Table 7 Allele and genotype frequencies of H19 rs217727 and its relationship with stroke subtypes
LAA | SVO | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
Case | Control | P | OR | 95%CI | Case | Control | P | OR | 95%CI | |
Genotype | ||||||||||
CC | 139 | 217 | Reference | 79 | 217 | Reference | ||||
CT | 168 | 274 | 0.765 | 0.957 | 0.719–1.275 | 91 | 274 | 0.607 | 0.912 | 0.643–1.295 |
TT | 49 | 61 | 0.304 | 1.254 | 0.814–1.932 | 41 | 61 | 0.010 | 1.846 | 1.151–2.961 |
Dominant effect | ||||||||||
CT + TT vs CC | 217/139 | 335/217 | 0.936 | 1.011 | 132/79 | 335/217 | 0.635 | 1.082 | 0.780–1.501 | |
Recessive effect | ||||||||||
TT vs CT + CC | 49/307 | 61/491 | 0.221 | 1.285 | 0.77–1.329 | 41/170 | 61/491 | 0.02 | 1.941 | 1.260–2.992 |
Allele | ||||||||||
T | 266 | 396 | Reference | 0.859–1.921 | 173 | 396 | Reference | |||
C | 446 | 708 | 0.520 | 1.066 | 0.877–1.296 | 249 | 708 | 0.064 | 1.242 | 0.987–1.563 |