ClinVar Miner

List of variants in gene KANSL1 reported as likely benign by Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_015443.4(KANSL1):c.1765G>A (p.Val589Met) rs1357621164
NM_015443.4(KANSL1):c.2981G>T (p.Ser994Ile) rs2146306637

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.