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    IA association results for the SNPs associated in the discovery, replication and combined datasets.

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    <p>Odds ratios (OR) and 95% confidence intervals (CI) are relative to the allele on the forward strand of the human genome reference sequence and are only shown for those markers with nominally significant associations (<i>P</i><sub><i>adj</i></sub>≤5.00E-02). Significant associations are highlighted in bold.</p><p>SNP: Single nucleotide polymorphism; kb: Kilobase pairs; F<sub>cases</sub> and F<sub>controls</sub>: Allele frequency in cases and controls, respectively; <i>P</i>: Allelic qui-square P-value. <i>P</i><sub><i>adj</i></sub>: <i>P</i>-values from logistic regression using log-additive model are adjusted for hypertension in the discovery dataset, for hypertension and smoking habits in the replication and combined datasets; <i>UBR3</i>: ubiquitin protein ligase E3 component n-recognin 3 gene; <i>MYO3B</i>: myosin IIIB gene; <i>SCN11A</i>: sodium channel, voltage-gated, type XI, alpha subunit gene; <i>WDR48</i>: WD repeat domain 48 gene; <i>PRDM9</i>: PR domain containing 9 gene; <i>HTR1B</i>: 5-hydroxytryptamine (serotonin) receptor 1B gene.</p><p>IA association results for the SNPs associated in the discovery, replication and combined datasets.</p
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