|
SNP/group
|
Genotypea (n (%))
|
χ2
|
p
|
Allele (n (%))
|
χ2
|
p
|
OR (95% CI)
|
|---|
|
rs1867624
|
CC
|
CT
|
TT
| | |
C
|
T
| | | |
|
Case
|
28 (0.07)
|
133 (0.33)
|
240 (0.60)
| | |
189 (0.24)
|
613 (0.76)
|
2.94
|
0.086
|
1.23 (0.97–1.23)
|
|
Control
|
18 (0.04)
|
128 (0.31)
|
263 (0.64)
|
0.88
|
0.349
|
164 (0.20)
|
654 (0.80)
|
|
rs2057482
|
TT
|
CT
|
CC
| | |
T
|
C
| | | |
|
Case
|
17 (0.04)
|
132 (0.33)
|
252 (0.63)
| | |
166 (0.21)
|
636 (0.79)
|
0.11
|
0.75
|
1.04 (0.82–1.33)
|
|
Control
|
22 (0.05)
|
120 (0.29)
|
267 (0.65)
|
2.94
|
0.09
|
164 (0.20)
|
654 (0.80)
| | | |
|
rs3739998
|
GG
|
GC
|
CC
| | |
G
|
C
| | | |
|
Case
|
20 (0.05)
|
132 (0.33)
|
249 (0.62)
| | |
172 (0.21)
|
630 (0.79)
|
0.26
|
0.611
|
0.94 (0.74–1.19)
|
|
Control
|
24 (0.06)
|
136 (0.33)
|
249 (0.61)
|
0.23
|
0.630
|
184 (0.22)
|
634 (0.78)
|
- aAll are in HWE. SNP Single nucleotide polymorphism, MI myocardial infarction