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. 2006 Nov;55(11):1679–1680. doi: 10.1136/gut.2006.104646

Table 2 Two marker haplotype frequencies, transmission, and association statistics for CARD4 (caspase recruitment domain family, member 4) in inflammatory bowel diseases.

Variation Haplotype* fcontrols fcases p Value‡ fT§ fNT§ p Value¶ D′**
rs2075822 + ND1+32656 1 – 1 0.771 0.762 0.846 0.455 0.486 0.094 0.91
1 – 2 0.042 0.040 0.140 0.101
2 – 1 0.013 0.015 0.026 0.057
2 – 2 0.174 0.184 0.380 0.357
ND1+32656 + rs2907748 1 – 1 0.784 0.775 0.727 0.473 0.519 0.719 0.98
1 – 2 0.002 0.002 0.011 0.011
2 – 1†† 0.006 0.004 0.014 0.008
2 – 2 0.208 0.220 0.503 0.462

*Allele 1 is defined as the major allele.

†Frequencies of haplotypes in cases and controls estimated by the expectation maximisation algorithm using COCAPHASE.[6]

‡Global significance value obtained after 10 000 permutations with COCAPHASE.

§Frequencies of transmitted (fT) and non‐transmitted (fNT) haplotypes observed using TDTPHASE.[6]

¶Global significance value obtained after 10 000 permutations with TDTPHASE.

**D′ value as a measure of linkage disequilibrium in the control sample.

††Protective haplotype previously identified by McGovern and colleagues.[2]