Variant: rs318240757 

    present in Gene: RTTN
    present in Chromosome: 18
    Position on Chromosome: 70135273
    Alleles of this Variant: T/A

rs318240757 in RTTN gene and MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES PMID 22939636 2012 RTTN mutations link primary cilia function to organization of the human cerebral cortex.