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

Table 1.

Association analysis of type 2 diabetes loci in type 1 diabetes cases and controls

Gene region SNP Cases, n Controls, n Minor allele, Number of chromosomes (allele frequency) OR (95% CI)a p value Power, %b Power, %c Type 2 diabetesd
Cases Controls OR Ref.
TCF7L2 rs7903146 (C>T)e 5,896 7,322 3,395 (0.29) 4,260 (0.29) 0.99 (0.94–1.05) 0.744 81 100 1.37 [8, 15]
rs12255372 (G>T) 7,776 8,847 4,421 (0.28) 5,125 (0.29) 0.97 (0.92–1.02) 0.235 92 100 1.52 [9]
CDKN2A–B rs10811661 (T>C) 7,634 7,148 2,754 (0.18) 2,498 (0.17) 1.03 (0.97–1.09) 0.354 68 100 0.83 [4, 8, 15]
FTO rs9939609 (T>A)e 7,655 7,182 6,098 (0.40) 5,644 (0.39) 1.03 (0.98–1.08) 0.252 92 100 1.17 [4, 8]
KCNJ11 rs5219 (C>T) 8,058 10,406 5,772 (0.36) 7,411 (0.36) 1.02 (0.97–1.06) 0.501 97 100 1.14 [8, 15]
HHEX–IDE rs1111875 (G>A) 7,968 9,675 6,369 (0.40) 8,042 (0.42) 0.94 (0.90–0.98) 0.003 97 100 0.88 [4, 8, 15]
IGF2BP2 rs4402960 (G>T) 7,554 7,101 4,755 (0.31) 4,546 (0.32) 0.98 (0.93–1.03) 0.457 89 99 1.14 [4, 8, 15]
CDKAL1 rs7756992 (A>G) 7,714 7,200 4,185 (0.27) 3,893 (0.27) 1.00 (0.95–1.05) 0.957 86 100 1.20 [11]
SLC30A8 rs13266634 (C>T) 7,680 7,200 4,879 (0.32) 4,463 (0.31) 1.04 (0.99–1.09) 0.146 89 93 0.89 [4, 8, 15]
WFS1 rs10010131 (G>A) 7,745 9,259 6,173 (0.40) 7,564 (0.41) 0.96 (0.92–1.00) 0.065 96 96 0.90 [12]
HNF1B rs7501939 (C>T) 7,712 7,217 6,249 (0.41) 5,800 (0.40) 1.01 (0.97–1.06) 0.554 93 85 1.10 [13]
PPARG rs1801282 (C>G) 8,229 9,342 1,880 (0.11) 2,304 (0.12) 0.91 (0.85–0.97) 0.004 60 82 0.88 [4, 8, 15]
THADA rs7578597 (T>C) 7,601 8,395 1,598 (0.11) 1,840 (0.11) 0.94 (0.88–1.01) 0.113 50 80 0.87 [5]
rs17031005(A>G) 7,256 8,760 1,481 (0.10) 1,878 (0.11) 0.94 (0.87–1.01) 0.078 50 80 NA

aThe ORs and 95% CIs are for the minor allele using the common allele as the reference allele

bPower calculated for an OR of 1.11 at an α level of 0.003, assuming a multiplicative allelic effects model, given the allele frequency and number of type 1 diabetes cases and controls genotyped

cPower calculated for the size of effect detected in type 2 diabetes at an α level of 0.003, assuming a multiplicative allelic effects model, using the number of type 1 diabetes cases and controls genotyped

dThe ORs are those reported in the literature for an association with type 2 diabetes

eNew analyses of previously published data [18, 19] are included for information (ESM Table 3)

CDKN2A–B denotes CDKN2A–CDKN2B

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