ClinVar Miner

List of variants in gene combination LOC110121269, SCN5A reported as likely benign 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.2788-6C>T rs41260344
NM_198056.2(SCN5A):c.2976C>T (p.Pro992=) rs193922725
NM_198056.2(SCN5A):c.3006C>G (p.Pro1002=) rs1553699716
NM_198056.2(SCN5A):c.3132C>T (p.Pro1044=) rs547709944
NM_198056.2(SCN5A):c.3183A>G (p.Glu1061=) rs7430407
NM_198056.2(SCN5A):c.3192G>A (p.Glu1064=) rs886039126
NM_198056.2(SCN5A):c.3270G>A (p.Pro1090=) rs752999955
NM_198056.2(SCN5A):c.3308C>A (p.Ser1103Tyr) rs7626962

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.