Skip to main content
Fig. 3 | BMC Genomics

Fig. 3

From: Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders

Fig. 3

Manhattan plots for RSM (a), IS (b) and RSM/IS (c) for the AGRE cohort. The x-axis indicates the position of each SNP on individual autosomal chromosomes and the y-axis indicates –log10 transformed GEMMA P-values. Red line: genome-wide significance threshold (P = 5.0E-08). Blue line: threshold for “suggestive significance” (P = 5.0E-05)

Back to article page

BMC Genomics

ISSN: 1471-2164

Contact us