Quantile-quantile plot of ~2.2 million SNPs for each of the six genome-wide association scans meta-analyzed. (a) DGI (n = 2,978). (b) FUSION (n = 2,371). (c) KORA (n = 1,644). (d) NHS (n = 2,286). (e) PLCO (n = 2,244). (f) SardiNIA (n = 4,305). Each black circle represents an observed statistic (defined as the -log₁₀(P)) versus the corresponding expected statistic. The gray line corresponds to the null distribution.

Analysis of combined effects. For each participant in the FINRISK97 panel with complete genotype at the 12 SNPs with P < 5 × 10^-7 in Table 1 (n = 7,566), we counted the number of height-increasing alleles to create a height score. Individuals with ≤8 or ≥16 ‘tall’ alleles were grouped. For each height score group, in men and women separately, the mean ± 95% confidence interval is plotted. The axis for men is on the left and the axis for women is on the right (same scale). The regression line in dark gray indicates that, for both men and women, each additional ‘tall’ allele increases height by 0.4 cm. The light gray histogram in the background represents the relative fraction of individuals in each height score group (height score ≤8: 4.7%; height score 9: 6.2%; height score 10: 11.1%; height score 11: 15.5%; height score 12: 17.5%; height score 13: 15.6%; height score 14: 13.7%; height score 15: 8.6%; height score ≥16: 7.1%).

Quantile-quantile plots supporting the presence of additional loci associated with height. (a) Plot of 2,260,683 SNPs from the meta-analysis of the six GWA scans (n = 15,821). Each black triangle represents an observed statistic (defined as the -log₁₀(P)) versus the corresponding expected statistic. The black squares correspond to the distribution of test statistics after removing markers correlated to the 12 height signals with P < 5 ×10^-7 described in Table 1. The gray line corresponds to the null distribution. (b) Association results from Weedon et al.18 provide independent evidence that the top 10,000 SNPs from our meta-analysis exceed the null expectations (gray line). We selected the top 10,000 SNPs from our meta-analysis before (black triangles) and after (black squares) removing SNPs marking the known height loci (identified by us and in the accompanying manuscript) and retrieved the corresponding P values from Weedon et al. We show one-tailed P values because we corrected for the direction of effects, if needed. Inflation factors are unusually high because the analysis is restricted to the top 10,000 SNPs, which are likely enriched for SNPs that are truly associated with height variation.