Variant: rs12552 

    present in Gene: OLFM4
    present in Chromosome: 13
    Position on Chromosome: 53051646
    Alleles of this Variant: A/G

rs12552 in OLFM4 gene and Child Development Disorders, Pervasive PMID 30804558 2019 Identification of common genetic risk variants for autism spectrum disorder.

rs12552 in OLFM4 gene and Intelligence PMID 29326435 2019 A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.

rs12552 in OLFM4 gene and Major Depressive Disorder PMID 29700475 2018 Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.

PMID 29942085 2018 Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.

PMID 27479909 2016 Identification of 15 genetic loci associated with risk of major depression in individuals of European descent.

PMID 30804558 2019 Identification of common genetic risk variants for autism spectrum disorder.