Background The association between rs13387042 polymorphism on 2q35 and breast cancer (BC) has been widely evaluated since it was first identified through genome-wide association approach. However, the
High myopia (HM) is one of the leading causes of visual impairment worldwide. In order to expand the myopia gene spectrum in the Chinese population, we investigated genetic mutations in a cohort of 27
*Numbering according to the genomic sequence of CCL22 (AC003665). Position 1 is the A of the initiation codon.‡Minor allele frequencies (MAF) in the screening population (N = 12).†NCBI, number from th