Variant: rs10866912

present in Gene: MROH6 present in Chromosome: 8 Position on Chromosome: 143573145 Alleles of this Variant: A/C;T

rs10866912 in MROH6 gene and Schizophrenia PMID 31268507 2019 Given this gene's role in niacin metabolism and the evidence for niacin deficiency provoking schizophrenialike symptoms in neuropsychiatric diseases such as pellagra and Hartnup disease, these results suggest that the rs10866912 genotype and niacin status may have implications for schizophrenia susceptibility and treatment.