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. 2010 Aug 26;6(8):e1001078. doi: 10.1371/journal.pgen.1001078

Table 2. The association of known risk alleles for T2D by race/ethnicity.a b .

SNP Risk Allelec Chr. NearestGene European Americans533 cases1,006 controls African Americans1,077 cases1,469 controls Latinos2,220 cases2,184 controls Japanese Americans1,736 cases1,761 controls Native Hawaiians576 cases983 controls Pooled6,142 cases7,403 controls P value Phet d
rs10923931 T 1 NOTCH2 OR(95%CI) 0.84 (0.64–1.10) 1.10 (0.97–1.25) 1.17 (1.01–1.35) 1.00 (0.70–1.44) 0.76 (0.50–1.15) 1.06 (0.98–1.16) 0.16 0.086
RAF 0.12 0.29 0.09 0.02 0.05 0.11
rs7578597 T 2 THADA OR(95%CI) 1.42 (1.06–1.91) 1.04 (0.90–1.19) 1.12 (0.93–1.35) 1.10 (0.68–1.78) 1.65 (1.01–2.70) 1.13 (1.02–1.25) 0.016 0.21
RAF 0.90 0.75 0.94 0.99 0.97 0.91
rs1801282 C 3 PPARG OR(95%CI) 1.26 (0.95–1.68) 1.95 (1.30–2.92) 1.03 (0.89–1.19) 1.05 (0.82–1.36) 1.14 (0.84–1.55) 1.13 (1.02–1.26) 0.018 0.048
RAF 0. 89 0.97 0.90 0.96 0.93 0.93
rs4607103 C 3 ADAMTS9 OR(95%CI) 1.11 (0.92–1.34) 1.03 (0.91–1.18) 0.99 (0.89–1.08) 1.05 (0.94–1.17) 0.98 (0.82–1.16) 1.02 (0.97–1.08) 0.45 0.78
RAF 0.73 0.70 0.69 0.61 0.72 0.68
rs4402960 T 3 IGF2BP2 OR(95%CI) 1.02 (0.85–1.23) 1.14 (1.01–1.28) 1.05 (0.95–1.16) 1.24 (1.11–1.38) 1.17 (0.99–1.39) 1.13 (1.07–1.19) 2.2×10−5 0.26
RAF 0.31 0.49 0.27 0.30 0.27 0.33
rs10010131 G 4 WFS1 OR(95%CI) 1.18 (0.99–1.40) 0.94 (0.83–1.07) 1.15 (1.04–1.27) 1.45 (0.98–2.13) 1.27 (1.03–1.56) 1.11 (1.04–1.19) 1.8×10−3 0.032
RAF 0.59 0.66 0.71 0.98 0. 81 0.76
rs7754840 C 6 CDKAL1 OR(95%CI) 1.26 (1.05–1.50) 1.03 (0.92–1.16) 1.09 (0.99–1.19) 1.37 (1.24–1.52) 1.39 (1.19–1.62) 1.20 (1.13–1.26) 4.1×10−11 6.2×10−4
RAF 0.29 0.55 0.31 0.40 0.52 0.40
rs864745 T 7 JAZF1 OR(95%CI) 0.98 (0.83–1.16) 1.16 (1.01–1.32) 1.30 (1.19–1.43) 1.19 (1.05–1.35) 1.13 (0.93–1.36) 1.20 (1.13–1.27) 1.3×10−9 0.054
RAF 0.51 0.73 0.61 0.77 0.75 0.68
rs13266634 C 8 SLC30A8 OR(95%CI) 1.28 (1.06–1.54) 1.21 (0.99–1.48) 1.11 (1.00–1.23) 1.18 (1.06–1.31) 1.04 (0.88–1.22) 1.15 (1.08–1.22) 9.7×10−6 0.47
RAF 0.68 0. 89 0.75 0.60 0.62 0.72
rs2383208 A 9 CDKN2B OR(95%CI) 1.35 (1.07–1.69) 1.14 (0.98–1.33) 1.15 (1.01–1.31) 1.26 (1.13–1.40) 1.02 (0.85–1.22) 1.18 (1.11–1.26) 2.1×10−7 0.27
RAF 0. 81 0. 81 0. 85 0.56 0.74 0.75
rs1111875 C 10 HHEX OR(95%CI) 0.93 (0.78–1.11) 1.10 (0.95–1.26) 1.03 (0.94–1.13) 1.21 (1.08–1.36) 0.93 (0.78–1.11) 1.07 (1.01–1.13) 0.028 0.037
RAF 0.61 0.74 0.63 0.28 0.28 0.52
rs7903146 T 10 TCF7L2 OR(95%CI) 1.55 (1.29–1.87) 1.32 (1.16–1.51) 1.31 (1.19–1.45) 1.74 (1.38–2.20) 1.12 (0.90–1.40) 1.36 (1.27–1.45) 1.1×10−19 0.068
RAF 0.27 0.28 0.23 0.04 0.14 0.19
rs12779790 G 10 CDC123 OR(95%CI) 1.02 (0.82–1.28) 1.09 (0.92–1.29) 1.19 (1.06–1.33) 1.01 (0.88–1.15) 1.16 (0.95–1.41) 1.10 (1.03–1.18) 5.9×10−3 0.36
RAF 0.17 0.14 0.17 0.17 0.18 0.17
rs2237895e C 11 KCNQ1 OR(95%CI) 0.98 (0.82–1.16) 1.04 (0.90–1.21) 1.15 (1.05–1.28) 1.12 (0.98–1.27) 1.16 (0.97–1.39) 1.11 (1.04–1.18) 7.8×10−4 0.17
RAF 0.42 0.20 0.40 0.35 0.33 0.34
rs2237897e C 11 KCNQ1 OR(95%CI) 0.86 (0.59–1.26) 1.13 (0.90–1.42) 1.23 (1.09–1.39) 1.26 (1.11–1.44) 1.06 (0.86–1.31) 1.21 (1.13–1.30) 3.2×10−7 0.10
RAF 0.95 0.92 0.76 0.62 0.78 0.79
rs5219 T 11 KCNJ11 OR(95%CI) 1.24 (1.05–1.47) 1.03 (0.84–1.26) 1.09 (1.00–1.20) 1.26 (1.13–1.40) 1.03 (0.88–1.21) 1.15 (1.08–1.21) 3.3×10−6 0.13
RAF 0.35 0.09 0.37 0.35 0.37 0.31
rs7961581 C 12 TSPAN8 OR(95%CI) 1.03 (0.86–1.24) 0.92 (0.80–1.06) 1.03 (0.93–1.15) 1.00 (0.88–1.14) 1.12 (0.94–1.33) 1.01 (0.95–1.08) 0.71 0.51
RAF 0.29 0.23 0.21 0.21 0.29 0.23
rs8050136 A 16 FTO OR(95%CI) 0.89 (0.75–1.06) 1.07 (0.95–1.20) 1.02 (0.92–1.12) 1.04 (0.92–1.18) 1.01 (0.84–1.21) 1.02 (0.96–1.08) 0.48 0.68
RAF 0.41 0.43 0.27 0.20 0.23 0.30
rs4430796 G 17 HNF1B OR(95%CI) 0.96 (0.82–1.14) 1.10 (0.97–1.25) 0.96 (0.88–1.05) 1.18 (1.06–1.32) 1.09 (0.92–1.30) 1.05 (1.00–1.11) 0.058 0.043
RAF 0.50 0.65 0.42 0.36 0.31 0.45
a

Odds ratios (and 95% confidence intervals) for allele dosage effects are adjusted for age (quartiles), BMI (quartiles), sex, and ethnicity (in pooled analysis).

b

Ethnic specific risk allele frequencies (RAF) calculated for each SNP.

c

NCBI build 36 (forward strand).

d

Phet = P value for heterogeneity of allelic effects across ethnic groups (4 df test).

e

rs2237895 and rs2237897 adjusted for each other.