Figure 1From: COMT genetic variation confers risk for psychotic and affective disorders: a case control studyRisk haplotypes identified in different studies and populations are shown. SNP IDs are indicated on top and the respective alleles are boxed underneath. "x" denotes a SNP that was not tested. * indicates a haplotype, which also included rs9265(A) and rs165849(A), both located distal to rs165599 in the ARVCF gene.Back to article page