a<p>Number of alleles for each SNP is given in parentheses.</p>b<p>Significant <i>P</i> value (<0.05) are in boldface.</p
a<p>Frequencies are shown in parentheses.</p>b<p>Significant <i>P</i> values (<0.05) are in bold.</p...
<p>Allele and genotype frequency is followed by percent values in parenthesis.</p>*<p>Indicates stat...
<p>The risk alleles considered are the variant alleles of rs7574865, rs3099844 and rs3024505 SNPs.</...
<p>The genotype and allele frequencies of identified SNPs in AS cases and healthy controls.</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...
<p>The genotype and allele frequency of three SNPs identified in 386 control subjects in his study.<...
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>Genotypic and allelic frequencies of the 10 SNPs in the 6 controls and 30 EC patients.</p
<p>Allele frequencies of the studied SNPs in our population and in the NCBI database.</p
Frequency and distribution of SNP allele and genotypes in cases (CD, ITB) and controls.</p
<p>*Five significant SNPs</p><p>Allele and genotype frequencies for 5 significant SNPs within PKM2.<...
<p>Significant p-values are in italic bold. Haplotypes are not shown, if frequency less than 2%.</p>...
<p> indicates the number of SNP markers used in the model being evaluated. All other values indicate...
<p>Major alleles are alleles with > 0.5 frequency across all populations</p><p>A: Major Allele frequ...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
a<p>Frequencies are shown in parentheses.</p>b<p>Significant <i>P</i> values (<0.05) are in bold.</p...
<p>Allele and genotype frequency is followed by percent values in parenthesis.</p>*<p>Indicates stat...
<p>The risk alleles considered are the variant alleles of rs7574865, rs3099844 and rs3024505 SNPs.</...
<p>The genotype and allele frequencies of identified SNPs in AS cases and healthy controls.</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...
<p>The genotype and allele frequency of three SNPs identified in 386 control subjects in his study.<...
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>Genotypic and allelic frequencies of the 10 SNPs in the 6 controls and 30 EC patients.</p
<p>Allele frequencies of the studied SNPs in our population and in the NCBI database.</p
Frequency and distribution of SNP allele and genotypes in cases (CD, ITB) and controls.</p
<p>*Five significant SNPs</p><p>Allele and genotype frequencies for 5 significant SNPs within PKM2.<...
<p>Significant p-values are in italic bold. Haplotypes are not shown, if frequency less than 2%.</p>...
<p> indicates the number of SNP markers used in the model being evaluated. All other values indicate...
<p>Major alleles are alleles with > 0.5 frequency across all populations</p><p>A: Major Allele frequ...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
a<p>Frequencies are shown in parentheses.</p>b<p>Significant <i>P</i> values (<0.05) are in bold.</p...
<p>Allele and genotype frequency is followed by percent values in parenthesis.</p>*<p>Indicates stat...
<p>The risk alleles considered are the variant alleles of rs7574865, rs3099844 and rs3024505 SNPs.</...
DOI
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