Table 1. Selected single nucleotide polymorphisms with evidence for association with sudden cardiac death and ventricular fibrillation due to coronary artery disease.

Gene	rsID	Chromosome locus	Most severe consequence	OR (95% CI)	Reference
NOS1AP	rs10918859	1q21	Intron variant		Westaway, et al.[58]
	rs12084280	1q23	Intergenetic variant
CASQ2	rs7521023 rs17500488 rs3010396 rs7366407	1p13 1q13 1q13 1q13	3 prime UTR Variant Intron variant Intron variant Intergenic variant	2.72 (1.44−5.13)	Refaat, et al.[79] Westaway, et al.[58]
ACYP2	rs1559040	2p16	Intron variant	1.54 (1.32−1.79)	Aouizerat, et al.[66]
ZNF385B	rs16866933	2q31	Intron variant	1.69 (1.48−1.93)	Aouizerat, et al.[66]
	rs4621553	5q22	Intergenic variant	1.40 (1.24−-1.58)
RAB3GAP1	rs6730157	2q21	Intron variant	1.60	Huertaz-Vazquez, et al.[74]
SCN5A	rs11720524	3p22	Intron variant	1.35 (1.05−1.74)	Albert, et al;[57] Marcsa, et al.[80]
GPD1L	rs9862154	3q22	Upstream gene variant		Westaway, et al.[58]
AGTR1	rs263936	3q24	Intergenic variant	1.13 (1.04−1.22)	Aouizerat, et al.[66]
GRIA1	rs12189362	5q33	Intron variant	1.50 (1.32−1.69)	Aouizerat, et al.[66]
ZNF365	rs2077316	10q21	Intron variant	2.41	Huertaz-Vazquez, et al.[74]
GPC5 (GLYPIAN 5)	rs3864180	13q31	Intron variant	0.85 (0.74−0.98)	Arking, et al.[65]
AP1G2	rs2281680	14q11	Splice region variant	1.38 (1.23−1.54)	Aouizerat, et al.[66]
	rs11624056	14q31	Intergeneic variant	1.43 (1.26−1.62)
DEGS2	rs7157599	14q32	Missense variant	1.13 (1.08−1.19)	Aouizerat, et al. [66]
	rs17718586	17q24	Intergeneic variant	1.53 (1.32−1.78)
	rs597503	18p11	Upstream gene variant	1.45 (1.27−1.65)
CXADR	rs2824292	21q21	Intergeneic variant	1.78 (1.47−2.13)	Bezzina, et al.[37]
KCTD1	rs16942421	18q11	Intron variant	1.68 (1.43−1.98)	Aouizerat, et al. [66]

OR: odds ratio; UTR: untranslated region.