Variant: rs1114167354 

    present in Gene: PARD3
    present in Chromosome: 10
    Position on Chromosome: 34341696
    Alleles of this Variant: T/C

rs1114167354 in PARD3 gene and NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO PMID 27925688 2017 Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation.