× 10−11). Since two of the unimputed variants (indel at chromosome 10, position 104 957 618 and rs7907645; p = 1.04 × 10−13 and p = 5.82 × 10−11, respectively) were within the same locus and we do not have access to conditional genetic association results from the PGC, we replaced those two variants with a single variant (rs12414028; PGC p = 1.96 × 10−12). In sum, we analysed 123 variants directly and four surrogate variants out of the 128 total target PGC schizophrenia-associated variants.
