nominally significantp = 5.14 × 10 −7
The first of these regions is located on chromosome 2 and includes nominally significant SCZ variant (top variant in PGC: rs10189857, p = 5.14 × 10 −7 ) 19 in an intron of BCL11A , and a T2D risk locus upstream of the same gene (top variant in DIAGRAMv3: rs243021, p = 3 × 10 −15 ) 46 .