ClinVar Miner

Submissions for variant NM_000214.3(JAG1):c.-299AAG[1]

dbSNP: rs147400796
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
Illumina Laboratory Services, Illumina RCV000317633 SCV000432971 likely benign Isolated Nonsyndromic Congenital Heart Disease 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000378964 SCV000432972 likely benign Arteriohepatic dysplasia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV002298574 SCV002588044 likely benign not provided 2021-11-08 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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.