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

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 (Padj≤5.00E-02). Significant associations are highlighted in bold.
SNP: Single nucleotide polymorphism; kb: Kilobase pairs; Fcases and Fcontrols: Allele frequency in cases and controls, respectively; P: Allelic qui-square P-value. Padj: P-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; UBR3: ubiquitin protein ligase E3 component n-recognin 3 gene; MYO3B: myosin IIIB gene; SCN11A: sodium channel, voltage-gated, type XI, alpha subunit gene; WDR48: WD repeat domain 48 gene; PRDM9: PR domain containing 9 gene; HTR1B: 5-hydroxytryptamine (serotonin) receptor 1B gene.
IA association results for the SNPs associated in the discovery, replication and combined datasets.