<p>CHR: Chromosome; SNP: Single Nucleotide Polymorphism. The last four columns show the allele reported frequency in cases (F A), in controls (F U) and, the p and the Odds Ratio (OR) values obtained in the NXC-GWAS sample.</p><p>In bold type, SNPs with a nominal p-value below 0.05.</p>†<p>The nearest gene or the gene where the SNP is located.</p><p>*SNPs genotyped (not imputed).</p
<p>Chr: Chromosome; OR:Odds Ratio; NA:not applicable or not available; European Data sets: previousl...
(SNP) is the most common variation of the human genome with more than 9 million reported in public d...
Single nucleotide polymorphisms (SNPs) are the most common form of human genetic variation, with mil...
<p>CHR: Chromosome; SNP: Single Nucleotide Polymorphism; BP: Base pair position; A1: Reference allel...
<p>CHR: Chromosome; SNP: Single Nucleotide Polymorphism; BP: Base pair position; A1: Reference allel...
<p>CHR: Chromosome; BP: Base pair position; SNP: Single Nucleotide Polymorphism; A1: Reference allel...
*<p>Numbers included after quality control of genotyping data.</p><p><i>Abbreviations</i>: <b>CHR</b...
<p>SNP, single nucleotide polymorphism; Chr, chromosome; bp, base pair; MAF, minor allele frequency ...
<p>All the positions are using NCBI build 36.3 as reference. Chr chromosome. The two alleles in a SN...
Single-Nucleotide Polymorphism (SNP) is a single nucleotide (A, C, G, and T) mutation in the genome....
<p>NSNP; Number of SNPs in this haplotype.</p><p>NHAP; Number of common haplotypes (f>0.01).</p><p>S...
<p>The first six SNPs were among those identified in the initial sequencing, and the remaining four ...
<p>Note gene is the best proximal candidate or closest gene to the locus and may not be the true pat...
<p>Abbreviations: SNP, single-nucleotide polymorphism; <i>OR</i>, odds ratio; <i>CI</i>, confidence ...
<p>Chr.: chromosome. GAIN, nonGAIN and ISC are three GWAS datasets for meta-analysis. ISHDSF min p w...
<p>Chr: Chromosome; OR:Odds Ratio; NA:not applicable or not available; European Data sets: previousl...
(SNP) is the most common variation of the human genome with more than 9 million reported in public d...
Single nucleotide polymorphisms (SNPs) are the most common form of human genetic variation, with mil...
<p>CHR: Chromosome; SNP: Single Nucleotide Polymorphism; BP: Base pair position; A1: Reference allel...
<p>CHR: Chromosome; SNP: Single Nucleotide Polymorphism; BP: Base pair position; A1: Reference allel...
<p>CHR: Chromosome; BP: Base pair position; SNP: Single Nucleotide Polymorphism; A1: Reference allel...
*<p>Numbers included after quality control of genotyping data.</p><p><i>Abbreviations</i>: <b>CHR</b...
<p>SNP, single nucleotide polymorphism; Chr, chromosome; bp, base pair; MAF, minor allele frequency ...
<p>All the positions are using NCBI build 36.3 as reference. Chr chromosome. The two alleles in a SN...
Single-Nucleotide Polymorphism (SNP) is a single nucleotide (A, C, G, and T) mutation in the genome....
<p>NSNP; Number of SNPs in this haplotype.</p><p>NHAP; Number of common haplotypes (f>0.01).</p><p>S...
<p>The first six SNPs were among those identified in the initial sequencing, and the remaining four ...
<p>Note gene is the best proximal candidate or closest gene to the locus and may not be the true pat...
<p>Abbreviations: SNP, single-nucleotide polymorphism; <i>OR</i>, odds ratio; <i>CI</i>, confidence ...
<p>Chr.: chromosome. GAIN, nonGAIN and ISC are three GWAS datasets for meta-analysis. ISHDSF min p w...
<p>Chr: Chromosome; OR:Odds Ratio; NA:not applicable or not available; European Data sets: previousl...
(SNP) is the most common variation of the human genome with more than 9 million reported in public d...
Single nucleotide polymorphisms (SNPs) are the most common form of human genetic variation, with mil...