Variant: rs1867503 

    present in Gene: INHCAP;TF
    present in Chromosome: 3
    Position on Chromosome: 133691804
    Alleles of this Variant: G/A

rs1867503 in INHCAP;TF gene and Child Development Disorders, Pervasive PMID 25534755 2015 A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?