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. 2016 Sep;13(9):789–797. doi: 10.11909/j.issn.1671-5411.2016.09.006

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.