ClinVar Miner

List of variants in gene KCNE3 reported as likely benign for Cardiovascular phenotype

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005472.5(KCNE3):c.116C>G (p.Pro39Arg) rs34604640 0.00014
NM_005472.5(KCNE3):c.296G>A (p.Arg99His) rs121908441 0.00007
NM_005472.5(KCNE3):c.94C>T (p.Arg32Trp) rs755300564 0.00003
NM_005472.5(KCNE3):c.49G>A (p.Val17Met) rs773287275 0.00002
NM_005472.5(KCNE3):c.150A>T (p.Leu50=) rs772767562 0.00001
NM_005472.5(KCNE3):c.21G>A (p.Thr7=) rs201582585 0.00001
NM_005472.5(KCNE3):c.117A>G (p.Pro39=)
NM_005472.5(KCNE3):c.183T>C (p.Ile61=)
NM_005472.5(KCNE3):c.240C>T (p.Thr80=)
NM_005472.5(KCNE3):c.242G>A (p.Arg81His)
NM_005472.5(KCNE3):c.279T>C (p.His93=) rs199972628
NM_005472.5(KCNE3):c.27C>G (p.Thr9=)
NM_005472.5(KCNE3):c.282G>A (p.Val94=)

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.