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. 2009 May 20;52(10):2109–2116. doi: 10.1007/s00125-009-1391-y

Table 2.

Association of PPARG and HHEX–IDE in type 1 diabetes families

Gene region SNP Families, n Allele or genotype Transmitteda, n (%) Not transmitteda, n (%) RR (95% CI) p value pcombined valued
PPARG rs1801282 3,312 G 862 (45.0) 988 (55.0) 0.87 (0.80–0.95) 0.003b 1.0 × 10−4
C/C 3,139 (77.4) 9,176 (75.4) 1.00 (reference)
C/G 853 (21.0) 2,789 (22.9) 0.86 (0.78–0.95)
G/G 65 (1.6) 206 (1.7) 0.84 (0.62–1.15) 0.010c
HHEX–IDE rs1111875 3,229 A 1,728 (49.8) 1,742 (50.2) 0.99 (0.93–1.06) 0.812b 0.017
G/G 1,283 (34.8) 3,855 (34.9) 1.00 (reference)
G/A 1,788 (48.6) 5,324 (48.2) 1.01 (0.92–1.10)
A/A 611 (16.6) 1,867 (16.9) 0.98 (0.85–1.12) 0.880c

aNote that the frequencies of genotypes in the cases and pseudo-controls are given, as well as the transmission counts from the transmission disequilibrium test analysis

bThe p value for association from the transmission disequilibrium test, which assumes a multiplicative model

cThe p value for association from the 2 df conditional logistic regression model, which does not assume a specific mode of inheritance

dThe p value obtained by combining the results of the case–control and family data set (please refer to the Methods for further details)

HHS Vulnerability Disclosure