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. 2012 Jul 13;91(1):185–192. doi: 10.1016/j.ajhg.2012.05.020

Table 2.

Evidence of Multiple Independent Effects in Disease-Associated Loci under Penalized and Conditional Regression Analyses

Chr Locus Reported Associations (p Value in Current Samples) Independent SNPs (and p Values Conditioned on All Other SNPs) Genomic Context of Independent SNPs
CD

6 CDKAL1(MIM 611259) rs6908425 (intron 3) rs6908425 (2.9 × 10−5), rs898165 (4.6 × 10−7) rs6908425 (intron 3), rs898165 (intron 13)
12 LRRK2 (MIM 609007)–MUC19 (MIM 612170) rs11175593 (intergenic) rs7962370 (9.2 × 10−7), rs11175593 (0.0025) rs7962370 (intergenic), rs11175593 (intergenic)

T1D

2 AFF3 (MIM 601464) rs9653442 (intergenic) rs11685258 (3.0 × 10−5), rs2309837 (2.1 × 10−5) rs11685258 (intron 1), rs2309837 (intergenic)
4 IL2 (MIM 147680) rs4505848 (intron 18 of KIAA1109 [MIM 611565]) rs4505848 (0.0059), rs13152362 (0.00029) rs4505848, rs13152362 (intron 59 of KIAA1109)

T2D

3 PPARG (MIM 601487)-SYN2 (MIM 600755) rs13081389a (intergenic) and rs17036101 (intergenic) rs6775191 (5.3 × 10−6), rs17036101 (0.017) rs6775191 (intergenic), rs17036101 (intergenic)

Only common SNPs with additive p ≤ 2.3 × 10−6 in the WTCCC data and those SNPs whose associations were confirmed in the literature were analyzed. The following abbreviations are used: chr, chromosome; CD, Crohn disease; T1D, type 1 diabetes; and T2D, type 2 diabetes.

a

rs13081389 is in perfect LD (r2 = 1) with rs17036101.