<p>For each of the nine SNP types, the likelihood of disease associations was estimated as the percentage of disease-associated SNPs among all SNPs measured in the HapMap 3 project. Similar likelihoods were observed among nsSNPs, sSNPs, and SNPs in the 5′-UTR. The number of disease-associated SNPs and SNPs measured in the HapMap 3 project were specified in the parenthesis.</p
We wished to investigate the ability of different SNP chipsets to detect association with a disease ...
<p>Statistically significant and replicated SNP associations at 3q25 and 4p16.</p
SNP markers involved in the association analysis for N146 and N280 populations.</p
<p>The median odds ratio±standard error was calculated for each of the nine SNP types using 9,574 cu...
<p>The median odds ratio of SNP-disease associations was plotted against the percentage of disease-a...
<p>*A hypothetical platform combined from the above six platforms to report the likelihood of SNPs b...
<p>NSNP; Number of SNPs in this haplotype.</p><p>NHAP; Number of common haplotypes (f>0.01).</p><p>S...
<p> indicates the number of SNP markers used in the model being evaluated. All other values indicate...
1<p>Number of PAGE study sites where both the SNP and phenotype were available for a given phenotype...
Many DNA variants have been identified on more than 300 diseases and traits using Genome-Wide Associ...
<p>Prevalence of the genotypes of the four studied SNPs in patients with different clinical severity...
<p>χ<sup>2</sup>-test was applied for testing genotype frequencies of SNPs in controls and patients ...
<p>*Two-sided χ<sup>2</sup> test, each haplotype compared with all other haplotypes.</p>#<p>Statisti...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
<p>Odds ratios (OR) and 95% confidence intervals (CI) are relative to the allele on the forward stra...
We wished to investigate the ability of different SNP chipsets to detect association with a disease ...
<p>Statistically significant and replicated SNP associations at 3q25 and 4p16.</p
SNP markers involved in the association analysis for N146 and N280 populations.</p
<p>The median odds ratio±standard error was calculated for each of the nine SNP types using 9,574 cu...
<p>The median odds ratio of SNP-disease associations was plotted against the percentage of disease-a...
<p>*A hypothetical platform combined from the above six platforms to report the likelihood of SNPs b...
<p>NSNP; Number of SNPs in this haplotype.</p><p>NHAP; Number of common haplotypes (f>0.01).</p><p>S...
<p> indicates the number of SNP markers used in the model being evaluated. All other values indicate...
1<p>Number of PAGE study sites where both the SNP and phenotype were available for a given phenotype...
Many DNA variants have been identified on more than 300 diseases and traits using Genome-Wide Associ...
<p>Prevalence of the genotypes of the four studied SNPs in patients with different clinical severity...
<p>χ<sup>2</sup>-test was applied for testing genotype frequencies of SNPs in controls and patients ...
<p>*Two-sided χ<sup>2</sup> test, each haplotype compared with all other haplotypes.</p>#<p>Statisti...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
<p>Odds ratios (OR) and 95% confidence intervals (CI) are relative to the allele on the forward stra...
We wished to investigate the ability of different SNP chipsets to detect association with a disease ...
<p>Statistically significant and replicated SNP associations at 3q25 and 4p16.</p
SNP markers involved in the association analysis for N146 and N280 populations.</p