Fig. 6. Significant associations observed in phenome-wide association study of lead and conditionally independent spQRSTa variants.

X-axis: Lead variant (RsID [Chromosome: Position (hg19): Allele1: Allele2]) or conditionally independent variant from the spatial QRS-T angle (spQRSTa) European ancestry meta-analysis that had a significant association with a clinical phenotype in UK Biobank. Y-axis: Phenotype derived from hospital episode statistics, with colour coding for each major group (circulatory system; red, digestive system; green, neoplasms; yellow, respiratory; blue). Odds ratios (OR) are color coded according to decreasing (blue) or increasing (green) odds. 3:38587306:A:G was a conditionally independent variant at the SCN5A locus.