<p>As samples of rs12118043 genotype AA were few, dominant model with AA+AC versus CC was applied. Likelihood ratio test was applied as more than 2 cells had expected count less than 5 in every Chi-square test.</p
<p>The most common haplotype of 4 major alleles (GCAT) is used as a reference to derive odds ratios ...
<p>Haplotypes indicated in Bold exhibited plausible association with CD. Rest of the haplotypes did ...
Copy number variation (CNV) is pervasive in the human genome and can play a causal role in genetic d...
a<p>Frequencies are shown in parentheses.</p>b<p>Significant <i>P</i> values (<0.05) are in bold.</p...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
<p>F<sub>cases</sub>/F<sub>controls</sub>, percent with that haplotype in the RC group/non-RC/ABD co...
<p>The odds ratios are computed by comparing each haplotype against all other haplotypes pooled. Cas...
<p>OR: odds ratio; CI: confidence intervals.</p><p>The association of haplotype CC in block 4 remain...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
<p>(A) Distribution of <i>CCR5</i> haplotypes and (B) Distribution of <i>CCL3L1</i> copy number. The...
<p>Only haplotypes with a frequency higher than 3% are listed.</p><p>OR: Odds ratio; CI: confidence ...
We investigated the effect of multiple susceptibility alleles at a single disease locus on the stati...
<p>The minimum sample size to achieve to detect association was calculated in simulated case-control...
<p>Odds ratios for each haplotype in the best-fitting model for each JIA subtypes, with 95% CI (grey...
<p>The most common haplotype of 4 major alleles (GCAT) is used as a reference to derive odds ratios ...
<p>Haplotypes indicated in Bold exhibited plausible association with CD. Rest of the haplotypes did ...
Copy number variation (CNV) is pervasive in the human genome and can play a causal role in genetic d...
a<p>Frequencies are shown in parentheses.</p>b<p>Significant <i>P</i> values (<0.05) are in bold.</p...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
<p>F<sub>cases</sub>/F<sub>controls</sub>, percent with that haplotype in the RC group/non-RC/ABD co...
<p>The odds ratios are computed by comparing each haplotype against all other haplotypes pooled. Cas...
<p>OR: odds ratio; CI: confidence intervals.</p><p>The association of haplotype CC in block 4 remain...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
<p>(A) Distribution of <i>CCR5</i> haplotypes and (B) Distribution of <i>CCL3L1</i> copy number. The...
<p>Only haplotypes with a frequency higher than 3% are listed.</p><p>OR: Odds ratio; CI: confidence ...
We investigated the effect of multiple susceptibility alleles at a single disease locus on the stati...
<p>The minimum sample size to achieve to detect association was calculated in simulated case-control...
<p>Odds ratios for each haplotype in the best-fitting model for each JIA subtypes, with 95% CI (grey...
<p>The most common haplotype of 4 major alleles (GCAT) is used as a reference to derive odds ratios ...
<p>Haplotypes indicated in Bold exhibited plausible association with CD. Rest of the haplotypes did ...
Copy number variation (CNV) is pervasive in the human genome and can play a causal role in genetic d...