ClinVar Miner

List of variants in gene combination LOC110121269, SCN5A reported as not provided for Brugada syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_198056.2(SCN5A):c.2804T>C (p.Leu935Pro) rs199473179
NM_198056.2(SCN5A):c.2893C>T (p.Arg965Cys) rs199473180
NM_198056.2(SCN5A):c.2894G>A (p.Arg965His) rs199473181
NM_198056.2(SCN5A):c.2989G>A (p.Ala997Thr) rs137854609
NM_198056.2(SCN5A):c.3068G>A (p.Arg1023His) rs199473592
NM_198056.2(SCN5A):c.3164A>G (p.Asp1055Gly) rs199473593
NM_198056.2(SCN5A):c.3236C>A (p.Ser1079Tyr) rs199473188
NM_198056.2(SCN5A):c.3338C>T (p.Ala1113Val) rs199473194

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.