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. 2006 Dec 21;80(2):273–390. doi: 10.1086/511051

Table 7. .

Two-Marker Haplotypes for the IL23R Gene[Note]

Discovery Sample SetGlobal P=.004
Replication 1 Sample SetGlobal P=.002
Replication 2 Sample SetGlobal P=.003
Combined AnalysisGlobala Pcomb=4.14×10-6
Haplotype
No. (Frequency) in
No. (Frequency) in
No. (Frequency) in
rs7530511 rs11209026 Case (n=467) Control (n=460) OR P Case
(n=498)
Control (n=498) OR P Case (n=481) Control (n=424) OR P ORcommon (95%CI)b Pcomba
C G 796 (.852) 730 (.793) 1.50 9.48×10−4 840 (.843) 794 (.797) 1.37 .006 824 (.857) 682 (.804) 1.45 .003 1.44 (1.25–1.65) 3.13×10−6
T G 96 (.103) 135 (.147) .67 .005 98 (.098) 113 (.113) .85 .249 104 (.108) 110 (.130) .81 .003 .77 (.65–.91) 3.22×10−4
C A 42 (.045) 55 (.060) .74 .134 56 (.056) 89 (.089) .61 .004 34 (.035) 56 (.066) .52 .153 .62 (.49–.77) .005
T A 0 0 2 (.002) 0 0 0

Note.— A pseudo-Gibbs sampling algorithm from the program SNPAnalyzer was used to estimate haplotype frequencies from unphased genotyping data, with cases and controls treated separately. The Haplo.Stats package was used to test for association between haplotypes and disease status.

a

Calculated using a Mantel-Haenszel common OR.

b

Calculated using Fisher’s combined test.