Variant: rs577948 

    present in Gene: MIR100HG
    present in Chromosome: 11
    Position on Chromosome: 122159482
    Alleles of this Variant: A/G

rs577948 in MIR100HG gene and Myopia, Degenerative PMID 19779542 2009 A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1.