Skip to main content
. 2019 Aug;14(8):1404–1411. doi: 10.4103/1673-5374.253525

Table 3.

Genotypes and allele frequencies between ischemic stroke cases and controls

SNP Allele/genotype Ischemic stroke Control Chi2/STAT OR (95% CI) P
rs6265 A 682(47.4) 709(44.8)
G 758(52.6) 873(55.2) 1.96 1.11(0.96–1.28) a0.162
AA 153(21.2) 172(21.7)
AG 376(52.2) 365(46.1)
GG 191(26.5) 254(32.1)
Dominantb 0.73 1.11(0.83–1.48) 0.467
Model
AA+GA
GG
Recessiveb –1.735 0.75(0.55–1.04) 0.083
Model
AA
GA+GG
rs7124442 C 126(8.7) 133(8.6)
T 1326(91.3) 1415(91.4) 0.01 1.01(0.78–1.31) 0.924
CC 3(0.4) 6(0.8)
TC 120(16.5) 121(15.6)
TT 603(83.1) 647(83.6)
Dominant –0.14 0.98(0.69–1.39) 0.89
Model
CC+TC
TT
Recessive –0.33 0.75(0.14–3.94) 0.739
Model
CC
TC+TT

SNP: Single-nucleotide polymorphism; STAT: logistic coefficient t statistic; CI: confidence interval; OR: odds ratio. aChi-square test; blogistic regression analyses adjusted on the basis of risk factors such as age, sex, hypertension, hyperlipidemia, diabetes, atrial fibrillation, smoking and drinking.