ClinVar Miner

List of variants in gene combination KCNQ1, KCNQ1OT1 reported as likely benign for atrial fibrillation (disease)

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_000218.3(KCNQ1):c.1394-14C>T rs28730758
NM_000218.3(KCNQ1):c.1455C>T (p.Phe485=) rs17215465
NM_181798.1(KCNQ1):c.1012+21526C>T rs72847701
NM_181798.1(KCNQ1):c.1012+21538C>T rs72850203
NM_181798.1(KCNQ1):c.1012+22646C>G rs146407692
NM_181798.1(KCNQ1):c.1133+4974G>A rs188083723

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.