Figure 1
Regional association plot of a negative logarithm of combined P-values for GRIN2B common variants.
The most significant SNP was rs7970177 (P = 1.73E-04), which showed strong LD with its nearby five SNPs (r2 > 0.8). The six SNPs constructed a strong LD block and showed strong associations with autism (P = 1.78E-06).
