ClinVar Miner

Submissions for variant NM_001744.6(CAMK4):c.981+1G>A (rs1561515242)

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
Institute of Neurogenomics,Technical University of Munich RCV000680276 SCV000804199 likely pathogenic Intellectual disability; Involuntary movements 2018-08-15 no assertion criteria provided research
OMIM RCV000754607 SCV000882520 uncertain significance not provided 2019-01-24 no assertion criteria provided literature only

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.