Skip to main content
. Author manuscript; available in PMC: 2017 Jan 1.
Published in final edited form as: Curr Probl Cardiol. 2015 Jun 11;41(1):7–57. doi: 10.1016/j.cpcardiol.2015.06.002

Table 1.

Brugada Syndrome Susceptibility Genes.

Locus Gene Ion Channel % of Probands
BrS1 3p21 SCN5A, Nav1.5 ↓ INa 11–28%
BrS2 3p24 GPD1L ↓ INa Rare
BrS3 12p13.3 CACNA1C, Cav1.2 ↓ ICa 6.6%
BrS4 10p12.33 CACNB2b, Cavβ2b ↓ ICa 4.8%
BrS5 19q13.1 SCN1B, Navβ1 ↓ INa 1.1%
BrS6 11q13–14 KCNE3, MiRP2 ↑ Ito Rare
BrS7 11q23.3 SCN3B, Navβ3 ↓ INa Rare
BrS8 12p11.23 KCNJ8, Kir6.1 ↑ IK-ATP 2%
BrS9 7q21.11 CACNA2D1, Cavα2δ ↓ ICa 1.8%
BrS10 1p13.2 KCND3, Kv4.3 ↑ Ito Rare
BrS11 17p13.1 RANGRF, MOG1 ↓ INa Rare
BrS12 3p21.2-p14.3 SLMAP ↓ INa Rare
BrS13 12p12.1 ABCC9, SUR2A ↑ IK-ATP Rare
BrS14 11q23 SCN2B, Navβ2 ↓ INa Rare
BrS15 12p11 PKP2, Plakophillin-2 ↓ INa Rare
BrS16 3q28 FGF12, FHAF1 ↓ INa Rare
BrS17 3p22.2 SCN10A, Nav1.8 ↓ INa 16.7%
BrS18 6q HEY2 (transcriptional factor) ↓ INa Rare
BrS19 7p12.1 SEMA3A, Semaphorin ↑ Ito Rare