Genome-Wide Association Study in an Admixed Case Series Reveals IL12A as a New Candidate in Behçet Disease
Fig 3
Behcet GWAS results using Linear Mixed Models Genomic approach.
Each dot represents an SNP in the dataset. QQ-plot (left). Associated SNPs deviating from the null hypothesis of no association (identity line). Manhattan plot (right). SNPs showing association with the disease map to two different signals in chromosome 6 and a singleton in chromosome 18.