Skip to main content
. Author manuscript; available in PMC: 2013 Sep 3.
Published in final edited form as: Obesity (Silver Spring). 2011 Jul 14;20(1):178–185. doi: 10.1038/oby.2011.200

Table 1.

Association analysis of SNP genotypes in the French Case-Control cohorts with obesity using PLINK

Genotype numbers and minor allele frequencies (MAF)
Results of association of SNP genotypes with obesity
Controls
Morbidly obese adults
Severely obese children
Morbidly obese adults
Severely obese children
SNP 1,1a 1,2 2,2 MAF 1,1 1,2 2,2 MAF 1,1 1,2 2,2 MAF Empirical
P value
Corrected
P value
Odds ratio
(95% CI)
Empirical
P value
Corrected
P value
Odds ratio
(95% CI)
rs33957861 874 254 21 12.9% 663 133 14 9.9% 482 121 8 11.2% 0.006 0.034 b 0.75
(0.61–0.91)
0.153 0.635 0.85
(0.69–1.06)
rs737477 1051 132 6 6.1% 449 56 1 5.7% 504 69 5 6.8% 0.716 1.000 0.94
(0.69–1.29)
0.382 0.945 1.14
(0.86–1.51)
rs2236318 319 568 223 45.7% 249 388 146 43.4% 176 282 124 45.5% 0.166 0.684 0.91
(0.8–1.04)
0.936 1.000 0.99
(0.86–1.15)
rs10823103 503 475 111 32.0% 378 311 66 29.3% 286 223 62 30.4% 0.086 0.430 0.88
(0.76–1.02)
0.348 0.924 0.93
(0.79–1.08)
rs12413112 876 238 22 12.4% 671 149 7 9.9% 457 119 7 11.4% 0.013 0.085 0.77
(0.63–0.95)
0.396 0.955 0.91
(0.73–1.13)
rs11599176 886 261 25 13.3% 684 156 8 10.1% 463 122 9 11.8% 0.003 0.019 b 0.74
(0.61–0.9)
0.217 0.767 0.87
(0.71–1.08)
rs10997865 480 511 129 34.3% 354 323 81 32.0% 249 264 71 34.8% 0.135 0.597 0.9
(0.78–1.03)
0.802 1.000 1.02
(0.88–1.18)
rs11596401 468 520 123 34.5% 339 329 70 31.8% 254 255 72 34.3% 0.083 0.443 0.89
(0.77–1.02)
0.936 1.000 0.99
(0.86–1.15)
rs35689145 948 187 9 9.0% 693 107 1 6.8% 526 80 4 7.2% 0.015 0.101 0.74
(0.58–0.94)
0.076 0.390 0.79
(0.61–1.03)
rs33955981 518 456 115 31.5% 389 333 76 30.4% 280 243 60 31.1% 0.474 0.984 0.95
(0.83–1.09)
0.830 1.000 0.98
(0.84–1.15)
rs2234975 952 220 7 9.9% 720 132 9 8.7% 499 75 6 7.5% 0.188 0.728 0.87
(0.7–1.07)
0.018 0.123 0.74
(0.57–0.95)

P values < 0.05 are shown in boldface.

Corrected P values result from one million permutations.

a

1 denotes the common allele and 2 denotes the rare allele.

b

Statistically significant P values.

CI, confidence interval.