ClinVar Miner

List of variants in gene TRPM4 reported as pathogenic for cardiac rhythm disease

Included ClinVar conditions (118):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_017636.4(TRPM4):c.2531G>A (p.Gly844Asp) rs200038418 0.00064
NM_017636.4(TRPM4):c.19G>A (p.Glu7Lys) rs267607142 0.00001
NM_017636.4(TRPM4):c.490C>T (p.Arg164Trp) rs387907216 0.00001
NM_017636.4(TRPM4):c.1127T>C (p.Ile376Thr) rs2122839457
NM_017636.4(TRPM4):c.2741A>G (p.Lys914Arg) rs172151858
NM_017636.4(TRPM4):c.3119T>C (p.Ile1040Thr) rs1369949906

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.