Variant: rs17802111 

    present in Gene: LOC101926974
    present in Chromosome: 2
    Position on Chromosome: 46282518
    Alleles of this Variant: C/G;T

rs17802111 in LOC101926974 gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.