ClinVar Miner

List of variants in gene DYRK1A, LOC130066653 studied for DYRK1A-related intellectual disability syndrome

Included ClinVar conditions (2):

DYRK1A-related intellectual disability syndrome
Intellectual disability syndrome due to a DYRK1A point mutation

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_000021.9:g.37347863_37423682del

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.