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. 2015 May 28;6:7060. doi: 10.1038/ncomms8060

Table 1. Characteristics of SNPs considered for use in Mendelian randomization analysis of the effect of T2D on CHD risk.

Locus SNP EA NEA OR T2D P value T2D OR CHD P value CHD Pleiotropic effect Physiologic cluster
ADCY5 rs11717195 T C 1.11 6.5E−14 1.00 8.3E−01 No BC
CDKAL1 rs7756992 G A 1.17 7.0E−35 1.02 7.2E−02 No BC
CDKN2A/B rs10811661 T C 1.18 3.7E−27 1.00 6.8E−01 No BC
DGKB rs17168486 T C 1.11 5.9E−11 1.00 6.6E−01 No BC
HHEX/IDE rs1111875 C T 1.11 2.0E−19 1.02 1.3E−02 No BC
PROX1 rs2075423 G T 1.07 8.1E−09 1.00 7.1E−01 No BC
SLC30A8 rs3802177 G A 1.14 1.3E−21 1.01 3.3E−01 No BC
THADA rs10203174 C T 1.14 9.5E−12 1.01 5.9E−01 No BC
MTNR1B rs10830963 G C 1.10 5.3E−13 1.01 2.6E−01 No HG
ANK1 rs516946 C T 1.09 2.5E−10 1.01 2.8E−01 No NA
BCAR1 rs7202877 T G 1.12 3.5E−08 1.07 2.7E−05 No NA
HMG20A rs7177055 A G 1.08 4.6E−09 1.01 2.1E−01 No NA
KLHDC5 rs10842994 C T 1.10 6.1E−10 0.99 2.4E−01 No NA
TLE1 rs2796441 G A 1.07 5.4E−09 1.02 9.5E−02 No NA
UBE2E2 rs1496653 A G 1.09 3.6E−09 1.01 5.8E−01 No NA
ZMIZ1 rs12571751 A G 1.08 1.0E−10 0.99 5.2E−01 No NA
ARAP1 (CENTD2) rs1552224 A C 1.11 1.8E−10 0.99 3.4E−01 No PI
BCL11A rs243088 T A 1.07 1.8E−08 1.02 3.8E−02 No UC
HMGA2 rs2261181 T C 1.13 1.2E−09 1.01 4.0E−01 No UC
IGF2BP2 rs4402960 T G 1.13 2.4E−23 1.02 1.5E−02 No UC
JAZF1 rs849135 G A 1.11 3.1E−17 1.02 5.8E−03 No UC
KCNQ1 rs163184 G T 1.09 1.2E−11 1.02 2.2E−02 No UC
PRC1 rs12899811 G A 1.08 6.3E−09 1.01 1.4E−01 No UC
TSPAN8/LGR5 rs7955901 C T 1.07 6.5E−09 0.99 4.6E−01 No UC
WFS1 rs4458523 G T 1.10 2.0E−15 1.01 4.6E−01 No UC
ZBED3 rs6878122 G A 1.10 5.0E−11 1.02 3.8E−01 No UC
TCF7L2 rs7903146 T C 1.39 1.2E−139 1.03 5.7E−03 Yes BC
IRS1 rs2943640 C A 1.10 2.7E−14 1.03 5.2E−04 Yes IR
PPARG rs1801282 C G 1.13 1.1E−12 1.00 7.8E−01 Yes IR
ANKRD55 rs459193 G A 1.08 6.0E−09 1.02 2.5E−02 Yes NA
CILP2 rs10401969 C T 1.13 7.0E−09 0.93 7.3E−05 Yes NA
FTO rs9936385 C T 1.13 2.6E−23 1.03 4.2E−03 Yes NA
GRB14 rs13389219 C T 1.07 1.0E−08 1.02 7.2E−02 Yes NA
MC4R rs12970134 A G 1.08 1.2E−08 1.03 1.8E−03 Yes NA
SPRY2 rs1359790 G A 1.08 1.4E−08 0.99 4.7E−01 Yes NA
ADAMTS9 rs6795735 C T 1.08 7.4E−11 0.98 1.8E−02 Yes UC
KCNJ11 rs5215 C T 1.07 8.5E−10 1.02 1.8E−02 Yes UC

BC, beta-cell dysfunction; CHD, coronary heart disease; CPMA, cross-phenotype meta-analysis; EA, effect allele; HG, hyperglycemic; IR, insulin resistance; NA, not available; NEA, non-effect allele; OR, odds ratio; PI, pro-insulin; SNP, single nucleotide polymorphism; T2D, type-2 diabetes; UC, unclassified.

Pleiotropic effect: ‘Yes' indicates that the SNP was associated with at least one confounding trait in the CPMA analysis. See Supplementary Table 2 for a full description of these pleiotropic associations. Physiologic Clusters: UC, IR, BC, PI, HG and NA. Note that the OR for CHD is not weighted for the effect of each SNP on T2D or fasting glucose. Figures report the OR for CHD weighted by their effect on T2D.