ClinVar Miner

List of variants in gene KCNJ8 reported as benign for Brugada syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NM_004982.4(KCNJ8):c.1001T>C (p.Val334Ala) rs34811413
NM_004982.4(KCNJ8):c.111C>T (p.Ile37=) rs112604741
NM_004982.4(KCNJ8):c.291C>G (p.Ala97=) rs34524779
NM_004982.4(KCNJ8):c.793T>C (p.Leu265=) rs16924297
NM_004982.4(KCNJ8):c.855G>A (p.Leu285=) rs34093632

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.