The first region contains missense and intron variants for GCKR gene (ENSG00000133962), a glucokinase regulator, with no previously reported associations for brain phenotypes, missense and intron variants for C2orf16 (ENSG00000221843) and intron variants for ZNF512 (ENSG00000243943) both protein coding genes with association with neurodegenerative diseases, T2D, and blood measurements. The gene discussed is SPATA31H1; the disease is neurodegenerative disease.