Variant: rs4683505

present in Gene: CLSTN2 present in Chromosome: 3 Position on Chromosome: 140528335 Alleles of this Variant: C/T

rs4683505 in CLSTN2 gene and Myopia, Degenerative PMID 23049088 2012 A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.