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.