c.1032_1034GGC[5] (p.Ala350dup) (rs764418312)

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
Ambry Genetics RCV000719872 SCV000850743 likely benign History of neurodevelopmental disorder 2016-06-29 criteria provided, single submitter clinical testing Other strong data supporting benign classification
Gharavi Laboratory,Columbia University RCV000722971 SCV000854102 uncertain significance not provided 2018-09-16 no assertion criteria provided research

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.