<p>Values are percentages of subjects (number) or haplotypes. NA not analysed because of small number of subjects (n≤3 per group).</p>*<p>ORs adjusted for PE risk factors.</p
<p>*Only haplotypes with estimated frequencies >1% are listed.</p><p>**Estimated numbers of informat...
<p>Only haplotypes with a frequency higher than 3% are listed.</p><p>OR: Odds ratio; CI: confidence ...
1<p>n: number of individuals with the respective polymorphism.</p>2<p>p-value: derived from Pearson ...
*<p>ORs (95% CI, p values) adjusted for PE risk factors, associated with the (II+VI) <i>versus</i> t...
<p>Values are the percentage of subjects (number) and haplotypes. PE, preeclampsia. NS, non severe.<...
<p>Frequencies of inferred haplotypes among the cases and controls and their association with risk N...
<p>The risk alleles considered are the variant alleles of rs7574865, rs3099844 and rs3024505 SNPs.</...
<p>Frequencies of the risk allele of 1p11-rs11249433 polymorphism among controls stratified by ethnic...
<p>Bold-faced values indicate significant difference.</p>*<p>Two-sided χ<sup>2</sup> test for the di...
<p>Genotype/allele frequencies of rs3834129 SNP in COGENT consortium cohorts and risk of CRC (logist...
<p>Only haplotypes with a frequency higher than 3% are listed.</p><p>OR: Odds ratio; CI: confidence ...
<p>Y-chromosome single nucleotide polymorphism (Y-SNP) haplogroup frequencies of the 3 EC high-risk ...
<p><i>Abbreviations:</i> CAD, coronary artery disease, P<sub>Sim</sub>, simulated P value; OR, odds ...
<p>Risk estimate and 95% confidence intervals are indicated for each genotype group in each study, a...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
<p>*Only haplotypes with estimated frequencies >1% are listed.</p><p>**Estimated numbers of informat...
<p>Only haplotypes with a frequency higher than 3% are listed.</p><p>OR: Odds ratio; CI: confidence ...
1<p>n: number of individuals with the respective polymorphism.</p>2<p>p-value: derived from Pearson ...
*<p>ORs (95% CI, p values) adjusted for PE risk factors, associated with the (II+VI) <i>versus</i> t...
<p>Values are the percentage of subjects (number) and haplotypes. PE, preeclampsia. NS, non severe.<...
<p>Frequencies of inferred haplotypes among the cases and controls and their association with risk N...
<p>The risk alleles considered are the variant alleles of rs7574865, rs3099844 and rs3024505 SNPs.</...
<p>Frequencies of the risk allele of 1p11-rs11249433 polymorphism among controls stratified by ethnic...
<p>Bold-faced values indicate significant difference.</p>*<p>Two-sided χ<sup>2</sup> test for the di...
<p>Genotype/allele frequencies of rs3834129 SNP in COGENT consortium cohorts and risk of CRC (logist...
<p>Only haplotypes with a frequency higher than 3% are listed.</p><p>OR: Odds ratio; CI: confidence ...
<p>Y-chromosome single nucleotide polymorphism (Y-SNP) haplogroup frequencies of the 3 EC high-risk ...
<p><i>Abbreviations:</i> CAD, coronary artery disease, P<sub>Sim</sub>, simulated P value; OR, odds ...
<p>Risk estimate and 95% confidence intervals are indicated for each genotype group in each study, a...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
<p>*Only haplotypes with estimated frequencies >1% are listed.</p><p>**Estimated numbers of informat...
<p>Only haplotypes with a frequency higher than 3% are listed.</p><p>OR: Odds ratio; CI: confidence ...
1<p>n: number of individuals with the respective polymorphism.</p>2<p>p-value: derived from Pearson ...