ClinVar Miner

List of variants studied for Intellectual disability, autosomal dominant 33 by New York Genome Center

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_130797.4(DPP6):c.1565A>G (p.Asn522Ser) rs774538369 0.00005
NM_130797.4(DPP6):c.1391C>T (p.Thr464Met) rs1054264418 0.00001
NM_001364497.2(DPP6):c.39T>A (p.Cys13Ter) rs2128935579
NM_130797.4(DPP6):c.1888G>A (p.Gly630Ser) rs2150654585

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.