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Chunk #6 — Meta-analysis identifies 12,111 height-associated SNPs

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A saturated map of common genetic variants associated with human height.
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We first performed separate meta-analyses in each of the five groups of cohorts. We identified 9,863, 1,511, 918, 453 and 69 quasi-independent genome-wide significant (GWS; P < 5 × 10−8) SNPs in the EUR, HIS, EAS, AFR and SAS groups, respectively (Table 1 and Supplementary Tables 4–8). Quasi-independent associations were obtained after performing approximate conditional and joint (COJO) multiple-SNP analyses6, as implemented in GCTA7 (Methods). Supplementary Note 1 presents sensitivity analyses of these COJO results, highlights biases due to relatively long-range linkage disequilibrium (LD) in admixed AFR and HIS individuals8 (Supplementary Fig. 3), and shows how to correct those biases by varying the GCTA input parameters (Supplementary Fig. 4). Moreover, previous studies have shown that confounding due to population stratification may remain uncorrected in large GWAS meta-analyses9,10. Therefore, we specifically investigated confounding effects in all ancestry-specific GWASs, and found that our results are minimally affected by population stratification (Supplementary Note 2 and Supplementary Figs. 5–7).Table 1 Summary of results from within-ancestry and trans-ancestry GWAS meta-analysesCohort ancestry or ethnic groupNumber of studiesMax n (mean n)Number of GWS COJO SNPs (PGWAS <