Variant: rs16872571

present in Gene: CLNK present in Chromosome: 4 Position on Chromosome: 10725229 Alleles of this Variant: C/T

rs16872571 in CLNK 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.

rs16872571 in CLNK gene and Vitiligo PMID 22561518 2012 Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.