Skip to main content
. 2009 Jun;20(6):1359–1367. doi: 10.1681/ASN.2008080842

Table 4.

Single SNP association analyses of SNPs 1–8 in 394 cases and 394 controlsa

SNP Genotype OR (95% CI)b Global Pc Corrected Pd
SNP 1 GG 1.46 (0.91–2.35) 6.0 × 10−5 4.8 × 10−4
(rs943887) AG 0.96 (0.59–1.56)
AA Reference
SNP 2 TT 1.60 (1.09–2.36) 0.0002 0.0017
(rs943888) CT 1.24 (0.88–1.75)
CC Reference
SNP 3 GG 1.66 (1.08–2.53) 0.0061 0.0476
(rs56131962) AG 1.27 (0.84–1.92)
AA Reference
SNP 4 CC 1.72 (1.12–2.64) 0.0036 0.0284
(rs55766725) CT 1.29 (0.85–1.96)
TT Reference
SNP 5 GG 1.61 (1.06–2.45) 0.0064 0.0499
(rs1263648) AG 1.22 (0.81–1.82)
AA Reference
SNP 6 AA 1.58 (1.04–2.39) 0.0080 0.0623
(rs1263649) AG 1.20 (0.80–1.79)
GG Reference
SNP 7 GG 1.07 (0.63–1.80) 0.1028 0.5803
(rs1263650) AG 0.97 (0.57–1.66)
AA Reference
SNP 8 TT 1.20 (0.72–2.01) 0.0668 0.4249
(rs1263651) CT 1.03 (0.61–1.74)
CC Reference
a

Data for single nucleotide polymorphisms (SNPs) 1 and 2 were missing in eight individuals, and SNP 3–8 data were missing in three individuals in the patient group. No missing data in the control group.

b

Odds ratio (OR) values after adjusting for age and gender by logistic regression.

c

Adjusting for age and gender by logistic regression, calculated by the likelihood ratio chi-square test (using genotype data) which compares the model with the marker and the model without the marker.

d

After Bonferroni correction for multiple testing.