From: Genetic variants of SLC6A4 and risk of coronary artery disease: insights from North Indian population
Haplotypes
Frequency
OR [95% C.I.]
p-value
CAD cases (n = 400)
Controls (n = 400)
S-12
0.47
0.48
0.96 (0.79–1.16)
0.7
L-12
0.24
0.18
1.45 (1.14–1.85)
0.002*
S-10
0.29
0.77 (0.62–0.96)
0.02*
L-10
0.05
0.047
1.03 (0.62–1.62)
0.9