Variant: rs7420812 

    present in Gene: PARD3B
    present in Chromosome: 2
    Position on Chromosome: 205570985
    Alleles of this Variant: T/C

rs7420812 in PARD3B gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.