PMID 22057235 2011 Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
rs7077335 in
LINC02649 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.