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. 2022 Sep 28;13(10):1755. doi: 10.3390/genes13101755

Table 1.

Genetics of Brugada syndrome.

BrS
Susceptibility Genes
Prevalence
in BrS Cases
BrS
Risk Loci
SNPs
SCN5A 20–25% SCN5A rs11708996
rs7638909a
rs62241190a
rs7374540a
rs7433206a
rs34760424a
rs41310232a
rs6782237a
SCN10A >5% SCN10A rs10428132
rs6801957
CACNA1C CACNB2 1–2% HEY2 rs9388451
rs9398791
PKP2 HCN4 <1% HDDC2 rs6913204a
KCNH2 KCNE3 rs6913204a
CACNA2D1 KCNJ8 TBX20 s11765936
KCND3 RANGFR rs340398a
SCN2B SCN1B GATA4 rs804281
KCND2 TRPM4 ZFPM2 rs72671655
KCNE5 ABCC9 WT1 rs72905083
SCN3B SLMAP TBX5 rs883079
FGF12 SEMA3A IRX3 rs11645463
GPD1L IRX5 rs72622262
References: [6,17,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43] PRKCA rs12945884
MAPRE2 rs476348
MYO18B rs133902

The current knowledge about genetics in BrS is shown, including susceptibility genes, prevalence, risk loci, and polymorphisms. BrS = Brugada syndrome; SNPs = single nucleotide polymorphisms [6,17,21,22,23,24,25,26,27,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43].