<p><sup>a</sup><i>P</i>-values <0.05 are shown in bold.</p><p><sup>b</sup> APN + ALN</p><p><sup>c</sup> Statistically significant with correction for multiple-SNP testing (<i>P</i> < 0.0055)</p><p>Genotypic analysis of the SNPs.</p
a<p>: The Fisher's exact test was used for SNP with a Minor Allele Frequency (MAF)<0.10.</p>b<p>: Pe...
*<p>Corrected <i>P-</i>values at the experiment-wise or chromosome-wise level are indicated for the ...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
a<p><i>P</i> values <0.05 are shown in bold.</p>b<p>APN+ALN.</p>c<p>Statistical significance with co...
<p><sup>a</sup><i>P</i>-values <0.05 are shown in bold.</p><p><sup>b</sup> APN + ALN</p><p>Allele fr...
a<p><i>P</i> values <0.05 are shown in bold.</p>b<p>APN+ALN.</p>c<p>Statistical non-significance wit...
<p>SNPs written in bold are significant after correcting for multiple testing.</p
<p><sup>a</sup><i>P-</i>values <0.05 are shown in bold.</p><p><sup>b</sup> APN + ALN</p><p>Allele fr...
a<p>Number of alleles for each SNP is given in parentheses.</p>b<p>Significant <i>P</i> value (<0.05...
<p>(To increase readability, the log<sub>10</sub>(BFs) are truncated at 20). (A) Genome-wide log<sub...
<p>The first six SNPs were among those identified in the initial sequencing, and the remaining four ...
<p>NSNP; Number of SNPs in this haplotype.</p><p>NHAP; Number of common haplotypes (f>0.01).</p><p>S...
<p>Genotype frequency of the tagging SNP A+930→G in the three study populations included in the meta...
<p>For nonsynonymous SNPs, the amino acid change and the Grantham score (ranging from 0 to 215), whi...
<p>Abbreviations: SNP, single-nucleotide polymorphism; <i>OR</i>, odds ratio; <i>CI</i>, confidence ...
a<p>: The Fisher's exact test was used for SNP with a Minor Allele Frequency (MAF)<0.10.</p>b<p>: Pe...
*<p>Corrected <i>P-</i>values at the experiment-wise or chromosome-wise level are indicated for the ...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
a<p><i>P</i> values <0.05 are shown in bold.</p>b<p>APN+ALN.</p>c<p>Statistical significance with co...
<p><sup>a</sup><i>P</i>-values <0.05 are shown in bold.</p><p><sup>b</sup> APN + ALN</p><p>Allele fr...
a<p><i>P</i> values <0.05 are shown in bold.</p>b<p>APN+ALN.</p>c<p>Statistical non-significance wit...
<p>SNPs written in bold are significant after correcting for multiple testing.</p
<p><sup>a</sup><i>P-</i>values <0.05 are shown in bold.</p><p><sup>b</sup> APN + ALN</p><p>Allele fr...
a<p>Number of alleles for each SNP is given in parentheses.</p>b<p>Significant <i>P</i> value (<0.05...
<p>(To increase readability, the log<sub>10</sub>(BFs) are truncated at 20). (A) Genome-wide log<sub...
<p>The first six SNPs were among those identified in the initial sequencing, and the remaining four ...
<p>NSNP; Number of SNPs in this haplotype.</p><p>NHAP; Number of common haplotypes (f>0.01).</p><p>S...
<p>Genotype frequency of the tagging SNP A+930→G in the three study populations included in the meta...
<p>For nonsynonymous SNPs, the amino acid change and the Grantham score (ranging from 0 to 215), whi...
<p>Abbreviations: SNP, single-nucleotide polymorphism; <i>OR</i>, odds ratio; <i>CI</i>, confidence ...
a<p>: The Fisher's exact test was used for SNP with a Minor Allele Frequency (MAF)<0.10.</p>b<p>: Pe...
*<p>Corrected <i>P-</i>values at the experiment-wise or chromosome-wise level are indicated for the ...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
DOI
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