List of variants in gene TRPM4 reported as benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_017636.4(TRPM4):c.375G>A (p.Ser125=)	rs34333830	0.05846
NM_017636.4(TRPM4):c.1041G>T (p.Leu347=)	rs61732831	0.03430
NM_017636.4(TRPM4):c.2982G>A (p.Ser994=)	rs1175810	0.03027
NM_017636.4(TRPM4):c.3024G>A (p.Ala1008=)	rs35145363	0.02710
NM_017636.4(TRPM4):c.2934T>C (p.Ile978=)	rs35516880	0.02629
NM_017636.4(TRPM4):c.783G>A (p.Lys261=)	rs111930830	0.01878
NM_017636.4(TRPM4):c.322C>T (p.Arg108Cys)	rs115335683	0.01074
NM_017636.4(TRPM4):c.3082C>T (p.Leu1028=)	rs79286201	0.01042
NM_017636.4(TRPM4):c.2619C>T (p.Thr873=)	rs144544237	0.00790
NM_017636.4(TRPM4):c.3405A>C (p.Ala1135=)	rs144647383	0.00426
NM_017636.4(TRPM4):c.870C>T (p.Asn290=)	rs141997826	0.00389

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.