Variant: rs10274279

present in Gene: PTPRN2 present in Chromosome: 7 Position on Chromosome: 157594749 Alleles of this Variant: T/C

rs10274279 in PTPRN2 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.