“…The phenotype of the lumican-deficient mouse and zebrafish implicates lumican as a functional candidate gene for high myopia [19,21]. Several high-frequency single-nucleotide polymorphisms have been identified in lumican [22,26], some of which may contribute to the pathogenesis of high myopia [2,22,23,24,25,26]; however, other genetic association studies suggest that lumican polymorphisms are not associated with this condition [3,6,27,28]. Some lumican SNPs such as rs17018718 and rs3759222 were described in only 1 or 2 studies [24,26,27].…”