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. Author manuscript; available in PMC: 2015 Feb 5.
Published in final edited form as: Mol Psychiatry. 2008 Jan 8;14(3):261–268. doi: 10.1038/sj.mp.4002141

Table 2. Genotypic association results.

Marker Allele frequencies (%) Genotypic association resultsa odds ratios (95% CI)

Homozygous major allele (reference) Heterozygous Homozygous minor allele P-valueb
rs1043805 A (85) 1.0 0.78 (0.49, 1.23) 0.76 (0.47, 1.24) 0.53
T (15)
rs3800373 A (72) 1.0 1.05 (0.82, 1.34) 1.66 (1.11, 2.46) 0.03
C (28)
rs7757037 G (52) 1.0 0.68 (0.53, 0.87) 0.63 (0.45, 0.89) 0.007
A (48)
rs3798346 A (78) 1.0 0.75 (0.44, 1.29) 0.67 (0.38, 1.19) 0.35
G (22)
rs9296158 G (70) 1.0 1.04 (0.82, 1.32) 1.53 (1.05, 2.22) 0.05
A (30)
rs1360780 C (70) 1.0 1.04 (0.81, 1.33) 1.81 (0.97, 2.13) 0.13
T (30)
rs4713902 T (70) 1.0 0.69 (0.55, 0.88) 0.47 (0.30, 0.74) 0.001
C (30)
rs6912833 T (73) 1.0 0.80 (0.58, 1.10) 0.77 (0.52, 1.15) 0.36
A (27)
rs9380525 C (68) 1.0 0.73 (0.54, 0.97) 0.69 (0.48, 1.01) 0.09
G (32)

Abbreviation: CI, confidence interval.

a

Odds ratios are calculated with respect to the reference group (the homozygous major allele for each marker). Odds ratios > 1.0 indicate that the genotype under examination (homozygous minor allele or heterozygous) is associated with higher risk. Odds ratios <1 indicate that the homozygous major allele is associated with higher risk.

b

Robust P-values are estimates of the overall trend for the data as calculated by the gtrr function using robust variance estimates.