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Figure 2 | Molecular Autism

Figure 2

From: Common variation contributes to the genetic architecture of social communication traits

Figure 2

Association plot for the association between social communication problems and common variation at 6p22.1. a). Chromosome ideogram for chromosome 6. b). Regional association plot for rs9257616 on chromosome 6p22.1. Directly genotyped and imputed variants are depicted by filled circles according to their GWAS P-value (−log10 P-value) and genomic position (NCBI Build 36). The local LD structure is reflected by HapMap CEU (Rel 22) recombination rates (blue line). The LD (r2) between the lead variant and surrounding SNPs is indicated by the colour code. c). Detailed genomic region near rs9257616 on chromosome 6p22.1 with variants in LD (r2 >0.3) including non-coding functional (Regulome score ≤2) and missense variation. The LD (r2) between the lead variant and surrounding SNPs is indicated by the colour code (0 (white)-1(black)). The local LD structure is reflected by HapMap CEU (Rel 22) r2 –based haplotype blocks. GWAS, genome-wide association studies; LD, linkage disequilibrium; SNPs, single nucleotide polymorphisms.

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